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AUSTRALIAN PHARMACIST
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    • risperidone
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                  [post_date] => 2025-05-21 12:44:53
                  [post_date_gmt] => 2025-05-21 02:44:53
                  [post_content] => The Therapeutic Goods Administration (TGA) has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18.
      
      In 2024 alone, 22 adverse events as a result of overdose of risperidone oral solution were reported to the TGA – most cases involved accidental administration of 10 times the prescribed dose (for example, 5 mL instead of 0.5 mL). 
      
      Although no deaths were recorded, adverse effects led to hospitalisations in most cases.
      

      Why are dosing errors occurring?

      An investigation by the TGA unearthed several drivers for dosing errors of risperidone oral solution including:
      • misinterpreting dosing instructions
      • incorrect use of the dosing syringe
      • medicine administration by non-primary caregivers (e.g. babysitters or other relatives).
      And the TGA is not the only national health agency to raise concerns about risperidone dosing confusion. The Spanish Agency for Medicines and Health Products issued a public alert after discovering that paediatric caregivers misread decimal points when administering a dose of 1 mg/mL risperidone solution, often inadvertently giving ten times the intended dose. Most (74%) of these incidents were serious, with children suffering sedation, hypotension, tachycardia, extrapyramidal symptoms, QT prolongation and, in some cases, seizures. In Ireland, the Health Products Regulatory Authority echoed these concerns, reporting ten‐fold overdoses in children aged 3–15 –  urging prescribers and pharmacists to provide clear dosing-device instructions and educate caregivers on recognising and responding to overdose symptoms.

      What’s changing?

      To address the identified risk, the Product Information (PI) and Consumer Medicines Information (CMI) for Risperdal have been revised, and generic manufacturers are now required to update PIs and CMIs to mirror these changes. The new versions for Risperdal include more detailed dosing guidance and illustrative diagrams to support accurate administration including:
      • use the supplied pipette only: do not substitute with another measuring device
      • open the child-resistant cap: push down on the plastic screw cap and turn counter-clockwise, then lift off
      • insert and draw up dose: place the pipette in the bottle; hold the bottom ring and pull up the top ring to the mark matching the prescribed dose (e.g. 0.25 mL for 0.25 mg, 0.5 mL for 0.5 mg)
      • dose equivalence: 1 mL of Risperdal solution = 1 mg risperidone; graduations on the plunger are in 0.25 mL (0.25 mg) increments
      • administer in a drink: remove the pipette, slide the top ring down to expel the dose into a non-alcoholic beverage (e.g. water, juice, milk, coffee – avoid tea)
      • after use: close the bottle; rinse the pipette with cold water, let it air dry in its case; avoid detergents or vigorous wiping to preserve the printed graduations.
      While each generic product should cover the same key details, the syringe and instructions can vary by brand. So pharmacists are advised to always double-check the individual PIs.

      What do pharmacists need to do?

      Dosing instructions need to be clearly printed on the label. According to the Australian Commission on Safety and Quality in Health Care’s National standard for labelling dispensed medicines (Standard 6), label wording  should:
      • have digits for dosage amounts (e.g. ‘Take 1 tablet,’ not ‘Take one tablet’ or ‘Take ONE tablet’)
      • express dose ranges with words between numbers (e.g. ‘1 to 2,’ not ‘1-2’ which could be read as ‘12’)
      • spell out common fractions to avoid confusion (e.g. ‘quarter,’ not ‘0.25’ or ‘¼’)
      • for small paediatric liquid doses, match the numbers on the oral dispenser (e.g. ‘0.5 mL’).
      Presenting numbers as digits generally improves clarity among patients. However, fractions written symbolically (e.g. ½’) may be misread as ‘1 or 2’ and decimal points can be overlooked (e.g. ‘1.5’ read as ‘15’). That’s why, when counselling patients prescribed risperidone oral solution, pharmacists should:
      • verify that all caregivers understand the prescribed dosing regimen
      • demonstrate precisely how to measure the required volume using the provided oral syringe
      • instruct caregivers to review the dosing label before each administration and confirm their understanding, especially with those administering the medicine for the first time.
      [post_title] => Paediatric risperidone errors prompt TGA safety update [post_excerpt] => The TGA has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => paediatric-risperidone-errors-prompt-tga-safety-update [to_ping] => [pinged] => [post_modified] => 2025-05-21 15:02:24 [post_modified_gmt] => 2025-05-21 05:02:24 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29429 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Paediatric risperidone errors prompt TGA safety update [title] => Paediatric risperidone errors prompt TGA safety update [href] => https://www.australianpharmacist.com.au/paediatric-risperidone-errors-prompt-tga-safety-update/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29433 [authorType] => )

      Paediatric risperidone errors prompt TGA safety update

      interruptions
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                  [post_date] => 2025-05-19 13:56:56
                  [post_date_gmt] => 2025-05-19 03:56:56
                  [post_content] => New research has found that pharmacists are interrupted at alarming rates when dispensing medicines.
      
      Led by Monash University’s Faculty of Pharmacy and Pharmaceutical Sciences, the study aimed to review existing evidence on how interruptions and distractions in pharmacy practice influence the occurrence of dispensing errors.
      
      [caption id="attachment_29414" align="alignright" width="260"] Dan Malone MPS[/caption]
      
      The review, which analysed 51 Australian and international studies, found that pharmacists can experience interruptions and distractions more than 20 times per hour.
      
      Phone calls were the biggest disruptor, said co-author Associate/Professor Dan Malone MPS, Course Director of the Undergraduate Pharmacy Degree.
      
      ‘For example, where a pharmacist would be dispensing or talking to someone, and either the phone was ringing or they would be interrupted by a colleague who said there was a phone call for the pharmacist,’ he said.
      
      Other key disruptors during dispensing included:
      • consumers interrupting pharmacists to ask a question
      • interruptions and distractions from pharmacy staff who needed to manage customer queries that were out of their scope.

      What are the impacts of interruptions?

      While most studies included in the review identified what the interruptions were and how frequently they occurred, few looked at the impact of interruptions and strategies to mitigate them. But of those that did, medication errors were the most serious issue identified. ‘While no medication error should occur, some are relatively minor whereas others are potentially fatal,’ A/Prof Malone said. Other identified impacts included: 
      • taking longer to dispense a script
      • poorer performance 
      • mental fatigue.

      What about self-interruptions?

      It’s not always external interruptions that are the culprits. Sometimes, it’s the pharmacists themselves who self-interrupt, the review team found. ‘They might be working on a particular task, then start searching the internet on an unrelated topic,’ A/Prof Malone said. ‘Or talk to their colleague while dispensing – initiating an interruption themselves.’  The term that's often used for this phenomenon is ‘multi-tasking’. But A/Prof Malone said it’s more akin to task-switching. ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,’ he said.

      What are the key intervention strategies?

      Should pharmacists be better trained to deal with inevitable interruptions, or should pharmacy teams try to reduce those interruptions in practice?  A bit of both, A/Prof Malone thinks. ‘Our pharmacy students do a lot of practice in terms of role playing the pharmacist in a workshop, for example,’ he said. ‘But when they go out on placement, they often complain that “it's really noisy, there's all these distractions and it’s hard to concentrate”,’ he said. 
      ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,.' DAN MALONE MPS 
      Better preparing students for that environment by stimulating situations where interruptions occur should help them to cope with future interruptions, A/Prof Mr Malone said. And while interruptions can’t be eliminated completely, systems can be put in place to reduce them, including:
      • having a set time where the pharmacist can't be interrupted
      • making sure there's workflow processes to ensure the pharmacist is less likely to be interrupted.
      ‘For example, when a prescription is dispensed, having a process whereby communication is such that the pharmacist is able to focus on the dispensing process,’ A/Prof Malone said. ‘When another prescription comes in, unless it's urgent, the pharmacist isn't interrupted – so they can go through the dispensing process with one prescription before they start the next.’ Or it might just be a matter of staffing. ‘Where possible, having two pharmacists on, with one focusing on tasks such as patient queries – limiting direct access to the other pharmacist during dispensing time,’ he said. However, in practice this isn’t always possible. When more urgent matters arise – as they inevitably do – pharmacists often have to park what they’re doing and switch tasks.  ‘That's understandable, but it’s preferable to minimise these occurrences, if possible,’ A/Prof Malone said.

      What about training other staff?

      There’s a ‘huge benefit’ in having well-trained pharmacy assistants on staff to reduce interruptions, and therefore errors, A/Prof Malone said. ‘I've worked with a lot of really experienced pharmacy assistants who know a lot about disease states, and are able to handle queries that come in and field questions over the phone without necessarily having to speak with the pharmacist,’ he said. But there are limitations to this approach, including making recommendations about Schedule 3 medicines. ‘This requires the pharmacist to be interrupted,’ A/Prof Malone added. PSA’s Pharmacists in 2030 recommends recognising and formalising the role of pharmacy assistants as well as technicians by establishing clear development pathways, such as:
      • registering support technicians to perform final-checking duties
      • embedding Certificate II, III and IV dispensary technician qualifications into practice to free pharmacists for direct patient care.
      To safeguard pharmacist wellbeing and minimise medicine errors, Pharmacists in 2030  advocates for:
      • enforcing safe-dispensing limits through patient-to-pharmacist ratios
      • building mandatory rest breaks into rosters
      • providing Employee Assistance Programs 
      • redesigning workspaces to enhance comfort and support mental health.

      What’s next on the horizon?

      The paper, led by pharmacist and PhD student Meaza Ayanaw, is a scoping review that’s paving the way for further research into how interruptions and distractions affect pharmacists’ decision-making ability, and how pharmacists prioritise different tasks.  ‘For example, should pharmacists switch tasks when they're in a pharmacy environment? If so, when should they switch? And what are the high- and low-priority tasks that require pharmacists to switch?’ A/Prof Malone said. From the results of the findings, more assessments and training will be developed using simulations such as Monash’s MyDispense. ‘This will help students to prepare for [pharmacy practice] by reflecting on real-world interruptions and distractions in a simulated environment. So that when they make mistakes, there's no consequence associated,’ A/Prof Malone said. For more information on streaming workflows and operations, don’t miss the poster presentation ‘Optimising pharmacy operations’ at PSA25, from 1–3 August 2025. Register here to attend. [post_title] => High interruption rates threaten patient safety [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => high-interruption-rates-threaten-patient-safety [to_ping] => [pinged] => [post_modified] => 2025-05-19 15:45:44 [post_modified_gmt] => 2025-05-19 05:45:44 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29407 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => High interruption rates threaten patient safety [title] => High interruption rates threaten patient safety [href] => https://www.australianpharmacist.com.au/high-interruption-rates-threaten-patient-safety/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29408 [authorType] => )

      High interruption rates threaten patient safety

      palliative care
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                  [post_date] => 2025-05-14 15:03:20
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                  [post_content] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that. 
      
      It can be difficult to tell from a prescription that a patient is receiving palliative care, said Tanya Maloney MPS, a community pharmacist in Coffs Harbour, NSW.
      
      [caption id="attachment_29354" align="alignright" width="233"] Tanya Maloney MPS[/caption]
      
      ‘What we lack in pharmacy is training on how to approach those difficult conversations in the right way so we can ask them a few questions to determine that,’ she said. ‘We're often a bit nervous about saying the wrong thing.’
      
      Though passionate about palliative care, Ms Maloney and her team have had to learn on the job.
      
      ‘We haven’t had any extra training and want to know how we can contribute more.’
      
      This is a common issue through the profession, with a lack in palliative care education tailored specifically to pharmacists, leading to a knowledge gap, said PSA Senior Pharmacist (Consulting and Program Delivery) Megan Tremlett MPS – who has managed a number of palliative care projects through Primary Health Networks and at a state level in recent years.
      
      ‘As pharmacists, we don't learn a lot about palliative care in our undergraduate course. And the majority of pharmacists haven't done any extra palliative care education since their university days.’
      
      To address this, PSA launched the ASPIRE Palliative Care Foundation Training Program on 13 May. The free, CPD-accredited course – supported by Palliative Care Australia and funded under the National Palliative Care Grants Program – upskills pharmacists regardless of practice setting.
      
      ‘The training program has been created with extensive stakeholder consultation to provide pharmacists with a thorough introduction to palliative care across the eight modules’ Ms Tremlett said.
      
      Rather than training pharmacists to specialise in palliative care, the training program is intended to lift the baseline knowledge of the profession, said Leah Robinson, Project Manager at PSA, who worked on the development of the program with Ms Tremlett.
      
      ‘It’s about understanding the different settings and phases of palliative care and at which points pharmacists can provide practical support to help families, patients and healthcare professionals in supporting palliative care.’
      
      A foundational understanding of palliative and end-of-life care across the health workforce is essential to meeting community needs, said Camilla Rowland, CEO of Palliative Care Australia.
      
      ‘Supporting people to live, and die well, means building palliative care capability across the entire health system. That includes pharmacists, often among the first healthcare professional patients and carers turn to for advice.’
      

      Learning about symptom management

      The ASPIRE training program has a module dedicated to symptoms and the trajectory of people living with life-limiting illness. Under a subsequent symptom management module, pharmacists can access resources and references for pharmacological management of the symptoms associated with dying that covers:
      • Pharmaceutical Benefits Scheme (PBS) and non-PBS medicines 
      • Special Access Scheme medications
      • Medicines used off-label.
      Experts, from pharmacists to prescribers, guide learners on handling sensitive conversations with patients and families – linking to Safer Care Victoria resources for monitoring and managing adverse effects, especially with continuous subcutaneous infusions.
      ‘We point pharmacists to a range of resources to support them with understanding medicines compatibilities in subcutaneous infusion devices and the adverse effects that might be expected,’ Ms Tremlett said. As illness progresses, medication regimens often grow more complex. ‘Pharmacists need to be able to step in and make recommendations around those [medicines] that could potentially be weaned or stopped to reduce that burden and the chance of side effects and interactions,’ Ms Tremlett said. The training program also helps pharmacists with information, tools and resources for conversions of medicines and different formulations, including switching from some or all of their opioids, to a replacement opioid delivered by another route, Ms Robinson said.  ‘It’s also [around] practical things pharmacists can offer such as providing a list of current medicines, home medication review, staged supply, support with prescription management, home delivery or flexibility around dose administration aids to help manage those medicines and the complexity of the changes they go through during the different phases of palliative care,’ Ms Robinson said.

      Developing interdisciplinary care skills

      At the moment, Ms Maloney feels as though community pharmacy is a missing piece in palliative care that’s uncertain where it fits. ‘We want to be able to fit into that wider team of their health carers so we can look at the holistic care and goals of the person and provide them with more than just medication,’ she said.
      ASPIRE emphasises collaboration with GPs, specialist palliative care teams, community nurses, paramedics and residential aged care staff. ‘In the module that's dedicated to interdisciplinary palliative care, pharmacists learn the broad range of people who are involved in palliative care, and some they might not expect – from death doulas to chaplains, music therapists and diversional therapists,’ Ms Tremlett said.

      Focusing on patient-centred care

      Once pharmacists identify a palliative care patient, they need knowledge and skills to determine how best to help at each stage, Ms Maloney said. ‘How do we know how to help them in all these different stages that they're going to go through?’ Pharmacists may think they know what’s best for a patient based on their clinical background, Ms Tremlett said. ‘But at the end of the day, what's important to the person or the patient is the single most important thing.’ ‘ASPIRE reminds pharmacists to be mindful of their own biases to meet the person where they are and help them achieve their goals of care, which might change over time as their condition progresses,’ Ms Robinson added. The patient-centred care module also highlights Australia’s cultural diversity – including First Nations peoples, migrants and those from non-English speaking backgrounds. ‘There is no such thing as a consistent cultural need in palliative care,’ Ms Tremlett said. ‘It's very different within cultures, between cultures and within communities, so pharmacists need to be able to adapt the care and services they provide without making assumptions.’ The need for translation services, what’s deemed an inappropriate conversation or who is the next of kin or carer can vary from person to person, Ms Robinson said. ‘It’s important to be mindful of how and what to communicate to align with those goals of care.’

      Helping families through grief and bereavement

      Being confident talking about death is something many pharmacists struggle with, Ms Maloney said. ‘You might prompt them a little bit, and they do get upset, and that’s often what puts us off,’ she said. ‘But it’s not necessarily a bad thing as they’re getting to open up and talk to you.’ The final ASPIRE module on grief, bereavement and self-care aims to normalise conversations about death and dying. Being comfortable enough to embed those conversations in day-to-day practice – including supporting people after their loved one has died – is crucial, Ms Tremlett said. ‘It's really important for pharmacists to be prepared to still speak about the person who's died, if that's what the person wants to do, and to recognise that grieving is very normal, and there's no right or wrong way to grieve.’ Pharmacists also need to be able to recognise prolonged grief and know when referrals  for extra support are needed. ‘If the pharmacist has the knowledge and skills to refer that person on for some extra help in the grieving process, that's really impactful,’ she said. Throughout the palliative care process, it’s crucial for pharmacists to look after themselves and to know when to check in on their colleagues too. ‘When we're constantly supporting people who are unwell … it's very natural for pharmacists to feel a burden of care,’ Ms Tremlett said. ‘Learning to recognise when you or your colleagues might be feeling a little overwhelmed, need extra support or to engage in self-care activities is really important.

      Embedding the training into practice

      Now that the ASPIRE training program is available, Ms Maloney wants all her pharmacists to complete it to lift their confidence and knowledge in palliative care. ‘As part of that, there's all the resources you can print out and revisit,’ she said. ‘They will be active documents that become part of our internal processes rather than training you just do and forget.’ The experience  of supporting palliative care patients also builds trust and loyalty among family members and carers. ‘You get to know them on a different level and see them when they're vulnerable,’ Ms Maloney said. ‘That rapport you can build up in that time by being there for them definitely builds that lifetime customer for the future.’ [post_title] => Bridging the palliative care education gap for pharmacists [post_excerpt] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that.  [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => bridging-the-palliative-care-education-gap-for-pharmacists [to_ping] => [pinged] => [post_modified] => 2025-05-14 16:27:55 [post_modified_gmt] => 2025-05-14 06:27:55 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29352 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Bridging the palliative care education gap for pharmacists [title] => Bridging the palliative care education gap for pharmacists [href] => https://www.australianpharmacist.com.au/bridging-the-palliative-care-education-gap-for-pharmacists/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29358 [authorType] => )

      Bridging the palliative care education gap for pharmacists

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                  [post_date] => 2025-05-13 16:45:40
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                  [post_content] => 

      Case scenario

      Amra, 80 years old and a regular patient of yours, has been discharged from hospital after an admission for a fall. She presents at the pharmacy with a bag of medicines and hands you a discharge medicines list. She appears to have been initiated on some new medicines in hospital and expresses confusion on which of her pre-hospital medicines to continue. You view her dispense history and My Health Record and notice discrepancies. It is unclear to you or Amra why some medicines have been initiated. She has an appointment with her GP in a couple of days.

      Learning objectives

      After reading this article, pharmacists should be able to:
      • Define transitions of care
      • Discuss medicines safety during transitions of care
      • Explain principles of safe and high-quality transitions of care
      • Discuss the role of the pharmacist across transitions of care.
      Competency standards (2016) addressed: 1.1, 1.4, 1.5, 2.2, 3.5 Accreditation number: CAP2505SYPMA Accreditation expiry: 31/04/2028
      Already read the CPD in the journal? Scroll to the bottom to SUBMIT ANSWERS.

      Medicines safety during transitions of care

      The Australian Commission on Safety and Quality in Health Care (ACSQHC) defines transitions of care as the period when all or part of a person’s healthcare is transferred between care providers or care settings.1

      Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. When medicines safety is not prioritised at transitions of care, the risk of adverse events is increased, such as readmission to hospital and adverse drug reactions.  A Cochrane review found that more than 50% of patients experience a medication error during transitions of care.2  A systematic review found that following hospital discharge to the community, 53% of adult patients experience at least one medication error, 50% experience one or more unintentional medication discrepancies (a subset of medication errors), and 19% experience one or more adverse drug events.3 A systematic review and meta-analysis found the prevalence of medication-related readmissions and adverse drug reaction-related readmissions in older people were 9% and 6%, respectively, with about one-fifth of these preventable.4

      Preventing medication-related harm at transitions of care is a key priority in the World Health Organization’s (WHO) third Global Patient Safety Challenge (Medication Without Harm).5 The ACSQHC’s response to the Challenge, published in 2020, described prioritising medication reconciliation at all transitions of care to reduce the risk of medication errors.6 Its response also recommended the use of My Health Record to engage patients and carers in curation and communication of medication regimen information.

      The ACSQHC’s response focused on transitions from hospital, a period known to be particularly high risk, and also recommended standardising the presentation of discharge summaries.6 For people with complex care needs, initiatives to reduce preventable medication-related readmissions were encouraged, such as early post-discharge medication reviews (hospital outreach or primary care led), and cross-sector case conferencing.6 Refinement of risk criteria or indicators was recommended to direct interventions towards patients at the greatest risk of medication-related harm.6

      The ACSQHC’s response did not specifically address other known contributors to medication-related harm during transitions of care, such as ensuring timely access to medicines and the tools that are sometimes required to use them, such as interim medication administration charts when discharged to residential care, dose administration aids, and adequate quantities of medicines supply.7,8

      Principles of safe and high-quality transitions of care

      The ACSQHC has recently published a set of principles to guide safe and high-quality transitions of care that highlight the need for multidisciplinary collaboration and coordination that relies on shared responsibility and accountability.9 The consistent application of these principles within practice, standards, policy and guidance are fundamental for safe transitions of care and apply to transitions of care wherever healthcare is received including primary, community, acute, subacute, aged and disability care.9

      The principles and their enablers are shown in Table 1.

      Australia’s priority actions to address medicines safety at transitions of care

      Progress toward Australia’s priority actions to address medicines safety at transitions of care has been mixed.10 Embedding medication reconciliation at admission and discharge from hospital has advanced and is now part of medicines safety standards that hospitals need to meet for accreditation.

      My Health Record has improved access to patients’ medication histories; however, patient engagement remains low, and, like all medication records, verification of data with the patient and other sources is required.11,12 Implementation of the Pharmacist Shared Medicines List (a verified medication history that can be uploaded to My Health Record) has been limited. Discharge summaries continue to have deficiencies, including inaccurate medicine lists and inadequate explanations of medicine changes.13 Primary care medicine lists and dose administration aid medicine labels, which are often used by hospital doctors to chart medicines on admission, are also frequently inaccurate.14,15

      Australian research highlights concerns about lack of awareness and uptake of post-discharge Home Medicines Reviews (HMRs) and Residential Medication Management Reviews (RMMRs) and the complexity in facilitating timely post-discharge medication reviews.16,17 Hospital outreach pharmacist medication review services and cross-sector multidisciplinary case conferencing are uncommon. There has been progress in developing validated criteria to identify patients at risk of medication-related readmission,18 though more work is needed to ensure generalisability and implementation.10

      Progress towards ensuring timely access to medicines following hospital discharge has been mixed.10 Reforms to enable medicines to be supplied by hospitals using the Pharmaceutical Benefits Scheme, and implementation of interim medication administration charts for patients discharged to residential care, have not occurred in all jurisdictions.

      Drivers for a stewardship approach to improve medicines safety at transitions of care

      In 2020, after decades of advocacy, Commonwealth-funded medication review program rules changed to allow hospital-based medical specialists to refer patients to credentialed pharmacists for collaborative post-discharge medication management reviews. In response, the Society of Hospital Pharmacists (now known as Advanced Pharmacy Australia [AdPha]) published a Hospital Pharmacy Practice Update, Hospital-Initiated Medication Reviews, which detailed information about pathways for patients to have post-discharge HMRs, RMMRs and Hospital Outreach Medication Reviews, as well as flagging MedsChecks as a medication reconciliation pathway.19 Unfortunately, resources were not provided by the Commonwealth or state health departments for promotion, training or implementation support for hospitals to implement hospital-initiated medication reviews, and uptake of these pathways has been low.

      An article published in 2022 presented barriers and enablers to hospital-initiated medication reviews, and highlighted the need for a stewardship approach to promote safe and high-quality medication management at transitions of care, with a key focus on facilitating early post-discharge medication reviews (within 10 days).20 The authors have continued to advocate for a hospital-led stewardship approach to address the perennial problem of medicines safety at transitions of care.10,21

      The recently published AdPha Standard of Practice for Pharmacy Services Specialising in Transitions of Care describes current best practice for the provision of pharmacy services that specialise in transitions of care, such as hospital outreach pharmacists and community liaison pharmacists, and supports the introduction of transitions of care stewardship programs into existing organisational clinical systems.22

      Medicines stewardship

      Stewardship in the context of health care refers to a structured program of strategies and interventions that address challenges within a specific clinical area, and ensure appropriate and efficient use of resources. Medicines stewardship programs focus on improving medicines use in areas where there is a high risk of inappropriate prescribing or adverse outcomes. Examples of successful programs include: antimicrobial, opioid analgesic, anticoagulation and psychotropic stewardship.21

      Medicines stewardship programs aim to improve medication management at individual and population levels to ensure consistent, appropriate care. At a population level, this may include developing guidelines and providing standardised processes and templates. At an individual level, it includes delivering tailored person-centred interventions to optimise medication outcomes. 

      Common elements of successful medicines stewardship programs include multidisciplinary leadership, stakeholder engagement, tailored communication strategies, behavioural changes, implementation science methodologies, and ongoing program monitoring, evaluation and reporting.21 Stewardship programs are often led or administered by a dedicated stewardship officer (usually a pharmacist) or team.21

      Medication Management at Transitions of Care Stewardship Framework

      Applying a stewardship approach to transitions of care may provide opportunities to focus organisational resources, foster multi- or interdisciplinary collaboration, and improve coordinated care when individuals transfer between care providers or settings.

      In 2023, the ACSQHC commissioned a rapid literature review and environmental scan examining Australian and international medication management strategies, including stewardship programs, at transitions of care focusing on admission to hospital and discharge to the community or residential care.23,24

      The literature review identified that, globally, there are no published studies or existing frameworks that describe a stewardship program specifically addressing medication management at transitions of care.24

      Given the evidence from the literature review and environmental scan, the ACSQHC set about developing a Medication Management at Transitions of Care Stewardship Framework (the Framework). The Framework is scheduled for release in the second quarter of 2025.

      The Framework is intended to provide healthcare organisations (hospitals) with a systematic approach for implementing coordinated medication management activities and interventions to optimise safe and high-quality transitions of care, with a focus on patients admitted to hospital and discharged to the community or residential aged care. The Framework will provide guidance that can be adapted to local context and the circumstances of individuals transitioning across care settings.

      The Framework will be supported by existing national standards and guidelines, including:

      • National Safety and Quality Health Service Standards25
      • Guiding Principles to Achieve Continuity in Medication Management8
      • National Medicines Policy 2022.26

      The ACSQHC’s principles of safe and high-quality transitions of care9 should also be considered in the local implementation of a medication management at transitions of care stewardship program.

      Leveraging digital health

      Digital health is a key enabler to achieve interoperable, accurate and timely communication between clinicians in the acute and primary care settings. The Framework will align with the National Digital Health Strategy 2023–202827 and the Strategy Delivery Roadmap.28

      Health facilities are encouraged to embed digitally enabled care to strengthen effective interdisciplinary communication and improve safe and high-quality medication management at transitions of care.29 

      Implementation of the Framework and the role of pharmacists across transitions of care

      The Framework is designed with a hospital focus, and it is intended that it will be used by hospitals to guide stewardship and coordination in collaboration with primary care practitioners.29

      General practice coordination of ongoing medical care prior to and following hospital discharge is vital, as is community pharmacist coordination of medication supply and management. Pharmacists embedded in general practice, onsite aged care pharmacists, and credentialed pharmacists providing HMRs and RMMRs, can also play an important role. However, it is not possible for general practice and primary care pharmacists to coordinate all time-critical aspects of medication management for complex hospital discharges that occur 7 days a week, and sometimes outside of business hours. In the first instance, hospitals need to take responsibility for bridging the gap by29:

      • ensuring that discharges are well planned
      • ensuring there is timely and accurate communication with primary care providers
      • providing an adequate supply of newly commenced medicines 
      • working with community-based healthcare professionals to ensure continuity of medication access
      • providing education to patients and carers, including a discharge medicines list
      • working with community-based healthcare professionals to ensure timely post-discharge medication review and follow-up as needed.
      Primary care and aged care pharmacists need to be aware of the risks associated with transitions of care and be prepared to work collaboratively with hospitals in a responsive and flexible way to ensure timely delivery of post-discharge transitions of care-related services such as medication reconciliation, medication supply and medication review.

      The authors encourage all pharmacists to engage with the Framework. It is a world-first document that will drive system improvements so Australians receive high-quality care, and is a pivotal response to the WHO’s third Global Patient Safety Challenge (Medication Without Harm) priority, transitions of care.

      Case scenario continued

      You phone the discharging hospital pharmacist (whose name was recorded on the patient’s discharge medicines list) to clarify Amra’s medicine changes and discharge medication management plan. You speak with Amra about your discussion and obtain consent to complete a MedsCheck and chat with her GP about any changes post-discharge. You go through each of her medicines and prepare her an updated medicines list. You also discuss the potential benefits of a Home Medicines Review (HMR) when there has been a hospital admission and medicine changes. You ask if she wishes for you to discuss an HMR referral with her GP which could be actioned at her upcoming GP appointment. She indicates an HMR would be welcome and thanks you for helping her.
      [cpd_submit_answer_button]

      Key points

      • A transition of care is when all or part of a person’s healthcare is transferred between care providers or care settings.
      • Preventing medication-related harm at transitions of care is a key priority in the WHO’s third Global Patient Safety Challenge (Medication Without Harm).
      • The ACSQHC has developed a Medication Management at Transitions of Care Stewardship Framework to optimise high-quality and safe medication management during transitions of care, focusing on hospital admissions and discharges to community and residential aged care.
      • Hospital and primary care pharmacists need to work collaboratively to improve the safety of transitions of care and ensure timely post-discharge medication reconciliation, medication supply and post-discharge medication review.   

      References

      1. Australian Commission on Safety and Quality in Health Care. Transitions of Care. 2024. At: www.safetyandquality.gov.au/our-work/transitions-care
      2. Redmond P, Grimes TC, McDonnell R, et al. Impact of medication reconciliation for improving transitions of care. Cochrane Database of Systematic Reviews 2018, Issue 8.
      3. Alqenae FA, Steinke D, Keers RN. Prevalence and nature of medication errors and medication-related harm following discharge from hospital to community settings: a systematic review. Drug Saf 2020;43(6):517–37.
      4. Prasad N, Lau ECY, Wojt I, et al. Prevalence of and risk factors for drug-related readmissions in older adults: a systematic review and meta-analysis. Drugs Aging 2024;41(1):1–11.
      5. World Health Organization. Medication Without Harm – Global Patient Safety Challenge on Medication Safety. Geneva: World Health Organization; 2017.
      6. Australian Commission on Safety and Quality in Health Care. Medication without harm – WHO Global Patient Safety Challenge. Australia’s response. Sydney: ACSQHC; 2020.
      7. Elliott RA, Tran T, Taylor SE, et al. Impact of a pharmacist-prepared interim residential care medication administration chart on gaps in continuity of medication management after discharge from hospital to residential care: a prospective pre- and post-intervention study (MedGap Study). BMJ Open 2012;2(3).
      8. Department of Health and Aged Care. Guiding Principles to Achieve Continuity in Medication Management. Canberra; 2022.
      9. Australian Commission on Safety and Quality in Health Care. Principles of safe and high-quality transitions of care (factsheet). 2024.
      10. Elliott RA, Angley M, Criddle DT, et al. Achieving safe medication management during transitions of care from hospital: time for a stewardship approach. Aust Prescr 2024;47(4):106–8.
      11. Elliott RA, Taylor SE, Koo SMK, et al. Accuracy of medication histories derived from an Australian cloud-based repository of prescribed and dispensed medication records. Intern Med J 2023;53:1002–9.
      12. Francis M, Francis P, Makeham M, et al. Using personal health records for medication continuity during transition of care: An observational study. Health Inf Manag 2024:18333583241270215.
      13. Wembridge P, Rashed S. Discharge summary medication list accuracy across five metropolitan hospitals: a retrospective medical record audit. Aust Health Rev 2022;46:338–45.
      14. Uzunbay Z, Elliott RA, Taylor S, et al. Accuracy of medication labels on community pharmacy-prepared dose administration aids: an observational study. Explor Res Clin Soc Pharm 2023;11:100318.
      15. Taylor S, Welch S, Harding A, et al. Accuracy of general practitioner medication histories for patients presenting to the emergency department. Aust Fam Physician 2014;43:728.
      16. Chen EY, Wang KN, Sluggett JK, et al. Process, impact and outcomes of medication review in Australian residential aged care facilities: a systematic review. Australas J Ageing 2019;38:9–25.
      17. Luetsch K, Rowett D, Twigg MJ. A realist synthesis of pharmacist-conducted medication reviews in primary care after leaving hospital: what works for whom and why? BMJ Qual Saf 2020;30(5):418–30.
      18. Criddle D, Devine B, Murray K, et al. Developing PHarmacie-R: a bedside risk prediction tool with a medicines management focus to identify risk of hospital readmission. Res Social Admin Pharm 2021;18 (7):3137–48.
      19. The Society of Hospital Pharmacists of Australia. Hospital-initiated medication reviews. Collingwood, Victoria: The Society of Hospital Pharmacists of Australia; 2020.
      20. Angley M, Criddle D, Rigby D, et al. Hospital-initiated post-discharge medication reviews in Australia: expert opinion on the barriers and enablers to implementation. J Pharm Pract Res 2022;52(6):446–53.
      21. Su E, Liew DFL, Donnelly J, et al. Medicines stewardship. Aust Prescr 2023;46(2):24–8.
      22. Advanced Pharmacy Australia Transition Care and Primary Care Specialty Practice Group. Standard of practice for pharmacy services specialising in transitions of care. J Pharm Pract Res 2024;54(5):417–35.
      23. Emadi F, Liu S, Yui C H, et al. Digital approaches that can be employed to facilitate safe medication management at transitions of care. Sydney: ACSQHC; 2024.
      24. Emadi F, Liu S, Yiu CH, et al. Medication management at transitions of care stewardship framework. Rapid literature review and environmental scan – final report. Sydney: Faculty of Medicine and Health, School of Pharmacy, University of Sydney; 2023.
      25. Australian Commission on Safety and Quality in Health Care. The National Safety and Quality Health Service (NSQHS) Standards (second edition) 2021. At: www.safetyandquality.gov.au/standards/nsqhs-standards
      26. Department of Health and Aged Care. National Medicines Policy 2022. Canberra; 2022.
      27. Australian Digital Health Agency. National Digital Health Strategy 2023-2028. Sydney; 2023.
      28. Australian Digital Health Agency. National Digital Health Strategy Delivery Roadmap 2023–2028. Sydney; 2023.
      29. Australian Commission on Safety and Quality in Health Care [DRAFT]. Medication Management at Transitions of Care Stewardship Framework. Sydney: ACSQHC; 2024.

      Our authors

      Manya Angley (she/her) BPharm, PhD, FPS, CredPharm (MMR), FAdPha is an Advanced Practice Pharmacist experienced in general practice, disability and aged care.

      Debbie Rigby (she/her) BPharm, GradDipClinPharm, FASCP, FPS, FACP, FAICD, FSHP, FANZCAP (GeriMed, Resp) is an Advanced Practice Pharmacist qualified in clinical pharmacy, geriatrics and respiratory medicine.

      Rohan Elliott (he/him) BPharm, BPharmSc(Hons), MClinPharm, PhD, FAdPhA, FANZCAP (GeriMed, Research) is an Advanced Practice Pharmacist with experience in hospitals, aged care and transitions of care.

      Our reviewer

      Elizabeth Manias (she/her) RN, BPharm, MPharm, MNStud, PhD, FANZCAP (Transitions of care, Geriatric Medicine)

      Conflict of interest declaration

      Manya Angley, Debbie Rigby and Rohan Elliott are co-investigators on a Medical Research Future Fund (MRFF) 2022 transitions of care project. MRFF is funded by the Australian Government. They are also co-authors of a literature review of transitions of care stewardship that was funded by the ACSQHC.

      Elizabeth Manias is a member of the Transitions of Care and Primary Care Leadership Committee of Advanced Pharmacy Australia.

      [post_title] => Improving medicines safety at transitions of care [post_excerpt] => Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => improving-medicines-safety-at-transitions-of-care [to_ping] => [pinged] => [post_modified] => 2025-05-14 13:04:04 [post_modified_gmt] => 2025-05-14 03:04:04 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29045 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Improving medicines safety at transitions of care [title] => Improving medicines safety at transitions of care [href] => https://www.australianpharmacist.com.au/improving-medicines-safety-at-transitions-of-care/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( [td_post_template] => single_template_4 ) [is_review:protected] => [post_thumb_id:protected] => 29343 [authorType] => )

      Improving medicines safety at transitions of care

      medicine storage
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                  [post_content] => Both Cautionary Advisory Label (CAL) 6 and CAL 13 have been overhauled to sharpen storage advice.
      
      CAL 6 explanatory notes advice in Digital Australian Pharmaceutical Formulary and Handbook (APF) now mentions considerations for room-temperature time windows for refrigerated medicines, while CAL 13’s tightened wording and advice flags truly sensitive formulations – ensuring pharmacists give patients clearer, more precise guidance.
      

      What’s changing?

      The familiar ‘Refrigerate, do not freeze’ warning of CAL 6 is not changing, however its explanatory notes have been expanded.  [caption id="attachment_29335" align="aligncenter" width="180"]CAL 6 CAL 6[/caption] There are many instances whereby refrigeration of temperature sensitive medicines may not be practical, for example travel days, power outages or ‘in-use’ multi-dose containers/devices. The updated explanatory notes advise pharmacists that they should refer to the medicines approved product information (PI) and counsel their patients on how to best store these medicines – covering when their temperature sensitive medicines may safely remain at room temperature (below 25 °C) – if applicable. [caption id="attachment_29336" align="aligncenter" width="176"] The old CAL 13[/caption] [caption id="attachment_29337" align="aligncenter" width="189"] The new CAL 13[/caption] Meanwhile, CAL 13 has been reworded. Previously ‘Do not remove from original packaging until dose required’, the new prompt, ‘Ask your pharmacist about the storage conditions for this medicine,’ applies only to dosage forms and active ingredients truly sensitive to light, moisture or temperature excursions.  This includes orally disintegrating tablets, effervescents, sublingual or buccal lozenges, dispersible granules, wafers and chewables, as well as amoxicillin/clavulanic acid, dabigatran, glyceryl trinitrate, nicorandil, nifedipine, phenothiazines, tamoxifen and sodium valproate. CAL 13 may also be applied in addition to other CALs relating to storage requirements (e.g. CALs 6, 7a or 7b) when complex storage instructions are applicable, and these other CALs do not adequately cover these. To support the change to CAL 13, the APF’s Good dispensing practice chapter has been updated with clearer and expanded guidance on providing advice to patients on how to store medicines, including that:
      • all medicines should be kept out of sight and out of reach of children at all times
      • unless specifically requiring refrigeration, and in the absence of special storage instructions outlined in the PI/consumer medicine information (CMI), medicines should be stored in their original packaging in a cool (preferably <25 °C), dry and secure place
      • medicines should generally not be removed from their original packaging until a dose is required – pharmacists should check how the patient intends to store their medicines (e.g. in a dosette box) and provide advice according to the storage instructions outlined in each medicines PI/CMI.
      CAL 13’s explanatory notes have also been updated in APF Digital to support pharmacists in applying the revised CAL. When packing medicines into Dose Administration Aids (DAAs) pharmacists should consider the approved PI of each medicine, and PSA’s Guidelines for pharmacists providing dose administration aid services.

      What led to this update?

      Medicine labels have traditionally relied on simple fridge-or-no-fridge advice. But today’s PIs are more complex.  Humira (adalimumab) is one good example. People using Humira are advised that they can store single pre-filled syringes or pens ‘below 25°C (room temperature) for a maximum period of 14 days, but must be protected from light. Once removed from the refrigerator for room temperature storage, the syringe must be used within 14 days or discarded, even if it is returned to the refrigerator’.  But CAL 6 doesn’t capture these nuances, so some patients are left guessing whether their medicines are safe to use or not during travel or at times when refrigeration is not available. The new explanatory notes prompt pharmacists to cover these scenarios as part of their routine counselling to promote safe and quality use of medicines. At the same time, the CAL 13 had become so ubiquitous – applicable to nearly all medicines – that its impact was diluted. What's more, most pharmacies didn’t even stock the printed sticker.  By narrowing its application, CAL 13’s power to prompt meaningful conversations about stability risks has been restored. Above all, when medicines are removed from their original packaging inappropriately, or stored incorrectly, this can translate into reduced potency or patient harm. These refinements give pharmacists clear, evidence-based cues to maintain medicine stability and efficacy. 

      How should pharmacists tailor storage advice?

      Pharmacists should personalise both verbal and written advice to the patient. Ensure every patient is counselled on how to best store their medicines including routinely asking how the patient plans to keep their medicines, for example will they use a dosette box? Is storage at an appropriate temperature an issue? If a medicine carries Label 6 but its PI indicates there is an appropriate room-temperature window, demonstrate the correct use of an insulated bag and explain the difference between ‘keep at 2–8 °C’ and ‘store below 25 °C’. Provide guidance on room temperature storage for their in-use multi dose container/device (if appropriate) and for times when refrigeration is unavailable or impractical. Pharmacists should also advise the patient to avoid storing medicines in the areas of a domestic refrigerator that may not maintain a temperature of 2–8 °C. This includes the door, top shelf or crisper; or within 40 mm of the back and sides of the main compartment. For CAL-13 affixed medicines, pharmacists should advise patients that these medications’ stability is protected by the original container and packaging, and that removing them prematurely can accelerate degradation and reduce efficacy. Work with the patient to address any barriers to this.

      What’s the implementation timeline?

      The revised explanatory notes for CAL 6 and CAL 13 are live in APF Digital as of 7 May 2025.  CAL printers will begin issuing the new CAL 13 labels on their next run. Until then, pharmacists should continue using the existing labels while equipping patients with the updated counselling points and advice outlined in the APF Digital.

      How should pharmacists put the new advice into practice?

      Let’s say Mrs L, 68, who has type 2 diabetes, atrial fibrillation and hypertension, presents to a pharmacy for her medicines. She picks up a prescription for insulin glargine pens, nifedipine and dabigatran. For her insulin glargine, you apply Label 6 and explain the medicine must be stored at 2–8 °C in the fridge’s main compartment, yet the in-use pen may remain at room temperature for up to 28 days. You provide her with an insulated bag and demonstrate how to use it. You then recognise that nifedipine is sensitive to light and dabigatran is moisture-sensitive, and apply Label 13 to each medicine’s packaging which prompts a PI check. You advise her to keep the medicines away from humid spots such as bathrooms or kitchen windowsills, and to keep them in their original packaging, out of direct light. Mrs L leaves confident in where to store each medicine, and you’ve pre-emptively safeguarded stability and efficacy. [post_title] => New CAL medicine storage guidance [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => new-cal-medicine-storage-guidance [to_ping] => [pinged] => [post_modified] => 2025-05-12 16:02:09 [post_modified_gmt] => 2025-05-12 06:02:09 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29331 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => New CAL medicine storage guidance [title] => New CAL medicine storage guidance [href] => https://www.australianpharmacist.com.au/new-cal-medicine-storage-guidance/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29332 [authorType] => )

      New CAL medicine storage guidance

  • Clinical
    • risperidone
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                  [post_content] => The Therapeutic Goods Administration (TGA) has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18.
      
      In 2024 alone, 22 adverse events as a result of overdose of risperidone oral solution were reported to the TGA – most cases involved accidental administration of 10 times the prescribed dose (for example, 5 mL instead of 0.5 mL). 
      
      Although no deaths were recorded, adverse effects led to hospitalisations in most cases.
      

      Why are dosing errors occurring?

      An investigation by the TGA unearthed several drivers for dosing errors of risperidone oral solution including:
      • misinterpreting dosing instructions
      • incorrect use of the dosing syringe
      • medicine administration by non-primary caregivers (e.g. babysitters or other relatives).
      And the TGA is not the only national health agency to raise concerns about risperidone dosing confusion. The Spanish Agency for Medicines and Health Products issued a public alert after discovering that paediatric caregivers misread decimal points when administering a dose of 1 mg/mL risperidone solution, often inadvertently giving ten times the intended dose. Most (74%) of these incidents were serious, with children suffering sedation, hypotension, tachycardia, extrapyramidal symptoms, QT prolongation and, in some cases, seizures. In Ireland, the Health Products Regulatory Authority echoed these concerns, reporting ten‐fold overdoses in children aged 3–15 –  urging prescribers and pharmacists to provide clear dosing-device instructions and educate caregivers on recognising and responding to overdose symptoms.

      What’s changing?

      To address the identified risk, the Product Information (PI) and Consumer Medicines Information (CMI) for Risperdal have been revised, and generic manufacturers are now required to update PIs and CMIs to mirror these changes. The new versions for Risperdal include more detailed dosing guidance and illustrative diagrams to support accurate administration including:
      • use the supplied pipette only: do not substitute with another measuring device
      • open the child-resistant cap: push down on the plastic screw cap and turn counter-clockwise, then lift off
      • insert and draw up dose: place the pipette in the bottle; hold the bottom ring and pull up the top ring to the mark matching the prescribed dose (e.g. 0.25 mL for 0.25 mg, 0.5 mL for 0.5 mg)
      • dose equivalence: 1 mL of Risperdal solution = 1 mg risperidone; graduations on the plunger are in 0.25 mL (0.25 mg) increments
      • administer in a drink: remove the pipette, slide the top ring down to expel the dose into a non-alcoholic beverage (e.g. water, juice, milk, coffee – avoid tea)
      • after use: close the bottle; rinse the pipette with cold water, let it air dry in its case; avoid detergents or vigorous wiping to preserve the printed graduations.
      While each generic product should cover the same key details, the syringe and instructions can vary by brand. So pharmacists are advised to always double-check the individual PIs.

      What do pharmacists need to do?

      Dosing instructions need to be clearly printed on the label. According to the Australian Commission on Safety and Quality in Health Care’s National standard for labelling dispensed medicines (Standard 6), label wording  should:
      • have digits for dosage amounts (e.g. ‘Take 1 tablet,’ not ‘Take one tablet’ or ‘Take ONE tablet’)
      • express dose ranges with words between numbers (e.g. ‘1 to 2,’ not ‘1-2’ which could be read as ‘12’)
      • spell out common fractions to avoid confusion (e.g. ‘quarter,’ not ‘0.25’ or ‘¼’)
      • for small paediatric liquid doses, match the numbers on the oral dispenser (e.g. ‘0.5 mL’).
      Presenting numbers as digits generally improves clarity among patients. However, fractions written symbolically (e.g. ½’) may be misread as ‘1 or 2’ and decimal points can be overlooked (e.g. ‘1.5’ read as ‘15’). That’s why, when counselling patients prescribed risperidone oral solution, pharmacists should:
      • verify that all caregivers understand the prescribed dosing regimen
      • demonstrate precisely how to measure the required volume using the provided oral syringe
      • instruct caregivers to review the dosing label before each administration and confirm their understanding, especially with those administering the medicine for the first time.
      [post_title] => Paediatric risperidone errors prompt TGA safety update [post_excerpt] => The TGA has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => paediatric-risperidone-errors-prompt-tga-safety-update [to_ping] => [pinged] => [post_modified] => 2025-05-21 15:02:24 [post_modified_gmt] => 2025-05-21 05:02:24 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29429 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Paediatric risperidone errors prompt TGA safety update [title] => Paediatric risperidone errors prompt TGA safety update [href] => https://www.australianpharmacist.com.au/paediatric-risperidone-errors-prompt-tga-safety-update/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29433 [authorType] => )

      Paediatric risperidone errors prompt TGA safety update

      interruptions
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                  [post_content] => New research has found that pharmacists are interrupted at alarming rates when dispensing medicines.
      
      Led by Monash University’s Faculty of Pharmacy and Pharmaceutical Sciences, the study aimed to review existing evidence on how interruptions and distractions in pharmacy practice influence the occurrence of dispensing errors.
      
      [caption id="attachment_29414" align="alignright" width="260"] Dan Malone MPS[/caption]
      
      The review, which analysed 51 Australian and international studies, found that pharmacists can experience interruptions and distractions more than 20 times per hour.
      
      Phone calls were the biggest disruptor, said co-author Associate/Professor Dan Malone MPS, Course Director of the Undergraduate Pharmacy Degree.
      
      ‘For example, where a pharmacist would be dispensing or talking to someone, and either the phone was ringing or they would be interrupted by a colleague who said there was a phone call for the pharmacist,’ he said.
      
      Other key disruptors during dispensing included:
      • consumers interrupting pharmacists to ask a question
      • interruptions and distractions from pharmacy staff who needed to manage customer queries that were out of their scope.

      What are the impacts of interruptions?

      While most studies included in the review identified what the interruptions were and how frequently they occurred, few looked at the impact of interruptions and strategies to mitigate them. But of those that did, medication errors were the most serious issue identified. ‘While no medication error should occur, some are relatively minor whereas others are potentially fatal,’ A/Prof Malone said. Other identified impacts included: 
      • taking longer to dispense a script
      • poorer performance 
      • mental fatigue.

      What about self-interruptions?

      It’s not always external interruptions that are the culprits. Sometimes, it’s the pharmacists themselves who self-interrupt, the review team found. ‘They might be working on a particular task, then start searching the internet on an unrelated topic,’ A/Prof Malone said. ‘Or talk to their colleague while dispensing – initiating an interruption themselves.’  The term that's often used for this phenomenon is ‘multi-tasking’. But A/Prof Malone said it’s more akin to task-switching. ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,’ he said.

      What are the key intervention strategies?

      Should pharmacists be better trained to deal with inevitable interruptions, or should pharmacy teams try to reduce those interruptions in practice?  A bit of both, A/Prof Malone thinks. ‘Our pharmacy students do a lot of practice in terms of role playing the pharmacist in a workshop, for example,’ he said. ‘But when they go out on placement, they often complain that “it's really noisy, there's all these distractions and it’s hard to concentrate”,’ he said. 
      ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,.' DAN MALONE MPS 
      Better preparing students for that environment by stimulating situations where interruptions occur should help them to cope with future interruptions, A/Prof Mr Malone said. And while interruptions can’t be eliminated completely, systems can be put in place to reduce them, including:
      • having a set time where the pharmacist can't be interrupted
      • making sure there's workflow processes to ensure the pharmacist is less likely to be interrupted.
      ‘For example, when a prescription is dispensed, having a process whereby communication is such that the pharmacist is able to focus on the dispensing process,’ A/Prof Malone said. ‘When another prescription comes in, unless it's urgent, the pharmacist isn't interrupted – so they can go through the dispensing process with one prescription before they start the next.’ Or it might just be a matter of staffing. ‘Where possible, having two pharmacists on, with one focusing on tasks such as patient queries – limiting direct access to the other pharmacist during dispensing time,’ he said. However, in practice this isn’t always possible. When more urgent matters arise – as they inevitably do – pharmacists often have to park what they’re doing and switch tasks.  ‘That's understandable, but it’s preferable to minimise these occurrences, if possible,’ A/Prof Malone said.

      What about training other staff?

      There’s a ‘huge benefit’ in having well-trained pharmacy assistants on staff to reduce interruptions, and therefore errors, A/Prof Malone said. ‘I've worked with a lot of really experienced pharmacy assistants who know a lot about disease states, and are able to handle queries that come in and field questions over the phone without necessarily having to speak with the pharmacist,’ he said. But there are limitations to this approach, including making recommendations about Schedule 3 medicines. ‘This requires the pharmacist to be interrupted,’ A/Prof Malone added. PSA’s Pharmacists in 2030 recommends recognising and formalising the role of pharmacy assistants as well as technicians by establishing clear development pathways, such as:
      • registering support technicians to perform final-checking duties
      • embedding Certificate II, III and IV dispensary technician qualifications into practice to free pharmacists for direct patient care.
      To safeguard pharmacist wellbeing and minimise medicine errors, Pharmacists in 2030  advocates for:
      • enforcing safe-dispensing limits through patient-to-pharmacist ratios
      • building mandatory rest breaks into rosters
      • providing Employee Assistance Programs 
      • redesigning workspaces to enhance comfort and support mental health.

      What’s next on the horizon?

      The paper, led by pharmacist and PhD student Meaza Ayanaw, is a scoping review that’s paving the way for further research into how interruptions and distractions affect pharmacists’ decision-making ability, and how pharmacists prioritise different tasks.  ‘For example, should pharmacists switch tasks when they're in a pharmacy environment? If so, when should they switch? And what are the high- and low-priority tasks that require pharmacists to switch?’ A/Prof Malone said. From the results of the findings, more assessments and training will be developed using simulations such as Monash’s MyDispense. ‘This will help students to prepare for [pharmacy practice] by reflecting on real-world interruptions and distractions in a simulated environment. So that when they make mistakes, there's no consequence associated,’ A/Prof Malone said. For more information on streaming workflows and operations, don’t miss the poster presentation ‘Optimising pharmacy operations’ at PSA25, from 1–3 August 2025. Register here to attend. [post_title] => High interruption rates threaten patient safety [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => high-interruption-rates-threaten-patient-safety [to_ping] => [pinged] => [post_modified] => 2025-05-19 15:45:44 [post_modified_gmt] => 2025-05-19 05:45:44 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29407 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => High interruption rates threaten patient safety [title] => High interruption rates threaten patient safety [href] => https://www.australianpharmacist.com.au/high-interruption-rates-threaten-patient-safety/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29408 [authorType] => )

      High interruption rates threaten patient safety

      palliative care
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                  [post_content] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that. 
      
      It can be difficult to tell from a prescription that a patient is receiving palliative care, said Tanya Maloney MPS, a community pharmacist in Coffs Harbour, NSW.
      
      [caption id="attachment_29354" align="alignright" width="233"] Tanya Maloney MPS[/caption]
      
      ‘What we lack in pharmacy is training on how to approach those difficult conversations in the right way so we can ask them a few questions to determine that,’ she said. ‘We're often a bit nervous about saying the wrong thing.’
      
      Though passionate about palliative care, Ms Maloney and her team have had to learn on the job.
      
      ‘We haven’t had any extra training and want to know how we can contribute more.’
      
      This is a common issue through the profession, with a lack in palliative care education tailored specifically to pharmacists, leading to a knowledge gap, said PSA Senior Pharmacist (Consulting and Program Delivery) Megan Tremlett MPS – who has managed a number of palliative care projects through Primary Health Networks and at a state level in recent years.
      
      ‘As pharmacists, we don't learn a lot about palliative care in our undergraduate course. And the majority of pharmacists haven't done any extra palliative care education since their university days.’
      
      To address this, PSA launched the ASPIRE Palliative Care Foundation Training Program on 13 May. The free, CPD-accredited course – supported by Palliative Care Australia and funded under the National Palliative Care Grants Program – upskills pharmacists regardless of practice setting.
      
      ‘The training program has been created with extensive stakeholder consultation to provide pharmacists with a thorough introduction to palliative care across the eight modules’ Ms Tremlett said.
      
      Rather than training pharmacists to specialise in palliative care, the training program is intended to lift the baseline knowledge of the profession, said Leah Robinson, Project Manager at PSA, who worked on the development of the program with Ms Tremlett.
      
      ‘It’s about understanding the different settings and phases of palliative care and at which points pharmacists can provide practical support to help families, patients and healthcare professionals in supporting palliative care.’
      
      A foundational understanding of palliative and end-of-life care across the health workforce is essential to meeting community needs, said Camilla Rowland, CEO of Palliative Care Australia.
      
      ‘Supporting people to live, and die well, means building palliative care capability across the entire health system. That includes pharmacists, often among the first healthcare professional patients and carers turn to for advice.’
      

      Learning about symptom management

      The ASPIRE training program has a module dedicated to symptoms and the trajectory of people living with life-limiting illness. Under a subsequent symptom management module, pharmacists can access resources and references for pharmacological management of the symptoms associated with dying that covers:
      • Pharmaceutical Benefits Scheme (PBS) and non-PBS medicines 
      • Special Access Scheme medications
      • Medicines used off-label.
      Experts, from pharmacists to prescribers, guide learners on handling sensitive conversations with patients and families – linking to Safer Care Victoria resources for monitoring and managing adverse effects, especially with continuous subcutaneous infusions.
      ‘We point pharmacists to a range of resources to support them with understanding medicines compatibilities in subcutaneous infusion devices and the adverse effects that might be expected,’ Ms Tremlett said. As illness progresses, medication regimens often grow more complex. ‘Pharmacists need to be able to step in and make recommendations around those [medicines] that could potentially be weaned or stopped to reduce that burden and the chance of side effects and interactions,’ Ms Tremlett said. The training program also helps pharmacists with information, tools and resources for conversions of medicines and different formulations, including switching from some or all of their opioids, to a replacement opioid delivered by another route, Ms Robinson said.  ‘It’s also [around] practical things pharmacists can offer such as providing a list of current medicines, home medication review, staged supply, support with prescription management, home delivery or flexibility around dose administration aids to help manage those medicines and the complexity of the changes they go through during the different phases of palliative care,’ Ms Robinson said.

      Developing interdisciplinary care skills

      At the moment, Ms Maloney feels as though community pharmacy is a missing piece in palliative care that’s uncertain where it fits. ‘We want to be able to fit into that wider team of their health carers so we can look at the holistic care and goals of the person and provide them with more than just medication,’ she said.
      ASPIRE emphasises collaboration with GPs, specialist palliative care teams, community nurses, paramedics and residential aged care staff. ‘In the module that's dedicated to interdisciplinary palliative care, pharmacists learn the broad range of people who are involved in palliative care, and some they might not expect – from death doulas to chaplains, music therapists and diversional therapists,’ Ms Tremlett said.

      Focusing on patient-centred care

      Once pharmacists identify a palliative care patient, they need knowledge and skills to determine how best to help at each stage, Ms Maloney said. ‘How do we know how to help them in all these different stages that they're going to go through?’ Pharmacists may think they know what’s best for a patient based on their clinical background, Ms Tremlett said. ‘But at the end of the day, what's important to the person or the patient is the single most important thing.’ ‘ASPIRE reminds pharmacists to be mindful of their own biases to meet the person where they are and help them achieve their goals of care, which might change over time as their condition progresses,’ Ms Robinson added. The patient-centred care module also highlights Australia’s cultural diversity – including First Nations peoples, migrants and those from non-English speaking backgrounds. ‘There is no such thing as a consistent cultural need in palliative care,’ Ms Tremlett said. ‘It's very different within cultures, between cultures and within communities, so pharmacists need to be able to adapt the care and services they provide without making assumptions.’ The need for translation services, what’s deemed an inappropriate conversation or who is the next of kin or carer can vary from person to person, Ms Robinson said. ‘It’s important to be mindful of how and what to communicate to align with those goals of care.’

      Helping families through grief and bereavement

      Being confident talking about death is something many pharmacists struggle with, Ms Maloney said. ‘You might prompt them a little bit, and they do get upset, and that’s often what puts us off,’ she said. ‘But it’s not necessarily a bad thing as they’re getting to open up and talk to you.’ The final ASPIRE module on grief, bereavement and self-care aims to normalise conversations about death and dying. Being comfortable enough to embed those conversations in day-to-day practice – including supporting people after their loved one has died – is crucial, Ms Tremlett said. ‘It's really important for pharmacists to be prepared to still speak about the person who's died, if that's what the person wants to do, and to recognise that grieving is very normal, and there's no right or wrong way to grieve.’ Pharmacists also need to be able to recognise prolonged grief and know when referrals  for extra support are needed. ‘If the pharmacist has the knowledge and skills to refer that person on for some extra help in the grieving process, that's really impactful,’ she said. Throughout the palliative care process, it’s crucial for pharmacists to look after themselves and to know when to check in on their colleagues too. ‘When we're constantly supporting people who are unwell … it's very natural for pharmacists to feel a burden of care,’ Ms Tremlett said. ‘Learning to recognise when you or your colleagues might be feeling a little overwhelmed, need extra support or to engage in self-care activities is really important.

      Embedding the training into practice

      Now that the ASPIRE training program is available, Ms Maloney wants all her pharmacists to complete it to lift their confidence and knowledge in palliative care. ‘As part of that, there's all the resources you can print out and revisit,’ she said. ‘They will be active documents that become part of our internal processes rather than training you just do and forget.’ The experience  of supporting palliative care patients also builds trust and loyalty among family members and carers. ‘You get to know them on a different level and see them when they're vulnerable,’ Ms Maloney said. ‘That rapport you can build up in that time by being there for them definitely builds that lifetime customer for the future.’ [post_title] => Bridging the palliative care education gap for pharmacists [post_excerpt] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that.  [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => bridging-the-palliative-care-education-gap-for-pharmacists [to_ping] => [pinged] => [post_modified] => 2025-05-14 16:27:55 [post_modified_gmt] => 2025-05-14 06:27:55 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29352 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Bridging the palliative care education gap for pharmacists [title] => Bridging the palliative care education gap for pharmacists [href] => https://www.australianpharmacist.com.au/bridging-the-palliative-care-education-gap-for-pharmacists/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29358 [authorType] => )

      Bridging the palliative care education gap for pharmacists

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      Case scenario

      Amra, 80 years old and a regular patient of yours, has been discharged from hospital after an admission for a fall. She presents at the pharmacy with a bag of medicines and hands you a discharge medicines list. She appears to have been initiated on some new medicines in hospital and expresses confusion on which of her pre-hospital medicines to continue. You view her dispense history and My Health Record and notice discrepancies. It is unclear to you or Amra why some medicines have been initiated. She has an appointment with her GP in a couple of days.

      Learning objectives

      After reading this article, pharmacists should be able to:
      • Define transitions of care
      • Discuss medicines safety during transitions of care
      • Explain principles of safe and high-quality transitions of care
      • Discuss the role of the pharmacist across transitions of care.
      Competency standards (2016) addressed: 1.1, 1.4, 1.5, 2.2, 3.5 Accreditation number: CAP2505SYPMA Accreditation expiry: 31/04/2028
      Already read the CPD in the journal? Scroll to the bottom to SUBMIT ANSWERS.

      Medicines safety during transitions of care

      The Australian Commission on Safety and Quality in Health Care (ACSQHC) defines transitions of care as the period when all or part of a person’s healthcare is transferred between care providers or care settings.1

      Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. When medicines safety is not prioritised at transitions of care, the risk of adverse events is increased, such as readmission to hospital and adverse drug reactions.  A Cochrane review found that more than 50% of patients experience a medication error during transitions of care.2  A systematic review found that following hospital discharge to the community, 53% of adult patients experience at least one medication error, 50% experience one or more unintentional medication discrepancies (a subset of medication errors), and 19% experience one or more adverse drug events.3 A systematic review and meta-analysis found the prevalence of medication-related readmissions and adverse drug reaction-related readmissions in older people were 9% and 6%, respectively, with about one-fifth of these preventable.4

      Preventing medication-related harm at transitions of care is a key priority in the World Health Organization’s (WHO) third Global Patient Safety Challenge (Medication Without Harm).5 The ACSQHC’s response to the Challenge, published in 2020, described prioritising medication reconciliation at all transitions of care to reduce the risk of medication errors.6 Its response also recommended the use of My Health Record to engage patients and carers in curation and communication of medication regimen information.

      The ACSQHC’s response focused on transitions from hospital, a period known to be particularly high risk, and also recommended standardising the presentation of discharge summaries.6 For people with complex care needs, initiatives to reduce preventable medication-related readmissions were encouraged, such as early post-discharge medication reviews (hospital outreach or primary care led), and cross-sector case conferencing.6 Refinement of risk criteria or indicators was recommended to direct interventions towards patients at the greatest risk of medication-related harm.6

      The ACSQHC’s response did not specifically address other known contributors to medication-related harm during transitions of care, such as ensuring timely access to medicines and the tools that are sometimes required to use them, such as interim medication administration charts when discharged to residential care, dose administration aids, and adequate quantities of medicines supply.7,8

      Principles of safe and high-quality transitions of care

      The ACSQHC has recently published a set of principles to guide safe and high-quality transitions of care that highlight the need for multidisciplinary collaboration and coordination that relies on shared responsibility and accountability.9 The consistent application of these principles within practice, standards, policy and guidance are fundamental for safe transitions of care and apply to transitions of care wherever healthcare is received including primary, community, acute, subacute, aged and disability care.9

      The principles and their enablers are shown in Table 1.

      Australia’s priority actions to address medicines safety at transitions of care

      Progress toward Australia’s priority actions to address medicines safety at transitions of care has been mixed.10 Embedding medication reconciliation at admission and discharge from hospital has advanced and is now part of medicines safety standards that hospitals need to meet for accreditation.

      My Health Record has improved access to patients’ medication histories; however, patient engagement remains low, and, like all medication records, verification of data with the patient and other sources is required.11,12 Implementation of the Pharmacist Shared Medicines List (a verified medication history that can be uploaded to My Health Record) has been limited. Discharge summaries continue to have deficiencies, including inaccurate medicine lists and inadequate explanations of medicine changes.13 Primary care medicine lists and dose administration aid medicine labels, which are often used by hospital doctors to chart medicines on admission, are also frequently inaccurate.14,15

      Australian research highlights concerns about lack of awareness and uptake of post-discharge Home Medicines Reviews (HMRs) and Residential Medication Management Reviews (RMMRs) and the complexity in facilitating timely post-discharge medication reviews.16,17 Hospital outreach pharmacist medication review services and cross-sector multidisciplinary case conferencing are uncommon. There has been progress in developing validated criteria to identify patients at risk of medication-related readmission,18 though more work is needed to ensure generalisability and implementation.10

      Progress towards ensuring timely access to medicines following hospital discharge has been mixed.10 Reforms to enable medicines to be supplied by hospitals using the Pharmaceutical Benefits Scheme, and implementation of interim medication administration charts for patients discharged to residential care, have not occurred in all jurisdictions.

      Drivers for a stewardship approach to improve medicines safety at transitions of care

      In 2020, after decades of advocacy, Commonwealth-funded medication review program rules changed to allow hospital-based medical specialists to refer patients to credentialed pharmacists for collaborative post-discharge medication management reviews. In response, the Society of Hospital Pharmacists (now known as Advanced Pharmacy Australia [AdPha]) published a Hospital Pharmacy Practice Update, Hospital-Initiated Medication Reviews, which detailed information about pathways for patients to have post-discharge HMRs, RMMRs and Hospital Outreach Medication Reviews, as well as flagging MedsChecks as a medication reconciliation pathway.19 Unfortunately, resources were not provided by the Commonwealth or state health departments for promotion, training or implementation support for hospitals to implement hospital-initiated medication reviews, and uptake of these pathways has been low.

      An article published in 2022 presented barriers and enablers to hospital-initiated medication reviews, and highlighted the need for a stewardship approach to promote safe and high-quality medication management at transitions of care, with a key focus on facilitating early post-discharge medication reviews (within 10 days).20 The authors have continued to advocate for a hospital-led stewardship approach to address the perennial problem of medicines safety at transitions of care.10,21

      The recently published AdPha Standard of Practice for Pharmacy Services Specialising in Transitions of Care describes current best practice for the provision of pharmacy services that specialise in transitions of care, such as hospital outreach pharmacists and community liaison pharmacists, and supports the introduction of transitions of care stewardship programs into existing organisational clinical systems.22

      Medicines stewardship

      Stewardship in the context of health care refers to a structured program of strategies and interventions that address challenges within a specific clinical area, and ensure appropriate and efficient use of resources. Medicines stewardship programs focus on improving medicines use in areas where there is a high risk of inappropriate prescribing or adverse outcomes. Examples of successful programs include: antimicrobial, opioid analgesic, anticoagulation and psychotropic stewardship.21

      Medicines stewardship programs aim to improve medication management at individual and population levels to ensure consistent, appropriate care. At a population level, this may include developing guidelines and providing standardised processes and templates. At an individual level, it includes delivering tailored person-centred interventions to optimise medication outcomes. 

      Common elements of successful medicines stewardship programs include multidisciplinary leadership, stakeholder engagement, tailored communication strategies, behavioural changes, implementation science methodologies, and ongoing program monitoring, evaluation and reporting.21 Stewardship programs are often led or administered by a dedicated stewardship officer (usually a pharmacist) or team.21

      Medication Management at Transitions of Care Stewardship Framework

      Applying a stewardship approach to transitions of care may provide opportunities to focus organisational resources, foster multi- or interdisciplinary collaboration, and improve coordinated care when individuals transfer between care providers or settings.

      In 2023, the ACSQHC commissioned a rapid literature review and environmental scan examining Australian and international medication management strategies, including stewardship programs, at transitions of care focusing on admission to hospital and discharge to the community or residential care.23,24

      The literature review identified that, globally, there are no published studies or existing frameworks that describe a stewardship program specifically addressing medication management at transitions of care.24

      Given the evidence from the literature review and environmental scan, the ACSQHC set about developing a Medication Management at Transitions of Care Stewardship Framework (the Framework). The Framework is scheduled for release in the second quarter of 2025.

      The Framework is intended to provide healthcare organisations (hospitals) with a systematic approach for implementing coordinated medication management activities and interventions to optimise safe and high-quality transitions of care, with a focus on patients admitted to hospital and discharged to the community or residential aged care. The Framework will provide guidance that can be adapted to local context and the circumstances of individuals transitioning across care settings.

      The Framework will be supported by existing national standards and guidelines, including:

      • National Safety and Quality Health Service Standards25
      • Guiding Principles to Achieve Continuity in Medication Management8
      • National Medicines Policy 2022.26

      The ACSQHC’s principles of safe and high-quality transitions of care9 should also be considered in the local implementation of a medication management at transitions of care stewardship program.

      Leveraging digital health

      Digital health is a key enabler to achieve interoperable, accurate and timely communication between clinicians in the acute and primary care settings. The Framework will align with the National Digital Health Strategy 2023–202827 and the Strategy Delivery Roadmap.28

      Health facilities are encouraged to embed digitally enabled care to strengthen effective interdisciplinary communication and improve safe and high-quality medication management at transitions of care.29 

      Implementation of the Framework and the role of pharmacists across transitions of care

      The Framework is designed with a hospital focus, and it is intended that it will be used by hospitals to guide stewardship and coordination in collaboration with primary care practitioners.29

      General practice coordination of ongoing medical care prior to and following hospital discharge is vital, as is community pharmacist coordination of medication supply and management. Pharmacists embedded in general practice, onsite aged care pharmacists, and credentialed pharmacists providing HMRs and RMMRs, can also play an important role. However, it is not possible for general practice and primary care pharmacists to coordinate all time-critical aspects of medication management for complex hospital discharges that occur 7 days a week, and sometimes outside of business hours. In the first instance, hospitals need to take responsibility for bridging the gap by29:

      • ensuring that discharges are well planned
      • ensuring there is timely and accurate communication with primary care providers
      • providing an adequate supply of newly commenced medicines 
      • working with community-based healthcare professionals to ensure continuity of medication access
      • providing education to patients and carers, including a discharge medicines list
      • working with community-based healthcare professionals to ensure timely post-discharge medication review and follow-up as needed.
      Primary care and aged care pharmacists need to be aware of the risks associated with transitions of care and be prepared to work collaboratively with hospitals in a responsive and flexible way to ensure timely delivery of post-discharge transitions of care-related services such as medication reconciliation, medication supply and medication review.

      The authors encourage all pharmacists to engage with the Framework. It is a world-first document that will drive system improvements so Australians receive high-quality care, and is a pivotal response to the WHO’s third Global Patient Safety Challenge (Medication Without Harm) priority, transitions of care.

      Case scenario continued

      You phone the discharging hospital pharmacist (whose name was recorded on the patient’s discharge medicines list) to clarify Amra’s medicine changes and discharge medication management plan. You speak with Amra about your discussion and obtain consent to complete a MedsCheck and chat with her GP about any changes post-discharge. You go through each of her medicines and prepare her an updated medicines list. You also discuss the potential benefits of a Home Medicines Review (HMR) when there has been a hospital admission and medicine changes. You ask if she wishes for you to discuss an HMR referral with her GP which could be actioned at her upcoming GP appointment. She indicates an HMR would be welcome and thanks you for helping her.
      [cpd_submit_answer_button]

      Key points

      • A transition of care is when all or part of a person’s healthcare is transferred between care providers or care settings.
      • Preventing medication-related harm at transitions of care is a key priority in the WHO’s third Global Patient Safety Challenge (Medication Without Harm).
      • The ACSQHC has developed a Medication Management at Transitions of Care Stewardship Framework to optimise high-quality and safe medication management during transitions of care, focusing on hospital admissions and discharges to community and residential aged care.
      • Hospital and primary care pharmacists need to work collaboratively to improve the safety of transitions of care and ensure timely post-discharge medication reconciliation, medication supply and post-discharge medication review.   

      References

      1. Australian Commission on Safety and Quality in Health Care. Transitions of Care. 2024. At: www.safetyandquality.gov.au/our-work/transitions-care
      2. Redmond P, Grimes TC, McDonnell R, et al. Impact of medication reconciliation for improving transitions of care. Cochrane Database of Systematic Reviews 2018, Issue 8.
      3. Alqenae FA, Steinke D, Keers RN. Prevalence and nature of medication errors and medication-related harm following discharge from hospital to community settings: a systematic review. Drug Saf 2020;43(6):517–37.
      4. Prasad N, Lau ECY, Wojt I, et al. Prevalence of and risk factors for drug-related readmissions in older adults: a systematic review and meta-analysis. Drugs Aging 2024;41(1):1–11.
      5. World Health Organization. Medication Without Harm – Global Patient Safety Challenge on Medication Safety. Geneva: World Health Organization; 2017.
      6. Australian Commission on Safety and Quality in Health Care. Medication without harm – WHO Global Patient Safety Challenge. Australia’s response. Sydney: ACSQHC; 2020.
      7. Elliott RA, Tran T, Taylor SE, et al. Impact of a pharmacist-prepared interim residential care medication administration chart on gaps in continuity of medication management after discharge from hospital to residential care: a prospective pre- and post-intervention study (MedGap Study). BMJ Open 2012;2(3).
      8. Department of Health and Aged Care. Guiding Principles to Achieve Continuity in Medication Management. Canberra; 2022.
      9. Australian Commission on Safety and Quality in Health Care. Principles of safe and high-quality transitions of care (factsheet). 2024.
      10. Elliott RA, Angley M, Criddle DT, et al. Achieving safe medication management during transitions of care from hospital: time for a stewardship approach. Aust Prescr 2024;47(4):106–8.
      11. Elliott RA, Taylor SE, Koo SMK, et al. Accuracy of medication histories derived from an Australian cloud-based repository of prescribed and dispensed medication records. Intern Med J 2023;53:1002–9.
      12. Francis M, Francis P, Makeham M, et al. Using personal health records for medication continuity during transition of care: An observational study. Health Inf Manag 2024:18333583241270215.
      13. Wembridge P, Rashed S. Discharge summary medication list accuracy across five metropolitan hospitals: a retrospective medical record audit. Aust Health Rev 2022;46:338–45.
      14. Uzunbay Z, Elliott RA, Taylor S, et al. Accuracy of medication labels on community pharmacy-prepared dose administration aids: an observational study. Explor Res Clin Soc Pharm 2023;11:100318.
      15. Taylor S, Welch S, Harding A, et al. Accuracy of general practitioner medication histories for patients presenting to the emergency department. Aust Fam Physician 2014;43:728.
      16. Chen EY, Wang KN, Sluggett JK, et al. Process, impact and outcomes of medication review in Australian residential aged care facilities: a systematic review. Australas J Ageing 2019;38:9–25.
      17. Luetsch K, Rowett D, Twigg MJ. A realist synthesis of pharmacist-conducted medication reviews in primary care after leaving hospital: what works for whom and why? BMJ Qual Saf 2020;30(5):418–30.
      18. Criddle D, Devine B, Murray K, et al. Developing PHarmacie-R: a bedside risk prediction tool with a medicines management focus to identify risk of hospital readmission. Res Social Admin Pharm 2021;18 (7):3137–48.
      19. The Society of Hospital Pharmacists of Australia. Hospital-initiated medication reviews. Collingwood, Victoria: The Society of Hospital Pharmacists of Australia; 2020.
      20. Angley M, Criddle D, Rigby D, et al. Hospital-initiated post-discharge medication reviews in Australia: expert opinion on the barriers and enablers to implementation. J Pharm Pract Res 2022;52(6):446–53.
      21. Su E, Liew DFL, Donnelly J, et al. Medicines stewardship. Aust Prescr 2023;46(2):24–8.
      22. Advanced Pharmacy Australia Transition Care and Primary Care Specialty Practice Group. Standard of practice for pharmacy services specialising in transitions of care. J Pharm Pract Res 2024;54(5):417–35.
      23. Emadi F, Liu S, Yui C H, et al. Digital approaches that can be employed to facilitate safe medication management at transitions of care. Sydney: ACSQHC; 2024.
      24. Emadi F, Liu S, Yiu CH, et al. Medication management at transitions of care stewardship framework. Rapid literature review and environmental scan – final report. Sydney: Faculty of Medicine and Health, School of Pharmacy, University of Sydney; 2023.
      25. Australian Commission on Safety and Quality in Health Care. The National Safety and Quality Health Service (NSQHS) Standards (second edition) 2021. At: www.safetyandquality.gov.au/standards/nsqhs-standards
      26. Department of Health and Aged Care. National Medicines Policy 2022. Canberra; 2022.
      27. Australian Digital Health Agency. National Digital Health Strategy 2023-2028. Sydney; 2023.
      28. Australian Digital Health Agency. National Digital Health Strategy Delivery Roadmap 2023–2028. Sydney; 2023.
      29. Australian Commission on Safety and Quality in Health Care [DRAFT]. Medication Management at Transitions of Care Stewardship Framework. Sydney: ACSQHC; 2024.

      Our authors

      Manya Angley (she/her) BPharm, PhD, FPS, CredPharm (MMR), FAdPha is an Advanced Practice Pharmacist experienced in general practice, disability and aged care.

      Debbie Rigby (she/her) BPharm, GradDipClinPharm, FASCP, FPS, FACP, FAICD, FSHP, FANZCAP (GeriMed, Resp) is an Advanced Practice Pharmacist qualified in clinical pharmacy, geriatrics and respiratory medicine.

      Rohan Elliott (he/him) BPharm, BPharmSc(Hons), MClinPharm, PhD, FAdPhA, FANZCAP (GeriMed, Research) is an Advanced Practice Pharmacist with experience in hospitals, aged care and transitions of care.

      Our reviewer

      Elizabeth Manias (she/her) RN, BPharm, MPharm, MNStud, PhD, FANZCAP (Transitions of care, Geriatric Medicine)

      Conflict of interest declaration

      Manya Angley, Debbie Rigby and Rohan Elliott are co-investigators on a Medical Research Future Fund (MRFF) 2022 transitions of care project. MRFF is funded by the Australian Government. They are also co-authors of a literature review of transitions of care stewardship that was funded by the ACSQHC.

      Elizabeth Manias is a member of the Transitions of Care and Primary Care Leadership Committee of Advanced Pharmacy Australia.

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      Improving medicines safety at transitions of care

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                  [post_date] => 2025-05-12 13:28:53
                  [post_date_gmt] => 2025-05-12 03:28:53
                  [post_content] => Both Cautionary Advisory Label (CAL) 6 and CAL 13 have been overhauled to sharpen storage advice.
      
      CAL 6 explanatory notes advice in Digital Australian Pharmaceutical Formulary and Handbook (APF) now mentions considerations for room-temperature time windows for refrigerated medicines, while CAL 13’s tightened wording and advice flags truly sensitive formulations – ensuring pharmacists give patients clearer, more precise guidance.
      

      What’s changing?

      The familiar ‘Refrigerate, do not freeze’ warning of CAL 6 is not changing, however its explanatory notes have been expanded.  [caption id="attachment_29335" align="aligncenter" width="180"]CAL 6 CAL 6[/caption] There are many instances whereby refrigeration of temperature sensitive medicines may not be practical, for example travel days, power outages or ‘in-use’ multi-dose containers/devices. The updated explanatory notes advise pharmacists that they should refer to the medicines approved product information (PI) and counsel their patients on how to best store these medicines – covering when their temperature sensitive medicines may safely remain at room temperature (below 25 °C) – if applicable. [caption id="attachment_29336" align="aligncenter" width="176"] The old CAL 13[/caption] [caption id="attachment_29337" align="aligncenter" width="189"] The new CAL 13[/caption] Meanwhile, CAL 13 has been reworded. Previously ‘Do not remove from original packaging until dose required’, the new prompt, ‘Ask your pharmacist about the storage conditions for this medicine,’ applies only to dosage forms and active ingredients truly sensitive to light, moisture or temperature excursions.  This includes orally disintegrating tablets, effervescents, sublingual or buccal lozenges, dispersible granules, wafers and chewables, as well as amoxicillin/clavulanic acid, dabigatran, glyceryl trinitrate, nicorandil, nifedipine, phenothiazines, tamoxifen and sodium valproate. CAL 13 may also be applied in addition to other CALs relating to storage requirements (e.g. CALs 6, 7a or 7b) when complex storage instructions are applicable, and these other CALs do not adequately cover these. To support the change to CAL 13, the APF’s Good dispensing practice chapter has been updated with clearer and expanded guidance on providing advice to patients on how to store medicines, including that:
      • all medicines should be kept out of sight and out of reach of children at all times
      • unless specifically requiring refrigeration, and in the absence of special storage instructions outlined in the PI/consumer medicine information (CMI), medicines should be stored in their original packaging in a cool (preferably <25 °C), dry and secure place
      • medicines should generally not be removed from their original packaging until a dose is required – pharmacists should check how the patient intends to store their medicines (e.g. in a dosette box) and provide advice according to the storage instructions outlined in each medicines PI/CMI.
      CAL 13’s explanatory notes have also been updated in APF Digital to support pharmacists in applying the revised CAL. When packing medicines into Dose Administration Aids (DAAs) pharmacists should consider the approved PI of each medicine, and PSA’s Guidelines for pharmacists providing dose administration aid services.

      What led to this update?

      Medicine labels have traditionally relied on simple fridge-or-no-fridge advice. But today’s PIs are more complex.  Humira (adalimumab) is one good example. People using Humira are advised that they can store single pre-filled syringes or pens ‘below 25°C (room temperature) for a maximum period of 14 days, but must be protected from light. Once removed from the refrigerator for room temperature storage, the syringe must be used within 14 days or discarded, even if it is returned to the refrigerator’.  But CAL 6 doesn’t capture these nuances, so some patients are left guessing whether their medicines are safe to use or not during travel or at times when refrigeration is not available. The new explanatory notes prompt pharmacists to cover these scenarios as part of their routine counselling to promote safe and quality use of medicines. At the same time, the CAL 13 had become so ubiquitous – applicable to nearly all medicines – that its impact was diluted. What's more, most pharmacies didn’t even stock the printed sticker.  By narrowing its application, CAL 13’s power to prompt meaningful conversations about stability risks has been restored. Above all, when medicines are removed from their original packaging inappropriately, or stored incorrectly, this can translate into reduced potency or patient harm. These refinements give pharmacists clear, evidence-based cues to maintain medicine stability and efficacy. 

      How should pharmacists tailor storage advice?

      Pharmacists should personalise both verbal and written advice to the patient. Ensure every patient is counselled on how to best store their medicines including routinely asking how the patient plans to keep their medicines, for example will they use a dosette box? Is storage at an appropriate temperature an issue? If a medicine carries Label 6 but its PI indicates there is an appropriate room-temperature window, demonstrate the correct use of an insulated bag and explain the difference between ‘keep at 2–8 °C’ and ‘store below 25 °C’. Provide guidance on room temperature storage for their in-use multi dose container/device (if appropriate) and for times when refrigeration is unavailable or impractical. Pharmacists should also advise the patient to avoid storing medicines in the areas of a domestic refrigerator that may not maintain a temperature of 2–8 °C. This includes the door, top shelf or crisper; or within 40 mm of the back and sides of the main compartment. For CAL-13 affixed medicines, pharmacists should advise patients that these medications’ stability is protected by the original container and packaging, and that removing them prematurely can accelerate degradation and reduce efficacy. Work with the patient to address any barriers to this.

      What’s the implementation timeline?

      The revised explanatory notes for CAL 6 and CAL 13 are live in APF Digital as of 7 May 2025.  CAL printers will begin issuing the new CAL 13 labels on their next run. Until then, pharmacists should continue using the existing labels while equipping patients with the updated counselling points and advice outlined in the APF Digital.

      How should pharmacists put the new advice into practice?

      Let’s say Mrs L, 68, who has type 2 diabetes, atrial fibrillation and hypertension, presents to a pharmacy for her medicines. She picks up a prescription for insulin glargine pens, nifedipine and dabigatran. For her insulin glargine, you apply Label 6 and explain the medicine must be stored at 2–8 °C in the fridge’s main compartment, yet the in-use pen may remain at room temperature for up to 28 days. You provide her with an insulated bag and demonstrate how to use it. You then recognise that nifedipine is sensitive to light and dabigatran is moisture-sensitive, and apply Label 13 to each medicine’s packaging which prompts a PI check. You advise her to keep the medicines away from humid spots such as bathrooms or kitchen windowsills, and to keep them in their original packaging, out of direct light. Mrs L leaves confident in where to store each medicine, and you’ve pre-emptively safeguarded stability and efficacy. [post_title] => New CAL medicine storage guidance [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => new-cal-medicine-storage-guidance [to_ping] => [pinged] => [post_modified] => 2025-05-12 16:02:09 [post_modified_gmt] => 2025-05-12 06:02:09 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29331 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => New CAL medicine storage guidance [title] => New CAL medicine storage guidance [href] => https://www.australianpharmacist.com.au/new-cal-medicine-storage-guidance/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29332 [authorType] => )

      New CAL medicine storage guidance

  • CPD
    • risperidone
      td_module_mega_menu Object
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          [post] => WP_Post Object
              (
                  [ID] => 29429
                  [post_author] => 3410
                  [post_date] => 2025-05-21 12:44:53
                  [post_date_gmt] => 2025-05-21 02:44:53
                  [post_content] => The Therapeutic Goods Administration (TGA) has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18.
      
      In 2024 alone, 22 adverse events as a result of overdose of risperidone oral solution were reported to the TGA – most cases involved accidental administration of 10 times the prescribed dose (for example, 5 mL instead of 0.5 mL). 
      
      Although no deaths were recorded, adverse effects led to hospitalisations in most cases.
      

      Why are dosing errors occurring?

      An investigation by the TGA unearthed several drivers for dosing errors of risperidone oral solution including:
      • misinterpreting dosing instructions
      • incorrect use of the dosing syringe
      • medicine administration by non-primary caregivers (e.g. babysitters or other relatives).
      And the TGA is not the only national health agency to raise concerns about risperidone dosing confusion. The Spanish Agency for Medicines and Health Products issued a public alert after discovering that paediatric caregivers misread decimal points when administering a dose of 1 mg/mL risperidone solution, often inadvertently giving ten times the intended dose. Most (74%) of these incidents were serious, with children suffering sedation, hypotension, tachycardia, extrapyramidal symptoms, QT prolongation and, in some cases, seizures. In Ireland, the Health Products Regulatory Authority echoed these concerns, reporting ten‐fold overdoses in children aged 3–15 –  urging prescribers and pharmacists to provide clear dosing-device instructions and educate caregivers on recognising and responding to overdose symptoms.

      What’s changing?

      To address the identified risk, the Product Information (PI) and Consumer Medicines Information (CMI) for Risperdal have been revised, and generic manufacturers are now required to update PIs and CMIs to mirror these changes. The new versions for Risperdal include more detailed dosing guidance and illustrative diagrams to support accurate administration including:
      • use the supplied pipette only: do not substitute with another measuring device
      • open the child-resistant cap: push down on the plastic screw cap and turn counter-clockwise, then lift off
      • insert and draw up dose: place the pipette in the bottle; hold the bottom ring and pull up the top ring to the mark matching the prescribed dose (e.g. 0.25 mL for 0.25 mg, 0.5 mL for 0.5 mg)
      • dose equivalence: 1 mL of Risperdal solution = 1 mg risperidone; graduations on the plunger are in 0.25 mL (0.25 mg) increments
      • administer in a drink: remove the pipette, slide the top ring down to expel the dose into a non-alcoholic beverage (e.g. water, juice, milk, coffee – avoid tea)
      • after use: close the bottle; rinse the pipette with cold water, let it air dry in its case; avoid detergents or vigorous wiping to preserve the printed graduations.
      While each generic product should cover the same key details, the syringe and instructions can vary by brand. So pharmacists are advised to always double-check the individual PIs.

      What do pharmacists need to do?

      Dosing instructions need to be clearly printed on the label. According to the Australian Commission on Safety and Quality in Health Care’s National standard for labelling dispensed medicines (Standard 6), label wording  should:
      • have digits for dosage amounts (e.g. ‘Take 1 tablet,’ not ‘Take one tablet’ or ‘Take ONE tablet’)
      • express dose ranges with words between numbers (e.g. ‘1 to 2,’ not ‘1-2’ which could be read as ‘12’)
      • spell out common fractions to avoid confusion (e.g. ‘quarter,’ not ‘0.25’ or ‘¼’)
      • for small paediatric liquid doses, match the numbers on the oral dispenser (e.g. ‘0.5 mL’).
      Presenting numbers as digits generally improves clarity among patients. However, fractions written symbolically (e.g. ½’) may be misread as ‘1 or 2’ and decimal points can be overlooked (e.g. ‘1.5’ read as ‘15’). That’s why, when counselling patients prescribed risperidone oral solution, pharmacists should:
      • verify that all caregivers understand the prescribed dosing regimen
      • demonstrate precisely how to measure the required volume using the provided oral syringe
      • instruct caregivers to review the dosing label before each administration and confirm their understanding, especially with those administering the medicine for the first time.
      [post_title] => Paediatric risperidone errors prompt TGA safety update [post_excerpt] => The TGA has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => paediatric-risperidone-errors-prompt-tga-safety-update [to_ping] => [pinged] => [post_modified] => 2025-05-21 15:02:24 [post_modified_gmt] => 2025-05-21 05:02:24 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29429 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Paediatric risperidone errors prompt TGA safety update [title] => Paediatric risperidone errors prompt TGA safety update [href] => https://www.australianpharmacist.com.au/paediatric-risperidone-errors-prompt-tga-safety-update/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29433 [authorType] => )

      Paediatric risperidone errors prompt TGA safety update

      interruptions
      td_module_mega_menu Object
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              (
                  [ID] => 29407
                  [post_author] => 3410
                  [post_date] => 2025-05-19 13:56:56
                  [post_date_gmt] => 2025-05-19 03:56:56
                  [post_content] => New research has found that pharmacists are interrupted at alarming rates when dispensing medicines.
      
      Led by Monash University’s Faculty of Pharmacy and Pharmaceutical Sciences, the study aimed to review existing evidence on how interruptions and distractions in pharmacy practice influence the occurrence of dispensing errors.
      
      [caption id="attachment_29414" align="alignright" width="260"] Dan Malone MPS[/caption]
      
      The review, which analysed 51 Australian and international studies, found that pharmacists can experience interruptions and distractions more than 20 times per hour.
      
      Phone calls were the biggest disruptor, said co-author Associate/Professor Dan Malone MPS, Course Director of the Undergraduate Pharmacy Degree.
      
      ‘For example, where a pharmacist would be dispensing or talking to someone, and either the phone was ringing or they would be interrupted by a colleague who said there was a phone call for the pharmacist,’ he said.
      
      Other key disruptors during dispensing included:
      • consumers interrupting pharmacists to ask a question
      • interruptions and distractions from pharmacy staff who needed to manage customer queries that were out of their scope.

      What are the impacts of interruptions?

      While most studies included in the review identified what the interruptions were and how frequently they occurred, few looked at the impact of interruptions and strategies to mitigate them. But of those that did, medication errors were the most serious issue identified. ‘While no medication error should occur, some are relatively minor whereas others are potentially fatal,’ A/Prof Malone said. Other identified impacts included: 
      • taking longer to dispense a script
      • poorer performance 
      • mental fatigue.

      What about self-interruptions?

      It’s not always external interruptions that are the culprits. Sometimes, it’s the pharmacists themselves who self-interrupt, the review team found. ‘They might be working on a particular task, then start searching the internet on an unrelated topic,’ A/Prof Malone said. ‘Or talk to their colleague while dispensing – initiating an interruption themselves.’  The term that's often used for this phenomenon is ‘multi-tasking’. But A/Prof Malone said it’s more akin to task-switching. ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,’ he said.

      What are the key intervention strategies?

      Should pharmacists be better trained to deal with inevitable interruptions, or should pharmacy teams try to reduce those interruptions in practice?  A bit of both, A/Prof Malone thinks. ‘Our pharmacy students do a lot of practice in terms of role playing the pharmacist in a workshop, for example,’ he said. ‘But when they go out on placement, they often complain that “it's really noisy, there's all these distractions and it’s hard to concentrate”,’ he said. 
      ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,.' DAN MALONE MPS 
      Better preparing students for that environment by stimulating situations where interruptions occur should help them to cope with future interruptions, A/Prof Mr Malone said. And while interruptions can’t be eliminated completely, systems can be put in place to reduce them, including:
      • having a set time where the pharmacist can't be interrupted
      • making sure there's workflow processes to ensure the pharmacist is less likely to be interrupted.
      ‘For example, when a prescription is dispensed, having a process whereby communication is such that the pharmacist is able to focus on the dispensing process,’ A/Prof Malone said. ‘When another prescription comes in, unless it's urgent, the pharmacist isn't interrupted – so they can go through the dispensing process with one prescription before they start the next.’ Or it might just be a matter of staffing. ‘Where possible, having two pharmacists on, with one focusing on tasks such as patient queries – limiting direct access to the other pharmacist during dispensing time,’ he said. However, in practice this isn’t always possible. When more urgent matters arise – as they inevitably do – pharmacists often have to park what they’re doing and switch tasks.  ‘That's understandable, but it’s preferable to minimise these occurrences, if possible,’ A/Prof Malone said.

      What about training other staff?

      There’s a ‘huge benefit’ in having well-trained pharmacy assistants on staff to reduce interruptions, and therefore errors, A/Prof Malone said. ‘I've worked with a lot of really experienced pharmacy assistants who know a lot about disease states, and are able to handle queries that come in and field questions over the phone without necessarily having to speak with the pharmacist,’ he said. But there are limitations to this approach, including making recommendations about Schedule 3 medicines. ‘This requires the pharmacist to be interrupted,’ A/Prof Malone added. PSA’s Pharmacists in 2030 recommends recognising and formalising the role of pharmacy assistants as well as technicians by establishing clear development pathways, such as:
      • registering support technicians to perform final-checking duties
      • embedding Certificate II, III and IV dispensary technician qualifications into practice to free pharmacists for direct patient care.
      To safeguard pharmacist wellbeing and minimise medicine errors, Pharmacists in 2030  advocates for:
      • enforcing safe-dispensing limits through patient-to-pharmacist ratios
      • building mandatory rest breaks into rosters
      • providing Employee Assistance Programs 
      • redesigning workspaces to enhance comfort and support mental health.

      What’s next on the horizon?

      The paper, led by pharmacist and PhD student Meaza Ayanaw, is a scoping review that’s paving the way for further research into how interruptions and distractions affect pharmacists’ decision-making ability, and how pharmacists prioritise different tasks.  ‘For example, should pharmacists switch tasks when they're in a pharmacy environment? If so, when should they switch? And what are the high- and low-priority tasks that require pharmacists to switch?’ A/Prof Malone said. From the results of the findings, more assessments and training will be developed using simulations such as Monash’s MyDispense. ‘This will help students to prepare for [pharmacy practice] by reflecting on real-world interruptions and distractions in a simulated environment. So that when they make mistakes, there's no consequence associated,’ A/Prof Malone said. For more information on streaming workflows and operations, don’t miss the poster presentation ‘Optimising pharmacy operations’ at PSA25, from 1–3 August 2025. Register here to attend. [post_title] => High interruption rates threaten patient safety [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => high-interruption-rates-threaten-patient-safety [to_ping] => [pinged] => [post_modified] => 2025-05-19 15:45:44 [post_modified_gmt] => 2025-05-19 05:45:44 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29407 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => High interruption rates threaten patient safety [title] => High interruption rates threaten patient safety [href] => https://www.australianpharmacist.com.au/high-interruption-rates-threaten-patient-safety/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29408 [authorType] => )

      High interruption rates threaten patient safety

      palliative care
      td_module_mega_menu Object
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          [post] => WP_Post Object
              (
                  [ID] => 29352
                  [post_author] => 3410
                  [post_date] => 2025-05-14 15:03:20
                  [post_date_gmt] => 2025-05-14 05:03:20
                  [post_content] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that. 
      
      It can be difficult to tell from a prescription that a patient is receiving palliative care, said Tanya Maloney MPS, a community pharmacist in Coffs Harbour, NSW.
      
      [caption id="attachment_29354" align="alignright" width="233"] Tanya Maloney MPS[/caption]
      
      ‘What we lack in pharmacy is training on how to approach those difficult conversations in the right way so we can ask them a few questions to determine that,’ she said. ‘We're often a bit nervous about saying the wrong thing.’
      
      Though passionate about palliative care, Ms Maloney and her team have had to learn on the job.
      
      ‘We haven’t had any extra training and want to know how we can contribute more.’
      
      This is a common issue through the profession, with a lack in palliative care education tailored specifically to pharmacists, leading to a knowledge gap, said PSA Senior Pharmacist (Consulting and Program Delivery) Megan Tremlett MPS – who has managed a number of palliative care projects through Primary Health Networks and at a state level in recent years.
      
      ‘As pharmacists, we don't learn a lot about palliative care in our undergraduate course. And the majority of pharmacists haven't done any extra palliative care education since their university days.’
      
      To address this, PSA launched the ASPIRE Palliative Care Foundation Training Program on 13 May. The free, CPD-accredited course – supported by Palliative Care Australia and funded under the National Palliative Care Grants Program – upskills pharmacists regardless of practice setting.
      
      ‘The training program has been created with extensive stakeholder consultation to provide pharmacists with a thorough introduction to palliative care across the eight modules’ Ms Tremlett said.
      
      Rather than training pharmacists to specialise in palliative care, the training program is intended to lift the baseline knowledge of the profession, said Leah Robinson, Project Manager at PSA, who worked on the development of the program with Ms Tremlett.
      
      ‘It’s about understanding the different settings and phases of palliative care and at which points pharmacists can provide practical support to help families, patients and healthcare professionals in supporting palliative care.’
      
      A foundational understanding of palliative and end-of-life care across the health workforce is essential to meeting community needs, said Camilla Rowland, CEO of Palliative Care Australia.
      
      ‘Supporting people to live, and die well, means building palliative care capability across the entire health system. That includes pharmacists, often among the first healthcare professional patients and carers turn to for advice.’
      

      Learning about symptom management

      The ASPIRE training program has a module dedicated to symptoms and the trajectory of people living with life-limiting illness. Under a subsequent symptom management module, pharmacists can access resources and references for pharmacological management of the symptoms associated with dying that covers:
      • Pharmaceutical Benefits Scheme (PBS) and non-PBS medicines 
      • Special Access Scheme medications
      • Medicines used off-label.
      Experts, from pharmacists to prescribers, guide learners on handling sensitive conversations with patients and families – linking to Safer Care Victoria resources for monitoring and managing adverse effects, especially with continuous subcutaneous infusions.
      ‘We point pharmacists to a range of resources to support them with understanding medicines compatibilities in subcutaneous infusion devices and the adverse effects that might be expected,’ Ms Tremlett said. As illness progresses, medication regimens often grow more complex. ‘Pharmacists need to be able to step in and make recommendations around those [medicines] that could potentially be weaned or stopped to reduce that burden and the chance of side effects and interactions,’ Ms Tremlett said. The training program also helps pharmacists with information, tools and resources for conversions of medicines and different formulations, including switching from some or all of their opioids, to a replacement opioid delivered by another route, Ms Robinson said.  ‘It’s also [around] practical things pharmacists can offer such as providing a list of current medicines, home medication review, staged supply, support with prescription management, home delivery or flexibility around dose administration aids to help manage those medicines and the complexity of the changes they go through during the different phases of palliative care,’ Ms Robinson said.

      Developing interdisciplinary care skills

      At the moment, Ms Maloney feels as though community pharmacy is a missing piece in palliative care that’s uncertain where it fits. ‘We want to be able to fit into that wider team of their health carers so we can look at the holistic care and goals of the person and provide them with more than just medication,’ she said.
      ASPIRE emphasises collaboration with GPs, specialist palliative care teams, community nurses, paramedics and residential aged care staff. ‘In the module that's dedicated to interdisciplinary palliative care, pharmacists learn the broad range of people who are involved in palliative care, and some they might not expect – from death doulas to chaplains, music therapists and diversional therapists,’ Ms Tremlett said.

      Focusing on patient-centred care

      Once pharmacists identify a palliative care patient, they need knowledge and skills to determine how best to help at each stage, Ms Maloney said. ‘How do we know how to help them in all these different stages that they're going to go through?’ Pharmacists may think they know what’s best for a patient based on their clinical background, Ms Tremlett said. ‘But at the end of the day, what's important to the person or the patient is the single most important thing.’ ‘ASPIRE reminds pharmacists to be mindful of their own biases to meet the person where they are and help them achieve their goals of care, which might change over time as their condition progresses,’ Ms Robinson added. The patient-centred care module also highlights Australia’s cultural diversity – including First Nations peoples, migrants and those from non-English speaking backgrounds. ‘There is no such thing as a consistent cultural need in palliative care,’ Ms Tremlett said. ‘It's very different within cultures, between cultures and within communities, so pharmacists need to be able to adapt the care and services they provide without making assumptions.’ The need for translation services, what’s deemed an inappropriate conversation or who is the next of kin or carer can vary from person to person, Ms Robinson said. ‘It’s important to be mindful of how and what to communicate to align with those goals of care.’

      Helping families through grief and bereavement

      Being confident talking about death is something many pharmacists struggle with, Ms Maloney said. ‘You might prompt them a little bit, and they do get upset, and that’s often what puts us off,’ she said. ‘But it’s not necessarily a bad thing as they’re getting to open up and talk to you.’ The final ASPIRE module on grief, bereavement and self-care aims to normalise conversations about death and dying. Being comfortable enough to embed those conversations in day-to-day practice – including supporting people after their loved one has died – is crucial, Ms Tremlett said. ‘It's really important for pharmacists to be prepared to still speak about the person who's died, if that's what the person wants to do, and to recognise that grieving is very normal, and there's no right or wrong way to grieve.’ Pharmacists also need to be able to recognise prolonged grief and know when referrals  for extra support are needed. ‘If the pharmacist has the knowledge and skills to refer that person on for some extra help in the grieving process, that's really impactful,’ she said. Throughout the palliative care process, it’s crucial for pharmacists to look after themselves and to know when to check in on their colleagues too. ‘When we're constantly supporting people who are unwell … it's very natural for pharmacists to feel a burden of care,’ Ms Tremlett said. ‘Learning to recognise when you or your colleagues might be feeling a little overwhelmed, need extra support or to engage in self-care activities is really important.

      Embedding the training into practice

      Now that the ASPIRE training program is available, Ms Maloney wants all her pharmacists to complete it to lift their confidence and knowledge in palliative care. ‘As part of that, there's all the resources you can print out and revisit,’ she said. ‘They will be active documents that become part of our internal processes rather than training you just do and forget.’ The experience  of supporting palliative care patients also builds trust and loyalty among family members and carers. ‘You get to know them on a different level and see them when they're vulnerable,’ Ms Maloney said. ‘That rapport you can build up in that time by being there for them definitely builds that lifetime customer for the future.’ [post_title] => Bridging the palliative care education gap for pharmacists [post_excerpt] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that.  [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => bridging-the-palliative-care-education-gap-for-pharmacists [to_ping] => [pinged] => [post_modified] => 2025-05-14 16:27:55 [post_modified_gmt] => 2025-05-14 06:27:55 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29352 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Bridging the palliative care education gap for pharmacists [title] => Bridging the palliative care education gap for pharmacists [href] => https://www.australianpharmacist.com.au/bridging-the-palliative-care-education-gap-for-pharmacists/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29358 [authorType] => )

      Bridging the palliative care education gap for pharmacists

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                  [post_date] => 2025-05-13 16:45:40
                  [post_date_gmt] => 2025-05-13 06:45:40
                  [post_content] => 

      Case scenario

      Amra, 80 years old and a regular patient of yours, has been discharged from hospital after an admission for a fall. She presents at the pharmacy with a bag of medicines and hands you a discharge medicines list. She appears to have been initiated on some new medicines in hospital and expresses confusion on which of her pre-hospital medicines to continue. You view her dispense history and My Health Record and notice discrepancies. It is unclear to you or Amra why some medicines have been initiated. She has an appointment with her GP in a couple of days.

      Learning objectives

      After reading this article, pharmacists should be able to:
      • Define transitions of care
      • Discuss medicines safety during transitions of care
      • Explain principles of safe and high-quality transitions of care
      • Discuss the role of the pharmacist across transitions of care.
      Competency standards (2016) addressed: 1.1, 1.4, 1.5, 2.2, 3.5 Accreditation number: CAP2505SYPMA Accreditation expiry: 31/04/2028
      Already read the CPD in the journal? Scroll to the bottom to SUBMIT ANSWERS.

      Medicines safety during transitions of care

      The Australian Commission on Safety and Quality in Health Care (ACSQHC) defines transitions of care as the period when all or part of a person’s healthcare is transferred between care providers or care settings.1

      Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. When medicines safety is not prioritised at transitions of care, the risk of adverse events is increased, such as readmission to hospital and adverse drug reactions.  A Cochrane review found that more than 50% of patients experience a medication error during transitions of care.2  A systematic review found that following hospital discharge to the community, 53% of adult patients experience at least one medication error, 50% experience one or more unintentional medication discrepancies (a subset of medication errors), and 19% experience one or more adverse drug events.3 A systematic review and meta-analysis found the prevalence of medication-related readmissions and adverse drug reaction-related readmissions in older people were 9% and 6%, respectively, with about one-fifth of these preventable.4

      Preventing medication-related harm at transitions of care is a key priority in the World Health Organization’s (WHO) third Global Patient Safety Challenge (Medication Without Harm).5 The ACSQHC’s response to the Challenge, published in 2020, described prioritising medication reconciliation at all transitions of care to reduce the risk of medication errors.6 Its response also recommended the use of My Health Record to engage patients and carers in curation and communication of medication regimen information.

      The ACSQHC’s response focused on transitions from hospital, a period known to be particularly high risk, and also recommended standardising the presentation of discharge summaries.6 For people with complex care needs, initiatives to reduce preventable medication-related readmissions were encouraged, such as early post-discharge medication reviews (hospital outreach or primary care led), and cross-sector case conferencing.6 Refinement of risk criteria or indicators was recommended to direct interventions towards patients at the greatest risk of medication-related harm.6

      The ACSQHC’s response did not specifically address other known contributors to medication-related harm during transitions of care, such as ensuring timely access to medicines and the tools that are sometimes required to use them, such as interim medication administration charts when discharged to residential care, dose administration aids, and adequate quantities of medicines supply.7,8

      Principles of safe and high-quality transitions of care

      The ACSQHC has recently published a set of principles to guide safe and high-quality transitions of care that highlight the need for multidisciplinary collaboration and coordination that relies on shared responsibility and accountability.9 The consistent application of these principles within practice, standards, policy and guidance are fundamental for safe transitions of care and apply to transitions of care wherever healthcare is received including primary, community, acute, subacute, aged and disability care.9

      The principles and their enablers are shown in Table 1.

      Australia’s priority actions to address medicines safety at transitions of care

      Progress toward Australia’s priority actions to address medicines safety at transitions of care has been mixed.10 Embedding medication reconciliation at admission and discharge from hospital has advanced and is now part of medicines safety standards that hospitals need to meet for accreditation.

      My Health Record has improved access to patients’ medication histories; however, patient engagement remains low, and, like all medication records, verification of data with the patient and other sources is required.11,12 Implementation of the Pharmacist Shared Medicines List (a verified medication history that can be uploaded to My Health Record) has been limited. Discharge summaries continue to have deficiencies, including inaccurate medicine lists and inadequate explanations of medicine changes.13 Primary care medicine lists and dose administration aid medicine labels, which are often used by hospital doctors to chart medicines on admission, are also frequently inaccurate.14,15

      Australian research highlights concerns about lack of awareness and uptake of post-discharge Home Medicines Reviews (HMRs) and Residential Medication Management Reviews (RMMRs) and the complexity in facilitating timely post-discharge medication reviews.16,17 Hospital outreach pharmacist medication review services and cross-sector multidisciplinary case conferencing are uncommon. There has been progress in developing validated criteria to identify patients at risk of medication-related readmission,18 though more work is needed to ensure generalisability and implementation.10

      Progress towards ensuring timely access to medicines following hospital discharge has been mixed.10 Reforms to enable medicines to be supplied by hospitals using the Pharmaceutical Benefits Scheme, and implementation of interim medication administration charts for patients discharged to residential care, have not occurred in all jurisdictions.

      Drivers for a stewardship approach to improve medicines safety at transitions of care

      In 2020, after decades of advocacy, Commonwealth-funded medication review program rules changed to allow hospital-based medical specialists to refer patients to credentialed pharmacists for collaborative post-discharge medication management reviews. In response, the Society of Hospital Pharmacists (now known as Advanced Pharmacy Australia [AdPha]) published a Hospital Pharmacy Practice Update, Hospital-Initiated Medication Reviews, which detailed information about pathways for patients to have post-discharge HMRs, RMMRs and Hospital Outreach Medication Reviews, as well as flagging MedsChecks as a medication reconciliation pathway.19 Unfortunately, resources were not provided by the Commonwealth or state health departments for promotion, training or implementation support for hospitals to implement hospital-initiated medication reviews, and uptake of these pathways has been low.

      An article published in 2022 presented barriers and enablers to hospital-initiated medication reviews, and highlighted the need for a stewardship approach to promote safe and high-quality medication management at transitions of care, with a key focus on facilitating early post-discharge medication reviews (within 10 days).20 The authors have continued to advocate for a hospital-led stewardship approach to address the perennial problem of medicines safety at transitions of care.10,21

      The recently published AdPha Standard of Practice for Pharmacy Services Specialising in Transitions of Care describes current best practice for the provision of pharmacy services that specialise in transitions of care, such as hospital outreach pharmacists and community liaison pharmacists, and supports the introduction of transitions of care stewardship programs into existing organisational clinical systems.22

      Medicines stewardship

      Stewardship in the context of health care refers to a structured program of strategies and interventions that address challenges within a specific clinical area, and ensure appropriate and efficient use of resources. Medicines stewardship programs focus on improving medicines use in areas where there is a high risk of inappropriate prescribing or adverse outcomes. Examples of successful programs include: antimicrobial, opioid analgesic, anticoagulation and psychotropic stewardship.21

      Medicines stewardship programs aim to improve medication management at individual and population levels to ensure consistent, appropriate care. At a population level, this may include developing guidelines and providing standardised processes and templates. At an individual level, it includes delivering tailored person-centred interventions to optimise medication outcomes. 

      Common elements of successful medicines stewardship programs include multidisciplinary leadership, stakeholder engagement, tailored communication strategies, behavioural changes, implementation science methodologies, and ongoing program monitoring, evaluation and reporting.21 Stewardship programs are often led or administered by a dedicated stewardship officer (usually a pharmacist) or team.21

      Medication Management at Transitions of Care Stewardship Framework

      Applying a stewardship approach to transitions of care may provide opportunities to focus organisational resources, foster multi- or interdisciplinary collaboration, and improve coordinated care when individuals transfer between care providers or settings.

      In 2023, the ACSQHC commissioned a rapid literature review and environmental scan examining Australian and international medication management strategies, including stewardship programs, at transitions of care focusing on admission to hospital and discharge to the community or residential care.23,24

      The literature review identified that, globally, there are no published studies or existing frameworks that describe a stewardship program specifically addressing medication management at transitions of care.24

      Given the evidence from the literature review and environmental scan, the ACSQHC set about developing a Medication Management at Transitions of Care Stewardship Framework (the Framework). The Framework is scheduled for release in the second quarter of 2025.

      The Framework is intended to provide healthcare organisations (hospitals) with a systematic approach for implementing coordinated medication management activities and interventions to optimise safe and high-quality transitions of care, with a focus on patients admitted to hospital and discharged to the community or residential aged care. The Framework will provide guidance that can be adapted to local context and the circumstances of individuals transitioning across care settings.

      The Framework will be supported by existing national standards and guidelines, including:

      • National Safety and Quality Health Service Standards25
      • Guiding Principles to Achieve Continuity in Medication Management8
      • National Medicines Policy 2022.26

      The ACSQHC’s principles of safe and high-quality transitions of care9 should also be considered in the local implementation of a medication management at transitions of care stewardship program.

      Leveraging digital health

      Digital health is a key enabler to achieve interoperable, accurate and timely communication between clinicians in the acute and primary care settings. The Framework will align with the National Digital Health Strategy 2023–202827 and the Strategy Delivery Roadmap.28

      Health facilities are encouraged to embed digitally enabled care to strengthen effective interdisciplinary communication and improve safe and high-quality medication management at transitions of care.29 

      Implementation of the Framework and the role of pharmacists across transitions of care

      The Framework is designed with a hospital focus, and it is intended that it will be used by hospitals to guide stewardship and coordination in collaboration with primary care practitioners.29

      General practice coordination of ongoing medical care prior to and following hospital discharge is vital, as is community pharmacist coordination of medication supply and management. Pharmacists embedded in general practice, onsite aged care pharmacists, and credentialed pharmacists providing HMRs and RMMRs, can also play an important role. However, it is not possible for general practice and primary care pharmacists to coordinate all time-critical aspects of medication management for complex hospital discharges that occur 7 days a week, and sometimes outside of business hours. In the first instance, hospitals need to take responsibility for bridging the gap by29:

      • ensuring that discharges are well planned
      • ensuring there is timely and accurate communication with primary care providers
      • providing an adequate supply of newly commenced medicines 
      • working with community-based healthcare professionals to ensure continuity of medication access
      • providing education to patients and carers, including a discharge medicines list
      • working with community-based healthcare professionals to ensure timely post-discharge medication review and follow-up as needed.
      Primary care and aged care pharmacists need to be aware of the risks associated with transitions of care and be prepared to work collaboratively with hospitals in a responsive and flexible way to ensure timely delivery of post-discharge transitions of care-related services such as medication reconciliation, medication supply and medication review.

      The authors encourage all pharmacists to engage with the Framework. It is a world-first document that will drive system improvements so Australians receive high-quality care, and is a pivotal response to the WHO’s third Global Patient Safety Challenge (Medication Without Harm) priority, transitions of care.

      Case scenario continued

      You phone the discharging hospital pharmacist (whose name was recorded on the patient’s discharge medicines list) to clarify Amra’s medicine changes and discharge medication management plan. You speak with Amra about your discussion and obtain consent to complete a MedsCheck and chat with her GP about any changes post-discharge. You go through each of her medicines and prepare her an updated medicines list. You also discuss the potential benefits of a Home Medicines Review (HMR) when there has been a hospital admission and medicine changes. You ask if she wishes for you to discuss an HMR referral with her GP which could be actioned at her upcoming GP appointment. She indicates an HMR would be welcome and thanks you for helping her.
      [cpd_submit_answer_button]

      Key points

      • A transition of care is when all or part of a person’s healthcare is transferred between care providers or care settings.
      • Preventing medication-related harm at transitions of care is a key priority in the WHO’s third Global Patient Safety Challenge (Medication Without Harm).
      • The ACSQHC has developed a Medication Management at Transitions of Care Stewardship Framework to optimise high-quality and safe medication management during transitions of care, focusing on hospital admissions and discharges to community and residential aged care.
      • Hospital and primary care pharmacists need to work collaboratively to improve the safety of transitions of care and ensure timely post-discharge medication reconciliation, medication supply and post-discharge medication review.   

      References

      1. Australian Commission on Safety and Quality in Health Care. Transitions of Care. 2024. At: www.safetyandquality.gov.au/our-work/transitions-care
      2. Redmond P, Grimes TC, McDonnell R, et al. Impact of medication reconciliation for improving transitions of care. Cochrane Database of Systematic Reviews 2018, Issue 8.
      3. Alqenae FA, Steinke D, Keers RN. Prevalence and nature of medication errors and medication-related harm following discharge from hospital to community settings: a systematic review. Drug Saf 2020;43(6):517–37.
      4. Prasad N, Lau ECY, Wojt I, et al. Prevalence of and risk factors for drug-related readmissions in older adults: a systematic review and meta-analysis. Drugs Aging 2024;41(1):1–11.
      5. World Health Organization. Medication Without Harm – Global Patient Safety Challenge on Medication Safety. Geneva: World Health Organization; 2017.
      6. Australian Commission on Safety and Quality in Health Care. Medication without harm – WHO Global Patient Safety Challenge. Australia’s response. Sydney: ACSQHC; 2020.
      7. Elliott RA, Tran T, Taylor SE, et al. Impact of a pharmacist-prepared interim residential care medication administration chart on gaps in continuity of medication management after discharge from hospital to residential care: a prospective pre- and post-intervention study (MedGap Study). BMJ Open 2012;2(3).
      8. Department of Health and Aged Care. Guiding Principles to Achieve Continuity in Medication Management. Canberra; 2022.
      9. Australian Commission on Safety and Quality in Health Care. Principles of safe and high-quality transitions of care (factsheet). 2024.
      10. Elliott RA, Angley M, Criddle DT, et al. Achieving safe medication management during transitions of care from hospital: time for a stewardship approach. Aust Prescr 2024;47(4):106–8.
      11. Elliott RA, Taylor SE, Koo SMK, et al. Accuracy of medication histories derived from an Australian cloud-based repository of prescribed and dispensed medication records. Intern Med J 2023;53:1002–9.
      12. Francis M, Francis P, Makeham M, et al. Using personal health records for medication continuity during transition of care: An observational study. Health Inf Manag 2024:18333583241270215.
      13. Wembridge P, Rashed S. Discharge summary medication list accuracy across five metropolitan hospitals: a retrospective medical record audit. Aust Health Rev 2022;46:338–45.
      14. Uzunbay Z, Elliott RA, Taylor S, et al. Accuracy of medication labels on community pharmacy-prepared dose administration aids: an observational study. Explor Res Clin Soc Pharm 2023;11:100318.
      15. Taylor S, Welch S, Harding A, et al. Accuracy of general practitioner medication histories for patients presenting to the emergency department. Aust Fam Physician 2014;43:728.
      16. Chen EY, Wang KN, Sluggett JK, et al. Process, impact and outcomes of medication review in Australian residential aged care facilities: a systematic review. Australas J Ageing 2019;38:9–25.
      17. Luetsch K, Rowett D, Twigg MJ. A realist synthesis of pharmacist-conducted medication reviews in primary care after leaving hospital: what works for whom and why? BMJ Qual Saf 2020;30(5):418–30.
      18. Criddle D, Devine B, Murray K, et al. Developing PHarmacie-R: a bedside risk prediction tool with a medicines management focus to identify risk of hospital readmission. Res Social Admin Pharm 2021;18 (7):3137–48.
      19. The Society of Hospital Pharmacists of Australia. Hospital-initiated medication reviews. Collingwood, Victoria: The Society of Hospital Pharmacists of Australia; 2020.
      20. Angley M, Criddle D, Rigby D, et al. Hospital-initiated post-discharge medication reviews in Australia: expert opinion on the barriers and enablers to implementation. J Pharm Pract Res 2022;52(6):446–53.
      21. Su E, Liew DFL, Donnelly J, et al. Medicines stewardship. Aust Prescr 2023;46(2):24–8.
      22. Advanced Pharmacy Australia Transition Care and Primary Care Specialty Practice Group. Standard of practice for pharmacy services specialising in transitions of care. J Pharm Pract Res 2024;54(5):417–35.
      23. Emadi F, Liu S, Yui C H, et al. Digital approaches that can be employed to facilitate safe medication management at transitions of care. Sydney: ACSQHC; 2024.
      24. Emadi F, Liu S, Yiu CH, et al. Medication management at transitions of care stewardship framework. Rapid literature review and environmental scan – final report. Sydney: Faculty of Medicine and Health, School of Pharmacy, University of Sydney; 2023.
      25. Australian Commission on Safety and Quality in Health Care. The National Safety and Quality Health Service (NSQHS) Standards (second edition) 2021. At: www.safetyandquality.gov.au/standards/nsqhs-standards
      26. Department of Health and Aged Care. National Medicines Policy 2022. Canberra; 2022.
      27. Australian Digital Health Agency. National Digital Health Strategy 2023-2028. Sydney; 2023.
      28. Australian Digital Health Agency. National Digital Health Strategy Delivery Roadmap 2023–2028. Sydney; 2023.
      29. Australian Commission on Safety and Quality in Health Care [DRAFT]. Medication Management at Transitions of Care Stewardship Framework. Sydney: ACSQHC; 2024.

      Our authors

      Manya Angley (she/her) BPharm, PhD, FPS, CredPharm (MMR), FAdPha is an Advanced Practice Pharmacist experienced in general practice, disability and aged care.

      Debbie Rigby (she/her) BPharm, GradDipClinPharm, FASCP, FPS, FACP, FAICD, FSHP, FANZCAP (GeriMed, Resp) is an Advanced Practice Pharmacist qualified in clinical pharmacy, geriatrics and respiratory medicine.

      Rohan Elliott (he/him) BPharm, BPharmSc(Hons), MClinPharm, PhD, FAdPhA, FANZCAP (GeriMed, Research) is an Advanced Practice Pharmacist with experience in hospitals, aged care and transitions of care.

      Our reviewer

      Elizabeth Manias (she/her) RN, BPharm, MPharm, MNStud, PhD, FANZCAP (Transitions of care, Geriatric Medicine)

      Conflict of interest declaration

      Manya Angley, Debbie Rigby and Rohan Elliott are co-investigators on a Medical Research Future Fund (MRFF) 2022 transitions of care project. MRFF is funded by the Australian Government. They are also co-authors of a literature review of transitions of care stewardship that was funded by the ACSQHC.

      Elizabeth Manias is a member of the Transitions of Care and Primary Care Leadership Committee of Advanced Pharmacy Australia.

      [post_title] => Improving medicines safety at transitions of care [post_excerpt] => Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => improving-medicines-safety-at-transitions-of-care [to_ping] => [pinged] => [post_modified] => 2025-05-14 13:04:04 [post_modified_gmt] => 2025-05-14 03:04:04 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29045 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Improving medicines safety at transitions of care [title] => Improving medicines safety at transitions of care [href] => https://www.australianpharmacist.com.au/improving-medicines-safety-at-transitions-of-care/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( [td_post_template] => single_template_4 ) [is_review:protected] => [post_thumb_id:protected] => 29343 [authorType] => )

      Improving medicines safety at transitions of care

      medicine storage
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                  [post_content] => Both Cautionary Advisory Label (CAL) 6 and CAL 13 have been overhauled to sharpen storage advice.
      
      CAL 6 explanatory notes advice in Digital Australian Pharmaceutical Formulary and Handbook (APF) now mentions considerations for room-temperature time windows for refrigerated medicines, while CAL 13’s tightened wording and advice flags truly sensitive formulations – ensuring pharmacists give patients clearer, more precise guidance.
      

      What’s changing?

      The familiar ‘Refrigerate, do not freeze’ warning of CAL 6 is not changing, however its explanatory notes have been expanded.  [caption id="attachment_29335" align="aligncenter" width="180"]CAL 6 CAL 6[/caption] There are many instances whereby refrigeration of temperature sensitive medicines may not be practical, for example travel days, power outages or ‘in-use’ multi-dose containers/devices. The updated explanatory notes advise pharmacists that they should refer to the medicines approved product information (PI) and counsel their patients on how to best store these medicines – covering when their temperature sensitive medicines may safely remain at room temperature (below 25 °C) – if applicable. [caption id="attachment_29336" align="aligncenter" width="176"] The old CAL 13[/caption] [caption id="attachment_29337" align="aligncenter" width="189"] The new CAL 13[/caption] Meanwhile, CAL 13 has been reworded. Previously ‘Do not remove from original packaging until dose required’, the new prompt, ‘Ask your pharmacist about the storage conditions for this medicine,’ applies only to dosage forms and active ingredients truly sensitive to light, moisture or temperature excursions.  This includes orally disintegrating tablets, effervescents, sublingual or buccal lozenges, dispersible granules, wafers and chewables, as well as amoxicillin/clavulanic acid, dabigatran, glyceryl trinitrate, nicorandil, nifedipine, phenothiazines, tamoxifen and sodium valproate. CAL 13 may also be applied in addition to other CALs relating to storage requirements (e.g. CALs 6, 7a or 7b) when complex storage instructions are applicable, and these other CALs do not adequately cover these. To support the change to CAL 13, the APF’s Good dispensing practice chapter has been updated with clearer and expanded guidance on providing advice to patients on how to store medicines, including that:
      • all medicines should be kept out of sight and out of reach of children at all times
      • unless specifically requiring refrigeration, and in the absence of special storage instructions outlined in the PI/consumer medicine information (CMI), medicines should be stored in their original packaging in a cool (preferably <25 °C), dry and secure place
      • medicines should generally not be removed from their original packaging until a dose is required – pharmacists should check how the patient intends to store their medicines (e.g. in a dosette box) and provide advice according to the storage instructions outlined in each medicines PI/CMI.
      CAL 13’s explanatory notes have also been updated in APF Digital to support pharmacists in applying the revised CAL. When packing medicines into Dose Administration Aids (DAAs) pharmacists should consider the approved PI of each medicine, and PSA’s Guidelines for pharmacists providing dose administration aid services.

      What led to this update?

      Medicine labels have traditionally relied on simple fridge-or-no-fridge advice. But today’s PIs are more complex.  Humira (adalimumab) is one good example. People using Humira are advised that they can store single pre-filled syringes or pens ‘below 25°C (room temperature) for a maximum period of 14 days, but must be protected from light. Once removed from the refrigerator for room temperature storage, the syringe must be used within 14 days or discarded, even if it is returned to the refrigerator’.  But CAL 6 doesn’t capture these nuances, so some patients are left guessing whether their medicines are safe to use or not during travel or at times when refrigeration is not available. The new explanatory notes prompt pharmacists to cover these scenarios as part of their routine counselling to promote safe and quality use of medicines. At the same time, the CAL 13 had become so ubiquitous – applicable to nearly all medicines – that its impact was diluted. What's more, most pharmacies didn’t even stock the printed sticker.  By narrowing its application, CAL 13’s power to prompt meaningful conversations about stability risks has been restored. Above all, when medicines are removed from their original packaging inappropriately, or stored incorrectly, this can translate into reduced potency or patient harm. These refinements give pharmacists clear, evidence-based cues to maintain medicine stability and efficacy. 

      How should pharmacists tailor storage advice?

      Pharmacists should personalise both verbal and written advice to the patient. Ensure every patient is counselled on how to best store their medicines including routinely asking how the patient plans to keep their medicines, for example will they use a dosette box? Is storage at an appropriate temperature an issue? If a medicine carries Label 6 but its PI indicates there is an appropriate room-temperature window, demonstrate the correct use of an insulated bag and explain the difference between ‘keep at 2–8 °C’ and ‘store below 25 °C’. Provide guidance on room temperature storage for their in-use multi dose container/device (if appropriate) and for times when refrigeration is unavailable or impractical. Pharmacists should also advise the patient to avoid storing medicines in the areas of a domestic refrigerator that may not maintain a temperature of 2–8 °C. This includes the door, top shelf or crisper; or within 40 mm of the back and sides of the main compartment. For CAL-13 affixed medicines, pharmacists should advise patients that these medications’ stability is protected by the original container and packaging, and that removing them prematurely can accelerate degradation and reduce efficacy. Work with the patient to address any barriers to this.

      What’s the implementation timeline?

      The revised explanatory notes for CAL 6 and CAL 13 are live in APF Digital as of 7 May 2025.  CAL printers will begin issuing the new CAL 13 labels on their next run. Until then, pharmacists should continue using the existing labels while equipping patients with the updated counselling points and advice outlined in the APF Digital.

      How should pharmacists put the new advice into practice?

      Let’s say Mrs L, 68, who has type 2 diabetes, atrial fibrillation and hypertension, presents to a pharmacy for her medicines. She picks up a prescription for insulin glargine pens, nifedipine and dabigatran. For her insulin glargine, you apply Label 6 and explain the medicine must be stored at 2–8 °C in the fridge’s main compartment, yet the in-use pen may remain at room temperature for up to 28 days. You provide her with an insulated bag and demonstrate how to use it. You then recognise that nifedipine is sensitive to light and dabigatran is moisture-sensitive, and apply Label 13 to each medicine’s packaging which prompts a PI check. You advise her to keep the medicines away from humid spots such as bathrooms or kitchen windowsills, and to keep them in their original packaging, out of direct light. Mrs L leaves confident in where to store each medicine, and you’ve pre-emptively safeguarded stability and efficacy. [post_title] => New CAL medicine storage guidance [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => new-cal-medicine-storage-guidance [to_ping] => [pinged] => [post_modified] => 2025-05-12 16:02:09 [post_modified_gmt] => 2025-05-12 06:02:09 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29331 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => New CAL medicine storage guidance [title] => New CAL medicine storage guidance [href] => https://www.australianpharmacist.com.au/new-cal-medicine-storage-guidance/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29332 [authorType] => )

      New CAL medicine storage guidance

  • People
    • risperidone
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                  [post_content] => The Therapeutic Goods Administration (TGA) has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18.
      
      In 2024 alone, 22 adverse events as a result of overdose of risperidone oral solution were reported to the TGA – most cases involved accidental administration of 10 times the prescribed dose (for example, 5 mL instead of 0.5 mL). 
      
      Although no deaths were recorded, adverse effects led to hospitalisations in most cases.
      

      Why are dosing errors occurring?

      An investigation by the TGA unearthed several drivers for dosing errors of risperidone oral solution including:
      • misinterpreting dosing instructions
      • incorrect use of the dosing syringe
      • medicine administration by non-primary caregivers (e.g. babysitters or other relatives).
      And the TGA is not the only national health agency to raise concerns about risperidone dosing confusion. The Spanish Agency for Medicines and Health Products issued a public alert after discovering that paediatric caregivers misread decimal points when administering a dose of 1 mg/mL risperidone solution, often inadvertently giving ten times the intended dose. Most (74%) of these incidents were serious, with children suffering sedation, hypotension, tachycardia, extrapyramidal symptoms, QT prolongation and, in some cases, seizures. In Ireland, the Health Products Regulatory Authority echoed these concerns, reporting ten‐fold overdoses in children aged 3–15 –  urging prescribers and pharmacists to provide clear dosing-device instructions and educate caregivers on recognising and responding to overdose symptoms.

      What’s changing?

      To address the identified risk, the Product Information (PI) and Consumer Medicines Information (CMI) for Risperdal have been revised, and generic manufacturers are now required to update PIs and CMIs to mirror these changes. The new versions for Risperdal include more detailed dosing guidance and illustrative diagrams to support accurate administration including:
      • use the supplied pipette only: do not substitute with another measuring device
      • open the child-resistant cap: push down on the plastic screw cap and turn counter-clockwise, then lift off
      • insert and draw up dose: place the pipette in the bottle; hold the bottom ring and pull up the top ring to the mark matching the prescribed dose (e.g. 0.25 mL for 0.25 mg, 0.5 mL for 0.5 mg)
      • dose equivalence: 1 mL of Risperdal solution = 1 mg risperidone; graduations on the plunger are in 0.25 mL (0.25 mg) increments
      • administer in a drink: remove the pipette, slide the top ring down to expel the dose into a non-alcoholic beverage (e.g. water, juice, milk, coffee – avoid tea)
      • after use: close the bottle; rinse the pipette with cold water, let it air dry in its case; avoid detergents or vigorous wiping to preserve the printed graduations.
      While each generic product should cover the same key details, the syringe and instructions can vary by brand. So pharmacists are advised to always double-check the individual PIs.

      What do pharmacists need to do?

      Dosing instructions need to be clearly printed on the label. According to the Australian Commission on Safety and Quality in Health Care’s National standard for labelling dispensed medicines (Standard 6), label wording  should:
      • have digits for dosage amounts (e.g. ‘Take 1 tablet,’ not ‘Take one tablet’ or ‘Take ONE tablet’)
      • express dose ranges with words between numbers (e.g. ‘1 to 2,’ not ‘1-2’ which could be read as ‘12’)
      • spell out common fractions to avoid confusion (e.g. ‘quarter,’ not ‘0.25’ or ‘¼’)
      • for small paediatric liquid doses, match the numbers on the oral dispenser (e.g. ‘0.5 mL’).
      Presenting numbers as digits generally improves clarity among patients. However, fractions written symbolically (e.g. ½’) may be misread as ‘1 or 2’ and decimal points can be overlooked (e.g. ‘1.5’ read as ‘15’). That’s why, when counselling patients prescribed risperidone oral solution, pharmacists should:
      • verify that all caregivers understand the prescribed dosing regimen
      • demonstrate precisely how to measure the required volume using the provided oral syringe
      • instruct caregivers to review the dosing label before each administration and confirm their understanding, especially with those administering the medicine for the first time.
      [post_title] => Paediatric risperidone errors prompt TGA safety update [post_excerpt] => The TGA has tightened dosing advice for the antipsychotic risperidone after an alarming number of overdoses occurred in patients under 18. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => paediatric-risperidone-errors-prompt-tga-safety-update [to_ping] => [pinged] => [post_modified] => 2025-05-21 15:02:24 [post_modified_gmt] => 2025-05-21 05:02:24 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29429 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Paediatric risperidone errors prompt TGA safety update [title] => Paediatric risperidone errors prompt TGA safety update [href] => https://www.australianpharmacist.com.au/paediatric-risperidone-errors-prompt-tga-safety-update/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29433 [authorType] => )

      Paediatric risperidone errors prompt TGA safety update

      interruptions
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                  [post_content] => New research has found that pharmacists are interrupted at alarming rates when dispensing medicines.
      
      Led by Monash University’s Faculty of Pharmacy and Pharmaceutical Sciences, the study aimed to review existing evidence on how interruptions and distractions in pharmacy practice influence the occurrence of dispensing errors.
      
      [caption id="attachment_29414" align="alignright" width="260"] Dan Malone MPS[/caption]
      
      The review, which analysed 51 Australian and international studies, found that pharmacists can experience interruptions and distractions more than 20 times per hour.
      
      Phone calls were the biggest disruptor, said co-author Associate/Professor Dan Malone MPS, Course Director of the Undergraduate Pharmacy Degree.
      
      ‘For example, where a pharmacist would be dispensing or talking to someone, and either the phone was ringing or they would be interrupted by a colleague who said there was a phone call for the pharmacist,’ he said.
      
      Other key disruptors during dispensing included:
      • consumers interrupting pharmacists to ask a question
      • interruptions and distractions from pharmacy staff who needed to manage customer queries that were out of their scope.

      What are the impacts of interruptions?

      While most studies included in the review identified what the interruptions were and how frequently they occurred, few looked at the impact of interruptions and strategies to mitigate them. But of those that did, medication errors were the most serious issue identified. ‘While no medication error should occur, some are relatively minor whereas others are potentially fatal,’ A/Prof Malone said. Other identified impacts included: 
      • taking longer to dispense a script
      • poorer performance 
      • mental fatigue.

      What about self-interruptions?

      It’s not always external interruptions that are the culprits. Sometimes, it’s the pharmacists themselves who self-interrupt, the review team found. ‘They might be working on a particular task, then start searching the internet on an unrelated topic,’ A/Prof Malone said. ‘Or talk to their colleague while dispensing – initiating an interruption themselves.’  The term that's often used for this phenomenon is ‘multi-tasking’. But A/Prof Malone said it’s more akin to task-switching. ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,’ he said.

      What are the key intervention strategies?

      Should pharmacists be better trained to deal with inevitable interruptions, or should pharmacy teams try to reduce those interruptions in practice?  A bit of both, A/Prof Malone thinks. ‘Our pharmacy students do a lot of practice in terms of role playing the pharmacist in a workshop, for example,’ he said. ‘But when they go out on placement, they often complain that “it's really noisy, there's all these distractions and it’s hard to concentrate”,’ he said. 
      ‘There's a lot of evidence that suggests jumping from one task to another is not an efficient way to work, and it's also more likely to introduce errors into the process,.' DAN MALONE MPS 
      Better preparing students for that environment by stimulating situations where interruptions occur should help them to cope with future interruptions, A/Prof Mr Malone said. And while interruptions can’t be eliminated completely, systems can be put in place to reduce them, including:
      • having a set time where the pharmacist can't be interrupted
      • making sure there's workflow processes to ensure the pharmacist is less likely to be interrupted.
      ‘For example, when a prescription is dispensed, having a process whereby communication is such that the pharmacist is able to focus on the dispensing process,’ A/Prof Malone said. ‘When another prescription comes in, unless it's urgent, the pharmacist isn't interrupted – so they can go through the dispensing process with one prescription before they start the next.’ Or it might just be a matter of staffing. ‘Where possible, having two pharmacists on, with one focusing on tasks such as patient queries – limiting direct access to the other pharmacist during dispensing time,’ he said. However, in practice this isn’t always possible. When more urgent matters arise – as they inevitably do – pharmacists often have to park what they’re doing and switch tasks.  ‘That's understandable, but it’s preferable to minimise these occurrences, if possible,’ A/Prof Malone said.

      What about training other staff?

      There’s a ‘huge benefit’ in having well-trained pharmacy assistants on staff to reduce interruptions, and therefore errors, A/Prof Malone said. ‘I've worked with a lot of really experienced pharmacy assistants who know a lot about disease states, and are able to handle queries that come in and field questions over the phone without necessarily having to speak with the pharmacist,’ he said. But there are limitations to this approach, including making recommendations about Schedule 3 medicines. ‘This requires the pharmacist to be interrupted,’ A/Prof Malone added. PSA’s Pharmacists in 2030 recommends recognising and formalising the role of pharmacy assistants as well as technicians by establishing clear development pathways, such as:
      • registering support technicians to perform final-checking duties
      • embedding Certificate II, III and IV dispensary technician qualifications into practice to free pharmacists for direct patient care.
      To safeguard pharmacist wellbeing and minimise medicine errors, Pharmacists in 2030  advocates for:
      • enforcing safe-dispensing limits through patient-to-pharmacist ratios
      • building mandatory rest breaks into rosters
      • providing Employee Assistance Programs 
      • redesigning workspaces to enhance comfort and support mental health.

      What’s next on the horizon?

      The paper, led by pharmacist and PhD student Meaza Ayanaw, is a scoping review that’s paving the way for further research into how interruptions and distractions affect pharmacists’ decision-making ability, and how pharmacists prioritise different tasks.  ‘For example, should pharmacists switch tasks when they're in a pharmacy environment? If so, when should they switch? And what are the high- and low-priority tasks that require pharmacists to switch?’ A/Prof Malone said. From the results of the findings, more assessments and training will be developed using simulations such as Monash’s MyDispense. ‘This will help students to prepare for [pharmacy practice] by reflecting on real-world interruptions and distractions in a simulated environment. So that when they make mistakes, there's no consequence associated,’ A/Prof Malone said. For more information on streaming workflows and operations, don’t miss the poster presentation ‘Optimising pharmacy operations’ at PSA25, from 1–3 August 2025. Register here to attend. [post_title] => High interruption rates threaten patient safety [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => high-interruption-rates-threaten-patient-safety [to_ping] => [pinged] => [post_modified] => 2025-05-19 15:45:44 [post_modified_gmt] => 2025-05-19 05:45:44 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29407 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => High interruption rates threaten patient safety [title] => High interruption rates threaten patient safety [href] => https://www.australianpharmacist.com.au/high-interruption-rates-threaten-patient-safety/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29408 [authorType] => )

      High interruption rates threaten patient safety

      palliative care
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                  [post_content] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that. 
      
      It can be difficult to tell from a prescription that a patient is receiving palliative care, said Tanya Maloney MPS, a community pharmacist in Coffs Harbour, NSW.
      
      [caption id="attachment_29354" align="alignright" width="233"] Tanya Maloney MPS[/caption]
      
      ‘What we lack in pharmacy is training on how to approach those difficult conversations in the right way so we can ask them a few questions to determine that,’ she said. ‘We're often a bit nervous about saying the wrong thing.’
      
      Though passionate about palliative care, Ms Maloney and her team have had to learn on the job.
      
      ‘We haven’t had any extra training and want to know how we can contribute more.’
      
      This is a common issue through the profession, with a lack in palliative care education tailored specifically to pharmacists, leading to a knowledge gap, said PSA Senior Pharmacist (Consulting and Program Delivery) Megan Tremlett MPS – who has managed a number of palliative care projects through Primary Health Networks and at a state level in recent years.
      
      ‘As pharmacists, we don't learn a lot about palliative care in our undergraduate course. And the majority of pharmacists haven't done any extra palliative care education since their university days.’
      
      To address this, PSA launched the ASPIRE Palliative Care Foundation Training Program on 13 May. The free, CPD-accredited course – supported by Palliative Care Australia and funded under the National Palliative Care Grants Program – upskills pharmacists regardless of practice setting.
      
      ‘The training program has been created with extensive stakeholder consultation to provide pharmacists with a thorough introduction to palliative care across the eight modules’ Ms Tremlett said.
      
      Rather than training pharmacists to specialise in palliative care, the training program is intended to lift the baseline knowledge of the profession, said Leah Robinson, Project Manager at PSA, who worked on the development of the program with Ms Tremlett.
      
      ‘It’s about understanding the different settings and phases of palliative care and at which points pharmacists can provide practical support to help families, patients and healthcare professionals in supporting palliative care.’
      
      A foundational understanding of palliative and end-of-life care across the health workforce is essential to meeting community needs, said Camilla Rowland, CEO of Palliative Care Australia.
      
      ‘Supporting people to live, and die well, means building palliative care capability across the entire health system. That includes pharmacists, often among the first healthcare professional patients and carers turn to for advice.’
      

      Learning about symptom management

      The ASPIRE training program has a module dedicated to symptoms and the trajectory of people living with life-limiting illness. Under a subsequent symptom management module, pharmacists can access resources and references for pharmacological management of the symptoms associated with dying that covers:
      • Pharmaceutical Benefits Scheme (PBS) and non-PBS medicines 
      • Special Access Scheme medications
      • Medicines used off-label.
      Experts, from pharmacists to prescribers, guide learners on handling sensitive conversations with patients and families – linking to Safer Care Victoria resources for monitoring and managing adverse effects, especially with continuous subcutaneous infusions.
      ‘We point pharmacists to a range of resources to support them with understanding medicines compatibilities in subcutaneous infusion devices and the adverse effects that might be expected,’ Ms Tremlett said. As illness progresses, medication regimens often grow more complex. ‘Pharmacists need to be able to step in and make recommendations around those [medicines] that could potentially be weaned or stopped to reduce that burden and the chance of side effects and interactions,’ Ms Tremlett said. The training program also helps pharmacists with information, tools and resources for conversions of medicines and different formulations, including switching from some or all of their opioids, to a replacement opioid delivered by another route, Ms Robinson said.  ‘It’s also [around] practical things pharmacists can offer such as providing a list of current medicines, home medication review, staged supply, support with prescription management, home delivery or flexibility around dose administration aids to help manage those medicines and the complexity of the changes they go through during the different phases of palliative care,’ Ms Robinson said.

      Developing interdisciplinary care skills

      At the moment, Ms Maloney feels as though community pharmacy is a missing piece in palliative care that’s uncertain where it fits. ‘We want to be able to fit into that wider team of their health carers so we can look at the holistic care and goals of the person and provide them with more than just medication,’ she said.
      ASPIRE emphasises collaboration with GPs, specialist palliative care teams, community nurses, paramedics and residential aged care staff. ‘In the module that's dedicated to interdisciplinary palliative care, pharmacists learn the broad range of people who are involved in palliative care, and some they might not expect – from death doulas to chaplains, music therapists and diversional therapists,’ Ms Tremlett said.

      Focusing on patient-centred care

      Once pharmacists identify a palliative care patient, they need knowledge and skills to determine how best to help at each stage, Ms Maloney said. ‘How do we know how to help them in all these different stages that they're going to go through?’ Pharmacists may think they know what’s best for a patient based on their clinical background, Ms Tremlett said. ‘But at the end of the day, what's important to the person or the patient is the single most important thing.’ ‘ASPIRE reminds pharmacists to be mindful of their own biases to meet the person where they are and help them achieve their goals of care, which might change over time as their condition progresses,’ Ms Robinson added. The patient-centred care module also highlights Australia’s cultural diversity – including First Nations peoples, migrants and those from non-English speaking backgrounds. ‘There is no such thing as a consistent cultural need in palliative care,’ Ms Tremlett said. ‘It's very different within cultures, between cultures and within communities, so pharmacists need to be able to adapt the care and services they provide without making assumptions.’ The need for translation services, what’s deemed an inappropriate conversation or who is the next of kin or carer can vary from person to person, Ms Robinson said. ‘It’s important to be mindful of how and what to communicate to align with those goals of care.’

      Helping families through grief and bereavement

      Being confident talking about death is something many pharmacists struggle with, Ms Maloney said. ‘You might prompt them a little bit, and they do get upset, and that’s often what puts us off,’ she said. ‘But it’s not necessarily a bad thing as they’re getting to open up and talk to you.’ The final ASPIRE module on grief, bereavement and self-care aims to normalise conversations about death and dying. Being comfortable enough to embed those conversations in day-to-day practice – including supporting people after their loved one has died – is crucial, Ms Tremlett said. ‘It's really important for pharmacists to be prepared to still speak about the person who's died, if that's what the person wants to do, and to recognise that grieving is very normal, and there's no right or wrong way to grieve.’ Pharmacists also need to be able to recognise prolonged grief and know when referrals  for extra support are needed. ‘If the pharmacist has the knowledge and skills to refer that person on for some extra help in the grieving process, that's really impactful,’ she said. Throughout the palliative care process, it’s crucial for pharmacists to look after themselves and to know when to check in on their colleagues too. ‘When we're constantly supporting people who are unwell … it's very natural for pharmacists to feel a burden of care,’ Ms Tremlett said. ‘Learning to recognise when you or your colleagues might be feeling a little overwhelmed, need extra support or to engage in self-care activities is really important.

      Embedding the training into practice

      Now that the ASPIRE training program is available, Ms Maloney wants all her pharmacists to complete it to lift their confidence and knowledge in palliative care. ‘As part of that, there's all the resources you can print out and revisit,’ she said. ‘They will be active documents that become part of our internal processes rather than training you just do and forget.’ The experience  of supporting palliative care patients also builds trust and loyalty among family members and carers. ‘You get to know them on a different level and see them when they're vulnerable,’ Ms Maloney said. ‘That rapport you can build up in that time by being there for them definitely builds that lifetime customer for the future.’ [post_title] => Bridging the palliative care education gap for pharmacists [post_excerpt] => Dedicated palliative care training for pharmacists is not commonplace. This PSA-developed course aims to change that.  [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => bridging-the-palliative-care-education-gap-for-pharmacists [to_ping] => [pinged] => [post_modified] => 2025-05-14 16:27:55 [post_modified_gmt] => 2025-05-14 06:27:55 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29352 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Bridging the palliative care education gap for pharmacists [title] => Bridging the palliative care education gap for pharmacists [href] => https://www.australianpharmacist.com.au/bridging-the-palliative-care-education-gap-for-pharmacists/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29358 [authorType] => )

      Bridging the palliative care education gap for pharmacists

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      Case scenario

      Amra, 80 years old and a regular patient of yours, has been discharged from hospital after an admission for a fall. She presents at the pharmacy with a bag of medicines and hands you a discharge medicines list. She appears to have been initiated on some new medicines in hospital and expresses confusion on which of her pre-hospital medicines to continue. You view her dispense history and My Health Record and notice discrepancies. It is unclear to you or Amra why some medicines have been initiated. She has an appointment with her GP in a couple of days.

      Learning objectives

      After reading this article, pharmacists should be able to:
      • Define transitions of care
      • Discuss medicines safety during transitions of care
      • Explain principles of safe and high-quality transitions of care
      • Discuss the role of the pharmacist across transitions of care.
      Competency standards (2016) addressed: 1.1, 1.4, 1.5, 2.2, 3.5 Accreditation number: CAP2505SYPMA Accreditation expiry: 31/04/2028
      Already read the CPD in the journal? Scroll to the bottom to SUBMIT ANSWERS.

      Medicines safety during transitions of care

      The Australian Commission on Safety and Quality in Health Care (ACSQHC) defines transitions of care as the period when all or part of a person’s healthcare is transferred between care providers or care settings.1

      Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. When medicines safety is not prioritised at transitions of care, the risk of adverse events is increased, such as readmission to hospital and adverse drug reactions.  A Cochrane review found that more than 50% of patients experience a medication error during transitions of care.2  A systematic review found that following hospital discharge to the community, 53% of adult patients experience at least one medication error, 50% experience one or more unintentional medication discrepancies (a subset of medication errors), and 19% experience one or more adverse drug events.3 A systematic review and meta-analysis found the prevalence of medication-related readmissions and adverse drug reaction-related readmissions in older people were 9% and 6%, respectively, with about one-fifth of these preventable.4

      Preventing medication-related harm at transitions of care is a key priority in the World Health Organization’s (WHO) third Global Patient Safety Challenge (Medication Without Harm).5 The ACSQHC’s response to the Challenge, published in 2020, described prioritising medication reconciliation at all transitions of care to reduce the risk of medication errors.6 Its response also recommended the use of My Health Record to engage patients and carers in curation and communication of medication regimen information.

      The ACSQHC’s response focused on transitions from hospital, a period known to be particularly high risk, and also recommended standardising the presentation of discharge summaries.6 For people with complex care needs, initiatives to reduce preventable medication-related readmissions were encouraged, such as early post-discharge medication reviews (hospital outreach or primary care led), and cross-sector case conferencing.6 Refinement of risk criteria or indicators was recommended to direct interventions towards patients at the greatest risk of medication-related harm.6

      The ACSQHC’s response did not specifically address other known contributors to medication-related harm during transitions of care, such as ensuring timely access to medicines and the tools that are sometimes required to use them, such as interim medication administration charts when discharged to residential care, dose administration aids, and adequate quantities of medicines supply.7,8

      Principles of safe and high-quality transitions of care

      The ACSQHC has recently published a set of principles to guide safe and high-quality transitions of care that highlight the need for multidisciplinary collaboration and coordination that relies on shared responsibility and accountability.9 The consistent application of these principles within practice, standards, policy and guidance are fundamental for safe transitions of care and apply to transitions of care wherever healthcare is received including primary, community, acute, subacute, aged and disability care.9

      The principles and their enablers are shown in Table 1.

      Australia’s priority actions to address medicines safety at transitions of care

      Progress toward Australia’s priority actions to address medicines safety at transitions of care has been mixed.10 Embedding medication reconciliation at admission and discharge from hospital has advanced and is now part of medicines safety standards that hospitals need to meet for accreditation.

      My Health Record has improved access to patients’ medication histories; however, patient engagement remains low, and, like all medication records, verification of data with the patient and other sources is required.11,12 Implementation of the Pharmacist Shared Medicines List (a verified medication history that can be uploaded to My Health Record) has been limited. Discharge summaries continue to have deficiencies, including inaccurate medicine lists and inadequate explanations of medicine changes.13 Primary care medicine lists and dose administration aid medicine labels, which are often used by hospital doctors to chart medicines on admission, are also frequently inaccurate.14,15

      Australian research highlights concerns about lack of awareness and uptake of post-discharge Home Medicines Reviews (HMRs) and Residential Medication Management Reviews (RMMRs) and the complexity in facilitating timely post-discharge medication reviews.16,17 Hospital outreach pharmacist medication review services and cross-sector multidisciplinary case conferencing are uncommon. There has been progress in developing validated criteria to identify patients at risk of medication-related readmission,18 though more work is needed to ensure generalisability and implementation.10

      Progress towards ensuring timely access to medicines following hospital discharge has been mixed.10 Reforms to enable medicines to be supplied by hospitals using the Pharmaceutical Benefits Scheme, and implementation of interim medication administration charts for patients discharged to residential care, have not occurred in all jurisdictions.

      Drivers for a stewardship approach to improve medicines safety at transitions of care

      In 2020, after decades of advocacy, Commonwealth-funded medication review program rules changed to allow hospital-based medical specialists to refer patients to credentialed pharmacists for collaborative post-discharge medication management reviews. In response, the Society of Hospital Pharmacists (now known as Advanced Pharmacy Australia [AdPha]) published a Hospital Pharmacy Practice Update, Hospital-Initiated Medication Reviews, which detailed information about pathways for patients to have post-discharge HMRs, RMMRs and Hospital Outreach Medication Reviews, as well as flagging MedsChecks as a medication reconciliation pathway.19 Unfortunately, resources were not provided by the Commonwealth or state health departments for promotion, training or implementation support for hospitals to implement hospital-initiated medication reviews, and uptake of these pathways has been low.

      An article published in 2022 presented barriers and enablers to hospital-initiated medication reviews, and highlighted the need for a stewardship approach to promote safe and high-quality medication management at transitions of care, with a key focus on facilitating early post-discharge medication reviews (within 10 days).20 The authors have continued to advocate for a hospital-led stewardship approach to address the perennial problem of medicines safety at transitions of care.10,21

      The recently published AdPha Standard of Practice for Pharmacy Services Specialising in Transitions of Care describes current best practice for the provision of pharmacy services that specialise in transitions of care, such as hospital outreach pharmacists and community liaison pharmacists, and supports the introduction of transitions of care stewardship programs into existing organisational clinical systems.22

      Medicines stewardship

      Stewardship in the context of health care refers to a structured program of strategies and interventions that address challenges within a specific clinical area, and ensure appropriate and efficient use of resources. Medicines stewardship programs focus on improving medicines use in areas where there is a high risk of inappropriate prescribing or adverse outcomes. Examples of successful programs include: antimicrobial, opioid analgesic, anticoagulation and psychotropic stewardship.21

      Medicines stewardship programs aim to improve medication management at individual and population levels to ensure consistent, appropriate care. At a population level, this may include developing guidelines and providing standardised processes and templates. At an individual level, it includes delivering tailored person-centred interventions to optimise medication outcomes. 

      Common elements of successful medicines stewardship programs include multidisciplinary leadership, stakeholder engagement, tailored communication strategies, behavioural changes, implementation science methodologies, and ongoing program monitoring, evaluation and reporting.21 Stewardship programs are often led or administered by a dedicated stewardship officer (usually a pharmacist) or team.21

      Medication Management at Transitions of Care Stewardship Framework

      Applying a stewardship approach to transitions of care may provide opportunities to focus organisational resources, foster multi- or interdisciplinary collaboration, and improve coordinated care when individuals transfer between care providers or settings.

      In 2023, the ACSQHC commissioned a rapid literature review and environmental scan examining Australian and international medication management strategies, including stewardship programs, at transitions of care focusing on admission to hospital and discharge to the community or residential care.23,24

      The literature review identified that, globally, there are no published studies or existing frameworks that describe a stewardship program specifically addressing medication management at transitions of care.24

      Given the evidence from the literature review and environmental scan, the ACSQHC set about developing a Medication Management at Transitions of Care Stewardship Framework (the Framework). The Framework is scheduled for release in the second quarter of 2025.

      The Framework is intended to provide healthcare organisations (hospitals) with a systematic approach for implementing coordinated medication management activities and interventions to optimise safe and high-quality transitions of care, with a focus on patients admitted to hospital and discharged to the community or residential aged care. The Framework will provide guidance that can be adapted to local context and the circumstances of individuals transitioning across care settings.

      The Framework will be supported by existing national standards and guidelines, including:

      • National Safety and Quality Health Service Standards25
      • Guiding Principles to Achieve Continuity in Medication Management8
      • National Medicines Policy 2022.26

      The ACSQHC’s principles of safe and high-quality transitions of care9 should also be considered in the local implementation of a medication management at transitions of care stewardship program.

      Leveraging digital health

      Digital health is a key enabler to achieve interoperable, accurate and timely communication between clinicians in the acute and primary care settings. The Framework will align with the National Digital Health Strategy 2023–202827 and the Strategy Delivery Roadmap.28

      Health facilities are encouraged to embed digitally enabled care to strengthen effective interdisciplinary communication and improve safe and high-quality medication management at transitions of care.29 

      Implementation of the Framework and the role of pharmacists across transitions of care

      The Framework is designed with a hospital focus, and it is intended that it will be used by hospitals to guide stewardship and coordination in collaboration with primary care practitioners.29

      General practice coordination of ongoing medical care prior to and following hospital discharge is vital, as is community pharmacist coordination of medication supply and management. Pharmacists embedded in general practice, onsite aged care pharmacists, and credentialed pharmacists providing HMRs and RMMRs, can also play an important role. However, it is not possible for general practice and primary care pharmacists to coordinate all time-critical aspects of medication management for complex hospital discharges that occur 7 days a week, and sometimes outside of business hours. In the first instance, hospitals need to take responsibility for bridging the gap by29:

      • ensuring that discharges are well planned
      • ensuring there is timely and accurate communication with primary care providers
      • providing an adequate supply of newly commenced medicines 
      • working with community-based healthcare professionals to ensure continuity of medication access
      • providing education to patients and carers, including a discharge medicines list
      • working with community-based healthcare professionals to ensure timely post-discharge medication review and follow-up as needed.
      Primary care and aged care pharmacists need to be aware of the risks associated with transitions of care and be prepared to work collaboratively with hospitals in a responsive and flexible way to ensure timely delivery of post-discharge transitions of care-related services such as medication reconciliation, medication supply and medication review.

      The authors encourage all pharmacists to engage with the Framework. It is a world-first document that will drive system improvements so Australians receive high-quality care, and is a pivotal response to the WHO’s third Global Patient Safety Challenge (Medication Without Harm) priority, transitions of care.

      Case scenario continued

      You phone the discharging hospital pharmacist (whose name was recorded on the patient’s discharge medicines list) to clarify Amra’s medicine changes and discharge medication management plan. You speak with Amra about your discussion and obtain consent to complete a MedsCheck and chat with her GP about any changes post-discharge. You go through each of her medicines and prepare her an updated medicines list. You also discuss the potential benefits of a Home Medicines Review (HMR) when there has been a hospital admission and medicine changes. You ask if she wishes for you to discuss an HMR referral with her GP which could be actioned at her upcoming GP appointment. She indicates an HMR would be welcome and thanks you for helping her.
      [cpd_submit_answer_button]

      Key points

      • A transition of care is when all or part of a person’s healthcare is transferred between care providers or care settings.
      • Preventing medication-related harm at transitions of care is a key priority in the WHO’s third Global Patient Safety Challenge (Medication Without Harm).
      • The ACSQHC has developed a Medication Management at Transitions of Care Stewardship Framework to optimise high-quality and safe medication management during transitions of care, focusing on hospital admissions and discharges to community and residential aged care.
      • Hospital and primary care pharmacists need to work collaboratively to improve the safety of transitions of care and ensure timely post-discharge medication reconciliation, medication supply and post-discharge medication review.   

      References

      1. Australian Commission on Safety and Quality in Health Care. Transitions of Care. 2024. At: www.safetyandquality.gov.au/our-work/transitions-care
      2. Redmond P, Grimes TC, McDonnell R, et al. Impact of medication reconciliation for improving transitions of care. Cochrane Database of Systematic Reviews 2018, Issue 8.
      3. Alqenae FA, Steinke D, Keers RN. Prevalence and nature of medication errors and medication-related harm following discharge from hospital to community settings: a systematic review. Drug Saf 2020;43(6):517–37.
      4. Prasad N, Lau ECY, Wojt I, et al. Prevalence of and risk factors for drug-related readmissions in older adults: a systematic review and meta-analysis. Drugs Aging 2024;41(1):1–11.
      5. World Health Organization. Medication Without Harm – Global Patient Safety Challenge on Medication Safety. Geneva: World Health Organization; 2017.
      6. Australian Commission on Safety and Quality in Health Care. Medication without harm – WHO Global Patient Safety Challenge. Australia’s response. Sydney: ACSQHC; 2020.
      7. Elliott RA, Tran T, Taylor SE, et al. Impact of a pharmacist-prepared interim residential care medication administration chart on gaps in continuity of medication management after discharge from hospital to residential care: a prospective pre- and post-intervention study (MedGap Study). BMJ Open 2012;2(3).
      8. Department of Health and Aged Care. Guiding Principles to Achieve Continuity in Medication Management. Canberra; 2022.
      9. Australian Commission on Safety and Quality in Health Care. Principles of safe and high-quality transitions of care (factsheet). 2024.
      10. Elliott RA, Angley M, Criddle DT, et al. Achieving safe medication management during transitions of care from hospital: time for a stewardship approach. Aust Prescr 2024;47(4):106–8.
      11. Elliott RA, Taylor SE, Koo SMK, et al. Accuracy of medication histories derived from an Australian cloud-based repository of prescribed and dispensed medication records. Intern Med J 2023;53:1002–9.
      12. Francis M, Francis P, Makeham M, et al. Using personal health records for medication continuity during transition of care: An observational study. Health Inf Manag 2024:18333583241270215.
      13. Wembridge P, Rashed S. Discharge summary medication list accuracy across five metropolitan hospitals: a retrospective medical record audit. Aust Health Rev 2022;46:338–45.
      14. Uzunbay Z, Elliott RA, Taylor S, et al. Accuracy of medication labels on community pharmacy-prepared dose administration aids: an observational study. Explor Res Clin Soc Pharm 2023;11:100318.
      15. Taylor S, Welch S, Harding A, et al. Accuracy of general practitioner medication histories for patients presenting to the emergency department. Aust Fam Physician 2014;43:728.
      16. Chen EY, Wang KN, Sluggett JK, et al. Process, impact and outcomes of medication review in Australian residential aged care facilities: a systematic review. Australas J Ageing 2019;38:9–25.
      17. Luetsch K, Rowett D, Twigg MJ. A realist synthesis of pharmacist-conducted medication reviews in primary care after leaving hospital: what works for whom and why? BMJ Qual Saf 2020;30(5):418–30.
      18. Criddle D, Devine B, Murray K, et al. Developing PHarmacie-R: a bedside risk prediction tool with a medicines management focus to identify risk of hospital readmission. Res Social Admin Pharm 2021;18 (7):3137–48.
      19. The Society of Hospital Pharmacists of Australia. Hospital-initiated medication reviews. Collingwood, Victoria: The Society of Hospital Pharmacists of Australia; 2020.
      20. Angley M, Criddle D, Rigby D, et al. Hospital-initiated post-discharge medication reviews in Australia: expert opinion on the barriers and enablers to implementation. J Pharm Pract Res 2022;52(6):446–53.
      21. Su E, Liew DFL, Donnelly J, et al. Medicines stewardship. Aust Prescr 2023;46(2):24–8.
      22. Advanced Pharmacy Australia Transition Care and Primary Care Specialty Practice Group. Standard of practice for pharmacy services specialising in transitions of care. J Pharm Pract Res 2024;54(5):417–35.
      23. Emadi F, Liu S, Yui C H, et al. Digital approaches that can be employed to facilitate safe medication management at transitions of care. Sydney: ACSQHC; 2024.
      24. Emadi F, Liu S, Yiu CH, et al. Medication management at transitions of care stewardship framework. Rapid literature review and environmental scan – final report. Sydney: Faculty of Medicine and Health, School of Pharmacy, University of Sydney; 2023.
      25. Australian Commission on Safety and Quality in Health Care. The National Safety and Quality Health Service (NSQHS) Standards (second edition) 2021. At: www.safetyandquality.gov.au/standards/nsqhs-standards
      26. Department of Health and Aged Care. National Medicines Policy 2022. Canberra; 2022.
      27. Australian Digital Health Agency. National Digital Health Strategy 2023-2028. Sydney; 2023.
      28. Australian Digital Health Agency. National Digital Health Strategy Delivery Roadmap 2023–2028. Sydney; 2023.
      29. Australian Commission on Safety and Quality in Health Care [DRAFT]. Medication Management at Transitions of Care Stewardship Framework. Sydney: ACSQHC; 2024.

      Our authors

      Manya Angley (she/her) BPharm, PhD, FPS, CredPharm (MMR), FAdPha is an Advanced Practice Pharmacist experienced in general practice, disability and aged care.

      Debbie Rigby (she/her) BPharm, GradDipClinPharm, FASCP, FPS, FACP, FAICD, FSHP, FANZCAP (GeriMed, Resp) is an Advanced Practice Pharmacist qualified in clinical pharmacy, geriatrics and respiratory medicine.

      Rohan Elliott (he/him) BPharm, BPharmSc(Hons), MClinPharm, PhD, FAdPhA, FANZCAP (GeriMed, Research) is an Advanced Practice Pharmacist with experience in hospitals, aged care and transitions of care.

      Our reviewer

      Elizabeth Manias (she/her) RN, BPharm, MPharm, MNStud, PhD, FANZCAP (Transitions of care, Geriatric Medicine)

      Conflict of interest declaration

      Manya Angley, Debbie Rigby and Rohan Elliott are co-investigators on a Medical Research Future Fund (MRFF) 2022 transitions of care project. MRFF is funded by the Australian Government. They are also co-authors of a literature review of transitions of care stewardship that was funded by the ACSQHC.

      Elizabeth Manias is a member of the Transitions of Care and Primary Care Leadership Committee of Advanced Pharmacy Australia.

      [post_title] => Improving medicines safety at transitions of care [post_excerpt] => Transitions of care are periods of high risk for medication errors and miscommunication, leading to patient harm. [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => improving-medicines-safety-at-transitions-of-care [to_ping] => [pinged] => [post_modified] => 2025-05-14 13:04:04 [post_modified_gmt] => 2025-05-14 03:04:04 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29045 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => Improving medicines safety at transitions of care [title] => Improving medicines safety at transitions of care [href] => https://www.australianpharmacist.com.au/improving-medicines-safety-at-transitions-of-care/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( [td_post_template] => single_template_4 ) [is_review:protected] => [post_thumb_id:protected] => 29343 [authorType] => )

      Improving medicines safety at transitions of care

      medicine storage
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                  [post_content] => Both Cautionary Advisory Label (CAL) 6 and CAL 13 have been overhauled to sharpen storage advice.
      
      CAL 6 explanatory notes advice in Digital Australian Pharmaceutical Formulary and Handbook (APF) now mentions considerations for room-temperature time windows for refrigerated medicines, while CAL 13’s tightened wording and advice flags truly sensitive formulations – ensuring pharmacists give patients clearer, more precise guidance.
      

      What’s changing?

      The familiar ‘Refrigerate, do not freeze’ warning of CAL 6 is not changing, however its explanatory notes have been expanded.  [caption id="attachment_29335" align="aligncenter" width="180"]CAL 6 CAL 6[/caption] There are many instances whereby refrigeration of temperature sensitive medicines may not be practical, for example travel days, power outages or ‘in-use’ multi-dose containers/devices. The updated explanatory notes advise pharmacists that they should refer to the medicines approved product information (PI) and counsel their patients on how to best store these medicines – covering when their temperature sensitive medicines may safely remain at room temperature (below 25 °C) – if applicable. [caption id="attachment_29336" align="aligncenter" width="176"] The old CAL 13[/caption] [caption id="attachment_29337" align="aligncenter" width="189"] The new CAL 13[/caption] Meanwhile, CAL 13 has been reworded. Previously ‘Do not remove from original packaging until dose required’, the new prompt, ‘Ask your pharmacist about the storage conditions for this medicine,’ applies only to dosage forms and active ingredients truly sensitive to light, moisture or temperature excursions.  This includes orally disintegrating tablets, effervescents, sublingual or buccal lozenges, dispersible granules, wafers and chewables, as well as amoxicillin/clavulanic acid, dabigatran, glyceryl trinitrate, nicorandil, nifedipine, phenothiazines, tamoxifen and sodium valproate. CAL 13 may also be applied in addition to other CALs relating to storage requirements (e.g. CALs 6, 7a or 7b) when complex storage instructions are applicable, and these other CALs do not adequately cover these. To support the change to CAL 13, the APF’s Good dispensing practice chapter has been updated with clearer and expanded guidance on providing advice to patients on how to store medicines, including that:
      • all medicines should be kept out of sight and out of reach of children at all times
      • unless specifically requiring refrigeration, and in the absence of special storage instructions outlined in the PI/consumer medicine information (CMI), medicines should be stored in their original packaging in a cool (preferably <25 °C), dry and secure place
      • medicines should generally not be removed from their original packaging until a dose is required – pharmacists should check how the patient intends to store their medicines (e.g. in a dosette box) and provide advice according to the storage instructions outlined in each medicines PI/CMI.
      CAL 13’s explanatory notes have also been updated in APF Digital to support pharmacists in applying the revised CAL. When packing medicines into Dose Administration Aids (DAAs) pharmacists should consider the approved PI of each medicine, and PSA’s Guidelines for pharmacists providing dose administration aid services.

      What led to this update?

      Medicine labels have traditionally relied on simple fridge-or-no-fridge advice. But today’s PIs are more complex.  Humira (adalimumab) is one good example. People using Humira are advised that they can store single pre-filled syringes or pens ‘below 25°C (room temperature) for a maximum period of 14 days, but must be protected from light. Once removed from the refrigerator for room temperature storage, the syringe must be used within 14 days or discarded, even if it is returned to the refrigerator’.  But CAL 6 doesn’t capture these nuances, so some patients are left guessing whether their medicines are safe to use or not during travel or at times when refrigeration is not available. The new explanatory notes prompt pharmacists to cover these scenarios as part of their routine counselling to promote safe and quality use of medicines. At the same time, the CAL 13 had become so ubiquitous – applicable to nearly all medicines – that its impact was diluted. What's more, most pharmacies didn’t even stock the printed sticker.  By narrowing its application, CAL 13’s power to prompt meaningful conversations about stability risks has been restored. Above all, when medicines are removed from their original packaging inappropriately, or stored incorrectly, this can translate into reduced potency or patient harm. These refinements give pharmacists clear, evidence-based cues to maintain medicine stability and efficacy. 

      How should pharmacists tailor storage advice?

      Pharmacists should personalise both verbal and written advice to the patient. Ensure every patient is counselled on how to best store their medicines including routinely asking how the patient plans to keep their medicines, for example will they use a dosette box? Is storage at an appropriate temperature an issue? If a medicine carries Label 6 but its PI indicates there is an appropriate room-temperature window, demonstrate the correct use of an insulated bag and explain the difference between ‘keep at 2–8 °C’ and ‘store below 25 °C’. Provide guidance on room temperature storage for their in-use multi dose container/device (if appropriate) and for times when refrigeration is unavailable or impractical. Pharmacists should also advise the patient to avoid storing medicines in the areas of a domestic refrigerator that may not maintain a temperature of 2–8 °C. This includes the door, top shelf or crisper; or within 40 mm of the back and sides of the main compartment. For CAL-13 affixed medicines, pharmacists should advise patients that these medications’ stability is protected by the original container and packaging, and that removing them prematurely can accelerate degradation and reduce efficacy. Work with the patient to address any barriers to this.

      What’s the implementation timeline?

      The revised explanatory notes for CAL 6 and CAL 13 are live in APF Digital as of 7 May 2025.  CAL printers will begin issuing the new CAL 13 labels on their next run. Until then, pharmacists should continue using the existing labels while equipping patients with the updated counselling points and advice outlined in the APF Digital.

      How should pharmacists put the new advice into practice?

      Let’s say Mrs L, 68, who has type 2 diabetes, atrial fibrillation and hypertension, presents to a pharmacy for her medicines. She picks up a prescription for insulin glargine pens, nifedipine and dabigatran. For her insulin glargine, you apply Label 6 and explain the medicine must be stored at 2–8 °C in the fridge’s main compartment, yet the in-use pen may remain at room temperature for up to 28 days. You provide her with an insulated bag and demonstrate how to use it. You then recognise that nifedipine is sensitive to light and dabigatran is moisture-sensitive, and apply Label 13 to each medicine’s packaging which prompts a PI check. You advise her to keep the medicines away from humid spots such as bathrooms or kitchen windowsills, and to keep them in their original packaging, out of direct light. Mrs L leaves confident in where to store each medicine, and you’ve pre-emptively safeguarded stability and efficacy. [post_title] => New CAL medicine storage guidance [post_excerpt] => [post_status] => publish [comment_status] => open [ping_status] => open [post_password] => [post_name] => new-cal-medicine-storage-guidance [to_ping] => [pinged] => [post_modified] => 2025-05-12 16:02:09 [post_modified_gmt] => 2025-05-12 06:02:09 [post_content_filtered] => [post_parent] => 0 [guid] => https://www.australianpharmacist.com.au/?p=29331 [menu_order] => 0 [post_type] => post [post_mime_type] => [comment_count] => 0 [filter] => raw ) [title_attribute] => New CAL medicine storage guidance [title] => New CAL medicine storage guidance [href] => https://www.australianpharmacist.com.au/new-cal-medicine-storage-guidance/ [module_atts:td_module:private] => Array ( ) [td_review:protected] => Array ( ) [is_review:protected] => [post_thumb_id:protected] => 29332 [authorType] => )

      New CAL medicine storage guidance

AUSTRALIAN PHARMACIST Australian Pharmacist
Home People Highlights from PSA19, day one

Highlights from PSA19, day one

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Ruth Cooper
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July 27, 2019
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In case you missed it, here’s some of the action from the first day of PSA19 – from the Welcome Reception, Early Career Pharmacists Party and Fellows Dinner.

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