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Published: 19th June, 2026
Contents
Welcome to the 150th edition of Best Practice Bulletin

Today marks a special milestone in the history of Best Practice Bulletin: the 150th time we have announced our latest resources, reported on important news for primary care and delivered a curated selection of other items of interest.
Let’s take a look back through the archives to see what was news when this all first began
- May, 2020
- 1st Issue of Best Practice Bulletin published
- Previously called “The COVID-19 Bulletin”; eight editions were published under this banner
- In this Issue we reported that an extra-large number of influenza vaccinations had been obtained to meet high demand for “flu season” and spirometry requirements were being temporarily removed as a funding criterion for some inhalers as this increased the risk of exposure to COVID-19. We announced the launch of BPACRx prescribing software and our latest topic in our Primary Care Update series. Medicine supply issues were starting to become commonplace.
- June, 2020
- First appearance of the now regular “Paper of the Week” segment in Issue 2 of the Bulletin: Is there a gene for thinness?
- March, 2021
- First “Podcast of the Week” published in Issue 21 (although it wasn’t called that until Issue 35): clinicians speaking out about their own mental health struggles
- December, 2021
- May, 2022
- 50th Issue of Best Practice Bulletin published
- In this Issue we profiled a new bpacnz publication on low back pain, we noted the current “onslaught” of respiratory illness being managed by primary care, we reported a trial of a new preventative treatment for children at high risk of respiratory syncytial virus (palivizumab: now funded for select children) and updated on changes to COVID-19 vaccinations
- May, 2024
- August, 2024
- Introduced the Medical Factorium, our popular occasional segment where we answer questions about curious medical oddities such as why do we yawn; why do joints ache when it’s cold; why do songs get stuck in our head; why is gout called gout; and the case of the crimson nose
- June, 2026
- Today we publish our 150th Issue 🥳
We publish Best Practice Bulletin as a way to connect our audience with the most important bits of information from primary care. We try to keep it about the clinical news and education and steer clear of the political. As much as possible, we also like to make it an enjoyable read, something to look forward to on a Friday.
Thank you for joining us in our sesquicentennial (we like big words around here). We were going to end with “See you for our 200th”, but actually, we would prefer to see you again for Issue 151, and the next one, and the one after that…
If you have ideas for topics for the Bulletin or any of our segments, email: editor@bpac.org.nz
Latest resources from bpacnz

It has been a busy first half of the year for the bpacnz publications team, with many articles published on a range of topics, including urinary tract infections in children, reporting adverse reactions, chronic kidney disease, genital herpes, pharmacological management of ADHD and migraine. View our latest articles here. CPD activities, including clinical audits, peer group discussions and quizzes/case studies are also available.
Stay tuned for our upcoming articles on SGLT-2 inhibitors, and Beyond breathlessness: Diagnosis and management of patients with COPD
Rewind: Wrap-up of recent key messages
Key dates and updates on news items from recent editions of Best Practice Bulletin:
- New HbA1c diagnostic thresholds for diabetes and pre-diabetes come into effect from 1st July to align with international standards. For further information, see Bulletin 144.
- Stock of progesterone 100 mg capsules (Utrogestan) has arrived in the country, following a period of limited supply (as last reported in Bulletin 147). Monthly dispensing of Utrogestan has applied since May; Pharmac are working to return stat dispensing; a date is yet to be announced.
Medicine news
The following news relating to medicine supply has recently been announced. These items are selected based on their relevance to primary care and where issues for patients are anticipated, e.g. no alternative medicine available or changing to the alternative presents issues. Information about medicine supply is available in the New Zealand Formulary at the top of the individual monograph for any affected medicine and summarised here.
Colchicine 500 microgram brand change
The funded brand of colchicine 500 microgram tablets, used for the treatment of gout, is changing from Colgout to Indoco. Indoco 500 microgram tablets will be listed on the Pharmaceutical Schedule from 1st July. Colgout will be delisted on 30th November. A brand switch fee will be available to pharmacists from 1st December.
Advise patients taking colchicine that their brand will change between July and December, and that the packaging will look different: the medicine will now come in blister packs rather than a bottle as this may reduce the likelihood of colchicine overdose. Reassure patients that there has been no change to the active ingredient and the tablet appearance will be similar. Patients are recommended to talk to their pharmacist if they have dexterity problems with opening blister packs.
A patient information sheet about the brand change is available here
Supply issue affecting lansoprazole 30 mg capsules (Lanzol Relief)
There is a supply issue affecting lansoprazole 30 mg capsules (Lanzol Relief), a proton pump inhibitor, due to manufacturing issues. A re-supply date is unknown; the 15 mg presentation is not currently affected. An alternative brand (Lansoprazole Viatris; orodispersible tablet) has been funded since 12th June;* however, it is not approved by Medsafe, therefore will need to be prescribed for supply under Section 29A of the Medicines Act. This brand contains phenylalanine which will not be suitable for all patients. Pharmacists may be able to dispense 2 × 15 mg capsules of the Lanzol Relief brand for patients in whom Lansoprazole Viatris is not suitable or tolerated.
* The listing should appear automatically in dispensing software; it will not appear in the online Pharmaceutical Schedule until 1st July. Pharmac advises that claims for Lansoprazole Viatris in June will be processed.
Rizatriptan 10 mg tablets supply issue
There is a supply issue affecting rizatriptan 10 mg tablets (Rizamelt), used for the treatment of acute migraine, due to manufacturing issues. Re-supply is expected in November. An alternative brand (Rizatriptan Rising) has been funded since 12th June;* however, it will not be available to order until later this month. Rizatriptan Rising is not approved by Medsafe, therefore will need to be prescribed for supply under Section 29A of the Medicines Act.
* The listing should appear automatically in dispensing software; it will not appear in the online Pharmaceutical Schedule until 1st July. Pharmac advises that claims for Rizatriptan Rising in June will be processed.
Valaciclovir 1,000 mg tablets (Vaclovir) to go out of stock
Stock of valaciclovir 1,000 mg tablets (Vaclovir), used for shingles and herpes, are limited due to manufacturing delays. Re-supply is expected in July. Two alternative brands (Valaciclovir Mylan and Valaciclovir Viatris) have been listed on the Pharmaceutical Schedule, however, neither brand is approved by Medasfe, therefore will need to be prescribed for supply under Section 29A of the Medicines Act.
Pharmac is asking pharmacists to dispense either of these brands where possible, rather than 2 × 500 mg tablets to avoid a supply issue with the 500 mg strength. Pharmacists should also be aware that Valaciclovir Mylan and Viatris come in a pack size of 21 rather than 30 tablets (Vaclovir).
Supply issue affecting benzathine benzylpenicillin (Bicillin LA)
Benzathine benzylpenicillin (Bicillin LA) is expected to go out of stock later this year due to delays at the manufacturer. Re-supply is scheduled for November. This antibiotic is primarily used for the prevention of acute rheumatic fever and the treatment of syphilis. An alternative brand (Benzetacil)* has been listed on the Pharmaceutical Schedule. It contains the same quantity of active ingredient; however, it comes in the form of a dry powder for reconstitution, rather than a pre-filled syringe. When reconstituted, the volume administered to patients is larger than Bicillin LA (4.8 mL compared to 2.3 mL).
Health New Zealand, Te Whatu Ora, is advising clinicians to prioritise stock of Bicillin LA to patients who need smaller injection volumes (e.g. younger children; view all priority groups here). Guidance on when to use Bicillin LA and Benzetacil for specific conditions is available here. Primary care clinicians are asked to prescribe oral alternatives to benzathine benzylpenicillin for patients with sore throats and skin infections due to Group A Streptococcus (where appropriate).
* Benzetacil is currently listed as Section 29 in the Pharmaceutical Schedule, however, it has received provisional Medsafe approval. The Schedule will be updated in the July release allowing Benzetacil to be supplied on standing order and PSO.
Ongoing supply issues affecting efavirenz + emtricitabine + tenofovir disoproxil
Supply issues affecting efavirenz with emtricitabine and tenofovir disoproxil (Viatris), used for HIV infection, have been ongoing for some time due to manufacturing delays. A re-supply date is unknown. Stock of the currently listed alternative brand (Teevir; Section 29) is expected to be exhausted this month. A temporary new brand, Tenofovir Efavirenz Emtricitabine (Mylan), has been available since 12th June;* however, it is not approved by Medsafe, therefore will need to be prescribed for supply under Section 29A of the Medicines Act.
* The listing should appear automatically in dispensing software; it will not appear in the online Pharmaceutical Schedule until 1st July. Pharmac advises that claims for the Mylan brand in June will be processed.
Upcoming changes to HPV vaccination schedule
From Monday, 27th July, HPV vaccination (Gardasil 9) provided through the School-Based Immunisation Programme will change to a one-dose course. Currently, the approved HPV vaccination course in New Zealand is two doses for children aged 9 – 14 years; therefore, a single-dose course will be off-label. However, evidence has demonstrated that a single HPV dose provides comparable protection to a two-dose course, with studies showing approximately 97 – 98% effectiveness against HPV infection and related cancers. This has led to many countries, including Australia, switching to a single-dose course in recent years.
A second dose can still be administered (funded) at least six months after the first in general practices or other community health providers if requested. Primary care is not expected to recall or actively follow-up children aged 9 – 14 years for a second dose. However, opportunistic catch-up vaccination (funded) should be offered to older children and adults aged up to 26 years who have not received any HPV doses.
IMAC and Health New Zealand are hosting an upcoming webinar on vaccinations to prevent cancer, covering HPV (including evidence for one dose) and hepatitis B. This free webinar is being held on Tuesday, 30th June, from 5:00 pm. Click here to register.
Consultation for paramedic prescriber medicines lists + ambulance medicines funding change
The Ministry of Health, Manatū Hauora, is seeking feedback on a proposed specified prescription medicines list for designated paramedic prescribers. Earlier this month, the decision to enable some paramedics to become designated prescribers was announced. This followed a consultation that was conducted at the end of 2025 by the Paramedic Council of New Zealand to determine whether paramedics in New Zealand should be granted prescribing authority (as reported in Bulletin 138). Feedback from this consultation is available here.
The proposed list includes a range of medicines for:
- Infections, e.g. amoxicillin, cefalexin, anti-infective ear and eye preparations containing framycetin or ciprofloxacin
- Analgesia, e.g. naproxen, celecoxib, codeine, tramadol
- Asthma, e.g. bronchodilators
- Cardiovascular disease, e.g. beta blockers, calcium channel blockers, antiarrhythmic medicines, statins
- Gout, e.g. allopurinol, colchicine, prednisone
- Diabetes, e.g. metformin
- Gastroesophageal reflux disease, e.g. omeprazole
View the full proposed list here
Extended Care Paramedics are increasingly being utilised in general practice clinics as part of the multidisciplinary team supporting patients with urgent, unscheduled community care needs. Proposed benefits of introducing paramedic prescribers include patients being able to access medicines and treatments in a timelier manner, the potential to reduce health inequities for certain groups, e.g. those who live rurally, and reducing the burden of work on other health care providers.
Consultation on the medicines list closes Sunday, 5th July. Feedback can be submitted here.
Medicines on ambulances to be funded via Pharmac
In a separate news release, Pharmac has announced that from 1st July, it will be responsible for funding medicines used in ambulances. Previously, ambulance providers would purchase medicines via funding from Health New Zealand and ACC. A series of changes will be made to the Pharmaceutical Schedule on 1st July, including the addition of a new section (Section E), where all funded ambulance medicines will be listed. Read more here.
Also from 1st July, tenecteplase, used for the treatment of ST-elevation myocardial infarction (STEMI), will be funded for emergency ambulance and PRIME services. This change is anticipated to reduce logistical barriers associated with obtaining the medicine; previously, tenecteplase was provided to PRIME and ambulance service providers from Health New Zealand hospitals.
Webinar on ACC Medical Certification Dashboard
Collaborative Aotearoa is hosting an upcoming webinar, presented by BPAC Clinical Solutions and ACC, on the ACC Medical Certification Dashboard. This interactive dashboard is offered through BPAC CareSuite, and provides information on your medical certification practice, including the ratio of ‘fully unfit’ and ‘fit for selected work’ certificates, average incapacity durations and return-to-work timeframes. This information can be used for self-reflection of practice and peer group discussion. The webinar is expected to cover how to access and use the Dashboard and how to interpret the data.
This free webinar will be held on Wednesday, 24th June, from 12:00 pm. Click here to register.
June is Bowel Cancer Awareness Month
This month (June) is Bowel Cancer Awareness Month. New Zealand has one of the highest incidences of bowel cancer in the world; approximately 3,000 people are diagnosed with bowel cancer each year. It is also a leading cause of cancer mortality (after lung cancer) with more than 1,200 deaths per year.
People aged 58* – 74 years (who are not already part of a high-risk surveillance bowel screening programme) are currently eligible for funded bowel cancer screening every two years using the faecal immunohistochemical test (FIT). The Government recently announced that the eligibility age is to be lowered again from the end of September, 2026, to 56 years for all people; the timeline for nationwide roll-out of this change has not yet been announced.
* Eligibility age in the MidCentral district is 60 – 74 years; this is reportedly being lowered to age 58 – 74 years in the coming months
Opportunistically check if eligible patients have received a bowel cancer screening kit and identify and address any barriers to completing the test.
For information on the referral of patients with features suggestive of bowel cancer, see: https://bpac.org.nz/2020/bowel-cancer.aspx
For information on the follow-up and surveillance for people after treatment for bowel cancer, and surveillance for people with polyps or inflammatory bowel disease, see: https://bpac.org.nz/2021/bowel-cancer.aspx and https://bpac.org.nz/2021/bowel-polyps.aspx
Cancer Control Agency: New look for cancer insights
In a recent email to the sector, Te Aho o Te Kahu, Cancer Control Agency, has announced the addition of a new section on their website: CanStats. CanStats features national and international cancer data and other resources on aspects of cancer control, including prevention, screening, diagnosis, treatment, survivorship as well as population insights. This replaces “Reports and numbers” and “Cancer in Numbers” sections of the website.
For example:
- “Screening” includes links to the BreastScreen Aotearoa Coverage, National Bowel Screening Programme Participation and National Cervical Screening Programme Coverage data
- “Diagnosis” includes links to the cancer data web tool (cancer registrations, diagnoses and deaths in New Zealand), cancer care data explorer (quality of life and outcomes of people with cancer in New Zealand) and the diagnostic dashboard (wait times for the past three years for diagnostic procedures that can be part of the cancer pathway)
- “Population Insights” includes reports on disability and cancer, state of cancer and links to the New Zealand Health Survey and New Zealand population data
Paper of the Week: Muscling in on muscle loss
Maintaining muscle mass is crucial for healthy ageing and as the saying goes “use it or lose it”. Muscle loss typically begins after the age of 40 years with a more marked decline in people aged 60 years and over. This gradual reduction in muscle mass and impaired physical function can progress to a formal diagnosis of sarcopenia, which is associated with worse health outcomes in later life, e.g. increased risk of falls. Most older adults need to increase their physical activity, with a particular emphasis on maintaining and developing muscle mass; resistance training is now recommended as part of non-pharmacological management for many chronic conditions. It is also important to acknowledge that reduced muscle mass is not solely a concern for older adults. Younger patients with chronic conditions, reduced mobility or a history of malnutrition may be at risk of reduced muscles mass. The recent increased use of glucagon-like peptide-1 (GLP-1) receptor agonists has prompted warnings about the risk of muscle loss and advice to increase protein intake and resistance training. Despite the potential consequences, primary care clinicians currently have limited guidance on who to assess for muscle loss and how this should be carried out.
An article published in the Australian Journal of General Practice describes a practical approach to evaluating and monitoring muscle mass in older patients. Clinicians should be aware of the various risk factors for low muscle mass; patients with at least one risk factor should undergo further assessment, e.g. five-times sit-to-stand, three-metre timed-up-and-go, hand grip strength test. The results of this assessment determine whether a prevention (i.e. general advice about exercise and nutrition) or management approach (referral to nutrition and activity support) is appropriate. Identifying patients with lower muscle mass earlier allows intervention to reduce further muscle loss, and in some cases reverse muscle loss, improving quality of life.
Is lean muscle mass a primary concern for you when treating older patients with chronic conditions? Are patients generally aware of the relationship between muscle mass and healthy ageing? How confident do you feel with providing advice around physical activity, nutrition and maintaining/increasing muscle mass? What are some of the recommendations you give to patients?
Read more
The approach to identifying and addressing low muscle mass is broken down into four stages (view a summary algorithm here):
Suspect
- All patients aged 50 years and over should be evaluated periodically for low muscle mass
- Assess for:
- Risk factors for muscle loss, including struggling to stand from a chair, particularly slow walking speed or poor balance observed during consultations
- Medicines (e.g. GLP-1 receptor agonists, chronic opioid or oral corticosteroid use), chronic conditions or other co-morbidities (e.g. cardiovascular, respiratory and kidney disease, depression, osteoporosis) associated with muscle loss
- Additional factors associated with sarcopenia that may make assessment for low muscle mass more appropriate in older adults, e.g. recent weight loss, low baseline BMI, history of malnutrition, early menopause, limited physical activity or a sedentary lifestyle
- Use clinical judgement when deciding which patients should undergo further assessment for muscle loss, however, proceeding to the next stage is likely appropriate in any patient with one or more of the risk factors listed above
Ask and/or assess
- The 5-item Strength, Assistance in walking, Rise from chair, Climb stairs and Falls (SARC-F) screening questionnaire can be used to identify patients who may be at increased risk of low muscle mass
- Patients with a SARC-F score ≥ 2 should undergo further assessment for muscle strength and function (while a score ≥ 4 is predictive of sarcopenia and poor outcomes)
- Objective methods for assessing muscle health and their proposed thresholds for indicating low muscle strength include:
- These thresholds represent scores below the 20 – 25th percentile of normative ranges for adults aged 60 years and over. Younger patients at higher risk of low muscle mass may not meet these thresholds but still require intervention; use clinical judgement.
Prevent or manage
- Patients who meet the thresholds indicating low muscle strength (above) should be strongly encouraged to increase their physical activity, i.e. a green prescription for resistance training, and protein intake (see below)
- Consider referral to community nutrition and physical activity services depending on local availability (see HealthPathways)
- Patients with risk factors for muscle loss but who do not meet thresholds should be provided with general education and recommendations for nutrition and physical activity
- General advice for patients with low muscle mass:
- Guidelines recommend at least two progressive resistance training sessions per week focusing on major muscle groups, e.g. body weight exercises, resistance bands, free weights
- Most older patients should aim for an increased daily protein intake of 1.0 – 1.5 g/kg/day (divided over multiple meals). N.B. A normal protein intake of 0.8 g/kg/day is typically encouraged in New Zealand for people with end-stage renal disease.
- Patient information on dietary protein is available here
- Consider nutritional supplements if patients cannot reach their daily protein target with whole foods
Review
- Reassess patients annually and following diagnosis of a new health condition or initiation of a medicine associated with muscle loss or other significant health event, e.g. fall, fracture, hospital admission
- As part of this review, re-examine patient risk factors for muscle loss and repeat SARC-F or strength assessment
Daly RM, Scott D, Govan L, et al. Muscle matters: A proposed algorithm to guide screening, assessment and management of poor muscle health in primary care. Aust J Gen Pract 2026;55:369–72. doi:10.31128/AJGP-06-25-7703.
This Bulletin is supported by the South Link Education Trust
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