A survey of prefilled, bolus-dose syringes containing single medications compounded in community pharmacies for palliative care patients in Tāmaki Makaurau Auckland, Aotearoa New Zealand
E. C. Griffiths 1 , S. M. Hanning 1 , S. S. Thakur 1 , D. A. Gargiulo
1
Abstract
In Aotearoa New Zealand, prefilled syringes for patients receiving palliative care in the community can be prepared (compounded) by certain pharmacies. Currently, there is limited information regarding the scope of compounding these prefilled syringes.
The study aimed to explore the range of subcutaneous bolus-dose medications and the compounding processes used in community pharmacies in Tāmaki Makaurau Auckland when preparing prefilled syringes used for anticipatory needs in patients receiving palliative care.
A convenience sample of community pharmacies contracted to prepare prefilled syringes was invited to complete an online survey. Information was requested on the medications compounded for bolus-dose syringes over the previous 6-month period, including what medications and facilities were used, how expiration dates were determined, and the time spent preparing these syringes.
Data were requested on compounding between 1 September 2022 and 28 February 2023 with complete responses received from 8 of the 40 pharmacies invited to participate. The top four medications compounded, in rank order, were midazolam, oxycodone, haloperidol, and morphine sulfate. All eight pharmacies compounded syringes in a still air box, and ‘published guidance’ was the most common source of expiration dates. Most respondents each reported spending 5–10 h per week preparing the compounded products.
Community pharmacies in Tāmaki Makaurau Auckland compounded a range of medications as bolus-dose prefilled syringes for patients receiving palliative care. These results will inform future planned studies on the stability and sterility of these syringes.
Keywords: aseptic services, bolus-dose, community pharmacies, compounding, electronic survey, palliative care, prefilled syringes, subcutaneous.
WHAT GAP THIS FILLS |
What is already known about the topic: Prefilled syringes of bolus-dose, single medications for anticipatory subcutaneous administration are prepared for patients receiving palliative care by certain community pharmacies in Aotearoa New Zealand. Current guidelines for the prefilled syringes recommend an expiry of 3 days if they are stored in refrigerated conditions. There are significant financial and environmental costs if these syringes are discarded unused. |
What this study adds: The medications compounded for bolus-dose administration by eight pharmacies in a 180-day period were in line with international guidelines for the anticipatory needs of patients receiving palliative care. ‘Published guidance’ was the most common source of the assigned expiry, but there was uncertainty about the sterility and stability of the compounded syringes. There is a need for improved funding for the service and enhanced communication with prescribers and palliative care staff about what is involved from the pharmacy’s perspective. |
Introduction
The standard international practice when patients receiving palliative care are unable to take medications orally is to administer them via a continuous subcutaneous infusion using a portable device.1
In Aotearoa New Zealand (NZ), syringes for this purpose can be prepared in community pharmacies contracted to provide aseptic services by Te Whatu Ora Health New Zealand.2 Specific training in this area is available.3 The operators use aseptic techniques in an apparatus called a ‘still air box’, which maintains a separate, clean compounding environment and is unique to NZ (Fig. 1).4
A pharmacist in training to prepare (compound) prefilled syringes in a still air box at Waipapa Taumata Rau University of Auckland, NZ.

For every medication contained in the continuous subcutaneous infusion syringe, a corresponding bolus-dose syringe is usually prescribed in anticipation of worsening symptoms.5 These bolus-dose syringes are compounded as single medications in 0.1–2 mL volumes, and current NZ guidelines recommend storage in the refrigerator with an expiry date of 3 days when the syringes are compounded in a still air box.6 Tāmaki Makaurau Auckland (Auckland) is the largest region in NZ where this service is available.
The availability of these bolus-dose syringes enables patients’ families to manage patients’ symptoms at home in a responsive way and has the potential to reduce the need for hospital admission during times of high symptom burden.7
Bolus-dose syringes are often dispensed in anticipation of need but not always used, and extending the expiry dates could help reduce material wastage. However, limited information exists on community pharmacy compounding processes – such as facilities used, preparation time, or how expiry dates are determined – despite the availability of guidelines.6 There is also a lack of data on the stability of unmixed medications over time, as in the preparation of continuous subcutaneous infusions.1 Therefore, we investigated the range of medications and the compounding process of these bolus-dose syringes prepared by community pharmacies in Auckland.
Methods
A cross-sectional, online survey with 11 questions was conducted among community pharmacies that prepare prefilled syringes. The tool was adapted from an unpublished hospital pharmacy survey previously used to inform pharmacy curricula in NZ. The current version was revised to capture data from community pharmacies and pre-tested by a pharmacy academic experienced in survey design. The survey was created and administered using Qualtrics (Provo, UT, USA).
An electronic database of Auckland community pharmacies known to compound prefilled syringes is maintained by the region’s hospice pharmacists via Auckland Regional HealthPathways, a web-based source of information for clinicians.8 At the time of the survey, the database was only available for the Auckland region. A link to the survey (see Supplementary material S1), including an information sheet, was emailed to all 40 pharmacies listed on the database by a researcher known to the pharmacies. Information was requested on the name and number of medications compounded as bolus-dose syringes during a 180-day retrospective period; the method used to determine expiry dates; the facilities used for compounding; and the time spent preparing the syringes. The data requested were derived from pharmacy dispensing records. Opportunities for free-text comments were included after selected questions, and the final question invited further feedback regarding aseptic services in community pharmacy in NZ. Data were also collected on pharmacy location and on the number and type of staff employed.
To ensure anonymity and confidentiality, survey responses were collated via the survey tool by a researcher unfamiliar to the participants. Participation was voluntary, and consent was assumed upon completion of the survey. A reminder email was sent to all pharmacies after 2 weeks by the initial researcher, and no incentives were offered.
Approval for the study was granted from the University of Auckland Human Participants Ethics Committee (Ref. UAHPEC25605).
Data were analysed quantitatively using frequencies; no statistical tests were used due to the small sample size. In preparing this manuscript, we followed the reporting guidelines set forth by the Checklist for Reporting of Survey Studies (CROSS).9
Results
A total of 40 community pharmacies were sent the email containing the link to the electronic survey; eight (20%) returned completed surveys. Incomplete surveys were excluded from analysis.
Most respondents were in a suburban precinct of five or more shops (n = 5, 62.5%), and pharmacies were from all geographical locations across Auckland. The pharmacies employed an average of four pharmacists, one intern pharmacist, two pharmacy technicians, and one other staff member, eg shop assistant.
All the respondents (n = 8, 100%) used a still air box to aseptically compound syringes in the study period (1 September 2022 to 28 February 2023). There was no indication that other aseptic facilities were used to prepare the syringes.
Two medications all eight respondents reported compounding as bolus doses were midazolam and haloperidol, comprising 1016 and 733 syringes respectively (Table 1).
Medication name | Number of respondents | Minimum number of syringes | Maximum number of syringes | Total number of syringes | |
---|---|---|---|---|---|
Midazolam | 8 | 16 | 286 | 1016 | |
Oxycodone | 7 | 30 | 300 | 785 | |
Haloperidol | 8 | 30 | 225 | 733 | |
Morphine sulfate | 7 | 22 | 244 | 686 | |
Levomepromazine | 5 | 10 | 200 | 435 | |
Hyoscine butylbromide | 4 | 30 | 100 | 251 | |
Dexamethasone | 6 | 4 | 20 | 62 | |
Methadone | 2 | 10 | 20 | 30 |
Minimum and maximum represent the lowest and highest numbers reported by individual respondents.
The same two medications (midazolam and haloperidol) were each compounded as the same concentration by all eight respondents. Conversely, levomepromazine was compounded as four different concentrations by five respondents (Table 2).
Medication name | Compounded concentration of the prefilled syringes | Number of respondents | |
---|---|---|---|
Midazolam | 2.5 mg/0.5 mL | 8 | |
Oxycodone | 2.5 mg/0.25 mL | 3 | |
5 mg/0.5 mL | 2 | ||
10 mg/1 mL | 2 | ||
Haloperidol | 0.5 mg/0.1 mL | 8 | |
Morphine sulfate | 2.5 mg/0.5 mL | 1 | |
5 mg/0.5 mL | 3 | ||
10 mg/1 mL | 3 | ||
Levomepromazine | 0.25 mg/0.1 mL | 1 | |
3.125 mg/0.125 mL | 1 | ||
6.25 mg/0.25 mL | 2 | ||
12.5 mg/0.5 mL | 1 | ||
Hyoscine butylbromide | 10 mg/0.5 mL | 1 | |
20 mg/1 mL | 3 | ||
Dexamethasone | 2 mg/0.5 mL | 1 | |
4 mg/1 mL | 4 | ||
Methadone | 5 mg/0.5 mL | 2 |
One respondent indicated that diluents were added to all the medications, and a second added diluents for only haloperidol, levomepromazine, and dexamethasone.
All respondents reported that they assigned an expiry date to the syringes based on published guidance (more than one option could be selected), such as ‘textbook, journal reference or website’ (n = 7); ‘clinical experience’ (n = 3); or ‘microbiological testing’ (n = 1). Free-text comments were: ‘hospice guidelines’, ‘training – 72 h’, ‘palliativedrugs.com, sterility testing data’, and ‘3-day expiry assigned as per recommendations, microbiological testing indicates stability [sterility] for 7 days, but uncertainty around chemical stability’.
The average weekly time spent preparing aseptic products – including time spent on paperwork and phone calls – ranged from 5 to 10 h. One respondent reported spending over 20 h per week, whereas another spent less than 5 h. A third respondent noted that this question was ‘very difficult to answer as it is determined by the number of patients we might have at any one time. Could be 3–4 h on weekends or public holidays, but it is not a regular request’. Another respondent indicated that the syringes were ‘often prepared before or after opening hours’.
Three free-text comments were submitted in response to the final question, which invited additional remarks on aseptic services in community pharmacy. One respondent requested: ‘better funding to account for time after hours preparing, also to account for stock and consumables to be held in readiness for preparation’. A second respondent wanted: ‘better communication with prescribers and hospice staff about what is involved – they want to collect in 10 mins’. A third respondent stated that their number of bolus-dose syringes supplied could have been higher: ‘Normally the December period is busy with palliative care and would be a third higher on the numbers I supplied. We had severe staffing issues for the Dec/Jan period.’
Discussion
The preparation of injections for patients to use in the home setting by pharmacists is regarded as the ‘gold standard’ of practice.10 Our study describes a service in Auckland where a subset of community pharmacies prepare prefilled syringes containing single-medication, bolus doses for palliative care patients. We believe this service is unique to NZ, and hence our study is the first of its kind.
Main findings and what this study adds
We identified medicines compounded as single-medication, bolus-dose syringes by community pharmacies over a 180-day period. These were midazolam, oxycodone, haloperidol, morphine sulfate, levomepromazine, hyoscine butylbromide, dexamethasone, and methadone.
The medications specified in the survey have known indications for pain, nausea and vomiting, anxiety, agitation, breathlessness, and respiratory secretions. This is in line with guidelines for anticipatory prescribing for patients receiving palliative care.11,12 While not usually considered an anticipatory medication, dexamethasone was commonly compounded, with six of the eight respondents preparing a total of 82 prefilled syringes during the survey period. Due to its long duration of action, dexamethasone can be administered once daily as a regular medication and is used to protect the skin at continuous subcutaneous infusion sites.1,13 Consequently, prefilled syringes containing dexamethasone may have been used for ongoing treatment rather than for anticipatory purposes.
Midazolam and haloperidol were each compounded at a single concentration by all eight respondents (Table 2). This is valuable information as it supports a case for proprietary syringes to be manufactured at these concentrations with extended expiry dates, which could significantly reduce pharmacy workload and product wastage.
We did not explicitly ask for the expiry date used, but all respondents followed the recommended NZ guidelines and assigned an expiry date. Although not mandated in the NZ guidelines, it was interesting to note that two respondents carried out microbiological testing. One respondent raised concerns about the stability of the medications in the compounded syringes.
Two respondents reported adding diluent to all or some of their bolus-dose syringes, although this practice is not mandated in the NZ guidelines. We speculate this may be due to specific patient needs or local in-house policies.
The variation observed in weekly compounding time across respondents is expected, given the natural ebb and flow of palliative care needs in a relatively small patient population, specifically those requiring subcutaneous medications.
Strengths and weaknesses/limitations of the study
Our study was only carried out in Auckland and so may not necessarily reflect those of community pharmacies in other areas of NZ. However, the information gained is unique because the service provided by community pharmacies is exclusive to NZ.
There were only 8 respondents from the 40 pharmacies known to compound prefilled syringes in Auckland. However, the medications listed in our study reflect those that are recommended for palliation of symptoms in end-of-life care.11,12 In addition, the eight pharmacies covered all geographical areas of Auckland, therefore we believe our results reflect most palliative care aseptic services within the region.
Conclusion
This study provides valuable insight into current data on the bolus-dose single medications compounded as prefilled syringes by community pharmacies in Auckland. There is some consistency with the reported medications and concentrations, but there is variation in time spent on the service with concerns raised about the stability of the compounded medications. Using these results, we plan to undertake studies to determine the stability and sterility of the medications compounded in these prefilled syringes with a view to re-examining their length of expiry.
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Declaration of funding
This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
Acknowledgements
The authors acknowledge the pharmacists who took the time to complete the survey and Sheng-Ting (Selena) Chiu for commenting on a final draft.
Author contributions
D. A. Gargiulo: made a substantial contribution to the concept and design of the work and analysis and interpretation of data; drafted the manuscript and revised it; approved the version to be published; has participated sufficiently in the work to take public responsibility for appropriate portions of the content. E. C. Griffiths: made a substantial contribution to the concept and design of the work; revised the manuscript; approved the version to be published; has participated sufficiently in the work to take public responsibility for appropriate portions of the content. S. M. Hanning: made a substantial contribution to the concept and design of the work; revised the manuscript; approved the version to be published; has participated sufficiently in the work to take public responsibility for appropriate portions of the content. S. S. Thakur: made a substantial contribution to the concept and design of the work; revised the manuscript; approved the version to be published; has participated sufficiently in the work to take public responsibility for appropriate portions of the content.
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