Evidence map›Paper›PMID 32978220›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2022

Assessment of the stability of citrate-buffered piperacillin/tazobactam for continuous infusion when stored in two commercially available elastomeric devices for outpatient parenteral antimicrobial chemotherapy: a study compliant with the NHS Yellow Cover Document requirements.

Conor Jamieson, Laima Ozolina, R Andrew Seaton, Mark Gilchrist, Tim Hills, F Drummond, Alan Shaun Wilkinson, BSAC Drug Stability Testing Working Group

Open access · hybridAbstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Conor JamiesonPharmacy Department, Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK conor.jamieson@nhs.net.
Laima OzolinaR&D, Biopharma Stability Testing Laboratory Ltd, Nottingham, UK.
R Andrew SeatonDepartment of Infectious Diseases, Queen Elizabeth University Hospital, Glasgow, UK.
Mark GilchristDepartment of Pharmacy/Infection, Imperial College Healthcare NHS Trust, London, UK.
Tim HillsPharmacy Department and OPAT Service, Nottingham University Hospitals NHS Trust, Nottingham, UK.
F DrummondBritish Society for Antimicrobial Chemotherapy, Birmingham, UK.
Alan Shaun WilkinsonR&D, Biopharma Stability Testing Laboratory Ltd, Nottingham, UK.
BSAC Drug Stability Testing Working Group
British Society for Antimicrobial Chemotherapy · GBImperial College Healthcare NHS Trust · GBNottingham University Hospitals NHS Trust · GBQueen Elizabeth University Hospital · GBSandwell & West Birmingham Hospitals NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the effect of pH control through the use of a citrate-buffered saline diluent pH 7 on the degradation rate of piperacillin/tazobactam solutions for infusion and to determine if an extended shelf-life of up to 13 days fridge 2°C-8°C plus 24 hours 'in-use' at 32°C in two elastomeric devices: FOLFusor LV10 (Baxter Healthcare, Thetford, UK) and Easypump II (B. Braun Medical Ltd, Sheffield, UK) can be achieved.

methodsTesting was as per the latest National Health Service (NHS) Pharmaceutical Quality Assurance Committee Yellow Cover Document (YCD) requirements.A validated stability indicating high-performance liquid chromatography method was used for assessing the stability of the solutions of piperacillin/tazobactam at a combined concentration of 25 mg/mL and 90 mg/mL respectively. Solutions were tested in two batches in replicate (n=3) at five time points according to the requirements of the YCD.

resultsPiperacillin/tazobactam stability was significantly improved when 0.3% w/v citrate-buffered saline pH 7 was used as the diluent, compared with using 0.9% w/v saline as diluent. Greater than 95% of the zero-time concentration of both actives remained following storage at 2°C-8°C for up to 13 days plus 24 hours at 32°C in both devices. The data support extended storage of up to 13 days 2°C-8°C plus 24 hours at 32°C 'in-use' when using FOLFusor LV10 (Baxter) or Easypump II (B. Braun) pump devices.

conclusionsThe enhanced stability complies with UK national standards as stated in the YCD for stability testing of aseptically produced small molecules and supports the storage of piperacillin/tazobactam for up to 13 days 2°C-8°C plus 24 hours at 32°C 'in-use' within two elastomeric pump devices. The extended shelf-life provides a significant advantage over the stability of piperacillin/tazobactam solutions for infusion when reconstituted and diluted in 0.9% w/v saline as diluent. The data open up the possibility of a continuous infusion of piperacillin/tazobactam delivered by elastomeric pump devices over 24 hours in an outpatient parenteral antimicrobial therapy setting.

Indexed as

OutpatientsState MedicineAnti-Bacterial AgentsCitratesDrug StabilityHumansPiperacillin, Tazobactam Drug CombinationAnti-Bacterial AgentsCitratesPiperacillin, Tazobactam Drug Combinationdrug analysisdrug stabilitydrug storageIV administrationshelf life

Identifiers

PMID32978220
PMCPMC9251159
OpenAlexW3088252315

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.