Plasma-Lyte 148 and Plasma-Lyte 148 + 5% glucose compatibility with commonly used critical care drugs.

Compatibility Drug stability Intensive care Pharmacostability Plasmalyte

Journal

Intensive care medicine experimental
ISSN: 2197-425X
Titre abrégé: Intensive Care Med Exp
Pays: Germany
ID NLM: 101645149

Informations de publication

Date de publication:
23 Jun 2020
Historique:
received: 11 11 2019
accepted: 26 05 2020
entrez: 25 6 2020
pubmed: 25 6 2020
medline: 25 6 2020
Statut: epublish

Résumé

Plasma-Lyte is a balanced, crystalloid intravenous fluid which has been shown to avoid the hyperchloremic metabolic acidosis associated with 0.9% sodium chloride. Data on physical, pH and chemical compatibility with other medicines are essential. The compatibility of adrenaline, dobutamine, dopamine, furosemide, midazolam, morphine and milrinone with Plasma-Lyte 148 (PLA) and Plasma-Lyte 148 with 5% glucose (PLA-G) was investigated. Control solutions were 0.9% sodium chloride and 5% glucose. Chemical stability was defined as < 5% concentration change with high-performance liquid chromatography (HPLC). Physical compatibility was assessed by checking for colour changes and precipitate formation. The pH of the admixtures was considered acceptable if between 5 and 9 at all time points. Six repeats were carried out for HPLC, 2 for physical compatibility checks and pH measurements, with all admixtures being tested at 0, 2 and 24 h after mixing. All combinations were found to be chemically stable at 0, 2 and 24 h apart from furosemide with PLA-G at 24 h and midazolam with PLA or PLA-G at both 2 and 24 h. Only midazolam was physically incompatible when mixed with both Plasma-Lyte solutions. The pH remained stable in all admixtures, although not all pH values recorded were within the range of 5-9. All drugs excluding furosemide and midazolam were shown to be chemically, physically and pH stable at the tested concentrations when diluted with PLA and PLA-G.

Identifiants

pubmed: 32577941
doi: 10.1186/s40635-020-00311-5
pii: 10.1186/s40635-020-00311-5
pmc: PMC7311557
doi:

Types de publication

Journal Article

Langues

eng

Pagination

25

Subventions

Organisme : Nottingham University Hospitals Charity
ID : N/A

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Auteurs

Sophie Hammond (S)

School of Medicine, University of Nottingham, Nottingham, UK.
Paediatric Critical Care Unit, Nottingham Children's Hospital, Derby Road, Nottingham, UK.

Andrew Wignell (A)

Paediatric Critical Care Unit, Nottingham Children's Hospital, Derby Road, Nottingham, UK.
Pharmacy Department, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Paul Cooling (P)

Division of Advanced Materials and Healthcare Technologies, School of Pharmacy, University of Nottingham, Nottingham, UK.

David A Barrett (DA)

Division of Advanced Materials and Healthcare Technologies, School of Pharmacy, University of Nottingham, Nottingham, UK.

Patrick Davies (P)

School of Medicine, University of Nottingham, Nottingham, UK. Patrick.davies@nuh.nhs.uk.
Paediatric Critical Care Unit, Nottingham Children's Hospital, Derby Road, Nottingham, UK. Patrick.davies@nuh.nhs.uk.

Classifications MeSH