Stability and compatibility of parenteral nutrition solutions; a review of influencing factors.

Amino acids Compatibility Glucose Intravenous medication Lipid Parenteral nutrition solutions Stability

Journal

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 05 01 2023
revised: 30 03 2023
accepted: 03 04 2023
medline: 17 5 2023
pubmed: 16 4 2023
entrez: 15 4 2023
Statut: ppublish

Résumé

Both stability and compatibility of parenteral nutrition solutions (PNS) with drug products are major concerns for clinicians and clinical pharmacists, especially when concurrent administration of PNS with intravenous medications (IVM) is unavoidable. Since the same physicochemical principles apply to both adult's and paediatrics' PNS, concerns about stability and compatibility may still apply to both. However, these concerns are relatively more common in paediatrics and neonatal clinical settings, where limited vascular access can be problematic and the coadministration of PNS and drugs is more common. In neonatal and paediatric populations, there have been few experimental studies and comprehensive evaluations looking at medication compatibility with frequently used PNS. This work is part of a larger research project concerned for compatibility of PNS with commonly used intravenous medication in paediatric and neonates. This paper captures and reviews published data on factors influencing stability and compatibility of parenteral nutrition solutions. This information will help clinicians and clinical pharmacists to understand the principals of the stability and compatibility of PNS, furthermore, it will inform better design of future compatibility studies, as it highlights the complexity of PNS and the multiple factors influencing the stability of PNS, and hence its compatibility with IVM. When preparing, prescribing, and administering the PNS, especially when co-administration with IVM is unavoidable, it is important to take into account the physicochemical properties of the PNS components and IVM as well as administration conditions and environmental factors. These factors should also be considered in the design of the compatibility studies of the PNS with the IVM.

Identifiants

pubmed: 37061100
pii: S0939-6411(23)00082-6
doi: 10.1016/j.ejpb.2023.04.002
pii:
doi:

Substances chimiques

Parenteral Nutrition Solutions 0
Pharmaceutical Preparations 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

87-95

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The research leading to these results received funding from Pfizer, R&D, UK Ltd.

Auteurs

Mahmoud Farhan (M)

School of Postgraduate Studies, Royal College of Surgeons in Ireland, Dublin, Ireland. Electronic address: mahmoudfarhan21@rcsi.ie.

Naomi McCallion (N)

Department of Pediatrics, Rotunda Hospital, Dublin, Ireland; Department of Pediatrics, Royal College of Surgeons in Ireland, Dublin, Ireland; Department of Neonatology, Children Hospital Ireland, Dublin, Ireland. Electronic address: naomimccallion@rcsi.ie.

Joanne Bennett (J)

Pfizer, R&D, UK Ltd, United Kingdom. Electronic address: joanne.bennett@pfizer.com.

Anne Cram (A)

Pfizer, R&D, UK Ltd, United Kingdom. Electronic address: anne.cram@pfizer.com.

Fiona O'Brien (F)

School of Pharmacy, Royal College of Surgeons in Ireland, Dublin, Ireland. Electronic address: fionaobrien@rcsi.ie.

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Classifications MeSH