Randomised, controlled, feasibility trial comparing vasopressor infusion administered via peripheral cannula versus central venous catheter for critically ill adults: A study protocol.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 19 11 2023
accepted: 11 03 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: epublish

Résumé

When clinicians need to administer a vasopressor infusion, they are faced with the choice of administration via either peripheral intravenous catheter (PIVC) or central venous catheter (CVC). Vasopressor infusions have traditionally been administered via central venous catheters (CVC) rather than Peripheral Intra Venous Catheters (PIVC), primarily due to concerns of extravasation and resultant tissue injury. This practice is not guided by contemporary randomised controlled trial (RCT) evidence. Observational data suggests safety of vasopressor infusion via PIVC. To address this evidence gap, we have designed the "Vasopressors Infused via Peripheral or Central Access" (VIPCA) RCT. The VIPCA trial is a single-centre, feasibility, parallel-group RCT. Eligible critically ill patients requiring a vasopressor infusion will be identified by emergency department (ED) or intensive care unit (ICU) staff and randomised to receive vasopressor infusion via either PIVC or CVC. Primary outcome is feasibility, a composite of recruitment rate, proportion of eligible patients randomised, protocol fidelity, retention and missing data. Primary clinical outcome is days alive and out of hospital up to day-30. Secondary outcomes will include safety and other clinical outcomes, and process and cost measures. Specific aspects of safety related to vasopressor infusions such as extravasation, leakage, device failure, tissue injury and infection will be assessed. VIPCA is a feasibility RCT whose outcomes will inform the feasibility and design of a multicentre Phase-3 trial comparing routes of vasopressor delivery. The exploratory economic analysis will provide input data for the full health economic analysis which will accompany any future Phase-3 RCT.

Sections du résumé

BACKGROUND BACKGROUND
When clinicians need to administer a vasopressor infusion, they are faced with the choice of administration via either peripheral intravenous catheter (PIVC) or central venous catheter (CVC). Vasopressor infusions have traditionally been administered via central venous catheters (CVC) rather than Peripheral Intra Venous Catheters (PIVC), primarily due to concerns of extravasation and resultant tissue injury. This practice is not guided by contemporary randomised controlled trial (RCT) evidence. Observational data suggests safety of vasopressor infusion via PIVC. To address this evidence gap, we have designed the "Vasopressors Infused via Peripheral or Central Access" (VIPCA) RCT.
METHODS METHODS
The VIPCA trial is a single-centre, feasibility, parallel-group RCT. Eligible critically ill patients requiring a vasopressor infusion will be identified by emergency department (ED) or intensive care unit (ICU) staff and randomised to receive vasopressor infusion via either PIVC or CVC. Primary outcome is feasibility, a composite of recruitment rate, proportion of eligible patients randomised, protocol fidelity, retention and missing data. Primary clinical outcome is days alive and out of hospital up to day-30. Secondary outcomes will include safety and other clinical outcomes, and process and cost measures. Specific aspects of safety related to vasopressor infusions such as extravasation, leakage, device failure, tissue injury and infection will be assessed.
DISCUSSION CONCLUSIONS
VIPCA is a feasibility RCT whose outcomes will inform the feasibility and design of a multicentre Phase-3 trial comparing routes of vasopressor delivery. The exploratory economic analysis will provide input data for the full health economic analysis which will accompany any future Phase-3 RCT.

Identifiants

pubmed: 38739611
doi: 10.1371/journal.pone.0295347
pii: PONE-D-23-36879
doi:

Substances chimiques

Vasoconstrictor Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Randomized Controlled Trial Comparative Study Clinical Trial Protocol

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0295347

Informations de copyright

Copyright: © 2024 Watts et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Stacey Watts (S)

Caboolture Hospital, Caboolture, Australia.

Yogesh Apte (Y)

Caboolture Hospital, Caboolture, Australia.
James Mayne Academy of Critical Care, The University of Queensland, Brisbane, Australia.

Thomas Holland (T)

Caboolture Hospital, Caboolture, Australia.

April Hatt (A)

Caboolture Hospital, Caboolture, Australia.

Alison Craswell (A)

Caboolture Hospital, Caboolture, Australia.
School of Health, University of the Sunshine Coast, Sippy Downs, Australia.

Frances Lin (F)

Caring Futures Institute, College of Nursing and Health Sciences, Flinders University, Adelaide, Australia.
Sunshine Coast Health Institute, School of Health, University of the Sunshine Coast, Sippy Downs, Australia.

Alexis Tabah (A)

James Mayne Academy of Critical Care, The University of Queensland, Brisbane, Australia.
Intensive Care Unit, Redcliffe Hospital, Brisbane, Australia.
Faculty of Health, Queensland University of Technology, Brisbane, Australia.
Queensland Critical Care Research Network, Herston, Australia.

Robert Ware (R)

Menzies Health Institute Queensland and School of Medicine and Dentistry, Griffith University, Southport, Australia.

Joshua Byrnes (J)

Centre for Applied Health Economics, School of Medicine and Dentistry, Griffith University, Southport, Australia.

Christopher Anstey (C)

Menzies Health Institute Queensland and School of Medicine and Dentistry, Griffith University, Southport, Australia.

Gerben Keijzers (G)

Menzies Health Institute Queensland and School of Medicine and Dentistry, Griffith University, Southport, Australia.
Department of Emergency Medicine, Gold Coast Hospital and Health Service, Southport, Australia.
Faculty of Health Sciences and Medicine Bond University, Robina, Australia.

Mahesh Ramanan (M)

Caboolture Hospital, Caboolture, Australia.
Queensland Critical Care Research Network, Herston, Australia.
Critical Care Division, The George Institute for Global Health, University of New South Wales, Kensington, Australia.
Faculty of Health, Queensland of Technology, Brisbane, Australia.

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