Peripheral and Central/Intraosseous Vasoactive Infusions During and After Pediatric Critical Care Transport: Retrospective Cohort Study of Extravasation Injury.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
01 08 2022
Historique:
pubmed: 29 4 2022
medline: 30 9 2022
entrez: 28 4 2022
Statut: ppublish

Résumé

To compare the prevalence of adverse events related to vasoactive drug infusions administered via a peripheral venous catheter versus a central venous or intraosseous catheter. Retrospective observational study. A pediatric critical care transport team, and the PICUs and regional hospitals within the North Thames and East Anglia regions of the United Kingdom. Children (up to 18 yr old) transported by the Children's Acute Transport Service receiving an infusion of a vasoactive drug (epinephrine, dobutamine, dopamine, norepinephrine, and vasopressin). None. The medical records of all children transported between April 2017 and May 2020 receiving a vasoactive drug infusion were reviewed and cross-referenced with the service critical incident database. The outcome measure was anatomic catheter-related adverse events (including extravasation) reported during transport or in the first 24 hours on the PICU. During the study period, the service undertook 3,836 transports. Vasoactive drugs were administered during 558 patient transports (14.5%). During 198 of 558 transports (35.5%), vasoactive drugs were administered via a peripheral venous catheter, with seven of 198 (3.5%) adverse events. One extravasation event resulted in tissue necrosis. The median time to injury after the infusion was commenced was 60 minutes (interquartile range, 30-60 min). During 360 of 558 transports (64.5%), vasoactive infusions were administered by central venous or intraosseous catheter, with nine of 360 (2.5%) adverse events. During pediatric critical care transport, we did not find a difference in prevalence of adverse events following the administration of vasoactive drugs via peripheral venous catheters or via central venous and intraosseous catheters.

Identifiants

pubmed: 35481954
doi: 10.1097/PCC.0000000000002972
pii: 00130478-202208000-00006
doi:

Substances chimiques

Dobutamine 3S12J47372
Dopamine VTD58H1Z2X
Norepinephrine X4W3ENH1CV
Epinephrine YKH834O4BH

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

626-634

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Déclaration de conflit d'intérêts

The authors have disclosed that they do not have any potential conflicts of interest.

Références

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Auteurs

Niha Peshimam (N)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

Kara Bruce-Hickman (K)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

Katrina Crawford (K)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

Gaurang Upadhyay (G)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

Elise Randle (E)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

Padmanabhan Ramnarayan (P)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.
Anaesthetics, Pain Medicine and Intensive Care Division, Department of Surgery and Cancer, Imperial College London, London, United Kingdom.

Andrew J Jones (AJ)

Children's Acute Transport Service, Great Ormond Street Hospital, London, United Kingdom.

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Classifications MeSH