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Sedation Management for Critically Ill Children with Pre-Existing Cognitive Impairment

Authors :
Kaitlin M. Best
Lisa A. Asaro
Martha A.Q. Curley
David Wypij
Geoffrey L. Allen
Derek C. Angus
Judy A. Ascenzi
Scot T. Bateman
Santiago Borasino
Cindy Darnell Bowens
G. Kris Bysani
Ira M. Cheifetz
Allison S. Cowl
Brenda L. Dodson
E. Vincent S. Faustino
Lori D. Fineman
Heidi R. Flori
Linda S. Franck
Rainer G. Gedeit
Mary Jo C. Grant
Andrea L. Harabin
Catherine Haskins-Kiefer
James H. Hertzog
Larissa Hutchins
Aileen L. Kirby
Ruth M. Lebet
Michael A. Matthay
Gwenn E. McLaughlin
JoAnne E. Natale
Phineas P. Oren
Nagendra Polavarapu
James B. Schneider
Adam J. Schwarz
Thomas P. Shanley
Shari Simone
Lewis P. Singer
Lauren R. Sorce
Edward J. Truemper
Michele A. Vander Heyden
R. Scott Watson
Claire R. Wells
Source :
The Journal of pediatrics. 206
Publication Year :
2018

Abstract

To compare current analgesia and sedation management practices between critically ill children with pre-existing cognitive impairment and critically ill neurotypical children, including possible indicators of therapeutic efficacy.This study used secondary analysis of prospective data from the RESTORE clinical trial, with 2449 children admitted to the pediatric intensive care unit and receiving mechanical ventilation for acute respiratory failure. Subjects with a baseline Pediatric Cerebral Performance Category ≥3 were defined as subjects with cognitive impairment, and differences between groups were explored using regression methods accounting for pediatric intensive care unit as a cluster variable.This study identified 412 subjects (17%) with cognitive impairment. Compared with neurotypical subjects, subjects with cognitive impairment were older (median, years, 6.2 vs 1.4; P .001) with more severe pediatric acute respiratory distress syndrome (40% vs 33%; P = .009). They received significantly lower cumulative doses of opioids (median, mg/kg, 14.2 vs 16.2; P .001) and benzodiazepines (10.6 vs 14.4; P .001). Three nonverbal subjects with cognitive impairment received no analgesia or sedation. Subjects with cognitive impairment were assessed as having more study days awake and calm and fewer study days with an episode of pain. They were less likely to be assessed as having inadequate pain/sedation management or unplanned endotracheal/invasive tube removal. Subjects with cognitive impairment had more documented iatrogenic withdrawal symptoms than neurotypical subjects.Subjects with cognitive impairment in this study received less medication, but it is unclear whether they have authentically lower analgesic and/or sedative requirements or are vulnerable to inadequate assessment of discomfort because of the lack of validated assessment tools. We recommend the development of pain and sedation assessment tools specific to this patient population.

Details

ISSN :
10976833
Volume :
206
Database :
OpenAIRE
Journal :
The Journal of pediatrics
Accession number :
edsair.doi.dedup.....1c0ad8ac7efb4188174f64c210a8b5a3