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Inherent Risk Factors for Nosocomial Infection in the Long Stay Critically Ill Child Without Known Baseline Immunocompromise: A Post Hoc Analysis of the CRISIS Trial
Journal article   Peer reviewed

Inherent Risk Factors for Nosocomial Infection in the Long Stay Critically Ill Child Without Known Baseline Immunocompromise: A Post Hoc Analysis of the CRISIS Trial

Joseph A. Carcillo, J. Michael Dean, Richard Holubkov, John Berger, Kathleen L. Meert, Kanwaljeet J.S. Anand, Jerry Zimmerman, Christopher J. Newth, Rick Harrison, Jeri Burr, …
Pediatric Infectious Disease Journal, Vol.35(11)
2016

Abstract

Adolescent Child Child, Preschool Critical Illness Cross Infection Female Humans Infant Intensive Care Units, Pediatric Male Retrospective Studies Risk Factors Acinetobacter Acinetobacter baumannii adolescent alpha hemolytic Streptococcus Article Aspergillus niger bacterium identification bloodstream infection Candida albicans Candida glabrata Candida parapsilosis Candida tropicalis child childhood disease Citrobacter freundii coagulase negative Staphylococcus cohort analysis controlled study critical illness critically ill patient Eikenella Enterobacter Enterobacter cloacae Enterobacteraerogenes Enterococcus Enterococcus aerogenes Enterococcus cloacae Enterococcus faecalis Enterococcus faecium Enterococcus raffinosis Escherichia coli female Filobasidiella fungus identification Gram positive cocci Haemophilus influenzae Haemophilus parainfluenzae heart arrest hospital admission hospital infection human immunocompromised patient infection prevention infection risk Klebsiella oxytoca Klebsiella pneumoniae length of stay lymphocytopenia major clinical study male methicillin resistant Staphylococcus aureus Micrococcus mixed infection Moraxella catarrhalis neutropenia nonhuman Pantoea agglomerans pediatric intensive care unit Peptoclostridium difficile post hoc analysis priority journal Pseudomonas aeruginosa retrospective study Serratia marcescens skin infection soft tissue infection species identification Staphylococcus aureus Staphylococcus epidermidis Stenotrophomonas maltophilia Streptococcus pneumoniae urinary tract infection vancomycin resistant Enterococcus faecium yeast critical illness cross infection infant pediatric intensive care unit preschool child risk factor
Background: Nosocomial infection remains an important health problem in long stay (>3 days) pediatric intensive care unit (PICU) patients. Admission risk factors related to the development of nosocomial infection in long stay immune competent patients in particular are not known. Methods: Post-hoc analysis of the previously published Critical Illness Stress induced Immune Suppression (CRISIS) prevention trial database, to identify baseline risk factors for nosocomial infection. Because there was no difference between treatment arms of that study in nosocomial infection in the population without known baseline immunocompromise, both arms were combined and the cohort that developed nosocomial infection was compared with the cohort that did not. Results: There were 254 long stay PICU patients without known baseline immunocompromise. Ninety (35%) developed nosocomial infection, and 164 (65%) did not. Admission characteristics associated with increased nosocomial infection risk were increased age, higher Pediatric Risk of Mortality version III score, the diagnoses of trauma or cardiac arrest and lymphopenia (P < 0.05). The presence of sepsis or infection at admission was associated with reduced risk of developing nosocomial infection (P < 0.05). In multivariable analysis, only increasing age, cardiac arrest and existing lymphopenia remained significant admission risk factors (P < 0.05); whereas trauma tended to be related to nosocomial infection development (P = 0.07). Conclusions: These data suggest that increasing age, cardiac arrest and lymphopenia predispose long stay PICU patients without known baseline immunocompromise to nosocomial infection. These findings may inform pre-hoc stratification randomization strategies for prospective studies designed to prevent nosocomial infection in this population. Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.

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