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The use of antimicrobial susceptibility testing in pediatric cystic fibrosis pulmonary exacerbations.
- Source :
-
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society [J Cyst Fibros] 2019 Nov; Vol. 18 (6), pp. 851-856. Date of Electronic Publication: 2019 May 28. - Publication Year :
- 2019
-
Abstract
- Background: Although antimicrobial susceptibility testing (AST) frequently guides cystic fibrosis (CF) pulmonary exacerbation (PEx) management, its clinical utility is unclear. This study examined associations between AST and antimicrobial switching during PEx treatment and time and occurrence of next PEx as treatment outcomes.<br />Methods: This retrospective cohort study utilized Pediatric Health Information System data. Children and adolescents aged 1-18 years admitted for a PEx from 2011 to 2016 were studied. Antimicrobial switching was defined as any intra-admission change in intravenous (IV), oral, and/or inhaled antimicrobials. Time to next PEx was defined as the time between index PEx hospital discharge and subsequent hospital admission requiring IV antimicrobials. Odds of antimicrobial switching ≥5 days after treatment initiation were determined by generalized linear mixed models, and associations between AST and time to next PEx were studied using Kaplan-Meier curves and Cox proportional hazards regression.<br />Results: AST occurred in 2518 (39%) of 6451 PEx at 36 hospitals and was associated with increased odds of antimicrobial switching (OR 1.33, 95% CI 1.16-1.52; p = 0.001) and increased hazard of future PEx (HR 1.32, 95% CI 1.16-1.50; p < 0.001). However, antimicrobial switching was not associated with a longer time to next PEx.<br />Conclusions: AST was associated with both increased probability of antimicrobial regimen change and increased PEx hazard. There was no evidence that antimicrobial regimen change was associated with clinical benefit as assessed by time to next PEx. However, these results indicate residual indication bias remained after adjustment for available disease covariates. Additional studies of the clinical value of AST are warranted.<br /> (Copyright © 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Disease Progression
Female
Humans
Infant
Infant, Newborn
Male
Neonatal Screening methods
Neutrophils immunology
Practice Patterns, Physicians' statistics & numerical data
Respiratory Function Tests methods
Symptom Assessment methods
Symptom Assessment statistics & numerical data
Anti-Bacterial Agents therapeutic use
Bronchoalveolar Lavage Fluid cytology
Bronchoalveolar Lavage Fluid microbiology
Cystic Fibrosis diagnosis
Cystic Fibrosis drug therapy
Cystic Fibrosis physiopathology
Inflammation diagnosis
Inflammation virology
Respiratory Tract Infections diagnosis
Respiratory Tract Infections drug therapy
Respiratory Tract Infections virology
Rhinovirus isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5010
- Volume :
- 18
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
- Publication Type :
- Academic Journal
- Accession number :
- 31147301
- Full Text :
- https://doi.org/10.1016/j.jcf.2019.05.012