Literature DB >> 33037121

Prevalence of Clinically Significant Drug-Drug Interactions Across US Children's Hospitals.

James W Antoon1,2, Matt Hall3, Alison Herndon4,2, Alison Carroll4,2, My-Linh Ngo4,2, Katherine L Freundlich4,2, Justine C Stassun2, Patricia Frost4,2, David P Johnson4,2, Swati B Chokshi4,2, Charlotte M Brown4,2, Whitney L Browning4,2, James A Feinstein5, Carlos G Grijalva6, Derek J Williams4,2.   

Abstract

BACKGROUND: Little is known about the prescribing of medications with potential drug-drug interactions (DDIs) in the pediatric population. The objective of this study was to determine the prevalence and variation of prescribing medications with clinically significant DDIs across children's hospitals in the United States.
METHODS: We performed a retrospective cohort study of patients <26 years of age who were discharged from 1 of 52 US children's hospitals between January 2016 and December 2018. Fifty-three drug pairings with clinically significant DDIs in children were evaluated. We identified patient-level risk factors associated with DDI using multivariable logistic regression. Adjusted hospital-level rates of DDI exposure were derived by using a generalized linear mixed-effects model, and DDI exposure variations were examined across individual hospitals.
RESULTS: Across 52 children's hospitals, 47 414 (2.0%) hospitalizations included exposure to a DDI pairing (34.9 per 1000 patient-days) during the study period. One-quarter of pairings were considered contraindicated (risk grade X). After adjusting for hospital and clinical factors, there was wide variation in the percentage of DDI prescribing across hospitals, ranging from 1.05% to 4.92%. There was also substantial hospital-level variation of exposures to individual drug pairings. Increasing age, number of complex chronic conditions, length of stay, and surgical encounters were independently associated with an increased odds of DDI exposure.
CONCLUSIONS: Patients hospitalized at US children's hospitals are frequently exposed to medications with clinically significant DDIs. Exposure risk varied substantially across hospitals. Further study is needed to determine the rate of adverse events due to DDI exposures and factors amenable for interventions promoting safer medication use.
Copyright © 2020 by the American Academy of Pediatrics.

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Year:  2020        PMID: 33037121      PMCID: PMC7786820          DOI: 10.1542/peds.2020-0858

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  17 in total

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4.  Potential drug-drug interactions in infant, child, and adolescent patients in children's hospitals.

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Journal:  Pediatrics       Date:  2014-12-15       Impact factor: 7.124

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7.  Core drug-drug interaction alerts for inclusion in pediatric electronic health records with computerized prescriber order entry.

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Authors:  Marilyn D Paterno; Saverio M Maviglia; Paul N Gorman; Diane L Seger; Eileen Yoshida; Andrew C Seger; David W Bates; Tejal K Gandhi
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9.  Epidemiology of Polypharmacy and Potential Drug-Drug Interactions Among Pediatric Patients in ICUs of U.S. Children's Hospitals.

Authors:  Dingwei Dai; James A Feinstein; Wynne Morrison; Athena F Zuppa; Chris Feudtner
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Journal:  BMC Pediatr       Date:  2014-08-08       Impact factor: 2.125

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4.  Complexity of Medication Regimens for Children With Neurological Impairment.

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5.  Novel Method for Early Prediction of Clinically Significant Drug-Drug Interactions with a Machine Learning Algorithm Based on Risk Matrix Analysis in the NICU.

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6.  Clinically Significant Cytochrome P450-Mediated Drug-Drug Interactions in Children Admitted to Intensive Care Units.

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