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

Author:

Antoon James W.12,Hall Matt3,Herndon Alison12,Carroll Alison12,Ngo My-linh12,Freundlich Katherine L.12,Stassun Justine C.2,Frost Patricia12,Johnson David P.12,Chokshi Swati B.12,Brown Charlotte M.12,Browning Whitney L.12,Feinstein James A.4,Grijalva Carlos G.5,Williams Derek J.12

Affiliation:

1. Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, Tennessee;

2. Departments of Pediatrics and

3. Children’s Hospital Association, Lenexa, Kansas; and

4. Adult and Child Consortium for Health Outcomes Research and Delivery Science, Children’s Hospital Colorado and University of Colorado Anschutz Medical Campus, Aurora, Colorado

5. Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee;

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.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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