Opportunities for Pharmacogenetic Testing Among Hospitalized Children With Medical Complexity.

Document Type

Article

Publication Date

3-2025

Identifier

DOI: 10.1542/hpeds.2025-008751

Abstract

OBJECTIVE: Children with medical complexity (CMC), in whom drug efficacy and adverse drug events are difficult to assess, could benefit from pharmacogenetic (PGx) testing. We sought to determine the prevalence of prescribed medications with a high level of evidence for PGx-guided dosing and to identify their associated genes for testing among CMC.

PATIENTS AND METHODS: This cross-sectional study included patients discharged from a complex care inpatient team from June 2019 to June 2020. We identified medications with level A evidence for PGx-guided dosing per the Clinical Pharmacogenetics Implementation Consortium (CPIC) in January 2023 (N = 73) from medication lists. We determined frequency of CPIC level A scheduled and as-needed (PRN) prescriptions. We compared these findings with a secondary dataset of patients who attend a complex care clinic.

RESULTS: For CPIC level A medications prescribed to the inpatients, 60.2% were on at least 1 scheduled medication and 60.2% were on at least 1 PRN medication. The most commonly scheduled medications were lansoprazole (25.0%) and omeprazole (16.4%); the most common PRN medications were ibuprofen (50%), ondansetron (18.8%), and tramadol (3.9%). The outpatient cohort similarly had a large proportion on at least 1 scheduled or 1 PRN medication (44.4% and 47.6%, respectively), with proton pump inhibitors (PPIs) being commonly prescribed. The genes most highly associated with the medications prescribed to both populations were CYP2C19, CYP2C9, and CYP2D6.

CONCLUSIONS: PPIs were the most common CPIC level A medications and are metabolized by CYP2C19, making it the most highly implicated gene. PPI-CYP2C19 should be a PGx testing priority.

Journal Title

Hosp Pediatr

Volume

16

Issue

3

First Page

160

Last Page

165

MeSH Keywords

Humans; Cross-Sectional Studies; Pharmacogenomic Testing; Child; Male; Female; Child, Preschool; Child, Hospitalized; Adolescent; Infant; Cytochrome P-450 CYP2C19; Hospitalization

PubMed ID

41713489

Keywords

Cross-Sectional Studies; Pharmacogenomic Testing; Hospitalized Child; Cytochrome P-450 CYP2C19; Hospitalization

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