Opportunities for Pharmacogenetic Testing to Guide Dosing of Medications in Youths With Medicaid

Author:

Tang Girdwood Sonya123,Hall Matthew4,Antoon James W.56,Kyler Kathryn E.789,Williams Derek J.56,Shah Samir S.1310,Orth Lucas E.11,Goldman Jennifer8912,Feinstein James A.13,Ramsey Laura B.89

Affiliation:

1. Division of Hospital Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

2. Division of Translational and Clinical Pharmacology, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

3. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio

4. Children’s Hospital Association, Lenexa, Kansas

5. Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee

6. Division of Hospital Medicine, Monroe Carell Jr Children's Hospital at Vanderbilt University Medical Center, Nashville, Tennessee

7. Division of Hospital Medicine, Children’s Mercy Kansas City, Kansas City, Missouri

8. Division of Clinical Pharmacology, Children’s Mercy Kansas City, Kansas City, Missouri

9. School of Medicine, University of Missouri-Kansas City

10. Division of Infectious Diseases, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

11. Department of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy, Aurora

12. Division of Infectious Diseases, Children’s Mercy Kansas City, Kansas City, Missouri

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

Abstract

ImportanceThere are an increasing number of medications with a high level of evidence for pharmacogenetic-guided dosing (PGx drugs). Knowledge of the prevalence of dispensings of PGx drugs and their associated genes may allow hospitals and clinical laboratories to determine which pharmacogenetic tests to implement.ObjectivesTo investigate the prevalence of outpatient dispensings of PGx drugs among Medicaid-insured youths, determine genes most frequently associated with PGx drug dispenses, and describe characteristics of youths who were dispensed at least 1 PGx drug.Design, Setting, and ParticipantsThis serial cross-sectional study includes data from 2011 to 2019 among youths aged 0 to 17 years in the Marketscan Medicaid database. Data were analyzed from August to December 2022.Main Outcomes and MeasuresPGx drugs were defined as any medication with level A evidence as determined by the Clinical Pharmacogenetics Implementation Consortium (CPIC). The number of unique youths dispensed each PGx drug in each year was determined. PGx drugs were grouped by their associated genes for which there was CPIC level A evidence to guide dosing, and a dispensing rate (No. of PGx drugs/100 000 youths) was determined for each group for the year 2019. Demographics were compared between youths dispensed at least 1 PGx drug and those not dispensed any PGx drugs.ResultsThe number of Medicaid-insured youths queried ranged by year from 2 078 683 youths in 2011 to 4 641 494 youths in 2017, including 4 126 349 youths (median [IQR] age, 9 [5-13] years; 2 129 926 males [51.6%]) in 2019. The proportion of Medicaid-insured youths dispensed PGx drugs increased from 289 709 youths (13.9%; 95% CI, 13.8%-14.0%) in 2011 to 740 072 youths (17.9%; 95% CI, 17.9%-18.0%) in 2019. Genes associated with the most frequently dispensed medications were CYP2C9, CYP2D6, and CYP2C19 (9197.0 drugs [95% CI, 9167.7-9226.3 drugs], 8731.5 drugs [95% CI, 8702.5-8759.5 drugs], and 3426.8 drugs [95% CI, 3408.1-3443.9 drugs] per 100 000 youths, respectively). There was a higher percentage of youths with at least 1 chronic medical condition among youths dispensed at least 1 PGx drug (510 445 youths [69.0%; 95% CI, 68.8%-69.1%]) than among 3 386 277 youths dispensed no PGx drug (1 381 544 youths [40.8%; 95% CI, 40.7%-40.9%) (P < .001) in 2019.Conclusions and RelevanceIn this study, there was an increasing prevalence of dispensings for PGx drugs. This finding suggests that pharmacogenetic testing of specific drug-gene pairs should be considered for frequently prescribed PGx drugs and their implicated genes.

Publisher

American Medical Association (AMA)

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