Understanding the state of pharmacogenomic testing for thiopurine methyltransferase within a large health system.
Aim: To investigate the current state of TPMT testing at a single-academic medical center. Methods: Single-center, retrospective chart review for patients newly prescribed a thiopurine. Data collection and evaluation included the prevalence and timing of TPMT testing, correct dosage adjustment if applicable, and incidence of myelosuppression. Results: 121 patients (71%) received TPMT testing. Out of the tested patients, 110 (90.9%) were designated as wild-type with normal metabolism. Dosing modification was appropriate in applicable patients. In unadjusted analysis, there was a lower incidence of myelosuppression among patients who were tested versus those who were not (16.5 vs 36.7%). Conclusion: Based on the study results, TPMT testing opportunities exist for nearly 30% of patients. Testing may reduce the incidence of myelosuppression.
Duke Scholars
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Related Subject Headings
- Retrospective Studies
- Pharmacology & Pharmacy
- Pharmacogenomic Testing
- Pharmacogenetics
- North Carolina
- Middle Aged
- Methyltransferases
- Mercaptopurine
- Male
- Humans
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Retrospective Studies
- Pharmacology & Pharmacy
- Pharmacogenomic Testing
- Pharmacogenetics
- North Carolina
- Middle Aged
- Methyltransferases
- Mercaptopurine
- Male
- Humans