Adverse drug reactions (ADRs) contribute to hospitalization but data on its economic burden is scant. Pre-emptive pharmacogenetic (PGx) testing can potentially reduce ADRs and its associated costs. The objectives of this study were to quantify the economic burden of ADRs and to estimate the breakeven cost of pre-emptive PGx testing in Singapore. We collected itemized costs for 1000 random non-elective hospitalizations of adults admitted to a tertiary-care general hospital in Singapore. The presence of ADRs at admission and their clinical characteristics were reported previously. The economic burden of ADRs was assessed from two perspectives: (1) Total cost and (2) incremental costs. The breakeven cost of PGx testing was estimated by dividing avoidable hospitalization costs for ADRs due to selected drugs by the number of patients taking those drugs. The total cost of 81 admissions caused by ADRs was US$570,404. Costs were significantly higher for bleeding/elevated international normalized ratio (US$9906 vs. US$2251, p = 6.58 × 10−3) compared to other ADRs, and for drugs acting on the blood coagulation system (US$9884 vs. US$2229, p = 4.41 × 10−3) compared to other drug classes. There were higher incremental laboratory costs due to ADRs causing or being present at admission. The estimated breakeven cost of a pre-emptive PGx test for patients taking warfarin, clopidogrel, chemotherapeutic and neuropsychiatric drugs was US$114 per patient. These results suggest that future studies designed to directly measure the clinical and cost impact of a pre-emptive genotyping program will help inform clinical practice and health policy decisions.
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We are grateful to all patients who participated in the study. This study was partly supported by an Agency for Science, Technology and Research of Singapore (A*STAR) Biomedical Research Council grant to the SAPhIRE programme (SPF2014/001), and by the National University of Singapore. LRB is supported by a Canadian Institutes of Health Research New Investigator award. We also thank the staff at the Vigilance and Compliance Branch of the Health Sciences Authority for helpful discussions.
Conflict of interest
The authors declare that they have no conflict of interest.
Joint senior authors: Liam R Brunham, Hwee-Lin Wee
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Chan, S.L., Ng, H.Y., Sung, C. et al. Economic burden of adverse drug reactions and potential for pharmacogenomic testing in Singaporean adults. Pharmacogenomics J 19, 401–410 (2019) doi:10.1038/s41397-018-0053-1
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