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AuthorAbushanab, Dina
AuthorMohammed, Shaban
AuthorAbdel-latif, Rania
AuthorAl-Muftah, Wadha
AuthorIsmail, Said I.
AuthorAl Hail, Moza
AuthorAl-Marridi, Wafa
AuthorAbdallah, Oraib
AuthorAl-Khuzaei, Noriya
AuthorAl-Thani, Asma
AuthorAl-Badriyeh, Daoud
Available date2025-04-24T06:32:16Z
Publication Date2024
Publication NameJournal of Pharmaceutical Policy and Practice
ResourceScopus
Identifierhttp://dx.doi.org/10.1080/20523211.2024.2410197
ISSN20523211
URIhttp://hdl.handle.net/10576/64480
AbstractBackground Pharmacogenetic testing improves the efficacy and safety of antidepressant pharmacotherapy for moderate-severe major depressive disorder by identifying genetic variations that influence medication metabolism, and adjusting treatment regimens accordingly. This study aims to assess the cost-effectiveness of implementing a pharmacogenetic testing approach to guide the prescription of antidepressants. Methods From the public hospital perspective, we developed a two-stage decision tree diagram of a short-term 6-week follow up, and a lifetime Markov model with 3-month cycles. The analysis compared the current standard of care with the alternative strategy of Pharmacogenetic-guided (multi-gene panel) testing in adult patients with moderate-severe major depressive disorder. Clinical outcomes and utilities were obtained from published studies, while healthcare costs were locally available. The short-term incremental cost-effectiveness ratio was against treatment response without side effects and without relapse, and against treatment response with/without side effects and without relapse. The long-term incremental cost-effectiveness ratio was against the quality-adjusted life year gained and years of life saved. Results Adopting the pharmacogenetic-guided therapy for adult patients with moderate-severe major depressive disorder in Qatar resulted in cost savings of Qatari Riyal 2,289 (95% confidence interval, −22,654–26,340) for the health system. In the short term, the pharmacogenetic-guided testing was associated with higher response rates without side effects and without relapse (mean difference 0.10, 95% confidence interval 0.09–0.15) and higher response rates with or without side effects and without relapse (mean difference 0.05, 95% confidence interval 0.04–0.06). For long term, the pharmacogenetic-guided testing resulted in 0.13 years of life saved and 0.06 quality-adjusted life year gained, per person, along with cost savings of Qatari Riyal 46,215 (95% confidence interval-15,744–101,758). The sensitivity analyses confirmed the robustness of the model results. Conclusion Implementing pharmacogenetic testing to guide antidepressant use was found to improve population health outcomes, while also significantly reducing health system costs.
SponsorThe authors would like to acknowledge Dr Majed Al-Abdullah, a senior consultant psychiatrist and the Chair of the Psychiatry Department at the Hamad Medical Corporation, for his principal role in the national implementation project of the genotype-guided treatment of major depression initiative in Qatar.
Languageen
PublisherTaylor and Francis Ltd.
Subjectantidepressive agents
cost-effectiveness analysis
depressive disorder
Pharmacogenetics
quality-adjusted life years
TitleCost-effectiveness analysis of genotype-guided optimization of major depression treatment in Qatar
TypeArticle
Issue Number1
Volume Number17
dc.accessType Open Access


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