376 558

Cited 0 times in

Cited 3 times in

Cost-Benefit Analysis of Tafenoquine for Radical Cure of Plasmodium vivax Malaria in Korea

DC Field Value Language
dc.contributor.authorSuh, Jiyeon-
dc.contributor.authorKim, Jung Ho-
dc.contributor.authorKim, Jong-Dae-
dc.contributor.authorKim, Chang Soo-
dc.contributor.authorChoi, Jun Yong-
dc.contributor.authorLee, Jeehyun-
dc.contributor.authorYeom, Joon Sup-
dc.date.accessioned2022-12-22T02:46:46Z-
dc.date.available2022-12-22T02:46:46Z-
dc.date.created2023-01-27-
dc.date.issued2022-07-
dc.identifier.issn1011-8934-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/191688-
dc.description.abstractBackground: Plasmodium vivax malaria has a persistent liver stage that causes relapse, and introducing tafenoquine to suppress relapse could aid in disease eradication. Therefore, we assessed the impact of tafenoquine introduction on P. vivax malaria incidence and performed a cost-benefit analysis from the payer's perspective. Methods: We expanded the previously developed P. vivax malaria dynamic transmission model and calibrated it to weekly civilian malaria incidences in 2014-2018. Primaquine and tafenoquine scenarios were considered by assuming different relapse probabilities, and relapse and total P. vivax malaria cases were predicted over the next decade for each scenario. We then estimated the number of cases prevented by replacing primaquine with tafenoquine. The cost and benefit of introducing tafenoquine were obtained using medical expenditure from a nationwide database, and a cost-benefit analysis was conducted. A probabilistic sensitivity analysis was performed to assess the economic feasibility robustness of tafenoquine introduction under uncertainties of model parameters, costs, and benefits. Results: Under 0.04 primaquine relapse probability, the introduction of tafenoquine with relapse probability of 0.01 prevented 129 (12.27%) and 35 (77.78%) total and relapse cases, respectively, over the next decade. However, under the same relapse probability as primaquine, introducing tafenoquine had no additional preventative effect. The 14 -day primaquine treatment cost was 57.37 and 65.13. The average medical expenditure per malaria patient was estimated at $1444.79. The cost-benefit analysis results provided an incremental benefit-cost ratio (IBCR) from 0 to 3.21 as the tafenoquine relapse probability decreased from 0.04 to 0.01. The probabilistic sensitivity analysis showed an IBCR > 1, indicating that tafenoquine is beneficial, with a probability of 69.1%. Conclusion: Tafenoquine could reduce P. vivax malaria incidence and medical costs and bring greater benefits than primaquine.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisher대한의학회(The Korean Academy of Medical Sciences)-
dc.relation.isPartOfJournal of Korean Medical Science-
dc.relation.isPartOfJOURNAL OF KOREAN MEDICAL SCIENCE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleCost-Benefit Analysis of Tafenoquine for Radical Cure of Plasmodium vivax Malaria in Korea-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSuh, Jiyeon-
dc.contributor.googleauthorKim, Jung Ho-
dc.contributor.googleauthorKim, Jong-Dae-
dc.contributor.googleauthorKim, Chang Soo-
dc.contributor.googleauthorChoi, Jun Yong-
dc.contributor.googleauthorLee, Jeehyun-
dc.contributor.googleauthorYeom, Joon Sup-
dc.identifier.doi10.3346/jkms.2022.37.e212-
dc.relation.journalcodeJ01517-
dc.identifier.eissn1598-6357-
dc.identifier.pmid35818703-
dc.subject.keywordPlasmodium vivax-
dc.subject.keywordMalaria-
dc.subject.keywordModeling-
dc.subject.keywordTafenoquine-
dc.subject.keywordCost-Benefit Analysis-
dc.contributor.alternativeNameChoi, Jun Yong-
dc.contributor.affiliatedAuthorKim, Jung Ho-
dc.contributor.affiliatedAuthorKim, Chang Soo-
dc.contributor.affiliatedAuthorChoi, Jun Yong-
dc.contributor.affiliatedAuthorYeom, Joon Sup-
dc.identifier.scopusid2-s2.0-85133735491-
dc.identifier.wosid000826312400002-
dc.citation.volume37-
dc.citation.number27-
dc.identifier.bibliographicCitationJournal of Korean Medical Science, Vol.37(27), 2022-07-
dc.identifier.rimsid77412-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorPlasmodium vivax-
dc.subject.keywordAuthorMalaria-
dc.subject.keywordAuthorModeling-
dc.subject.keywordAuthorTafenoquine-
dc.subject.keywordAuthorCost-Benefit Analysis-
dc.subject.keywordPlusPREVENT RELAPSE-
dc.subject.keywordPlusPRIMAQUINE-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusADHERENCE-
dc.subject.keywordPlus2D6-
dc.type.docTypeArticle-
dc.identifier.kciidART002859933-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.identifier.articlenoe212-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.