Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0193112
DC Field | Value | |
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dc.title | Revisiting policy on chronic HCV treatment under the Thai Universal Health Coverage: An economic evaluation and budget impact analysis | |
dc.contributor.author | Rattanavipapong W. | |
dc.contributor.author | Anothaisintawee T. | |
dc.contributor.author | Teerawattananon Y. | |
dc.date.accessioned | 2020-03-27T01:05:18Z | |
dc.date.available | 2020-03-27T01:05:18Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Rattanavipapong W., Anothaisintawee T., Teerawattananon Y. (2018). Revisiting policy on chronic HCV treatment under the Thai Universal Health Coverage: An economic evaluation and budget impact analysis. PLoS ONE 13 (2) : e0193112. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0193112 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165968 | |
dc.description.abstract | Thailand is encountering challenges to introduce the high-cost sofosbuvir for chronic hepatitis C treatment as part of the Universal Health Care’s benefit package. This study was conducted in respond to policy demand from the Thai government to assess the value for money and budget impact of introducing sofosbuvir-based regimens in the tax-based health insurance scheme. The Markov model was constructed to assess costs and benefits of the four treatment options that include: (i) current practice–peginterferon alfa (PEG) and ribavirin (RBV) for 24 weeks in genotype 3 and 48 weeks for other genotypes; (ii) Sofosbuvir plus peginterferon alfa and ribavirin (SOF+PEG-RBV) for 12 weeks; (iii) Sofosbuvir and daclatasvir (SOF+DCV) for 12 weeks; (iv) Sofosbuvir and ledipasvir (SOF+LDV) for 12 weeks for non-3 genotypes and SOF+PEG-RBV for 12 weeks for genotype 3 infection. Given that policy options (ii) and (iii) are for pan-genotypic infection, the cost of genotype testing was applied only for policy options (i) and (iv). Results reveal that all sofosbuvir-based regimens had greater quality adjusted life years (QALY) gains compared with the current treatment, therefore associated with lower lifetime costs and more favourable health outcomes. Additionally, among the three regimens of sofosbuvir, SOF+PEG-RBV for genotype 3 and SOF+LDV for non-3 genotype are the most cost-effective treatment option with the threshold of 160,000 THB per QALY gained. The results of this study had been used in policy discussion which resulted in the recent inclusion of SOF+PEG-RBV for genotype 3 and SOF+LDV for non-3 genotype in the Thailand’s benefit package. © 2018 Rattanavipapong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | daclatasvir | |
dc.subject | ledipasvir | |
dc.subject | peginterferon alpha | |
dc.subject | ribavirin | |
dc.subject | sofosbuvir | |
dc.subject | antivirus agent | |
dc.subject | Article | |
dc.subject | budget | |
dc.subject | chronic hepatitis C | |
dc.subject | controlled study | |
dc.subject | cost benefit analysis | |
dc.subject | cost effectiveness analysis | |
dc.subject | cost utility analysis | |
dc.subject | drug cost | |
dc.subject | economic evaluation | |
dc.subject | health care cost | |
dc.subject | health care policy | |
dc.subject | health insurance | |
dc.subject | Hepatitis C virus genotype 3 | |
dc.subject | Markov chain | |
dc.subject | quality adjusted life year | |
dc.subject | quality of life | |
dc.subject | tax | |
dc.subject | Thailand | |
dc.subject | budget | |
dc.subject | chronic hepatitis C | |
dc.subject | combination drug therapy | |
dc.subject | cost | |
dc.subject | economic model | |
dc.subject | economics | |
dc.subject | female | |
dc.subject | genetics | |
dc.subject | genotype | |
dc.subject | genotyping technique | |
dc.subject | human | |
dc.subject | insurance | |
dc.subject | male | |
dc.subject | Antiviral Agents | |
dc.subject | Budgets | |
dc.subject | Costs and Cost Analysis | |
dc.subject | Drug Therapy, Combination | |
dc.subject | Female | |
dc.subject | Genotype | |
dc.subject | Genotyping Techniques | |
dc.subject | Hepatitis C, Chronic | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Models, Economic | |
dc.subject | Universal Coverage | |
dc.type | Article | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.description.doi | 10.1371/journal.pone.0193112 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 13 | |
dc.description.issue | 2 | |
dc.description.page | e0193112 | |
Appears in Collections: | Staff Publications Elements |
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