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Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment

OBJECTIVES: To conduct the benefit–risk assessment of 3-hydroxy-3-methyl-glutaryl (HMG) coenzyme A reductase inhibitors (statins) using a discrete choice experiment, based on 3 major stakeholders’ perspectives including patients, experts and policymakers in Thailand. DESIGN: A discrete choice experi...

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Autores principales: Wanishayakorn, Tanatape, Sornlertlumvanich, Korn, Ngorsuraches, Surachat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769438/
https://www.ncbi.nlm.nih.gov/pubmed/26916689
http://dx.doi.org/10.1136/bmjopen-2015-009387
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author Wanishayakorn, Tanatape
Sornlertlumvanich, Korn
Ngorsuraches, Surachat
author_facet Wanishayakorn, Tanatape
Sornlertlumvanich, Korn
Ngorsuraches, Surachat
author_sort Wanishayakorn, Tanatape
collection PubMed
description OBJECTIVES: To conduct the benefit–risk assessment of 3-hydroxy-3-methyl-glutaryl (HMG) coenzyme A reductase inhibitors (statins) using a discrete choice experiment, based on 3 major stakeholders’ perspectives including patients, experts and policymakers in Thailand. DESIGN: A discrete choice experiment questionnaire survey in three stakeholders’ perspectives. SETTING: Public hospitals in Thailand. PARTICIPANTS: A total of 353 policymakers, experts and patients. OUTCOMES: Stakeholders’ preferences for assessment criteria (stroke reduction, myocardial infarction reduction, myalgia and hepatotoxicity). Statins’ ranking and maximum acceptable risk in all perspectives were also calculated. RESULTS: For any perspective, the most and least important criteria were the risk of hepatotoxicity and the benefit of myocardial infarction reduction, respectively. Patients and experts agreed on the order of importance for myalgia and stroke reduction, but policymakers had different order of importance in these criteria. Overall, results showed that the highest and lowest chances of being chosen were atorvastatin and rosuvastatin, respectively. Only patients’ ranking order was different from others. Maximum acceptable risk of hepatotoxicity was lower than that of myalgia, reflecting the greater concern of all perspectives to statin consequence on liver. CONCLUSIONS: The results of benefit–risk assessment from every perspective were somewhat consistent. This study demonstrated the feasibility of applying a discrete choice experiment in the benefit–risk assessment of drugs and encouraged the engagement of multiple stakeholders in the decision-making process.
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spelling pubmed-47694382016-03-01 Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment Wanishayakorn, Tanatape Sornlertlumvanich, Korn Ngorsuraches, Surachat BMJ Open Health Policy OBJECTIVES: To conduct the benefit–risk assessment of 3-hydroxy-3-methyl-glutaryl (HMG) coenzyme A reductase inhibitors (statins) using a discrete choice experiment, based on 3 major stakeholders’ perspectives including patients, experts and policymakers in Thailand. DESIGN: A discrete choice experiment questionnaire survey in three stakeholders’ perspectives. SETTING: Public hospitals in Thailand. PARTICIPANTS: A total of 353 policymakers, experts and patients. OUTCOMES: Stakeholders’ preferences for assessment criteria (stroke reduction, myocardial infarction reduction, myalgia and hepatotoxicity). Statins’ ranking and maximum acceptable risk in all perspectives were also calculated. RESULTS: For any perspective, the most and least important criteria were the risk of hepatotoxicity and the benefit of myocardial infarction reduction, respectively. Patients and experts agreed on the order of importance for myalgia and stroke reduction, but policymakers had different order of importance in these criteria. Overall, results showed that the highest and lowest chances of being chosen were atorvastatin and rosuvastatin, respectively. Only patients’ ranking order was different from others. Maximum acceptable risk of hepatotoxicity was lower than that of myalgia, reflecting the greater concern of all perspectives to statin consequence on liver. CONCLUSIONS: The results of benefit–risk assessment from every perspective were somewhat consistent. This study demonstrated the feasibility of applying a discrete choice experiment in the benefit–risk assessment of drugs and encouraged the engagement of multiple stakeholders in the decision-making process. BMJ Publishing Group 2016-02-25 /pmc/articles/PMC4769438/ /pubmed/26916689 http://dx.doi.org/10.1136/bmjopen-2015-009387 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Health Policy
Wanishayakorn, Tanatape
Sornlertlumvanich, Korn
Ngorsuraches, Surachat
Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title_full Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title_fullStr Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title_full_unstemmed Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title_short Benefit–risk assessment of HMG-CoA reductase inhibitors (statins): a discrete choice experiment
title_sort benefit–risk assessment of hmg-coa reductase inhibitors (statins): a discrete choice experiment
topic Health Policy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769438/
https://www.ncbi.nlm.nih.gov/pubmed/26916689
http://dx.doi.org/10.1136/bmjopen-2015-009387
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