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韩国药物报销中应用卫生技术评估的八年经验

Eight-year experience of using HTA in drug reimbursement: South Korea.

作者信息

Bae Eun-Young, Hong Ji-Min, Kwon Hye-Young, Jang Suhyun, Lee Hye-Jae, Bae SeungJin, Yang Bong-Min

机构信息

School of Pharmacy, Gyeongsang National University, Jinju, South Korea; Institute of Pharmacy, Gyeongsang National University, Jinju, South Korea.

Graduate School of Public Health, Seoul National University, Seoul, South Korea.

出版信息

Health Policy. 2016 Jun;120(6):612-20. doi: 10.1016/j.healthpol.2016.03.013. Epub 2016 Apr 1.

Abstract

This study describes the process and results of drug reimbursement decision-making in South Korea and evaluates its performance from the perspectives of the various stakeholders involved. Data were retrieved from the evaluation report posted on the Health Insurance Review and Assessment Service (HIRA) website. As of 2014, 253 new drugs had been submitted to the HIRA for appraisal. Of these, 175 (69.2%) were recommended in favor of listing and 78 (30.8%) were rejected. Furthermore, 68 of these drugs were deemed clinically improved relative to existing drugs. For those drugs that did not demonstrate clinical superiority (which was most of them), a simple price comparison to the existing drug was utilized as a gate toward listing. On top of the base-line analysis, 104 stakeholders from the industry, academia, public office, and civic society responded to a questionnaire designed to obtain their opinions on the South Korean positive list system (PLS). Stakeholders agreed that the consistency of reimbursement decision-making has improved since 2007, while accessibility to new drugs has apparently decreased. Respondents also indicated a preference toward improved public access to decision-making information. This examination of reimbursement decisions in South Korea will illuminate critical issues for countries that are considering the introduction of similar policies.

摘要

本研究描述了韩国药品报销决策的过程和结果,并从相关各利益攸关方的角度评估了其绩效。数据取自医疗保险审查和评估服务局(HIRA)网站上发布的评估报告。截至2014年,已有253种新药提交给HIRA进行评估。其中,175种(69.2%)被建议批准上市,78种(30.8%)被拒绝。此外,这些药物中有68种被认为相对于现有药物在临床方面有所改进。对于那些未显示出临床优势的药物(大多数药物属于此类),与现有药物进行简单的价格比较被用作上市的一道门槛。在基线分析之外,来自行业、学术界、公职部门和民间社会的104名利益攸关方对一份旨在获取他们对韩国正面清单制度(PLS)看法的问卷进行了回复。利益攸关方一致认为,自2007年以来,报销决策的一致性有所提高,而新药的可及性明显下降。受访者还表示倾向于改善公众对决策信息的获取。对韩国报销决策的此次审查将为正在考虑引入类似政策的国家阐明关键问题。

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