Protecting the socioeconomic rights and interests of patients with rare diseases based on an innovative payment mechanism.

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL
Amei He, Minxing Chen, Peipei Song, Qingyi Wu, Chunlin Jin, Jiangjiang He
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引用次数: 0

Abstract

The pathogenesis of diseases in the field of rare diseases is complex. Many rare diseases have yet to be conquered worldwide, and there are still no effective treatments for most rare diseases, resulting in limited accessibility to medications. Over the past few years, China has been committed to ensuring the availability of drugs for rare diseases, both at the national level and in all sectors of society. Through National Healthcare Insurance Negotiations (hereinafter referred to as "national negotiations"), the National Healthcare Security Administration has included several drugs for rare diseases in medical insurance coverage, addressing some of the issues with medications for rare diseases. National Negotiations have reduced the prices of drugs for rare diseases to a certain extent, but they remain expensive for many patients. By the end of 2023, out of the 165 drugs for rare diseases that had been launched, 53 were still not covered by medical insurance, leaving patients with a significant financial burden. Addressing payment issues remains a current challenge, and various regions in China are actively exploring innovative methods of paying for rare disease care to protect the socioeconomic rights and interests of patients with rare diseases.

创新支付机制,保障罕见病患者社会经济权益。
罕见病领域的发病机制复杂。在世界范围内,许多罕见疾病尚未被征服,大多数罕见疾病仍然没有有效的治疗方法,导致药物的可及性有限。在过去几年中,中国一直致力于在国家一级和社会各部门确保罕见病药物的可得性。国家医疗保障局通过全民医保谈判(以下简称“全民医保谈判”),将几种罕见病药品纳入医保范围,解决了部分罕见病药品问题。国家谈判在一定程度上降低了罕见病药品的价格,但对许多患者来说仍然很贵。截至2023年底,在已上市的165种罕见病药物中,仍有53种未纳入医保,患者经济负担沉重。解决支付问题仍然是当前的挑战,中国各地区正在积极探索罕见病治疗的创新支付方式,以保护罕见病患者的社会经济权益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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