Marshall Alison D, Willing Alex R, Kairouz Abe, Cunningham Evan B, Wheeler Alice, O'Brien Nicholas, Perera Vidura, Ward John W, Hiebert Lindsey, Degenhardt Louisa, Hajarizadeh Behzad, Colledge Samantha, Hickman Matthew, Jawad Danielle, Lazarus Jeffrey V, Matthews Gail V, Scheibe Andrew, Vickerman Peter, Dore Gregory J, Grebely Jason
Viral Hepatitis Clinical Research Program, The Kirby Institute, University of New South Wales, Sydney, NSW, Australia; Centre for Social Research in Health, University of New South Wales, Sydney, NSW, Australia.
Viral Hepatitis Clinical Research Program, The Kirby Institute, University of New South Wales, Sydney, NSW, Australia.
Lancet Gastroenterol Hepatol. 2024 Apr;9(4):366-382. doi: 10.1016/S2468-1253(23)00335-7. Epub 2024 Feb 15.
Direct-acting antivirals (DAAs) for hepatitis C virus (HCV) infection have delivered high response rates (>95%) and simplified the management of HCV treatment, permitting non-specialists to manage patients without advanced liver disease. We collected and reviewed global data on the registration and reimbursement (government subsidised) of HCV therapies, including restrictions on reimbursement. Primary data collection occurred between Nov 15, 2021, and July 24, 2023, through the assistance of a global network of 166 HCV experts. We retrieved data for 160 (77%) of 209 countries and juristrictions. By mid-2023, 145 (91%) countries had registered at least one of the following DAA therapies: sofosbuvir-velpatasvir, sofosbuvir-velpatasvir-voxilaprevir, glecaprevir-pibrentasvir, sofosbuvir-daclatasvir, or sofosbuvir. 109 (68%) countries reimbursed at least one DAA therapy. Among 102 low-income and middle-income countries (LMICs), 89 (87%) had registered at least one HCV DAA therapy and 53 (52%) reimbursed at least one DAA therapy. Among all countries with DAA therapy reimbursement (n=109), 66 (61%) required specialist prescribing, eight (7%) had retreatment restrictions, seven (6%) had an illicit drug use restriction, five (5%) had an alcohol use restriction, and three (3%) had liver disease restrictions. Global access to DAA reimbursement remains uneven, with LMICs having comparatively low reimbursement compared with high-income countries. To meet WHO goals for HCV elimination, efforts should be made to assist countries, particularly LMICs, to increase access to DAA reimbursement and remove reimbursement restrictions-especially prescriber-type restrictions-to ensure universal access.
用于治疗丙型肝炎病毒(HCV)感染的直接抗病毒药物(DAAs)具有很高的治愈率(>95%),并简化了HCV治疗的管理,使非专科医生也能够管理无晚期肝病的患者。我们收集并审查了关于HCV治疗药物注册和报销(政府补贴)的全球数据,包括报销限制。主要数据收集于2021年11月15日至2023年7月24日期间,通过一个由166名HCV专家组成的全球网络协助完成。我们获取了209个国家和地区中160个(77%)的数据。截至2023年年中,145个(91%)国家已注册了以下至少一种DAA治疗药物:索磷布韦-维帕他韦、索磷布韦-维帕他韦-伏西瑞韦、格卡瑞韦-哌仑他韦、索磷布韦-达拉他韦或索磷布韦。109个(68%)国家报销了至少一种DAA治疗药物。在102个低收入和中等收入国家(LMICs)中,89个(87%)已注册了至少一种HCV DAA治疗药物,53个(52%)报销了至少一种DAA治疗药物。在所有报销DAA治疗药物的国家(n=109)中,66个(61%)要求专科医生开具处方,8个(7%)有再治疗限制,7个(6%)有非法药物使用限制,5个(5%)有酒精使用限制,3个(3%)有肝病限制。全球DAA报销的可及性仍然不均衡,与高收入国家相比,LMICs的报销比例相对较低。为实现世界卫生组织消除HCV的目标,应努力协助各国,特别是LMICs,增加DAA报销的可及性,并消除报销限制,尤其是开具处方者类型的限制,以确保普遍可及。