Snell Gaelen, Marshall Alison D, van Gennip Jennifer, Bonn Matthew, Butler-McPhee Janet, Cooper Curtis L, Kronfli Nadine, Williams Sarah, Bruneau Julie, Feld Jordan J, Janjua Naveed Z, Klein Marina, Cunningham Nance, Grebely Jason, Bartlett Sofia R
Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
The Kirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Can Liver J. 2023 Jul 26;6(2):190-200. doi: 10.3138/canlivj-2022-0040. eCollection 2023 Jul.
Direct-acting antiviral (DAA) therapies have simplified HCV treatment, and publicly funded Canadian drug plans have eliminated disease-stage restrictions for reimbursement of DAA therapies. However other policies which complicate, delay, or prevent treatment initiation still persist. We aim to describe these plans' existing reimbursement criteria and appraise whether they hinder treatment access.
We reviewed DAA reimbursement policies of 16 publicly funded drug plans published online and provided by contacts with in-depth knowledge of prescribing criteria. Data were collected from May to July 2022. Primary outcomes were: (1) if plans have arranged to accept point-of-care HCV RNA testing for diagnosis; testing requirements for (2) HCV genotype, (3) fibrosis stage, and (4) chronic infection; (5) time taken and method used to approve reimbursement requests; (6) providers eligible to prescribe DAAs; and (7) restrictions on re-treatment.
Fifteen (94%) plans have at least one policy in place which limits simplified HCV treatment. Many plans continue to require results of genotype or fibrosis staging, limit eligible prescribers, and take longer than 1 day to approve coverage requests. One plan discourages treatment for re-infection.
Reimbursement criteria set by publicly funded Canadian drug plans continue to limit timely, equitable access to HCV treatment. Eliminating clinically irrelevant pre-authorization testing, expanding eligible prescribers, expediting claims processing, and broadening coverage of treatment for reinfection will improve access to DAAs. The federal government could further enhance efforts by introducing a federal HCV elimination strategy or federal high-cost drug PharmaCare program.
直接抗病毒(DAA)疗法简化了丙型肝炎病毒(HCV)的治疗,加拿大的公共资助药物计划已取消了DAA疗法报销的疾病阶段限制。然而,其他使治疗开始复杂化、延迟或阻碍治疗开始的政策仍然存在。我们旨在描述这些计划现有的报销标准,并评估它们是否阻碍了治疗的可及性。
我们审查了16个公共资助药物计划的DAA报销政策,这些政策在线发布或由熟悉处方标准的联系人提供。数据收集于2022年5月至7月。主要结果包括:(1)计划是否已安排接受即时检验HCV RNA检测用于诊断;(2)HCV基因型、(3)纤维化阶段、(4)慢性感染的检测要求;(5)批准报销申请所需的时间和使用的方法;(6)有资格开具DAA药物的提供者;以及(7)再次治疗的限制。
15个(94%)计划至少有一项政策限制了简化的HCV治疗。许多计划仍然要求提供基因型或纤维化分期结果,限制合格的开处方者,并且批准承保申请的时间超过1天。有一个计划不鼓励对再次感染进行治疗。
加拿大公共资助药物计划设定的报销标准继续限制了及时、公平地获得HCV治疗的机会。消除临床无关的预先授权检测、扩大合格的开处方者范围、加快理赔处理以及扩大再次感染治疗的覆盖范围将改善DAA药物的可及性。联邦政府可以通过引入联邦HCV消除战略或联邦高成本药物药物保险计划进一步加大力度。