加拿大丙型肝炎病毒感染直接抗病毒治疗的公共报销政策:一项描述性研究。

Gaelen Snell, Alison D Marshall, Jennifer van Gennip, Matthew Bonn, Janet Butler-McPhee, Curtis L Cooper, Nadine Kronfli, Sarah Williams, Julie Bruneau, Jordan J Feld, Naveed Z Janjua, Marina Klein, Nance Cunningham, Jason Grebely, Sofia R Bartlett
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引用次数: 1

摘要

背景:直接作用抗病毒(DAA)疗法简化了HCV治疗,加拿大政府资助的药物计划取消了DAA疗法报销的疾病阶段限制。然而,其他使治疗复杂化、延迟或阻止治疗开始的政策仍然存在。我们的目的是描述这些计划的现有报销标准,并评估它们是否阻碍了治疗的获得。方法:对网上公布的16个公费药品计划的DAA报销政策进行审核,并对处方标准有深入了解。数据收集于2022年5月至7月。主要结局为:(1)是否计划接受即时诊断HCV RNA检测;(2) HCV基因型,(3)纤维化阶段,(4)慢性感染的检测要求;(五)批准报销申请的时间和方法;(6)有资格规定daa的提供者;(七)对再处理的限制。结果:15个(94%)计划至少有一项限制简化HCV治疗的政策。许多计划仍然需要基因型或纤维化分期的结果,限制合格的处方者,并且需要超过1天的时间来批准保险申请。一项计划不鼓励对再次感染进行治疗。结论:加拿大公共资助药物计划制定的报销标准继续限制丙型肝炎病毒治疗的及时、公平获取。消除与临床无关的预授权测试,扩大符合条件的处方者,加快索赔处理,扩大再感染治疗的覆盖范围,将改善daa的可及性。联邦政府可以通过引入联邦丙型肝炎病毒消除战略或联邦高成本药物保健计划来进一步加强努力。
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Public reimbursement policies in Canada for direct-acting antiviral treatment of hepatitis C virus infection: A descriptive study.

Background: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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