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Optimal Control of Hepatitis C Antiviral Treatment Programme Delivery for Prevention amongst a Population of Injecting Drug Users

机译:预防注射吸毒人群中预防丙型肝炎病毒治疗计划的最优控制

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摘要

In most developed countries, HCV is primarily transmitted by injecting drug users (IDUs). HCV antiviral treatment is effective, and deemed cost-effective for those with no re-infection risk. However, few active IDUs are currently treated. Previous modelling studies have shown antiviral treatment for active IDUs could reduce HCV prevalence, and there is emerging interest in developing targeted IDU treatment programmes. However, the optimal timing and scale-up of treatment is unknown, given the real-world constraints commonly existing for health programmes. We explore how the optimal programme is affected by a variety of policy objectives, budget constraints, and prevalence settings. We develop a model of HCV transmission and treatment amongst active IDUs, determine the optimal treatment programme strategy over 10 years for two baseline chronic HCV prevalence scenarios (30% and 45%), a range of maximum annual budgets (50,000–300,000 per 1,000 IDUs), and a variety of objectives: minimising health service costs and health utility losses; minimising prevalence at 10 years; minimising health service costs and health utility losses with a final time prevalence target; minimising health service costs with a final time prevalence target but neglecting health utility losses. The largest programme allowed for a given budget is the programme which minimises both prevalence at 10 years, and HCV health utility loss and heath service costs, with higher budgets resulting in greater cost-effectiveness (measured by cost per QALY gained compared to no treatment). However, if the objective is to achieve a 20% relative prevalence reduction at 10 years, while minimising both health service costs and losses in health utility, the optimal treatment strategy is an immediate expansion of coverage over 5–8 years, and is less cost-effective. By contrast, if the objective is only to minimise costs to the health service while attaining the 20% prevalence reduction, the programme is deferred until the final years of the decade, and is the least cost-effective of the scenarios.
机译:在大多数发达国家,HCV主要是通过注射毒品使用者(IDU)传播的。 HCV抗病毒治疗是有效的,并且对于那些没有再次感染风险的人来说,具有成本效益。但是,目前很少使用活动的IDU。先前的建模研究表明,针对活跃的注射毒品使用者的抗病毒治疗可以降低HCV的患病率,并且对开发有针对性的注射毒品使用者的治疗方案越来越感兴趣。但是,考虑到健康计划通常存在的现实世界的限制,最佳的治疗时机和扩大规模尚不清楚。我们探讨了各种政策目标,预算限制和流行率设置如何影响最佳计划。我们在活跃的注射毒品使用者之间建立了HCV传播和治疗模型,确定了两种基线慢性HCV流行情况(30%和45%),年度最高预算范围(每1,000个注射毒品使用者50,000–300,000范围)的十年最佳治疗方案策略)以及各种目标:最大程度地减少卫生服务成本和卫生事业损失;将10年的患病率降至最低;以最终的患病率目标最小化医疗服务成本和医疗事业损失;以最终的患病率目标将医疗服务成本降至最低,但忽略了医疗事业损失。给定预算所允许的最大计划是将10年的患病率以及HCV卫生事业损失和健康服务成本最小化的计划,更高的预算会产生更高的成本效益(以与未治疗相比获得的每QALY成本衡量) 。但是,如果目标是在10年内将相对患病率降低20%,同时将医疗服务成本和医疗效用损失最小化,则最佳治疗策略是在5-8年内立即扩大覆盖范围,并且成本更低-有效。相比之下,如果目标仅是在达到20%的患病率降低的同时将医疗服务的成本降至最低,则该计划将推迟到该十年的最后几年,并且在该方案中成本效益最低。

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