Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.
Burnet Institute, Melbourne, Australia; Monash University, Melbourne, Australia.
Int J Drug Policy. 2022 Jan;99:103458. doi: 10.1016/j.drugpo.2021.103458. Epub 2021 Oct 6.
Compared to other countries in sub-Saharan Africa, Tanzania has a relatively progressive illicit drug harm reduction (HR) policy, through a predominantly opioid substitution therapy-based programme. However, access to hepatitis C virus (HCV) diagnosis and curative direct acting antiviral therapy remains elusive. We developed a cost-effectiveness model to evaluate a simplified HCV screening-and-treatment intervention amongst PWID in Dar-es-Salaam, Tanzania.
A decision tree and Markov state transition model compared existing practice (no access to HCV viral confirmation and treatment) with the integration of point-of-care HCV screening and treatment within (1) existing HR services and (2) expansion to include PWID not currently engaged in HR. Outcome measures were screening, treatment, HR and disease-related costs per PWID, quality-adjusted life years (QALY) and disability adjusted life years (DALY). Cost-effectiveness was evaluated from a healthcare payer's perspective over a 30-year time horizon over a range of willingness-to-pay thresholds (USD$273 to USD$1,050). Both deterministic and probabilistic sensitivity analyses have been conducted.
Assuming a chronic HCV prevalence of 18.8%, screening-and-treatment in existing HR settings resulted in an ICER per QALY-gained and DALY averted of USD$633 and USD$1,161, respectively. Expanding to include an outreach programme for unengaged PWID yielded an ICER per QALY-gained and DALY-averted of USD$4,091 and USD$10,288. Factors affecting the sensitivity of the ICER value included the cost of HR and the health utility of non-cirrhotic disease states.
Simplified HCV screening and treatment of PWID has the potential to be cost-effective in Dar-es-Salaam, Tanzania. In practice, synergism of human and financial resources with established health programmes may offer a pragmatic solution to minimise operational costs.
坦桑尼亚与撒哈拉以南非洲的其他国家相比,拥有相对进步的非法药物减少伤害(HR)政策,主要通过基于阿片类药物替代疗法的方案实施。然而,获得丙型肝炎病毒(HCV)诊断和治疗性直接作用抗病毒治疗仍然难以实现。我们开发了一种成本效益模型,以评估在坦桑尼亚达累斯萨拉姆的注射吸毒者(PWID)中实施简化 HCV 筛查和治疗干预的效果。
决策树和马尔可夫状态转移模型将现有的实践(无法获得 HCV 病毒确认和治疗)与在(1)现有 HR 服务中纳入即时 HCV 筛查和治疗,以及(2)扩大到包括目前未参与 HR 的 PWID 进行比较。结果衡量标准为每位 PWID 的筛查、治疗、HR 和疾病相关费用,质量调整生命年(QALY)和残疾调整生命年(DALY)。从医疗保健支付者的角度,在 30 年的时间范围内,对一系列支付意愿阈值(273 美元至 1050 美元)进行了成本效益评估。同时进行了确定性和概率敏感性分析。
假设慢性 HCV 流行率为 18.8%,在现有 HR 环境中进行筛查和治疗,每获得一个 QALY 和 DALY 分别需要花费 633 美元和 1161 美元。将范围扩大到包括未参与的 PWID 的外展计划,每获得一个 QALY 和 DALY 分别需要花费 4091 美元和 10288 美元。影响 ICER 值敏感性的因素包括 HR 成本和非肝硬化疾病状态的健康效用。
在达累斯萨拉姆,简化 PWID 的 HCV 筛查和治疗具有成本效益。在实践中,与既定卫生计划的人力和财务资源的协同作用可能是一种切实可行的解决方案,可以最大限度地降低运营成本。