Liu Shan, Watcha Daena, Holodniy Mark, Goldhaber-Fiebert Jeremy D
Ann Intern Med. 2014 Oct 21;161(8):546-53. doi: 10.7326/M14-0602.
Prevalence of chronic hepatitis C virus (HCV) infection is high among incarcerated persons in the United States. New, short-duration, high-efficacy therapies may expand treatment eligibility in this population.
To assess the cost-effectiveness of sofosbuvir for HCV treatment in incarcerated populations.
Markov model.
Published literature and expert opinion.
Treatment-naive men with chronic, genotype 1 HCV monoinfection.
Lifetime.
Societal.
No treatment, 2-drug therapy (pegylated interferon and ribavirin), or 3-drug therapy with either boceprevir or sofosbuvir. For inmates with short remaining sentences (<1.5 years), only no treatment or sofosbuvir 3-drug therapy was feasible; for those with long sentences (≥1.5 years; mean, 10 years), all strategies were considered. After release, eligible persons could receive sofosbuvir 3-drug therapy.
Discounted costs (in 2013 U.S. dollars), discounted quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratios.
RESULTS OF BASE-CASE ANALYSIS: The strategies yielded 13.12, 13.57, 14.43, and 15.18 QALYs, respectively, for persons with long sentences. Sofosbuvir produced the largest absolute reductions in decompensated cirrhosis (16%) and hepatocellular carcinoma (9%), resulting in 2.1 additional QALYs at an added cost exceeding $54,000 compared with no treatment. For persons with short sentences, sofosbuvir cost $25,700 per QALY gained compared with no treatment; for those with long sentences, it dominated other treatments, costing $28,800 per QALY gained compared with no treatment.
High reinfection rates in prison attenuated cost-effectiveness for persons with long sentences.
Data on sofosbuvir's long-term effectiveness and price are limited. The analysis did not consider women, Hispanic persons, or patients co-infected with HIV or hepatitis B virus.
Sofosbuvir-based treatment is cost-effective for incarcerated persons, but affordability is an important consideration.
National Institutes of Health.
在美国,丙型肝炎病毒(HCV)慢性感染在被监禁人群中很常见。新型、疗程短、疗效高的疗法可能会扩大该人群的治疗资格。
评估索磷布韦用于被监禁人群HCV治疗的成本效益。
马尔可夫模型。
已发表的文献和专家意见。
初治的慢性1型HCV单一感染男性。
终身。
社会。
不治疗、两药联合治疗(聚乙二醇干扰素和利巴韦林)或三药联合治疗(联合博赛匹韦或索磷布韦)。对于剩余刑期较短(<1.5年)的囚犯,仅不治疗或索磷布韦三药联合治疗可行;对于刑期较长(≥1.5年;平均10年)的囚犯,则考虑所有策略。释放后,符合条件的人员可接受索磷布韦三药联合治疗。
贴现成本(以2013年美元计)、贴现质量调整生命年(QALY)和增量成本效益比。
对于刑期较长的人员,这些策略分别产生了13.12、13.57、14.43和15.18个QALY。与不治疗相比,索磷布韦使失代偿性肝硬化(16%)和肝细胞癌(9%)的绝对减少量最大,额外产生2.1个QALY,但增加的成本超过54,000美元。对于刑期较短的人员,与不治疗相比,索磷布韦每获得一个QALY的成本为25,700美元;对于刑期较长的人员,它优于其他治疗方法,与不治疗相比,每获得一个QALY的成本为28,800美元。
监狱中高再感染率削弱了刑期较长人员的成本效益。
关于索磷布韦长期疗效和价格的数据有限。分析未考虑女性、西班牙裔人群或合并感染HIV或乙型肝炎病毒的患者。
基于索磷布韦的治疗对被监禁人员具有成本效益,但可负担性是一个重要考虑因素。
美国国立卫生研究院。