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评估在澳大利亚注射毒品人群中治疗慢性丙型肝炎病毒的成本效益。

Assessing the cost-effectiveness of treating chronic hepatitis C virus in people who inject drugs in Australia.

机构信息

School of Medicine, University of California, San Francisco, San Francisco, California 94143, USA.

出版信息

J Gastroenterol Hepatol. 2013 Apr;28(4):707-16. doi: 10.1111/jgh.12041.

Abstract

BACKGROUND AND AIM

To assess the cost-effectiveness of hepatitis C virus treatment with pegylated interferon alfa-2a and ribavirin in current and former people who inject drugs (PWID).

METHODS

A decision analytic model simulated the lifetime costs and outcomes of four treatment options: early treatment with mild fibrosis, standard treatment with moderate fibrosis, late treatment with compensated cirrhosis, and no treatment. Treatment modalities were simulated across current, former, and never-injector cohorts of 1000 hypothetical patients with chronic hepatitis C virus. The main outcome measures were incremental costs ($AUD) per quality-adjusted life years (QALYs) gained, and incremental cost-effectiveness ratios (ICERs) were calculated for each cohort.

RESULTS

Treatment of current PWID during mild fibrosis resulted in a discounted average gain of 1.60 QALYs (95% confidence interval 0.93-2.26) for an added cost of $12,723 ($11,153-$14,396) compared with no treatment, yielding an ICER of $7941 per QALY gained ($6347-$12,017). Former PWID gained 1.80 QALYs (1.29-2.33) for $10,441 ($8843-$12,074) for early treatment compared with no treatment, resulting in an ICER of $5808 per QALY gained ($5189-$6849). Never-injectors gained 2.33 QALYs (1.87-2.80) for $9290 ($7642-$10,912) compared with no treatment-an ICER of $3985 per QALY gained ($3896-$4080). Early treatment was more cost-effective than late treatment in all cohorts.

CONCLUSIONS

Despite comorbidities, increased mortality, and reduced adherence, treatment of both current and former PWID is cost-effective. Our estimates fall below the unofficial Australian cost-effectiveness threshold of $AUD 50,000 per QALY for public subsidies. Scaling up treatment for PWID can be justified on purely economic grounds.

摘要

背景与目的

评估聚乙二醇干扰素 alfa-2a 和利巴韦林治疗当前和既往吸毒者(PWID)丙型肝炎病毒的成本效益。

方法

通过决策分析模型模拟了四种治疗方案的终生成本和结果:轻度纤维化的早期治疗、中度纤维化的标准治疗、代偿性肝硬化的晚期治疗和无治疗。对 1000 名慢性丙型肝炎病毒的假设患者的当前、既往和从未注射者队列进行了治疗方式模拟。主要结局指标为每获得一个质量调整生命年(QALY)的增量成本(澳元),并为每个队列计算了增量成本效益比(ICER)。

结果

与不治疗相比,在轻度纤维化期间对当前 PWID 进行治疗,可使患者获得 1.60 个 QALY(95%置信区间 0.93-2.26),并增加 12723 澳元(11153-14396 澳元)的成本,其增量成本效益比为每获得一个 QALY 7941 澳元(6347-12017 澳元)。与不治疗相比,早期治疗可使既往 PWID 获得 1.80 个 QALY(1.29-2.33),并增加 10441 澳元(8843-12074 澳元)的成本,其增量成本效益比为每获得一个 QALY 5808 澳元(5189-6849 澳元)。与不治疗相比,从未注射者获得 2.33 个 QALY(1.87-2.80),并增加 9290 澳元(7642-10912 澳元)的成本,其增量成本效益比为每获得一个 QALY 3985 澳元(3896-4080 澳元)。在所有队列中,早期治疗均比晚期治疗更具成本效益。

结论

尽管存在合并症、死亡率增加和依从性降低,当前和既往 PWID 的治疗仍具有成本效益。我们的估计低于澳大利亚未经官方认可的 50000 澳元/QALY 的公共补贴成本效益阈值。扩大 PWID 的治疗可以在纯粹的经济基础上得到证明。

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