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英国类风湿性关节炎成年患者使用依那西普的成本效益建模。

Modelling the cost-effectiveness of etanercept in adults with rheumatoid arthritis in the UK.

作者信息

Brennan A, Bansback N, Reynolds A, Conway P

机构信息

Operational Research, School of Health and Related Research, University of Sheffield, Sheffield, South Yorkshire, UK.

出版信息

Rheumatology (Oxford). 2004 Jan;43(1):62-72. doi: 10.1093/rheumatology/keg451. Epub 2003 Jul 30.

Abstract

OBJECTIVES

This model examines the cost-effectiveness of etanercept monotherapy under British Society for Rheumatology guidelines, i.e. adults previously failing two disease-modifying anti-rheumatic drugs (DMARDs). It compares a DMARD sequence with etanercept third line against the same sequence excluding etanercept.

METHOD

The 6-monthly trend in Health Assessment Questionnaire (HAQ) disability score is simulated for 10 000 patients' lifetimes using clinical trial data and published literature. Switching to the next treatment is triggered by lack of response, loss of efficacy or adverse events. Patient mortality depends on rheumatoid arthritis life-tables and on epidemiological evidence relating reduced risk to HAQ improvement. Regression of HAQ/EuroQol (EQ-5D) utility provides quality-adjusted life years (QALY) gained. Primary analysis includes drug costs, monitoring and hospitalizations.

RESULTS

The central estimate cost per QALY is pound 16 330. Sensitivity analyses ( pound 7800 to pound 42 000) showed long-term HAQ progression (etanercept, DMARDs, non-responders) as most sensitive variables. The inclusion of potential avoided nursing home admissions and indirect costs/lost employment further improves the cost-effectiveness.

CONCLUSIONS

For adults in the UK, the results suggest that etanercept is cost-effective when compared with non-biologic agents. The National Institute for Clinical Excellence has accepted that etanercept is cost-effective and recommended its availability for use in patients who have failed at least two DMARDs. This model was an important component of that decision. The model is further suitable for use for a wide range of other cost-effectiveness questions in rheumatoid arthritis.

摘要

目的

该模型依据英国风湿病学会指南,研究了依那西普单药治疗的成本效益,即针对先前使用两种改善病情抗风湿药物(DMARDs)治疗失败的成年人。它将一种DMARD治疗顺序(依那西普作为三线用药)与排除依那西普的相同治疗顺序进行了比较。

方法

利用临床试验数据和已发表文献,模拟了10000名患者一生中健康评估问卷(HAQ)残疾评分的半年变化趋势。因无反应、疗效丧失或不良事件而触发更换为下一种治疗。患者死亡率取决于类风湿关节炎生命表以及与HAQ改善相关的降低风险的流行病学证据。HAQ/欧洲五维健康量表(EQ-5D)效用的回归得出获得的质量调整生命年(QALY)。主要分析包括药物成本、监测和住院费用。

结果

每获得一个QALY的核心估计成本为16330英镑。敏感性分析(7800英镑至42000英镑)表明,长期HAQ进展(依那西普、DMARDs、无反应者)是最敏感的变量。纳入潜在可避免的养老院入住费用和间接成本/就业损失进一步提高了成本效益。

结论

对于英国的成年人,结果表明与非生物制剂相比,依那西普具有成本效益。英国国家卫生与临床优化研究所已认可依那西普具有成本效益,并建议将其提供给至少两种DMARDs治疗失败的患者使用。该模型是该决策的一个重要组成部分。该模型还适用于类风湿关节炎中一系列其他成本效益问题。

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