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通过药物遗传学检测避免药物不良反应:对TPMT和AZA引起的副作用相关经济证据的系统评价

Avoiding adverse drug reactions by pharmacogenetic testing: a systematic review of the economic evidence in the case of TPMT and AZA-induced side effects.

作者信息

Compagni Amelia, Bartoli Simona, Buehrlen Bernhard, Fattore Giovanni, Ibarreta Dolores, de Mesa Emma Gutierrez

机构信息

Center for Research in Health and Social Care Management, Department of Institutional Analysis and Public Management, Università Bocconi, Milan, Italy.

出版信息

Int J Technol Assess Health Care. 2008 Summer;24(3):294-302. doi: 10.1017/S0266462308080392.

Abstract

OBJECTIVES

The study aims at evaluating the economic evidence related to testing for genetic variants of the drug-metabolizing enzyme, TPMT. Detecting TPMT genetic variants before the administration of azathioprine (AZA) has the potential to prevent serious and costly adverse drug reactions (ADRs), such as neutropenia. In particular, our analysis concentrated on assessing the reliability of data on costs of neutropenia and performing the tests, the two main cost categories that could inform an economic evaluation of TPMT pharmacogenetic testing.

METHODS

A systematic literature review was performed to gather evidence on the costs of testing and neutropenia. Articles were critically appraised for their comprehensiveness and quality. To better estimate costs of TPMT tests, a small-scale survey of European diagnostic laboratories was conducted.

RESULTS

Only seven articles were retrieved specifying the costs associated with the management and treatment of AZA-induced neutropenia. Most of these studies are based on theoretical modeling reconstructed with key-informants or on very few cases of ADRs, and either the methodology for cost calculation is not specified or costs are based on national cost databases and tariffs. After critical appraisal of these studies, we considered 2,116 euros as the most reliable estimate for the cost of a case of neutropenia. Literature review accompanied by the survey of several diagnostic laboratories also provided an estimate (68 euros) for TPMT testing. Based on these values, the net cost per prevented case of neutropenia equals to 5,300 euros.

CONCLUSIONS

Solid economic considerations related to TPMT pharmacogenetic testing are still limited by underreporting of ADRs and high level of approximation related to cost data. Ad hoc observational studies and the ADR recording process embedded in pharmacovigilance systems, established across Europe, should represent more reliable sources of cost data in the future.

摘要

目的

本研究旨在评估与药物代谢酶硫嘌呤甲基转移酶(TPMT)基因变异检测相关的经济学证据。在使用硫唑嘌呤(AZA)之前检测TPMT基因变异有可能预防严重且代价高昂的药物不良反应(ADR),如中性粒细胞减少症。特别是,我们的分析集中于评估中性粒细胞减少症成本数据的可靠性以及检测成本,这两个主要成本类别可为TPMT药物遗传学检测的经济学评估提供依据。

方法

进行了一项系统的文献综述,以收集检测和中性粒细胞减少症成本的证据。对文章的全面性和质量进行了严格评估。为了更好地估计TPMT检测的成本,对欧洲诊断实验室进行了一项小规模调查。

结果

仅检索到7篇文章,明确了与AZA诱导的中性粒细胞减少症管理和治疗相关的成本。这些研究大多基于与关键信息提供者重建的理论模型或极少的ADR病例,要么未指定成本计算方法,要么成本基于国家成本数据库和收费标准。在对这些研究进行严格评估后,我们认为2116欧元是一例中性粒细胞减少症成本的最可靠估计值。文献综述以及对多个诊断实验室的调查也提供了TPMT检测的估计成本(68欧元)。基于这些数值,每预防一例中性粒细胞减少症的净成本为5300欧元。

结论

与TPMT药物遗传学检测相关的可靠经济学考量仍受ADR报告不足以及成本数据高度近似性的限制。特设观察性研究以及欧洲各地建立的药物警戒系统中嵌入的ADR记录过程,未来应成为更可靠的成本数据来源。

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