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用于优先考虑冠状动脉血运重建患者的生物标志物的有效性和成本效益:系统评价和决策模型。

The effectiveness and cost-effectiveness of biomarkers for the prioritisation of patients awaiting coronary revascularisation: a systematic review and decision model.

机构信息

Department of Epidemiology and Public Health, University College London, UK.

出版信息

Health Technol Assess. 2010 Feb;14(9):1-151, iii-iv. doi: 10.3310/hta14090.

Abstract

OBJECTIVE

To determine the effectiveness and cost-effectiveness of a range of strategies based on conventional clinical information and novel circulating biomarkers for prioritising patients with stable angina awaiting coronary artery bypass grafting (CABG).

DATA SOURCES

MEDLINE and EMBASE were searched from 1966 until 30 November 2008.

REVIEW METHODS

We carried out systematic reviews and meta-analyses of literature-based estimates of the prognostic effects of circulating biomarkers in stable coronary disease. We assessed five routinely measured biomarkers and the eight emerging (i.e. not currently routinely measured) biomarkers recommended by the European Society of Cardiology Angina guidelines. The cost-effectiveness of prioritising patients on the waiting list for CABG using circulating biomarkers was compared against a range of alternative formal approaches to prioritisation as well as no formal prioritisation. A decision-analytic model was developed to synthesise data on a range of effectiveness, resource use and value parameters necessary to determine cost-effectiveness. A total of seven strategies was evaluated in the final model.

RESULTS

We included 390 reports of biomarker effects in our review. The quality of individual study reports was variable, with evidence of small study (publication) bias and incomplete adjustment for simple clinical information such as age, sex, smoking, diabetes and obesity. The risk of cardiovascular events while on the waiting list for CABG was 3 per 10,000 patients per day within the first 90 days (184 events in 9935 patients with a mean of 59 days at risk). Risk factors associated with an increased risk, and included in the basic risk equation, were age, diabetes, heart failure, previous myocardial infarction and involvement of the left main coronary artery or three-vessel disease. The optimal strategy in terms of cost-effectiveness considerations was a prioritisation strategy employing biomarker information. Evaluating shorter maximum waiting times did not alter the conclusion that a prioritisation strategy with a risk score using estimated glomerular filtration rate (eGFR) was cost-effective. These results were robust to most alternative scenarios investigating other sources of uncertainty. However, the cost-effectiveness of the strategy using a risk score with both eGFR and C-reactive protein (CRP) was potentially sensitive to the cost of the CRP test itself (assumed to be 6 pounds in the base-case scenario).

CONCLUSIONS

Formally employing more information in the prioritisation of patients awaiting CABG appears to be a cost-effective approach and may result in improved health outcomes. The most robust results relate to a strategy employing a risk score using conventional clinical information together with a single biomarker (eGFR). The additional prognostic information conferred by collecting the more costly novel circulating biomarker CRP, singly or in combination with other biomarkers, in terms of waiting list prioritisation is unlikely to be cost-effective.

摘要

目的

确定一系列基于常规临床信息和新型循环生物标志物的策略在为等待冠状动脉旁路移植术(CABG)的稳定型心绞痛患者进行优先排序方面的有效性和成本效益。

数据来源

从 1966 年到 2008 年 11 月 30 日,检索了 MEDLINE 和 EMBASE。

研究方法

我们对稳定型冠心病中循环生物标志物预后影响的文献估计进行了系统评价和荟萃分析。我们评估了五种常规测量的生物标志物和欧洲心脏病学会心绞痛指南推荐的八种新兴(即目前尚未常规测量)生物标志物。使用循环生物标志物对 CABG 等待名单上的患者进行优先排序的成本效益与一系列替代的正式排序方法以及不进行正式排序进行了比较。我们开发了一个决策分析模型,以综合一系列有效性、资源利用和价值参数的数据,以确定成本效益。最终模型评估了七种策略。

结果

我们的综述共纳入了 390 项生物标志物效应的报告。个别研究报告的质量参差不齐,存在小样本研究(发表)偏倚和对年龄、性别、吸烟、糖尿病和肥胖等简单临床信息的不完全调整。在 CABG 等待名单上的患者发生心血管事件的风险为每 10000 例患者每天 3 例(9935 例患者中有 184 例发生事件,平均风险期为 59 天)。与风险增加相关的危险因素包括年龄、糖尿病、心力衰竭、既往心肌梗死以及左主干冠状动脉或三血管疾病受累,这些危险因素被纳入基本风险方程。从成本效益角度来看,最佳策略是采用生物标志物信息的优先排序策略。评估较短的最长等待时间并没有改变使用估计肾小球滤过率(eGFR)的风险评分的优先排序策略具有成本效益的结论。这些结果在考虑其他不确定性来源的大多数替代方案中都是稳健的。然而,使用同时使用 eGFR 和 C 反应蛋白(CRP)的风险评分的策略的成本效益可能对 CRP 测试本身的成本敏感(在基本情况下假设为 6 英镑)。

结论

在为等待 CABG 的患者进行优先排序时,正式采用更多信息似乎是一种具有成本效益的方法,并且可能会带来更好的健康结果。最可靠的结果与采用基于常规临床信息和单个生物标志物(eGFR)的风险评分的策略有关。在等待名单上进行优先排序时,单独或结合其他生物标志物收集更昂贵的新型循环生物标志物 CRP 所带来的额外预后信息不太可能具有成本效益。

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