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药物经济学分析中协议驱动成本的问题。

The problem of protocol driven costs in pharmacoeconomic analysis.

作者信息

Coyle D, Lee K M

机构信息

Clinical Epidemiology Unit, Loeb Research Institute, Ottawa Civic Hospital, Ontario, Canada.

出版信息

Pharmacoeconomics. 1998 Oct;14(4):357-63. doi: 10.2165/00019053-199814040-00003.

Abstract

The increasing number of economic evaluations of healthcare interventions and of drug therapies in particular has been well documented. Surveys of the quality of studies have demonstrated that standards of conduct of such studies have not similarly increased. Concerns over the standards have led to increased calls that economic analyses be more closely linked to randomised controlled clinical trials (RCT). Seven potential threats to the external validity of results limit the generalisability of studies based on RCTs. One such threat is the existence of protocol driven costs. There are two main types of protocol driven costs. Protocol prescribed costs arise as a result of resource use mandated by the clinical trial design. Protocol derived costs occur when increased clinical investigations mandated by trial protocols lead to atypical disease management. Methods to control for protocol driven costs within pharmacoeconomic study designs are available. Modelling studies can be based on data within clinical trials combined with observational data representing more typical resource use. The adoption of pragmatic clinical trial designs provide greater external validity though reduced internal validity. Refinements to explanatory clinical trials can also lead to reduced protocol driven costs. The extent that current studies control for such costs is unclear due to the lack of transparency in the reporting of study methods. A review of published studies found little consideration of protocol driven costs although in several studies there was evidence of their existence. Future studies conducted alongside RCTs should explicitly address how the issue of protocol driven costs was handled within the study framework.

摘要

医疗保健干预措施,尤其是药物治疗的经济评估数量不断增加,这一点已有充分记录。对研究质量的调查表明,此类研究的 conduct 标准并未相应提高。对这些标准的担忧导致越来越多的呼声要求经济分析与随机对照临床试验(RCT)更紧密地联系起来。结果外部有效性的七个潜在威胁限制了基于RCT的研究的可推广性。其中一个威胁是方案驱动成本的存在。方案驱动成本主要有两种类型。方案规定成本是由于临床试验设计规定的资源使用而产生的。当试验方案要求增加临床研究导致非典型疾病管理时,就会产生方案衍生成本。在药物经济学研究设计中,有控制方案驱动成本的方法。建模研究可以基于临床试验中的数据,并结合代表更典型资源使用的观察数据。采用务实的临床试验设计虽然会降低内部有效性,但能提供更高的外部有效性。对解释性临床试验的改进也可以降低方案驱动成本。由于研究方法报告缺乏透明度,目前的研究在多大程度上控制了此类成本尚不清楚。对已发表研究的综述发现,很少有人考虑方案驱动成本,尽管在一些研究中有证据表明其存在。与RCT同时进行的未来研究应明确说明在研究框架内如何处理方案驱动成本问题。

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