Owens D K, Nease R F
Section of General Medicine (111A), VA Palo Alto Health Care System, CA 94304, USA.
Med Decis Making. 1997 Oct-Dec;17(4):409-26. doi: 10.1177/0272989X9701700406.
A central problem in practice guideline development is how to develop guidelines that appropriately account for variations in clinical populations and practice settings. Despite recognition of this problem, there is no formal mechanism for assessing what the need is for flexibility in guidelines, or for deciding how to incorporate such flexibility into recommendations.
This research sought to provide a formal basis to determine when clinical circumstances vary sufficiently that guideline recommendations should differ, how recommendations should be tailored for a specific clinical setting, and whether the benefit associated with such site-specific guidelines justifies the expense of their development.
The authors describe an approach for estimating the maximum health benefit that developers can obtain by eliminating uncertainty about differences in the patient populations and practice settings in which a guideline will be used. This estimate, the expected value of customization, provides a mechanism to evaluate the cost-effectiveness of the development of site-specific guidelines that account explicitly for variation in clinical circumstances. Application of this method to the development of screening guidelines for human immunodeficiency virus (HIV) infection indicates that the development of site-specific guidelines potentially is cost-effective. Site-specific guidelines either improve, or leave unchanged, the efficiency of HIV screening; whether they increase or decrease total expenditures and health benefits depends on the choice of a cost-effectiveness threshold, and the clinical problem.
Development of guideline recommendations based on decision models provides a normative approach for evaluating the need for and the cost-effectiveness of site-specific guidelines that have been tailored to specific practice settings. Such site-specific guidelines can improve substantially the expected health benefit and the economic efficiency of practice guidelines.
实践指南制定中的一个核心问题是如何制定能够适当考虑临床人群和实践环境差异的指南。尽管认识到了这个问题,但对于评估指南灵活性的需求以及决定如何将这种灵活性纳入建议中,并没有正式的机制。
本研究旨在提供一个正式的基础,以确定临床情况何时差异足够大以至于指南建议应该有所不同,如何针对特定临床环境调整建议,以及针对特定场所的指南所带来的益处是否证明其开发成本是合理的。
作者描述了一种方法,用于估计指南开发者通过消除指南所适用的患者人群和实践环境差异的不确定性所能获得的最大健康益处。这个估计值,即定制的预期价值,提供了一种机制来评估明确考虑临床情况差异的特定场所指南开发的成本效益。将这种方法应用于人类免疫缺陷病毒(HIV)感染筛查指南的制定表明,开发特定场所指南可能具有成本效益。特定场所指南要么提高,要么不改变HIV筛查的效率;它们是增加还是减少总支出和健康益处取决于成本效益阈值的选择以及临床问题。
基于决策模型制定指南建议为评估针对特定实践环境量身定制的特定场所指南的需求和成本效益提供了一种规范方法。这种特定场所指南可以显著提高实践指南的预期健康益处和经济效率。