Maclure Malcolm, Nguyen Anne, Carney Greg, Dormuth Colin, Roelants Hendrik, Ho Kendall, Schneeweiss Sebastian
School of Health Information Science, Faculty of Human and Social Development, University of Victoria, British Columbia (BC), Canada.
Basic Clin Pharmacol Toxicol. 2006 Mar;98(3):243-52. doi: 10.1111/j.1742-7843.2006.pto_301.x.
Randomized pragmatic trials of drugs, physician education and drug policies are needed to improve pharmacosurveillance and cost-effectiveness of prescribing. Since 1994, we have developed and tested methods for low-cost education and policy trials to improve prescribing in primary care in Canada. We review methodology for using drug claims and other health services data to evaluate prescribing improvement programs and policies. We apply the lessons to a proposed trial of physician education tools (PET) for quality improvement of prescribing. Design issues for the trial include defining the potential programme in causal terms using counterfactuals, narrowing the denominator to the population affected, excluding noise from the numerator, calculating the prescribing preference, adjusting for baseline differences, controlling for modifiers and confounders, accounting for uncertainty when measuring impacts, and grouping practices for feedback and recognition. Data from a randomized trial of academic detailing illustrate measurement challenges. A decade of progress on methods for evaluating prescribing improvement programs with drug claims data has enabled planning of routine randomized pragmatic trials of education and policies in primary care in Canada.
需要开展药物、医生教育和药物政策的随机实用试验,以改善药物监测和处方的成本效益。自1994年以来,我们已开发并测试了低成本教育和政策试验方法,以改善加拿大初级保健中的处方情况。我们回顾了使用药物报销申请及其他卫生服务数据来评估处方改善项目和政策的方法。我们将这些经验教训应用于一项拟议的医生教育工具(PET)试验,以提高处方质量。该试验的设计问题包括使用反事实从因果关系角度定义潜在项目、将分母缩小到受影响人群、从分子中排除干扰因素、计算处方偏好、调整基线差异、控制修饰因素和混杂因素、在衡量影响时考虑不确定性,以及将医疗机构分组以便进行反馈和表彰。一项学术推广随机试验的数据说明了测量方面的挑战。在利用药物报销申请数据评估处方改善项目的方法上取得的十年进展,使得在加拿大开展初级保健教育和政策的常规随机实用试验成为可能。