Institute of Vector-Borne Disease, Monash University, Melbourne, Australia.
MRC Tropical Epidemiology Group, Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Am J Epidemiol. 2018 Sep 1;187(9):2021-2028. doi: 10.1093/aje/kwy099.
Cluster-randomized controlled trials are the gold standard for assessing efficacy of community-level interventions, such as vector-control strategies against dengue. We describe a novel cluster-randomized trial methodology with a test-negative design (CR-TND), which offers advantages over traditional approaches. This method uses outcome-based sampling of patients presenting with a syndrome consistent with the disease of interest, who are subsequently classified as test-positive cases or test-negative controls on the basis of diagnostic testing. We used simulations of a cluster trial to demonstrate validity of efficacy estimates under the test-negative approach. We demonstrated that, provided study arms are balanced for both test-negative and test-positive illness at baseline and that other test-negative design assumptions are met, the efficacy estimates closely match true efficacy. Analytical considerations for an odds ratio-based effect estimate arising from clustered data and potential approaches to analysis are also discussed briefly. We concluded that application of the test-negative design to certain cluster-randomized trials could increase their efficiency and ease of implementation.
整群随机对照试验是评估社区层面干预措施(如登革热病媒控制策略)效果的金标准。我们描述了一种新颖的整群随机试验方法,即基于阴性检测的设计(CR-TND),这种方法比传统方法具有优势。该方法基于与目标疾病一致的综合征,对出现综合征的患者进行基于结果的抽样,然后根据诊断检测将患者分类为阳性检测病例或阴性检测对照。我们使用集群试验模拟来证明阴性检测方法下疗效估计的有效性。我们证明,只要在基线时研究组在阴性和阳性疾病方面保持平衡,并且满足其他阴性检测设计假设,那么疗效估计就与真实疗效非常接近。我们还简要讨论了基于比值比的聚类数据效应估计的分析注意事项和潜在的分析方法。我们得出的结论是,将阴性检测设计应用于某些整群随机试验可以提高其效率和实施的便利性。