Chang M N, Guess H A, Heyse J F
Department of Statistics, University of Florida, Gainesville 32611.
Stat Med. 1994 Sep 30;13(18):1807-14. doi: 10.1002/sim.4780131803.
A new efficacy measure is developed for use in prevention trials of interventions which may affect both disease incidence and disease severity. We assign a severity score to each incident case and sum severity scores over all incident cases within each treatment group to create a burden-of-illness score for each treatment group. Efficacy is evaluated by the difference between the burden-of-illness per randomized subject in the two randomized treatment groups. Since the numbers of summands in each burden-of-illness score is a random variable, standard methods of analysis are not directly applicable. The asymptotic distribution and sampling properties of the net reduction in the burden-of-illness score are derived for trials designed to stop either after a fixed length of follow-up or after the occurrence of a fixed number of cases. We illustrate the method with data from a clinical trial of a human rotavirus vaccine.
一种新的疗效测量方法被开发出来,用于可能影响疾病发病率和疾病严重程度的干预措施的预防试验。我们为每个发病病例分配一个严重程度评分,并对每个治疗组内所有发病病例的严重程度评分进行求和,以创建每个治疗组的疾病负担评分。疗效通过两个随机治疗组中每个随机受试者的疾病负担差异来评估。由于每个疾病负担评分中的求和项数量是一个随机变量,标准的分析方法不能直接应用。对于设计为在固定随访期后或固定病例数出现后停止的试验,推导了疾病负担评分净减少的渐近分布和抽样特性。我们用一项人类轮状病毒疫苗临床试验的数据来说明该方法。