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具有右截断泊松分布结局的整群随机试验的功效计算:来自疟疾媒介控制试验的一个实例

Power calculations for cluster randomized trials (CRTs) with right-truncated Poisson-distributed outcomes: a motivating example from a malaria vector control trial.

机构信息

Department of Infectious Disease Epidemiology, MRC Centre for Global Infectious Disease Analysis, Imperial College London, London, UK.

Department of Statistical Methodology and Consulting, Novartis Pharma AG, Basel, Switzerland.

出版信息

Int J Epidemiol. 2020 Jun 1;49(3):954-962. doi: 10.1093/ije/dyz277.

Abstract

BACKGROUND

Cluster randomized trials (CRTs) are increasingly used to study the efficacy of interventions targeted at the population level. Formulae exist to calculate sample sizes for CRTs, but they assume that the domain of the outcomes being considered covers the full range of values of the considered distribution. This assumption is frequently incorrect in epidemiological trials in which counts of infection episodes are right-truncated due to practical constraints on the number of times a person can be tested.

METHODS

Motivated by a malaria vector control trial with right-truncated Poisson-distributed outcomes, we investigated the effect of right-truncation on power using Monte Carlo simulations.

RESULTS

The results demonstrate that the adverse impact of right-truncation is directly proportional to the magnitude of the event rate, λ, with calculations of power being overestimated in instances where right-truncation was not accounted for. The severity of the adverse impact of right-truncation on power was more pronounced when the number of clusters was ≤30 but decreased the further the right-truncation point was from zero.

CONCLUSIONS

Potential right-truncation should always be accounted for in the calculation of sample size requirements at the study design stage.

摘要

背景

集群随机对照试验(CRTs)越来越多地被用于研究针对人群水平的干预措施的效果。目前已有公式可用于计算 CRT 的样本量,但它们假设所考虑的结果域涵盖了所考虑分布的所有值范围。在由于对一个人可以接受的检测次数有限而导致感染发作次数呈右截断的流行病学试验中,这种假设通常是不正确的。

方法

受一项针对疟疾媒介控制的试验中右截断泊松分布结果的启发,我们使用蒙特卡罗模拟方法研究了右截断对功效的影响。

结果

结果表明,右截断的不利影响与事件率λ的大小成正比,在未考虑右截断的情况下,功效的计算会被高估。当聚类数≤30 时,右截断对功效的不利影响更为明显,但随着右截断点离零越远,影响程度越小。

结论

在研究设计阶段,应始终考虑潜在的右截断对样本量需求的计算。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab1/7394957/cbe4da526ed3/dyz277f1.jpg

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