合并单侧和双侧相关数据的相对风险区间估计。

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Kejia Wang, Chang-Xing Ma
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引用次数: 0

摘要

在临床试验、流行病学或观察性研究中,测量数据通常以单侧或双侧数据的形式收集。例如,在眼科研究中,主要结果通常是从一个人的单眼或双眼获得的。在医学研究中,相对风险通常是感兴趣的参数,也是常用的参数。在本文中,我们根据等依赖性假设,为单侧和双侧相关数据的相对风险建立了三个置信区间。所提出的置信区间基于使用费雪评分法得出的参数最大似然估计值。我们进行了模拟研究,以评估所提出的置信区间在经验覆盖概率、平均区间宽度以及中侧非覆盖概率与远侧非覆盖概率之比方面的性能。我们还将所提出的方法与基于方差估计恢复法的置信区间以及根据修正的泊松回归模型得到的相关二元数据置信区间进行了比较。我们建议在一般应用中采用分数置信区间,因为它能最好地控制 95% 水平的收敛概率,同时具有合理的平均区间宽度。我们用一个实际例子来说明这些方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interval estimation of relative risks for combined unilateral and bilateral correlated data.

Measurements are generally collected as unilateral or bilateral data in clinical trials, epidemiology, or observational studies. For example, in ophthalmology studies, the primary outcome is often obtained from one eye or both eyes of an individual. In medical studies, the relative risk is usually the parameter of interest and is commonly used. In this article, we develop three confidence intervals for the relative risk for combined unilateral and bilateral correlated data under the equal dependence assumption. The proposed confidence intervals are based on maximum likelihood estimates of parameters derived using the Fisher scoring method. Simulation studies are conducted to evaluate the performance of proposed confidence intervals with respect to the empirical coverage probability, the mean interval width, and the ratio of mesial non-coverage probability to the distal non-coverage probability. We also compare the proposed methods with the confidence interval based on the method of variance estimates recovery and the confidence interval obtained from the modified Poisson regression model with correlated binary data. We recommend the score confidence interval for general applications because it best controls converge probabilities at the 95% level with reasonable mean interval width. We illustrate the methods with a real-world example.

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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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