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Journal of Clinical Epidemiology|February 16, 2021
A proposed framework to guide evidence synthesis practice for meta-analysis with zero-events studiesChang Xu, Luis Furuya-Kanamori, Liliane Zorzela, et al.BMC Medical Research Methodology|March 13, 2023
Measuring the impact of zero-cases studies in evidence synthesis practice using the harms index and benefits index (Hi-Bi)Chang Xu, Luis Furuya-Kanamori, Lifeng Lin, et al.Journal of Evidence-Based Medicine|July 1, 2026
Toward Evidence Synthesis of Adverse Events in Imbalanced Time-to-Event DataZhen Peng, Jingyi Jiang, Lifeng Lin, et al.BMJ (Clinical Research Ed.)|May 10, 2022
Validity of data extraction in evidence synthesis practice of adverse events: reproducibility studyChang Xu, Tianqi Yu, Luis Furuya-Kanamori, et al.BMC Medicine|October 11, 2024
Harm effects in non-registered versus registered randomized controlled trials of medications: a retrospective cohort study of clinical trialsChang Xu, Shiqi Fan, Luis Furuya-Kanamori, et al.BMC Medicine|June 15, 2021
Utilization of the evidence from studies with no events in meta-analyses of adverse events: an empirical investigationChang Xu, Xiaoqin Zhou, Liliane Zorzela, et al.Health Science Reports|July 31, 2020
Arcsine-based transformations for meta-analysis of proportions: Pros, cons, and alternativesLifeng Lin, Chang XuJournal of Clinical Epidemiology|May 7, 2025
Prospective registration was associated with a reduced risk of bias for randomized controlled trials: a meta-research studyYuan Tian, Haofei Lu, Wenxuan Zhou, et al.Journal of General Internal Medicine|September 10, 2021
Empirical Comparisons of 12 Meta-analysis Methods for Synthesizing Proportions of Binary OutcomesLifeng Lin, Chang Xu, Haitao ChuBMC Medicine|March 6, 2024
Influence of lack of blinding on the estimation of medication-related harms: a retrospective cohort study of randomized controlled trialsChang Xu, Fengying Zhang, Suhail A R Doi, et al.Pageof 197