建议使用益处风险方法,在报告试验时提高不良事件结果的突出性
Nikki Totton1, Ed Waddingham2, Ruth Owen3
1Sheffield Centre for Health and Related Research, School of Medicine and Population Health, University of Sheffield, Regent Court, 30 Regent Street, Sheffield, S1 4DA, UK. n.v.totton@sheffield.ac.uk.
在临床试验中报告不良事件与治疗有效性一起,提高了透明度. 像BRAT,NCB和OMERACT 3x3表这样的效益风险方法提高了试验结果的清晰度,以更好地做出决策.
科学领域:
- 临床试验方法论 临床试验方法论
- 基于证据的医学是基于证据的医学.
- 患者安全 患者安全
背景情况:
- 随机对照试验 (RCT) 往往低于报告不良事件,阻碍了全面的治疗评估.
- CONSORT危害检查清单旨在标准化不良事件报告.
- 将危害报告与有效性结果相结合,可以提供更完整的试验证据图像.
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