设治疗组事件发生率(experimental event rate)为EER,对照组事件发生率(control event rate)为CER,则相对危险度指标计算公式如下: 相对危险度(relative risk, RR),..
基于12个网页-相关网页
...m豆丁网 这些事件按 组别可表示为试验组事件发生率(experimental event rate,EER) 和对照组事件发生率(control event rate,CER); ②绝对危险降低率(absolute risk reduction, ARR):ARR=CER -...
基于4个网页-相关网页
...豆丁网 事件按 组别可表示为试验组事件发生率(experimental event rate,EER)和对 照组事件发生率(control event rate,CER); ②绝对危险降低率(absolute risk reduction,ARR):ARR=CER-...
基于2个网页-相关网页
两组住院期间心血管病事件发生率无明显统计学差别。
The incidence rate of major adverse cardiac events (MACE) was not significantly different between the two groups during hospitalization.
安非他酮组的与药物相关的不良事件发生率为65.2%、阿米替林组为88.6%。
Incidence of adverse events was 65.2% in bupropion and 88.6% in amitriptyline.
两组观察中无严重不良事件。两组间事件的发生率相似。
No severe adverse events were observed in either group. The frequency of events was generally similar between the two groups.
应用推荐