Division of Stroke and Cerebrovascular Diseases, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA (T.G., C.N., J.W., C.M.H., M.S.).
Data Coordination Unit, Department of Public Health Sciences, Medical University of South Carolina, Charleston (L.D.F., S.D.Y., A.T., J.G.).
Stroke. 2021 Jan;52(2):442-446. doi: 10.1161/STROKEAHA.120.032166. Epub 2021 Jan 25.
Fewer women than men tend to be enrolled in clinical trials of intracerebral hemorrhage. It is unclear whether this reflects lower prevalence of intracerebral hemorrhage in women, selection bias, or poor recruitment efforts. We undertook this study to examine differences between men and women in the reasons for exclusion from the iDEF trial (Intracerebral Hemorrhage Deferoxamine).
The screen failure log included 29 different reasons for exclusion. Chi-square statistics were used to evaluate the differences in reasons for exclusion between men and women.
A total of 38.2% of participants in iDEF were women. Three thousand nine hundred eighty-two women (45.7%) and 4736 men (54.3%) were screen failures (<0.0001). Similar proportions of women (1.28%) and men (1.73%) were excluded due to inability to obtain consent (=0.1). Patients or families declined participation in 1.26% of women versus 1.31% of men (=0.9). More women than men failed screening because of age>80 (22.40% versus 12.61%; adjusted =0.0007) and preexisting do-not-resuscitate/do-not-intubate (3.69% versus 2.83%; adjusted =0.067).
Lower rates of women enrollment in the iDEF trial may be attributed to older age. Inability to obtain consent or declining participation was similar between women and men, arguing against selection bias. Our findings should be confirmed in other intracerebral hemorrhage trials to determine best strategies to improve women's representation in future trials.
与男性相比,女性参与颅内出血临床试验的人数较少。目前尚不清楚这是反映了女性颅内出血的发病率较低,还是选择偏倚,或者招募工作不力。我们进行这项研究,旨在检查 iDEF 试验(脑出血去铁胺)中男性和女性排除的原因之间的差异。
筛选失败日志包括 29 种不同的排除原因。卡方检验用于评估男性和女性排除原因之间的差异。
iDEF 试验中共有 38.2%的参与者为女性。3982 名女性(45.7%)和 4736 名男性(54.3%)筛选失败(<0.0001)。由于无法获得同意,女性(1.28%)和男性(1.73%)的排除比例相似(=0.1)。患者或家属拒绝参与的女性占 1.26%,男性占 1.31%(=0.9)。由于年龄>80 岁(22.40%比 12.61%;调整后=0.0007)和预先存在的不复苏/不插管(3.69%比 2.83%;调整后=0.067),女性比男性更多地筛选失败。
iDEF 试验中女性参与率较低可能归因于年龄较大。无法获得同意或拒绝参与的情况在女性和男性之间相似,这表明不存在选择偏倚。我们的研究结果应在其他颅内出血试验中得到证实,以确定改善未来试验中女性代表性的最佳策略。