From the Department of Medicine (Neurology) (M.C.F.S.), University of Ottawa, Canada.
Ottawa Hospital Research Institute (M.C.F.S., B.D., S.C., C.-Q.W.), University of Ottawa, Canada.
Stroke. 2019 Apr;50(4):1017-1020. doi: 10.1161/STROKEAHA.118.024096.
Background and Purpose- The ESCAPE trial (The Endovascular Treatment for Small Core and Anterior Circulation Proximal Occlusion With Emphasis on Minimizing CT to Recanalization Times) was a multicentre, randomized controlled trial of endovascular thrombectomy versus standard care for patients with acute ischemic stroke that allowed patients to be enrolled with deferred consent. We investigated the knowledge and opinions of these patients or their authorized third parties about the consent process. Methods- All patients (or their authorized third parties) enrolled with deferral of consent in ESCAPE were invited to complete a 12-question survey within the first 4 days of enrollment and again at 90 days. Questions investigated knowledge of the ESCAPE trial and opinions on deferral of consent. Results- Of 56 patients enrolled with deferred consent, 33 (59%) completed the initial survey, and of these, 27 (81%) completed the 90-day follow-up. Enrollment with deferred consent was not associated with a significant difference in door-to-randomization times (50.5 versus 57 minutes; P=0.29) but allowed these 56 patients to participate in the trial. Only 52% of respondents understood that patients could be randomized to thrombectomy or standard care, although most understood the other basic principles of the trial. At baseline and at 90 days, respondents disagreed or strongly disagreed with deferred consent in acute stroke trials generally (82% and 78%) and in the ESCAPE trial specifically (93% and 91%). Conclusions- Respondents generally disagreed with the use of deferred consent for enrollment in the ESCAPE trial and in stroke trials more generally.
背景与目的-ESCPE 试验(强调最小化 CT 至再通时间的小核心和前循环近端闭塞的血管内治疗)是一项多中心、随机对照试验,比较了急性缺血性脑卒中患者血管内血栓切除术与标准治疗的效果,允许患者在延迟同意的情况下入组。我们研究了这些患者或其授权第三方对同意过程的了解和意见。方法-所有以延迟同意方式入组 ESCAPE 的患者(或其授权第三方)都被邀请在入组后的头 4 天内完成一项包含 12 个问题的调查,并在 90 天再次进行。调查问题包括对 ESCAPE 试验的了解和对延迟同意的看法。结果-在 56 名以延迟同意方式入组的患者中,有 33 名(59%)完成了初始调查,其中 27 名(81%)完成了 90 天的随访。延迟同意入组与门到随机分组时间(50.5 分钟与 57 分钟;P=0.29)之间无显著差异,但允许这 56 名患者参与试验。只有 52%的受访者理解患者可以随机分配到血栓切除术或标准治疗组,尽管大多数人理解了试验的其他基本原则。在基线和 90 天时,受访者不同意或强烈不同意急性脑卒中试验一般情况下(82%和 78%)和 ESCAPE 试验特定情况下(93%和 91%)的延迟同意。结论-受访者普遍不同意在 ESCAPE 试验和更广泛的脑卒中试验中使用延迟同意来入组。