Department of Neurology, University of Leipzig, Leipzig, Germany.
Department of Neurology, Universitätsklinikum Würzburg, Würzburg, Germany.
Eur Stroke J. 2023 Mar;8(1):241-250. doi: 10.1177/23969873221143856. Epub 2023 Jan 6.
Intravenous thrombolysis (IVT) is an on label treatment for selected patients with acute ischemic stroke (AIS). As major bleeding or allergic shock may occur, the need to ensure patients' informed consent for IVT is a matter of debate.
Prospective investigator-initiated multi-center observational study to assess the ability of AIS patients to recall information, provided by a physician during a standardized educational talk (SET) on IVT use. The recall of 20 pre-defined items was assessed in AIS after 60-90 min ( = 93) or 23-25 h ( = 40) after SET. About 40 patients with subacute stroke, 40 non-stroke patients, and 23 relatives of AIS patients served as controls, and were surveyed 60-90 min after SET.
Within 60-90 min after SET, AIS patients (median age 70 years, 31% female, median NIHSS score on admission 3 points) who were considered capable to provide informed consent recalled 55% (IQR 40%-66.7%) of the provided SET items. In multivariable linear regression analysis recapitulation by AIS patients was associated with their educational level (β = 6.497, < 0.001), self-reported excitement level (β = 1.879, = 0.011) and NIHSS score on admission (β = -1.186, = 0.001). Patients with subacute stroke (70 years, 40% female, median NIHSS = 2) recalled 70% (IQR 55.7%-83.6%), non-stroke patients (75 years, 40% female) 70% (IQR 60%-78.7%), and AIS relatives (58 years, 83% female) 70% (IQR 60%-85%). Compared to subacute stroke patients, AIS patients less often recalled the frequency of IVT-related bleeding (21% vs 43%), allergic shock (15% vs 39%), and bleeding-related morbidity and mortality (44% vs 78%). AIS patients recalled 50% (IQR 42.3%-67.5%) of the provided items 23-25 h after SET.
AIS patients eligible for IVT remember about half of all SET-items after 60-90 min or 23-25 h, respectively. The fact that the recapitulation of IVT-associated risks is particularly poor should be given special consideration.
静脉溶栓(IVT)是治疗急性缺血性脑卒中(AIS)的一种有适应证的治疗方法。由于可能发生大出血或过敏性休克,确保患者对 IVT 的知情同意是一个有争议的问题。
前瞻性研究者发起的多中心观察性研究,以评估 AIS 患者在接受标准化教育谈话(SET)后,对医生提供的关于 IVT 使用的信息的回忆能力。在 SET 后 60-90 分钟( = 93)或 23-25 小时( = 40)后,评估 AIS 患者对 20 个预先定义项目的回忆情况。约 40 名亚急性脑卒中患者、40 名非脑卒中患者和 23 名 AIS 患者的亲属作为对照,在 SET 后 60-90 分钟进行调查。
在 SET 后 60-90 分钟内,被认为有能力提供知情同意的 AIS 患者(中位年龄 70 岁,31%为女性,入院时 NIHSS 评分中位数为 3 分)回忆起 55%(IQR 40%-66.7%)的 SET 项目。在多变量线性回归分析中,AIS 患者的回忆与他们的教育水平(β=6.497, < 0.001)、自我报告的兴奋程度(β=1.879, = 0.011)和入院时的 NIHSS 评分(β=-1.186, = 0.001)相关。亚急性脑卒中患者(70 岁,40%为女性,中位 NIHSS=2)回忆起 70%(IQR 55.7%-83.6%),非脑卒中患者(75 岁,40%为女性)回忆起 70%(IQR 60%-78.7%),AIS 患者的亲属(58 岁,83%为女性)回忆起 70%(IQR 60%-85%)。与亚急性脑卒中患者相比,AIS 患者较少回忆起 IVT 相关出血的频率(21% vs 43%)、过敏性休克(15% vs 39%)和出血相关发病率和死亡率(44% vs 78%)。AIS 患者在 SET 后 23-25 小时回忆起 50%(IQR 42.3%-67.5%)的提供项目。
有资格接受 IVT 的 AIS 患者分别在 60-90 分钟或 23-25 小时后,分别能记住大约一半的 SET 项目。IVT 相关风险的回忆特别差,这一事实应特别考虑。