Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.
VASCage, Research Centre On Vascular Ageing and Stroke, Innsbruck, Austria.
BMC Cardiovasc Disord. 2022 Aug 1;22(1):347. doi: 10.1186/s12872-022-02785-5.
Patients with ischaemic stroke or transient ischaemic attack (TIA) are at high risk of incident cardiovascular events and recurrent stroke. Despite compelling evidence about the efficacy of secondary prevention, a substantial gap exists between risk factor management in real life and that recommended by international guidelines. We conducted the STROKE-CARD trial (NCT02156778), a multifaceted pragmatic disease management program between 2014 and 2018 with follow-up until 2019. This program successfully reduced cardiovascular risk and improved health-related quality of life and functional outcome in patients with acute ischaemic stroke or TIA within 12 months after the index event. To investigate potential long-term effects of STROKE-CARD care compared to standard care, an extension of follow-up is warranted.
We aim to include all patients from the STROKE-CARD trial (n = 2149) for long-term follow-up between 2019 and 2021 with the study visit scheduled 3-6 years after the stroke/TIA event. The co-primary endpoint is the composite of major recurrent cardiovascular events (nonfatal stroke, nonfatal myocardial infarction, and vascular death) from hospital discharge until the long-term follow-up visit and health-related quality of life measured with the European Quality of Life-5 Dimensions (EQ-5D-3L) at the final visit. Secondary endpoints include overall mortality, long-term functional outcome, and target-level achievement in risk factor management.
This long-term follow-up will provide evidence on whether the pragmatic post-stroke/TIA intervention program STROKE-CARD is capable of preventing recurrent cardiovascular events and improving quality-of-life in the long run. Trial registration clinicaltrials.gov: NCT04205006 on 19 December 2019.
缺血性卒中和短暂性脑缺血发作(TIA)患者发生心血管事件和复发性卒中的风险较高。尽管有大量关于二级预防效果的证据,但在现实生活中对危险因素的管理与国际指南推荐之间存在很大差距。我们于 2014 年至 2018 年开展了一项多方面的实用疾病管理计划——STROKE-CARD 试验(NCT02156778),并对其进行了随访,直至 2019 年。该计划成功降低了急性缺血性卒中和 TIA 患者在指数事件后 12 个月内的心血管风险,并改善了与健康相关的生活质量和功能结局。为了研究 STROKE-CARD 护理与标准护理相比的潜在长期效果,需要进行随访扩展。
我们计划在 2019 年至 2021 年期间对 STROKE-CARD 试验(n=2149)中的所有患者进行长期随访,研究访问时间安排在卒中/TIA 事件后 3-6 年。主要复合终点是从出院到长期随访就诊期间的主要复发性心血管事件(非致命性卒中、非致命性心肌梗死和血管性死亡)以及最终就诊时用欧洲生命质量五维量表(EQ-5D-3L)测量的健康相关生活质量。次要终点包括总死亡率、长期功能结局和危险因素管理的目标水平达标情况。
这项长期随访将提供证据,证明实用的卒中/TIA 后干预计划 STROKE-CARD 是否能够预防复发性心血管事件并从长远改善生活质量。试验注册:clinicaltrials.gov:NCT04205006,于 2019 年 12 月 19 日注册。