Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Division of Neurogeriatrics, Solna, Sweden.
Department of Neurology, University Medical Centre, Ljubljana, Slovenia.
J Alzheimers Dis. 2020;73(3):1013-1021. doi: 10.3233/JAD-191011.
Recurrent ischemic stroke (IS) increases the risk of cognitive decline. To lower the risk of recurrent IS, secondary prevention is essential.
Our aim was to compare post-discharge secondary IS prevention and its maintenance up to 3 years after first IS in patients with and without Alzheimer's disease and other dementia disorders.
Prospective open-cohort study 2007-2014 from the Swedish national dementia registry (SveDem) and the Swedish national stroke registry (Riksstroke). Patients with dementia who experienced an IS (n = 1410; 332 [23.5%] with Alzheimer's disease) were compared with matched non-dementia IS patients (n = 7150). We analyzed antiplatelet, anticoagulant, blood pressure lowering, and statin treatment as planned medication initiation at discharge and actual dispensation of medications at first, second, and third year post-stroke.
At discharge, planned initiation of medication was higher in patients with dementia compared to non-dementia patients for antiplatelets (OR with 95% CI for fully adjusted models 1.23 [1.02-1.48]) and lower for blood pressure lowering medication (BPLM; 0.57 [0.49-0.67]), statins (0.57 [0.50-0.66]), and anticoagulants (in patients with atrial fibrillation - AF; 0.41 [0.32-0.53]). When analysis for antiplatelets was stratified according to the presence of AF, ORs for receiving antiplatelets remained significant only in the presence of AF (in the presence of AF 1.56 [1.21-2.01], in patients without AF 0.99 [0.75-1.33]). Similar trends were observed in 1st, 2nd, and 3rd year post-stroke.
Dementia was a predictor of lower statin and BPLM use. Patients with dementia and AF were more likely to be prescribed antiplatelets and less likely to receive anticoagulants.
复发性缺血性中风(IS)会增加认知能力下降的风险。为降低复发性 IS 的风险,二级预防至关重要。
我们旨在比较有和无阿尔茨海默病及其他痴呆症的患者在首次 IS 后出院后的二级 IS 预防及其维持情况,最长可达 3 年。
2007-2014 年进行的一项来自瑞典国家痴呆症登记处(SveDem)和瑞典国家中风登记处(Riksstroke)的前瞻性开放队列研究。患有 IS 的痴呆症患者(n=1410;332 例[23.5%]患有阿尔茨海默病)与匹配的非痴呆症 IS 患者(n=7150)进行比较。我们分析了抗血小板、抗凝、降压和他汀类药物治疗作为出院时的计划药物起始治疗以及首次、第二次和第三次中风后实际药物分配情况。
出院时,与非痴呆症患者相比,痴呆症患者接受抗血小板药物治疗的计划起始率更高(完全调整模型的 OR 为 1.23 [1.02-1.48]),而降压药物治疗(BPLM)、他汀类药物(0.57 [0.50-0.66])和抗凝剂(房颤患者中 - AF;0.41 [0.32-0.53])的起始率更低。当根据是否存在 AF 对抗血小板药物进行分层分析时,仅在存在 AF 时,接受抗血小板药物治疗的 OR 仍然显著(存在 AF 时为 1.56 [1.21-2.01],不存在 AF 时为 0.99 [0.75-1.33])。在首次、第二次和第三次中风后也观察到类似的趋势。
痴呆是他汀类药物和 BPLM 使用率降低的预测因素。患有痴呆症和 AF 的患者更有可能接受抗血小板治疗,而不太可能接受抗凝治疗。