Ganesh Aravind, Volny Ondrej, Kovacova Ingrid, Tomek Aleš, Bar Michal, Pádr Radek, Cihlar Filip, Nevsimalova Miroslava, Jurak Lubomir, Havlicek Roman, Kovar Martin, Sevcik Petr, Rohan Vladimír, Fiksa Jan, Cerník David, Jura Rene, Vaclavik Daniel, Hill Michael D, Mikulík Robert
Calgary Stroke Program (AG, MDH), Departments of Clinical Neurosciences and Community Health Sciences, the Hotchkiss Brain Institute, and the O'Brien Institute for Public Health, University of Calgary Cumming School of Medicine, Canada; Department of Neurology (OV, MB), University Hospital Ostrava, Ostrava; International Clinical Research Centre (OV, IK, RM), Stroke Research Program, St. Anne's University Hospital, Brno; Faculty of Medicine (OV, MB), University Ostrava; Department of Neurology (OV), Charles University, 2nd Medical Faculty; Institute of Health Information and Statistics of the Czech Republic (AT), Prague; Department of Radiology (RP), 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital; Department of Radiology (FC), Masaryk Hospital, Usti nad Labem; Department of Neurology (MN), Hospital Ceske Budejovice; Neurocenter (LJ), Regional Hospital Liberec; Department of Neurology (RH), Military University Hospital; Department of Neurology (MK), Na Homolce Hospital, Prague; Department of Neurology (PS, VR), Faculty of Medicine in Pilsen, Charles University in Prague; Department of Neurology (JF), Charles University, First Faculty of Medicine and General University Hospital, Prague; Masaryk Hospital Usti nad Labem - KZ a.s. (DC), Department of Neurology-Comprehensive Stroke Center; Department of Neurology (RJ), University Hospital Brno and Faculty of Medicine Masaryk University, Brno; Department of Neurology (DV), AGEL Research and Training Institute, Ostrava Vitkovice Hospital, Czech Republic; Departments of Radiology and Medicine (MDH), University of Calgary Cumming School of Medicine, Alberta, Canada; and Department of Neurology (RM), Tomas Bata Regional Hospital Zlin, Czech Republic.
Neurol Clin Pract. 2024 Dec;14(6):e200341. doi: 10.1212/CPJ.0000000000200341. Epub 2024 Aug 16.
Given the paucity of high-quality safety/efficacy data on acute stroke therapies in patients with premorbid disability, they risk being routinely excluded from such therapies. We examined utilization of endovascular thrombectomy (EVT), associated workflow, and poststroke outcomes among patients with vs without premorbid disability.
We used national registry data on thrombolysis/EVT for the Czech Republic from 1 January 2016 to 31 December 2020. Premorbid disability was defined as prestroke modified Rankin Scale score (mRS) ≥3. We compared proportions of patients with vs without premorbid disability who received EVT and examined workflow times. We compared ΔmRS-change in mRS from prestroke to 3 months-in patients with vs without premorbid disability, in addition to intracerebral hemorrhage (ICH), mortality, and discharge NIHSS (National Institutes of Health Stroke Scale score), adjusting for age, sex, baseline NIHSS, and comorbidities, and verified using propensity score weighting (PSW) and matching for differences in treatment assignment. We stratified by age group (<65, 65-74, 75-84, ≥85 years) to explore outcome heterogeneity with vs without premorbid disability.
Among 22,405 patients with ischemic stroke who received thrombolysis/EVT/both, 1,712 (7.6%) had prestroke mRS ≥ 3. Patients with prestroke disability were less likely to receive EVT vs those without (10.1% vs 20.7%, aOR: 0.30, 95% CI 0.24-0.36). When treated, they had longer door-to-arterial puncture times (median: 75 minutes, IQR: 58-100 vs 54, IQR: 27-77, adjusted difference: 12.5, 95% CI 2.68-22.3). Patients with prestroke disability receiving thrombolysis/EVT/both had worse ΔmRS (adjusted rate ratio, aIRR on PSW: 1.57, 95% CI 1.43-1.72), rates of 3-month mRS 5-6, discharge NIHSS, and mortality (aOR-PSW [mortality]: 2.54, 95% CI 1.92-3.34), while ICH did not significantly differ. 32.1% of patients with prestroke disability receiving thrombolysis/EVT/both successfully returned to prestroke state, but this proportion ranged from 19.6% for those older than 85 years to 66.0% for those younger than 65 years. Regardless of premorbid disability, EVT was associated with better outcomes including lower ΔmRS (aIRR-PSW: 0.87, 95% CI 0.83-0.91) and mortality, with no interaction of treatment effect by premorbid disability status (e.g., mortality p = 0.73). EVT recipients with premorbid disability did not differ significantly for several outcomes including ΔmRS (aIRR: 0.99, 95% CI 0.84-1.17) but were more likely to have 3-month mRS 5-6 (70.1% vs 39.5% without premorbid disability, aOR: 1.85, 95% CI 1.12-3.04).
Patients with premorbid disability were less likely to receive EVT, had slower treatment times, and had worse outcomes compared with patients without premorbid disability. However, regardless of premorbid disability, patients fared better with EVT vs medical management and one-third with prestroke disability returned to their prestroke status.
鉴于关于病前残疾患者急性卒中治疗的高质量安全性/有效性数据匮乏,他们有被常规排除在这类治疗之外的风险。我们研究了病前有残疾与无残疾患者的血管内血栓切除术(EVT)使用情况、相关工作流程及卒中后结局。
我们使用了捷克共和国2016年1月1日至2020年12月31日期间溶栓/EVT的国家登记数据。病前残疾定义为卒中前改良Rankin量表评分(mRS)≥3。我们比较了接受EVT的病前有残疾与无残疾患者的比例,并检查了工作流程时间。我们比较了病前有残疾与无残疾患者从卒中前到3个月时mRS的变化(ΔmRS),以及脑出血(ICH)、死亡率和出院时美国国立卫生研究院卒中量表评分(NIHSS),并对年龄、性别、基线NIHSS和合并症进行了调整,还使用倾向评分加权(PSW)和匹配来验证治疗分配差异。我们按年龄组(<65岁、65 - 74岁、75 - 84岁、≥85岁)进行分层,以探讨病前有残疾与无残疾患者的结局异质性。
在22405例接受溶栓/EVT/两者治疗的缺血性卒中患者中,1712例(7.6%)卒中前mRS≥3。与无病前残疾的患者相比,病前有残疾的患者接受EVT的可能性较小(10.1%对20.7%,调整后比值比:0.30,95%置信区间0.24 - 0.36)。接受治疗时,他们的门到动脉穿刺时间更长(中位数:75分钟,四分位间距:58 - 100对54,四分位间距:27 - 77,调整后差异:12.5,95%置信区间2.68 - 22.3)。接受溶栓/EVT/两者治疗的病前有残疾患者的ΔmRS更差(PSW调整后的发生率比,aIRR:1.57,95%置信区间1.43 - 1.72),3个月时mRS为5 - 6的发生率、出院时NIHSS及死亡率(PSW调整后的比值比[死亡率]:2.54,95%置信区间1.92 - 3.34),而ICH无显著差异。接受溶栓/EVT/两者治疗的病前有残疾患者中,32.1%成功恢复到卒中前状态,但这一比例在85岁以上患者中为19.6%,在65岁以下患者中为66.0%。无论病前残疾情况如何,EVT与更好的结局相关,包括更低的ΔmRS(PSW调整后的aIRR:0.87,95%置信区间0.83 - 0.91)和死亡率,病前残疾状态对治疗效果无交互作用(如死亡率p = 0.73)。接受EVT的病前有残疾患者在包括ΔmRS在内的几个结局方面无显著差异(aIRR:0.99,95%置信区间0.84 - 1.17),但更有可能3个月时mRS为5 - 6(70.1%对无病前残疾患者的39.5%,调整后比值比:1.85,95%置信区间1.12 - 3.04)。
与无病前残疾的患者相比,病前有残疾的患者接受EVT的可能性较小,治疗时间较慢,结局较差。然而,无论病前残疾情况如何,与药物治疗相比,接受EVT的患者情况更好,三分之一有卒中前残疾的患者恢复到了卒中前状态。