Hotter Benjamin, Padberg Inken, Liebenau Andrea, Knispel Petra, Heel Sabine, Steube Diethard, Wissel Jörg, Wellwood Ian, Meisel Andreas
Center for Stroke Research Berlin and Department of Neurology, Charité University Hospital Berlin, Berlin, Germany.
Zentrum für ambulante Neuropsychologie und Verhaltenstherapie, Berlin, Germany.
Eur Stroke J. 2018 Sep;3(3):237-245. doi: 10.1177/2396987318771174. Epub 2018 Apr 19.
Detailed data on the long-term consequences and treatment of stroke are scarce. We aimed to assess the needs and disease burden of community-dwelling stroke patients and their carers and to compare their treatment to evidence-based guidelines by a stroke neurologist.
We invited long-term stroke patients from two previous acute clinical studies ( = 516) in Berlin, Germany to participate in an observational, cross-sectional study. Participants underwent a comprehensive interview and examination using the Post-Stroke Checklist and validated standard measures of: self-reported needs, quality of life, overall outcome, spasticity, pain, aphasia, cognition, depression, secondary prevention, social needs and caregiver burden.
Fifty-seven participants (median initial National Institutes of Health Stroke Scale score 10 interquartile range 4-12.75) consented to assessment (median 41 months (interquartile range 36-50) after stroke. Modified Rankin Scale was 2 (median; interquartile range 1-3), EuroQoL index value was 0.81 (median; interquartile range 0.70-1.00). The frequencies for disabilities in the major domains were: spasticity 35%; cognition 61%; depression 20%; medication non-compliance 14%. Spasticity ( = 0.008) and social needs ( < 0.001) had the strongest impact on quality of life. The corresponding items in the Post-Stroke Checklist were predictive for low mood ( < 0.001), impaired cognition ( = 0.015), social needs ( = 0.005) and caregiver burden ( = 0.031). In the comprehensive interview, we identified the following needs: medical review (30%), optimization of pharmacotherapy (18%), outpatient therapy (47%) and social work input (33%).
These results suggest significant unmet needs and gaps in health and social care in long-term stroke patients. Further research to develop a comprehensive model for managing stroke aftercare is warranted. clinicaltrials.gov NCT02320994.
关于中风长期后果及治疗的详细数据匮乏。我们旨在评估社区中风患者及其照料者的需求和疾病负担,并将他们接受的治疗与中风神经科医生基于循证指南的治疗进行比较。
我们邀请了德国柏林之前两项急性临床研究中的长期中风患者(n = 516)参与一项观察性横断面研究。参与者使用中风后检查表以及经过验证的标准测量方法接受了全面访谈和检查,这些测量方法涉及自我报告的需求、生活质量、总体结果、痉挛、疼痛、失语、认知、抑郁、二级预防、社会需求和照料者负担。
57名参与者(初始美国国立卫生研究院中风量表评分中位数为10,四分位间距为4 - 12.75)同意接受评估(中风后中位数为41个月(四分位间距为36 - 50))。改良Rankin量表评分为2(中位数;四分位间距为1 - 3),欧洲生活质量指数值为0.81(中位数;四分位间距为0.70 - 1.00)。主要领域的残疾发生率为:痉挛35%;认知61%;抑郁20%;药物治疗不依从14%。痉挛(P = 0.008)和社会需求(P < 0.001)对生活质量的影响最大。中风后检查表中的相应项目可预测情绪低落(P < 0.001)、认知障碍(P = 0.015)、社会需求(P = 0.005)和照料者负担(P = 0.031)。在全面访谈中,我们确定了以下需求:医学复查(30%)、药物治疗优化(18%)、门诊治疗(47%)和社会工作介入(33%)。
这些结果表明长期中风患者在健康和社会护理方面存在显著未满足的需求和差距。有必要开展进一步研究以制定一个全面的中风后续护理管理模型。clinicaltrials.gov NCT02320994 。