Department of Stroke Rehabilitation, National Cerebral and Cardiovascular Center, 6-1 Kishibeshinmachi, Suita, Osaka 564-8565, Japan; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, 6-1 Kishibeshinmachi, Suita, Osaka 564-8565, Japan.
Department of Stroke Rehabilitation, National Cerebral and Cardiovascular Center, 6-1 Kishibeshinmachi, Suita, Osaka 564-8565, Japan.
J Neurol Sci. 2019 Sep 15;404:11-15. doi: 10.1016/j.jns.2019.07.012. Epub 2019 Jul 10.
Robot-assisted gait training following acute stroke could allow patients with severe disability to receive a high dosage and intensity of gait training compared with conventional physical therapy (CP). However, given the limited data on gauging the efficacy of Hybrid Assistive Limb (HAL) on gait training in patients with acute stroke, we aimed to evaluate several outcome measures following gait training with HAL. Patients with first-ever stroke, who required a walking aid and were able to start gait training within 1 week of stroke onset were included in the current study. Patients were assigned to either the CP or HAL group. Outcome measures were collected at baseline, and at the 2nd (at 2-6 weeks), and 3rd (at 3-5 months) assessments. All patients underwent physical therapy until the 3rd assessment; patients in the HAL group underwent gait training using HAL until the 2nd assessment. Thirty-seven patients (19 from CP and 18 from HAL, median age = 69 years) completed the study. At the 2nd assessment, the total Functional Independence Measure (FIM) score was higher in the HAL group than in the CP group (90.1 vs. 79.0, p = 0.042). In conclusion, the FIM scale could be used to identify responsiveness to acute stroke rehabilitation using HAL.
机器人辅助步态训练在急性脑卒中后,可以让严重残疾的患者接受更高剂量和强度的步态训练,而不是传统的物理疗法(CP)。然而,由于关于评估 Hybrid Assistive Limb (HAL) 在急性脑卒中患者步态训练中的疗效的数据有限,我们旨在评估使用 HAL 进行步态训练后的几种结果测量。本研究纳入了首次中风、需要助行器且能够在中风发作后 1 周内开始步态训练的患者。患者被分配到 CP 或 HAL 组。在基线、第 2 次(2-6 周)和第 3 次(3-5 个月)评估时收集结果测量。所有患者都接受物理治疗,直到第 3 次评估;HAL 组的患者在第 2 次评估前使用 HAL 进行步态训练。37 名患者(CP 组 19 名,HAL 组 18 名,中位年龄 69 岁)完成了研究。在第 2 次评估时,HAL 组的总功能独立性测量(FIM)评分高于 CP 组(90.1 比 79.0,p=0.042)。总之,FIM 量表可用于识别使用 HAL 进行急性脑卒中康复的反应性。