Gailey Robert S, Gaunaurd Ignacio, Agrawal Vibhor, Finnieston Adam, O'Toole Christopher, Tolchin Ronald
Department of Physical Therapy, Miller School of Medicine, University of Miami, Coral Gables, FL 33146, USA.
J Rehabil Res Dev. 2012;49(4):597-612. doi: 10.1682/jrrd.2011.04.0077.
We examined the application of outcome measures to determine changes in function caused by standardized functional prosthetic gait training and the use of four different prosthetic feet in people with unilateral transtibial limb loss. Two self-report measures (Prosthetic Evaluation Questionnaire-Mobility Scale [PEQ-13] and Locomotor Capabilities Index [LCI]), and three performance-based measures (Amputee Mobility Predictor with a prosthesis [AMPPRO], 6-minute walk test [6MWT] and step activity monitor [SAM]) were used. Ten people with unilateral transtibial limb loss, five with peripheral vascular disease (PVD) and five without PVD, completed testing. Subjects were tested at baseline and after receiving training with their existing prosthesis and with the study socket and four prosthetic feet, i.e., SACH (solid ankle cushion heel), SAFE (stationary attachment flexible endoskeletal), Talux, and Proprio feet, over 8 to 10 weeks. Training was administered between testing sessions. No differences were detected by the PEQ-13, LCI, 6MWT, or SAM following training and after fitting with test feet. The AMPPRO demonstrated differences following training with the existing prosthesis in the PVD group and between selected feet from baseline testing ( p </= 0.05). Significant differences were found between the PVD and the non-PVD groups (p </= 0.05) in the AMPPRO and 6MWT when using the Proprio foot. Self-report measures were unable to detect differences between prosthetic feet.
我们研究了结局指标的应用,以确定标准化功能性假肢步态训练以及使用四种不同假肢脚对单侧胫骨截肢患者功能变化的影响。使用了两种自我报告指标(假肢评估问卷-活动量表[PEQ-13]和运动能力指数[LCI])以及三种基于表现的指标(佩戴假肢的截肢者运动预测器[AMPPRO]、6分钟步行试验[6MWT]和步数活动监测器[SAM])。十名单侧胫骨截肢患者,其中五名患有外周血管疾病(PVD),五名没有PVD,完成了测试。受试者在基线时以及在使用其现有假肢以及研究接受腔和四种假肢脚(即SACH(实心踝垫跟)、SAFE(固定连接柔性内骨骼)、Talux和本体感觉脚)进行8至10周的训练后接受测试。训练在测试阶段之间进行。训练后以及佩戴测试脚后,PEQ-13、LCI、6MWT或SAM均未检测到差异。在PVD组中,使用现有假肢训练后以及在基线测试中选定的脚之间,AMPPRO显示出差异(p≤0.05)。当使用本体感觉脚时,PVD组和非PVD组在AMPPRO和6MWT方面存在显著差异(p≤0.05)。自我报告指标无法检测到假肢脚之间的差异。