Roessingh Research and Development, Enschede, The Netherlands.
Artif Organs. 2010 May;34(5):366-76. doi: 10.1111/j.1525-1594.2009.00879.x.
The aim was to determine if the treatment of a drop foot by means of an implantable two-channel peroneal nerve stimulator improves health-related quality of life (HRQoL). All subjects were measured at baseline and after a follow-up period of 12 and 26 weeks. Twenty-nine stroke survivors with chronic hemiplegia with drop foot who fulfilled the predefined inclusion and exclusion criteria were included in the present randomized controlled trial. The intervention group received an implantable two-channel peroneal nerve stimulator for correction of their drop foot. The control group continued using their conventional walking device, consisting of an ankle-foot orthosis, orthopedic shoes, or no device. HRQoL was assessed in two different ways: (i) by taking descriptive measures, that is, the Short Form-36 (SF-36; generic measure) and the Disability Impact Profile (DIP; specific measure); and (ii) by obtaining preference-based utilities both measured with the time trade-off (direct way) and by calculating them from the EuroQol (EQ-5D) and SF-36. A significant positive effect of the implantable device was found on the physical functioning domain, the general health domain, and the physical component summary score of the SF-36. For the DIP, a significant improvement was found on the domains mobility, self-care, and psychological status in the intervention group. Regarding the preference-based utility measures, a significant effect was found for the utility index calculated from the EQ-5D. The implantable two-channel peroneal nerve stimulator seems to be efficient to improve HRQoL, mainly the domains related to physical functioning. A relation was present between the utility indexes calculated from the EQ-5D and SF-36.
目的是确定通过植入式双通道腓总神经刺激器治疗足下垂是否能提高健康相关生活质量(HRQoL)。所有受试者均在基线时和随访 12 周和 26 周后进行测量。29 名符合预定纳入和排除标准的慢性偏瘫伴足下垂的脑卒中幸存者被纳入本随机对照试验。干预组接受植入式双通道腓总神经刺激器治疗其足下垂。对照组继续使用传统的步行装置,包括踝足矫形器、矫形鞋或无装置。HRQoL 通过两种不同的方法进行评估:(i)通过采取描述性措施,即 36 项简短健康调查(SF-36;通用措施)和残疾影响概况(DIP;特定措施);(ii)通过时间权衡(直接方法)获得偏好为基础的效用,并通过计算从 EuroQol(EQ-5D)和 SF-36 获得。植入式设备对 SF-36 的生理功能、一般健康和生理成分总分有显著的积极影响。对于 DIP,干预组在移动、自理和心理状态等领域有显著改善。关于偏好为基础的效用措施,从 EQ-5D 计算出的效用指数有显著影响。植入式双通道腓总神经刺激器似乎能够有效提高 HRQoL,主要是与生理功能相关的领域。从 EQ-5D 和 SF-36 计算出的效用指数之间存在相关性。