Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH 44106, USA.
Arch Phys Med Rehabil. 2012 May;93(5):896-904. doi: 10.1016/j.apmr.2012.01.001.
To investigate the longitudinal performance of a surgically implanted neuroprosthesis for lower-extremity exercise, standing, and transfers after spinal cord injury.
Case series.
Research or outpatient physical therapy departments of 4 academic hospitals.
Subjects (N=15) with thoracic or low cervical level spinal cord injuries who had received the 8-channel neuroprosthesis for exercise and standing.
After completing rehabilitation with the device, the subjects were discharged to unrestricted home use of the system. A series of assessments were performed before discharge and at a follow-up appointment approximately 1 year later.
Neuroprosthesis usage, maximum standing time, body weight support, knee strength, knee fatigue index, electrode stability, and component survivability.
Levels of maximum standing time, body weight support, knee strength, and knee fatigue index were not statistically different from discharge to follow-up (P>.05). Additionally, neuroprosthesis usage was consistent with subjects choosing to use the system on approximately half of the days during each monitoring period. Although the number of hours using the neuroprosthesis remained constant, subjects shifted their usage to more functional standing versus more maintenance exercise, suggesting that the subjects incorporated the neuroprosthesis into their lives. Safety and reliability of the system were demonstrated by electrode stability and a high component survivability rate (>90%).
This group of 15 subjects is the largest cohort of implanted lower-extremity neuroprosthetic exercise and standing system users. The safety and efficiency data from this group, and acceptance of the neuroprosthesis as demonstrated by continued usage, indicate that future efforts toward commercialization of a similar device may be warranted.
研究一种用于下肢运动、站立和脊髓损伤后转移的植入式神经假体的纵向性能。
病例系列。
4 所学术医院的研究或门诊物理治疗科。
接受 8 通道神经假体进行运动和站立的胸段或低颈段脊髓损伤受试者(N=15)。
在完成设备康复后,将受试者出院并在家中不受限制地使用该系统。在出院前和大约 1 年后的随访预约中进行了一系列评估。
神经假体使用、最大站立时间、体重支持、膝关节力量、膝关节疲劳指数、电极稳定性和部件存活率。
最大站立时间、体重支持、膝关节力量和膝关节疲劳指数从出院到随访的水平无统计学差异(P>.05)。此外,神经假体的使用与受试者选择在每个监测期间的大约一半天数使用系统一致。尽管使用神经假体的时间保持不变,但受试者将其使用转移到更具功能性的站立,而不是更多的维持性运动,这表明受试者将神经假体融入了他们的生活。电极稳定性和高部件存活率(>90%)证明了系统的安全性和可靠性。
这组 15 名受试者是接受植入式下肢神经假体运动和站立系统的最大队列。该组的安全性和效率数据以及对神经假体的接受程度,如持续使用所示,表明未来可能有必要为类似设备的商业化做出努力。