Spine Service, Indian Spinal Injuries Center, Vasant Kunj, New Delhi, India.
Spinal Cord. 2009 Dec;47(12):887-95. doi: 10.1038/sc.2009.54. Epub 2009 Jun 2.
Prospective Pilot Study.
To determine the safety and feasibility of autologous olfactory mucosal transplantation into the spinal cord in chronic spinal cord injured using the technique developed by Carlos Lima et al.
Spinal Injury Center, New Delhi.
Five chronic, motor complete, traumatic spinal cord injury (SCI) patients with neurological level C5-T12 underwent the procedure. Participants were assessed at baseline and at 6 monthly intervals. Safety and tolerability were evaluated through monitoring for any adverse events and tests including magnetic resonance imaging (MRI) evaluation. Efficacy assessment was done through neurological, functional and psychological evaluation, electrophysiological studies and urodynamics.
Surgery was tolerated well by all American Spinal Injury Association (ASIA) Impairment Scale (AIS) A participants. The only AIS B participant lost sensory scores significantly after surgery but is gradually regaining it. MRI evaluation revealed a syrinx in one participant and increase in length of myelomalacia in four participants. There were no other adverse findings on MRI evaluation. There was no significant improvement in any of the neurological, electrophysiological or urodynamic efficacy variables. Statistically significant improvement was seen in functional scores as evaluated by Spinal Cord Independence Measure, Beck Depression Inventory scores and life impact scores on International Spinal Cord Injury Scale.
The procedure is relatively safe and feasible in AIS A participants with thoracic level injuries at 18 month follow-up. No efficacy could be demonstrated which could be attributed to the procedure.
前瞻性试点研究。
使用 Carlos Lima 等人开发的技术,确定自体嗅黏膜移植到慢性脊髓损伤脊髓中的安全性和可行性。
新德里脊髓损伤中心。
5 名慢性、运动完全性、创伤性脊髓损伤(SCI)患者,神经水平 C5-T12,接受了该手术。参与者在基线和每 6 个月进行评估。通过监测任何不良事件和测试,包括磁共振成像(MRI)评估,评估安全性和耐受性。通过神经学、功能和心理评估、电生理学研究和尿动力学评估来评估疗效。
所有美国脊髓损伤协会(ASIA)损伤量表(AIS)A 参与者均能很好地耐受手术。唯一的 AIS B 参与者手术后感觉评分显著下降,但正在逐渐恢复。MRI 评估显示 1 名参与者有脊髓空洞症,4 名参与者的脊髓软化长度增加。MRI 评估未发现其他不良发现。任何神经学、电生理学或尿动力学疗效变量均无显著改善。脊髓独立性测量、贝克抑郁量表评分和国际脊髓损伤量表生活影响评分评估的功能评分有显著改善。
在 18 个月随访时,该程序在 AIS A 参与者和胸段损伤中相对安全且可行。由于该程序,无法证明其有效性。