Barros Tarcísio Eloy Pessoa, Araujo Fernando Flores De, Higino Lucas Da Paz, Marcon Raphael Martus, Cristante Alexandre Fogaça
. Universidade de São Paulo, Faculdade de Medicina, Department of Orthopedics and Traumatology, São Paulo, SP, Brazil.
Acta Ortop Bras. 2016 May-Jun;24(3):123-6. doi: 10.1590/1413-785220162403160032.
To evaluate the effect of monosialoganglioside (GM-1) in spinal cord trauma patients seen in our service who have not been treated with methylprednisolone.
Thirty patients with acute spinal cord trauma were randomly divided into two groups. In Group 1, patients received 200 mg GM-1 in the initial assessment and thereafter received 100 mg intravenous per day for 30 days and Group 2 (control) received saline. Patients were evaluated periodically (at 6 weeks, 6 months, one year and two years), using a standardized neurological assessment of the American Spinal Injury Association / International Spinal Cord Society.
The comparative statistical analysis of motor indices, sensitive indices for pain and touch according to the standardization of ASIA / ISCOS showed that the assessments at 6 weeks, 6 months and 2 years, GM-Group 1 patients had higher rates than the control group regarding sensitivity to pain and touch, with no statistically significant difference from the motor index.
The functional assessment showed improvement in the sensitive indices of patients treated with GM1 after post-traumatic spinal cord injury compared to patients who received placebo. Level of Evidence IV, Prospective Case Studies Series.
评估单唾液酸神经节苷脂(GM-1)对我院未接受甲基强的松龙治疗的脊髓损伤患者的疗效。
30例急性脊髓损伤患者随机分为两组。第1组患者在初始评估时接受200mg GM-1,此后每天静脉注射100mg,共30天,第2组(对照组)接受生理盐水。定期(6周、6个月、1年和2年)使用美国脊髓损伤协会/国际脊髓学会的标准化神经学评估对患者进行评估。
根据ASIA/ISCOS标准化对运动指数、疼痛和触觉敏感指数进行的比较统计分析表明,在6周、6个月和2年的评估中,GM-1组1患者在疼痛和触觉敏感性方面的比率高于对照组,与运动指数无统计学显著差异。
功能评估显示,与接受安慰剂的患者相比,创伤后脊髓损伤后接受GM1治疗的患者敏感指数有所改善。证据等级IV,前瞻性病例研究系列。