期刊文献+

鼠神经生长因子联合神经节苷脂对脑损伤患者神经功能修复的影响 被引量:9

Efficiency of mouse nerve growth factor combined with ganglioside in treatment of patients with brain injury
下载PDF
导出
摘要 目的探讨鼠神经生长因子联合神经节苷脂对脑损伤患者神经功能修复的影响。方法将90例颅脑脑损伤患者采用随机数字表法分为A组、B组、C组,每组30例。在常规治疗基础上,A组患者加用神经节苷脂治疗,B组患者加用鼠神经生长因子治疗,C组患者加用神经节苷脂联合鼠神经生长因子治疗。比较3组患者的临床疗效、神经功能评分、日常生活能力评分及肌力评分。结果 C组患者的总有效率为93.33%,高于A、B组(P<0.05),而A组与B组的总有效率比较无统计学差异(P>0.05);3组患者治疗后的神经功能评分、日常生活能力评分、肌力评分均较治疗前显著增高(均P<0.05);C组患者治疗后神经功能评分、日常生活能力评分、肌力评分均高于A、B组(均P<0.05),A组与B组比较无统计学差异(P>0.05)。结论采用神经节苷脂、鼠神经生长因子联合治疗脑损伤患者的临床疗效显著,不仅可有效修复患者的神经功能及受损的肌力,还能提高其日常生活能力,可推广应用于临床。 Objective To investigate the efficacy of mouse nerve growth factor combined with ganglioside in treatment ofpatients with brain injury. Methods Ninety patients with brain injury patients admitted from January 2016 to June 2017 wererandomly assigned in three groups with 30 patients in each group. All patients were treated with conventional therapy; inaddition, patients in group A also received ganglioside, patients in group B received mouse nerve growth factor and patientsin group C received ganglioside plus mouse nerve growth factor. The clinical efficacy was evaluated with the neurologicalfunction score, ADL score and muscle strength score before and after treatment in three groups. Results The overalleffective rate of group C (93.33%) was higher than that of group A and group B (P〈0.05), while there was no significant differencein effective rate between group A and group B (P〉0.05). The neurological function score, ADL score and muscle strength scoreswere significantly improved after treatment in all three groups (P〈0.05); the scores in group C were higher than those of other twogroups (P〈0.05), however, there was no significant difference between groups A and B (P〉0.05). Conclusion Gangliosidecombined with mouse nerve growth can more effectively improve nerve function than use of single drug in treatment of patientswith brain Injury.
作者 张行泉 Zhang Xingquan(Department of Neurosurgery,Zhoushan Hospital,Zhoushan 316000,China)
出处 《浙江医学》 CAS 2018年第20期2220-2222,2226,共4页 Zhejiang Medical Journal
关键词 脑损伤 神经节苷脂 鼠神经生长因子 神经功能 Brain injury;Ganglioside;Nerve growth factor;Neural function
  • 相关文献

参考文献12

二级参考文献85

  • 1王维治.神经病学[M].北京:人民卫生出版社,2004.132.
  • 2Kawakami N,Kashiwagi S,Kitahara T, et al. Effect of local abmin- stration of basic fibroblast growth factor against neuronal damage caused by transient intracerebral mass lesion in rats[ J]. Brain Res, 1995,697 : 104.
  • 3Komacka MK. Magnesium sulphate in the treatment of ischemic-hy- poxic neonatal encephalopathy [ J ]. Neurol Neuroehir Pol,2001,35 ( 2 ) : 299 - 308.
  • 4Alfred LS. Management and treatment planning for the abnormally developing child[ M]//Alfred LS. Early diagnosis and intervention- al therapy in cerelbral palsy. 3ed. New York: Marcel Dekker Inc, 2001:95 - 119.
  • 5Michal AE,Amy GB,Kelsey B. Intrauterine inflammation,insufficient to induce parturition,still evokes fetal and neonatal brain injury[J].{H}International Journal of Developmental Neuroscience,2011,(6):663-671.
  • 6Van Velthoven CT,Kavelaars A,Van Bel F. Mesenchymal stem cell treatment after neonatal hypoxic-ischemic brain injury improves behavioral outcome and induces neuronal and oligodendrocyte regeneration[J].Brain Behavior Immun,2010,(3):387-393.
  • 7Julie AW,Hanna ER,Kathryn MB. Evidence that the serotonin transporter does not shift into the cytosol of remaining neurons after neonatal brain injury[J].{H}Neuroscience Research,2012,(3):252-256.
  • 8Tatyana V,Ali F,Michael VJ. Pluripotent possibilities:human umbilical cord blood cell treatment after neonatal brain injury[J].{H}PEDIATRIC NEUROLOGY,2013,(5):346-354.
  • 9Umral K,Tuzun F,Tuqyan K. Role of epigenetic regulatory mechanisms in neonatal hypoxic-ischemic brain injury[J].{H}EARLY HUMAN DEVELOPMENT,2013,(3):165-173.
  • 10Irina B,Kirstin L,Michael M. 45:Inflammation-induced preterm birth (Ⅱ-PTB):prenatal ILl β blockade prevents neonatal brain injury in a region specific manner but not preterm birth[J].{H}AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY,2012,(1):30-31.

共引文献127

同被引文献89

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部