期刊文献+

东菱迪芙治疗吉兰-巴雷综合征的临床观察

Batroxobin for Guillain-Barre syndrome:clinical observation
下载PDF
导出
摘要 目的探讨血浆中纤维蛋白原含量下降,是否能促进吉兰-巴雷综合征患者康复。方法 27例GBS患者,随机分为2组,治疗组在发病后除给予丙种球蛋白治疗外,静脉给予东菱迪芙首剂10u,并隔日给予5u,连续用药7次,对照组仅给予丙种球蛋白治疗。观察患者临床症状恢复情况,应用Hughes评分标准对不同时间点的临床神经功能进行评分;定期检测患者神经电生理改变。结果治疗组用药后,其血浆中纤维蛋白原含量明显低于对照组,治疗组在发病180d时Hughes评分明显低于对照组。神经电生理检查发现,在发病90d时,治疗组正中神经及尺神经传导速度较对照组恢复得更快。结论吉兰-巴雷综合征患者急性期血浆中纤维蛋白原含量下降,可能促进了患者神经功能恢复。 Objective To discuss the relationship between the low level fibrinogen and the healing of Guillain-Barre syndrome.Methods All patients were divided into two groups stochastically and treated with intravenous immunoglobulins(IVIg)at a dose of 0.4g/kg body weight per day for 5 days consecutively.In addition,the treatment group was administrated Batroxobin preparation 10u,hereafter 5u every other day,altogether continuously applied drugs for 7 times.The control group only got the IVIg treatment.The patients' clinical symptoms at different situation were observed,and the Hughes scale was used to grading the patients' clinical nerve function.The neuroelectricity physiology of patients was examined and compared between different groups.Results The fibrinogen levels of the treatment group in blood plasma was lower than the control group obviously.The Hughes grade of the treatment group was lower than the control group obviously 180 days after the onset.Electrophysiological examination showed that the median nerve and ulnar nerve conduction velocity of the treatment group recovered faster than the control group 90 days after the onset.Conclusion The patients of Guillain-Barre syndrome with decreased fibrinogen in blood plasma may promote patients recovery.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2010年第9期819-821,共3页 Journal of Apoplexy and Nervous Diseases
关键词 吉兰-巴雷综合征 纤维蛋白原 东菱迪芙 Guillain-Barre Syndrome Fibrinogen Batroxobin
  • 相关文献

参考文献15

  • 1Asbury AK, Arnason BGW, Karp HR, et al. Criteria for diagnosis of Guillain-Barre syndrome [ J]. Ann Neural,1978,3:565-566.
  • 2Randomised trial of plasma exchange, intravenous immunoglobulin, and combined treatments in Guillain-Barre syndrome. Plasma Exehange/Sandoglobulin Guillain-Barre Syndrome Trial Group [ J ]. Lancet, 1997,349:225-230.
  • 3Hadden RD, Cornblath DR, Hughes RA, et al. Electrophysiological classification of Guillain-Barre syndrome: clinical associations and outcome[ J]. Ann Neurol, 1998,44:780-788.
  • 4Homer PJ, Gage FH. Regenerating the damaged central nervous system [ J]. Nature,2000,407:963-970.
  • 5Silver J, Miller JH. Regeneration beyond the glial sear [ J]. Nat Rev Neurosci ,2004,5 : 146-156.
  • 6Jessen KR, Mirsky R. Schwann ceils and their precursors emerge as major regulators of nerve development [ J ]. Trends Neurosci, 1999, 22:402-410.
  • 7Jessen KR, Mirsky R. Developmental regulation in the Schwann cell lineage[J]. Adv Exp Med Bio1,1999,468:3-12.
  • 8Chen ZL, Striekland S. Laminin gammal is critical for Sehwann cell differentiation, axon myelination, and regeneration in the peripheral nerve [J]. J Cell Biol,2003,163(4) :889-899.
  • 9Anton ES, Sandrock AW Jr, Matthew WD. Merosin promotes neurite growth and Schwann cell migration in vitro and nerve regeneration in vivo : Evidence using an antibody to merosin, ARM-1 [ J ]. Dev Biol, 1994,164 ( 1 ) : 133-146.
  • 10Fernandez-Valle C, Gwynn L, Wood PM. Anti-beta 1 integrin anti- body inhibits Schwann cell myelination [ J]. J Neurobiol, 1994,25: 1207-1226.

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