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出 处:《中华神经科杂志》2009年第6期402-405,共4页Chinese Journal of Neurology
基 金:国家“985”计划课题资助项目(985-2-004-113);首都医学发展科研基金资助项目(2005-1007);国家自然科学基金资助项目(30672203)
摘 要:目的采取回顾性研究方法探讨肌萎缩侧索硬化(ALs)的预后相关因素。方法收集1994年1月至2004年12月于北京大学第三医院就诊的ALJS患者106例,记录其临床资料、肺活量和神经功能等级评分,每3个月到半年进行面访或电话随访,直至其死亡或气管切开。用Kaplan—Meier方法计算中位生存时间,用Logrank分析各单因素变量与生存时间的关系,用Cox风险比例模型分析多变量对生存时间的影响。结果106例ALS患者平均发病年龄为(52.1±10.5)岁,确诊52例,拟诊37例,可能17例。患者的中位生存时间为35个月(95%CI30~40个月)。单因素分析发现起病部位、发病到诊断的时间和诊断时的用力肺活量为生存时间的影响因素,差异有统计学意义(Logrank6.84、43.30、4.78,均P〈0.05)。进一步用Cox风险比例模型分析,发病到诊断的时间为最有力的影响因子(Wald值20.221,风险系数0.351,P〈0.05),而性别、年龄、诊断级别、诊断时的神经功能评分情况与生存时间无明显相关。结论发病到确诊的时间为生存时间最有力的影响因子,提示ALS患者诊断时的病情发展速度与生存时间高度相关,值得进一步研究。Objective To identify the factors related to amyotrophic lateral sclerosis (ALS) prognosis in a retrospective study. Methods One hundred and six patients were evaluated with ALS enrolled in our hospital from January 1994 to December 2004. The patients were monitored with a standard evaluation form, which recorded clinical features, function rating scale (FRS) and forced vital capacity (FVC) every 3 or 6 months from visit to death or having tracheostomy. Results Mean age at onset was (52. 1± 10. 5) years. According to revised E1 Escorial diagnostic criteria (EEDC), 52 patients had definite ALS, 37 probable ALS, 17 possible ALS. The median survival time from symptom onset was 35 months (95% CI 30-40 months). In the univariate analysis, survival was significantly related to lesion site, lag time from onset to diagnosis and predicted FVC at diagnosis ( Log rank 6. 84, 43.30, 4.78, all P 〈 0. 05 ). In the Cox multivariate model, lag time from onset to diagnosis was significantly related to survival ( Wald 20. 221, hazard ratio 0. 351, P 〈 0. 05 ). Age, sex, EEDC classification, FRS at diagnosis were not related to survival. Conclusion Lag time from onset to diagnosis is a strong predictor of survival, which suggests that progression rate is highly related to survival and further study is needed.
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