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Epidemiology of Amyotrophic Lateral Sclerosis and Effect of Riluzole on Disease Course

机译:肌萎缩性侧索硬化的流行病学和利鲁唑对疾病进程的影响

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Objectives:To assess the epidemiology of ALS in Austria and to evaluate the long-term effect of riluzole treatment on survival. Methods: Hospital discharge and riluzole prescription databases were used to identify ALS cases from January 2008 to June 2012. Using the capture-recapture method we evaluated the incidence and prevalence of ALS and patients' survival in dependence of age, gender and riluzole treatment. Results: The corrected incidence and prevalence of ALS were 3.13/100,000 person-years (95% CI, 2.77 to 3.50) and 9.14/100,000 persons (95% CI, 8.53 to 9.79), respectively. Median survival from diagnosis was 676 days (95% CI, 591 to 761). A younger age at diagnosis was associated with a longer survival. Gender did not appear to affect survival time. Riluzole therapy was associated with a survival advantage only for the initial treatment period. The adjusted hazard ratio of mortality for using riluzole increased continually over time resulting in an apparent reversal of its beneficial effect after 6 months of therapy. Conclusions: We report incidence and prevalence estimates that are on the upper end of the wide range discussed in literature. Riluzole seems to exert a beneficial effect only in the first 6 months of therapy. (C) 2015 S. Karger AG, Basel
机译:目的:评估奥地利ALS的流行病学并评估利鲁唑治疗对生存的长期影响。方法:使用出院和利鲁唑处方数据库鉴定2008年1月至2012年6月的ALS病例。我们采用捕获-再捕获方法评估ALS的发生率和患病率以及患者的年龄,性别和利鲁唑治疗的依赖性。结果:校正后的ALS发生率和患病率分别为3.13 / 100,000人年(95%CI,2.77至3.50)和9.14 / 100,000人(95%CI,8.53至9.79)。诊断后的中位生存期为676天(95%CI,591至761)。诊断年龄越小,生存期越长。性别似乎并未影响生存时间。利鲁唑治疗仅在初始治疗阶段才具有生存优势。使用利鲁唑调整后的死亡率致死率随时间持续增加,导致治疗6个月后其有益作用明显逆转。结论:我们报告的发病率和患病率估计值是文献中讨论的范围的上限。利鲁唑似乎仅在治疗的前6个月才发挥有益作用。 (C)2015 S.Karger AG,巴塞尔

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