Literature DB >> 27617889

Epidemiology of Amyotrophic Lateral Sclerosis: A Population-Based Study in Israel.

Clara Weil1, Neta Zach, Shay Rishoni, Varda Shalev, Gabriel Chodick.   

Abstract

BACKGROUND: Globally, the annual incidence and prevalence of amyotrophic lateral sclerosis (ALS) are estimated at 1.9 and 4.5 per 100,000 population, respectively. This study is aimed at describing the epidemiology of ALS in Israel in a real-world setting.
METHODS: A retrospective study was performed using the databases of Maccabi Healthcare Services (MHS), a 2-million-member health maintenance organization in Israel. The study included all MHS adults diagnosed with ALS between 1997 and 2013. In 2013, characteristics of ALS patients were compared to those of age-sex-matched patients without ALS. Survival after ALS diagnosis was assessed until death and until tracheostomy or death (follow-up through 2014).
RESULTS: In 2013 (n = 158), the prevalence of ALS was 8.1 per 100,000 population in MHS. In 1997-2013, a total of 375 ALS patients were diagnosed, corresponding to an average annual incidence of 1.8 per 100,000 population in MHS. The median survival from diagnosis to death was 3.5 years (95% CI 2.9-4.1), with approximately 28% surviving at least 10 years. Median tracheostomy-free survival was 2.5 years (95% CI 2.1-2.9).
CONCLUSIONS: Results suggest that there is a relatively high prevalence of ALS in Israel. Further research is needed to investigate factors that may contribute to the survival of patients with ALS in Israel.
© 2016 S. Karger AG, Basel.

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Year:  2016        PMID: 27617889     DOI: 10.1159/000448921

Source DB:  PubMed          Journal:  Neuroepidemiology        ISSN: 0251-5350            Impact factor:   3.282


  2 in total

1.  Medication use and risk of amyotrophic lateral sclerosis-a systematic review.

Authors:  Can Cui; Jiangwei Sun; Kyla A McKay; Caroline Ingre; Fang Fang
Journal:  BMC Med       Date:  2022-08-05       Impact factor: 11.150

2.  A retrospective study of the clinical phenotype and predictors of survival in non-Caucasian Hispanic patients with amyotrophic lateral sclerosis.

Authors:  Claudia Marisol Sánchez-Martínez; José Alberto Choreño-Parra; Lilia Nuñez-Orozco; Noel Placencia-Álvarez; Laura Marcela Alvis-Castaño; Parménides Guadarrama-Ortiz
Journal:  BMC Neurol       Date:  2019-10-29       Impact factor: 2.474

  2 in total

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