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Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
Published on: March 4, 2014
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Factors predicting survival in ALS: a multicenter Italian study
Andrea Calvo1, Cristina Moglia1, Christian Lunetta2,3
1"Rita Levi Montalcini" Department of Neuroscience, ALS Center, University of Torino, Turin, Italy.
Journal of Neurology
|October 26, 2016
Summary
This study reveals key factors influencing Amyotrophic Lateral Sclerosis (ALS) survival, including age at onset and diagnostic delay. These findings aid in clinical practice and designing future ALS clinical trials.
Area of Science:
- Neurology
- Epidemiology
- Clinical Research
Background:
- Amyotrophic Lateral Sclerosis (ALS) prognosis is influenced by various factors.
- Understanding these factors is crucial for patient care and research.
Purpose of the Study:
- To investigate the impact of clinical characteristics and therapeutic interventions on ALS prognosis.
- To identify independent prognostic factors for ALS survival.
Main Methods:
- Retrospective analysis of 2648 ALS patients diagnosed between 2009-2013 across 13 Italian centers.
- Data collection included phenotypic profiles, follow-up data, and diagnostic certainty (revised El Escorial criteria).
- Univariate and multivariate analyses were performed to identify survival predictors.
Main Results:
- Median survival time from onset to death/tracheostomy was 44 months.
- Independent prognostic factors identified include age at onset, diagnostic delay, and phenotype.
- Riluzole use and diagnostic certainty (R-EEC) were also significant predictors.
Conclusions:
- Clinical and demographic factors significantly impact ALS survival.
- Differences observed between referral center patients and the general ALS population warrant further investigation.
- Findings can inform clinical practice, trial design, and prognostic tool development for ALS.
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