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Current Status of the Diagnosis and Management of Amyotrophic Lateral Sclerosis in Korea: a Multi-center Cross-sectional Study

Overview
Journal J Clin Neurol
Specialty Neurology
Date 2013 Jan 17
PMID 23323138
Citations 6
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Abstract

Background And Purpose: Recently published, evidence-based guidelines should alter the management of amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND). However, the newest recommendations for ALS/MND therapy are not reflected in actual clinical practice. We sought to evaluate the current status of the diagnosis and management of ALS in Korea.

Methods: The Korean ALS/MND research group was organized in 2010, involving more than 50 neurologists from neuromuscular centers in Korea. Participating centers collected data from April to September 2010 on the diagnosis and management of patients with ALS. Data forms from the ALS patient care database, which is a component of the ALS clinical assessment, research, and education program (http://www.outcomes-umassmed.org/ALS/), were modified and used for data collection.

Results: In total, 373 sporadic ALS cases from 35 centers were enrolled. The demographic features and clinical findings were similar to those in previous reports from other countries. The mean age at onset was 50-60 years, and a slight male predominance was observed. The enrolled patients predominantly showed focal onset of cervical or lumbosacral symptoms. Only about one-half of the indicated patients (31.4%) received a physician's recommendation for a parenteral gastrostomy, and 18.1% underwent the procedure. Noninvasive ventilation was recommended in 23% of patients, but applied in only 9.5% of them. Tracheostomy was performed in 12.7% of patients.

Conclusions: The demographic and clinical features of the diagnosis and management of ALS in Korea are similar to those reported in other countries; however, supportive management, as recommended in evidence-based guidelines, are not yet widely recommended or performed for patients with ALS in Korea.

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References
1.
Mitsumoto H, Davidson M, Moore D, Gad N, Brandis M, Ringel S . Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunction. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003; 4(3):177-85. DOI: 10.1080/14660820310011728. View

2.
Bourke S, Bullock R, Williams T, Shaw P, Gibson G . Noninvasive ventilation in ALS: indications and effect on quality of life. Neurology. 2003; 61(2):171-7. DOI: 10.1212/01.wnl.0000076182.13137.38. View

3.
Moss A, Casey P, Stocking C, Roos R, Brooks B, Siegler M . Home ventilation for amyotrophic lateral sclerosis patients: outcomes, costs, and patient, family, and physician attitudes. Neurology. 1993; 43(2):438-43. DOI: 10.1212/wnl.43.2.438. View

4.
Bradley W, Anderson F, Bromberg M, Gutmann L, Harati Y, ROSS M . Current management of ALS: comparison of the ALS CARE Database and the AAN Practice Parameter. The American Academy of Neurology. Neurology. 2001; 57(3):500-4. DOI: 10.1212/wnl.57.3.500. View

5.
Haverkamp L, Appel V, Appel S . Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. Brain. 1995; 118 ( Pt 3):707-19. DOI: 10.1093/brain/118.3.707. View