A spatial analysis of amyotrophic lateral sclerosis (ALS) cases in the United States and their proximity to multidisciplinary ALS clinics, 2013.

Journal Article (Journal Article)

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease that typically results in death within 2-5 years of initial symptom onset. Multidisciplinary ALS clinics (MDCs) have been established to provide specialty care to people living with the disease. OBJECTIVE: To estimate the proximity of ALS prevalence cases to the nearest MDC in the US to help evaluate one aspect of access to care. METHODS: Using 2013 prevalence data from the National ALS Registry, cases were geocoded by city using geographic information system (GIS) software, along with the locations of all MDCs in operation during 2013. Case-to-MDC proximity was calculated and analyzed by sex, race, and age group. RESULTS: During 2013, there were 72 MDCs in operation in 30 different states. A total of 15,633 ALS cases were geocoded and were distributed throughout all 50 states. Of these, 62.6% were male, 77.9% were white, and 76.2% were 50-79 years old. For overall case-to-MDC proximity, nearly half (44.9%) of all geocoded cases in the US lived >50 miles from an MDC, including approximately a quarter who lived >100 miles from an MDC. There was a statistically significant difference between distance to MDC by race and age group. CONCLUSIONS: The high percentage of those living more than 50 miles from the nearest specialized clinic underscores one of the many challenges of ALS. Having better access to care, whether at MDCs or through other modalities, is likely key to increasing survivability and obtaining appropriate end-of-life treatment and support for people with ALS.

Full Text

Duke Authors

Cited Authors

  • Horton, DK; Graham, S; Punjani, R; Wilt, G; Kaye, W; Maginnis, K; Webb, L; Richman, J; Bedlack, R; Tessaro, E; Mehta, P

Published Date

  • February 2018

Published In

Volume / Issue

  • 19 / 1-2

Start / End Page

  • 126 - 133

PubMed ID

  • 29262737

Pubmed Central ID

  • 29262737

Electronic International Standard Serial Number (EISSN)

  • 2167-9223

Digital Object Identifier (DOI)

  • 10.1080/21678421.2017.1406953


  • eng

Conference Location

  • England