Suicide among veterans with amyotrophic lateral sclerosis

Emily M. Lund, Trisha A. Hostetter, Jeri E. Forster, Claire A. Hoffmire, Kelly A. Stearns-Yoder, Lisa A. Brenner, Maryam Tahmasbi Sohi

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Background: The purpose of this study was to estimate the risk of death by suicide for those with amyotrophic lateral sclerosis (ALS) seeking care within the Veterans Health Administration (VHA). Methods: This was a retrospective, cohort study. Extended Cox regression models were used to compare the hazard of suicide between the ALS and the unexposed groups. Results: The hazard of suicide was 3.98 times higher for those with ALS than for those without (95% confidence interval [CI], 2.64-6.00; P <.0001). After adjusting for covariates, those with ALS remained at increased risk (hazard ratio, 3.48; 95% CI, 2.31-5.24; P <.001). Conclusions: Among those seeking care in the VHA, individuals with ALS are at increased risk for dying by suicide. Additional suicide prevention efforts, including strategies for reducing access to lethal means, are warranted.

Original languageEnglish
Pages (from-to)807-811
Number of pages5
JournalMuscle and Nerve
Volume63
Issue number6
DOIs
StatePublished - Jun 2021

Bibliographical note

Publisher Copyright:
© 2021 Wiley Periodicals LLC. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

Keywords

  • amyotrophic lateral sclerosis
  • Lou Gehrig's disease
  • suicide
  • veterans

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