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Prognosis of amyotrophic lateral sclerosis patients after tracheostomy invasive ventilation in Korea

  • Jong Su Kim
  • , Minae Park
  • , Sojeong Park
  • , Juhee Chae
  • , Yoon Ho Hong
  • , Kyung Seok Park
  • , Jung Joon Sung*
  • , Seok Jin Choi*
  • *Corresponding author for this work
  • Seoul National University
  • Hanmi Pharmaceutical Co., Ltd.
  • SMG-SNU Seoul Boramae Medical Center

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background: Tracheostomy invasive ventilation (TIV) is applied to a subset of amyotrophic lateral sclerosis (ALS) patients; however, its frequency and impact on prognosis vary across countries. Methods: We conducted a nationwide retrospective cohort study using Korean National Health Insurance claims data. All patients diagnosed with sporadic ALS from 2012 to 2017 were included, with the observation period until 2020. The survival time between the TIV and non-TIV groups was compared using propensity score matching analysis, and prognostic factors were assessed within the TIV group. Results: This study included 3484 ALS patients (mean [standard deviation] age, 62.4 [11.9] years, 60.4% male), among whom 1230 (35.3%) underwent TIV. After 1:1 propensity score matching, the survival duration between the two groups was not significantly different (28 vs. 25 months, p = 0.057). Cox regression indicated that older age (hazard ratios [HRs] for each decade compared to <40 years: 3.89, 3.83, 5.30, 6.78, and 8.40 [(Formula presented.) 80 years]; p < 0.005 for all) and lower income (HR, 1.28; 95% confidence interval [CI], 1.09–1.52; p = 0.003) negatively impacted survival, while gastrostomy (HR, 0.57; 95% CI, 0.50–0.66; p < 0.001) and supportive care services (HR, 0.43; 95% CI, 0.32–0.59; p < 0.001) were associated with prolonged survival. Conclusions: TIV was administered to more than one-third of Korean ALS patients without significant survival prolongation. Older age, lower income, lack of gastrostomy, and insufficient supportive care were independent poor prognostic factors for survival, underscoring the importance of comprehensive management for ALS patients.

Original languageEnglish
Pages (from-to)271-281
Number of pages11
JournalAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Volume25
Issue number3-4
DOIs
StatePublished - 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 1 - No Poverty
    SDG 1 No Poverty

Keywords

  • Amyotrophic lateral sclerosis
  • prognosis
  • survival
  • tracheostomy

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