Risk of sepsis in patients with amyotrophic lateral sclerosis: a population-based retrospective cohort study in Taiwan.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 28093437.
- Also identified by DOI 10.1136/bmjopen-2016-013761 and PMC identifier 5253540.
- Licence recorded as CC BY-NC.
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Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease, and sepsis is a frequent cause of death in hospitalised patients. We investigated the relationship between ALS and the subsequent risk of sepsis. A retrospective cohort analysis. Patients with ALSs diagnosed between 2000 and 2010 in Taiwan National Health Insurance Research Database. We included 701 and 2804 patients as the ALS and the non-ALS groups, respectively. The risk of sepsis was calculated by Cox proportional hazards regression model. During the follow-up period, the incidence density rates were 77.8 and 11.1 per 1000 person-years in the ALS and non-ALS groups, respectively. After adjusting for sex, age, Charlson comorbidity index score, life-support measures, and β<sub>2</sub>-adrenoceptor agonists treatment, the ALS group had a higher risk of sepsis (HR=3.42; 95% CI 2.60 to 4.50) than the non-ALS group. An increase of the risk was observed in patients with ALS receiving life support treatment measures, whereas a decrease of the risk was associated with treatment of β<sub>2</sub>-adrenoceptor agonists. The risk of sepsis is associated with a prior ALS diagnosis, and may be increased by the use of life support measures and decreased by β<sub>2</sub>-adrenoceptor agonists.
Medical subject headings
- Amyotrophic Lateral Sclerosis
- Sepsis