Key result
Baseline anticholinergic burden shows no association with all-cause mortality in hemodialysis patients.
Why the study?
Does anticholinergic burden increase mortality and morbidity in patients undergoing hemodialysis?
Cohort (n=6,069)
Yes
Does anticholinergic burden increase mortality and morbidity in patients undergoing hemodialysis?
Hazard Ratio: 0.92 (95% CI 0.78–1.08)
p-value: p=0.31
In patients undergoing hemodialysis, anticholinergic burden was not associated with increased mortality or adverse outcomes, contrasting with findings in the general population.
Anticholinergic burden showed no mortality link in hemodialysis; challenges general population data but leaves open effects pending randomized confirmation.
Background Patients undergoing hemodialysis frequently receive medications with anticholinergic effects, yet evidence linking cumulative anticholinergic burden to outcomes in this population is scarce. While general population studies associate anticholinergic burden with adverse outcomes, it remains unknown whether the same holds true in patients undergoing hemodialysis. We examined whether anticholinergic burden is associated with mortality and morbidity in patients undergoing hemodialysis. Methods We analyzed data from 6069 adults (mean age 65 years, 34% women) in the Japan Dialysis Outcomes and Practice Patterns Study (J-DOPPS) cohort (2009–2018). Baseline anticholinergic burden was assessed using the Anticholinergic Cognitive Burden (ACB) score; patients were categorized as ACB ≥ 1 versus 0. The primary outcome was all-cause mortality; secondary outcomes included fracture-related hospitalization, cardiovascular events, self-reported falls, and quality of life (QOL) changes measured by the Short-Form 12-Item Health Survey (SF-12). Analyses used Cox and multivariable regression, adjusting for demographics, comorbidities, and polypharmacy. Results At baseline, 50.4% of patients had ACB scores ≥ 1. During 2.1-year mean follow-up, 707 deaths occurred. The adjusted hazard ratio for mortality (ACB ≥ 1 versus 0) was 0.92 (95% confidence interval [CI] 0.78–1.08; P = 0.31). No dose–response relationship was observed. Anticholinergic burden was not significantly associated with fracture-related hospitalization (adjusted odds ratio [OR] 1.31, 95% CI 0.94–1.83), cardiovascular events (OR 1.13, CI 0.96–1.33), falls (OR 0.92, CI 0.73–1.15), or QOL changes. Conclusions In this hemodialysis cohort, anticholinergic burden was not associated with increased mortality or adverse outcomes, contrasting with general population findings. These results do not establish safety of individual anticholinergic agents; rather, they suggest that overall burden did not drive adverse outcomes in this population. Judicious prescribing remains warranted until further evidence from studies incorporating dialysis-specific factors becomes available.
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Honda et al. (2026) conducted a cohort in Hemodialysis (n=6,069). Anticholinergic burden (ACB score ≥ 1) vs. ACB score = 0 was evaluated on All-cause mortality (HR 0.92, 95% CI 0.78-1.08, p=0.31). Baseline anticholinergic burden (ACB ≥ 1) was not significantly associated with all-cause mortality in patients undergoing hemodialysis (HR 0.92; 95% CI 0.78-1.08; P=0.31).
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