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April 11, 2026LUTS Lower Urinary Tract Symptoms2 citations

Association Between Frailty and Short‐Term Treatment‐Related Adverse Events in Patients With Overactive Bladder

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SISohei IwagamiHYHiraku YamamotoHMHaruka Miyai

Key Points

  • To evaluate the relationship between frailty at treatment initiation and the occurrence of treatment-related adverse events in patients with overactive bladder.
  • Retrospective cohort study of 122 patients initiating pharmacotherapy for OAB.
  • Frailty assessed using the Frailty Screening Index classified into robust, prefrail, and frail.
  • Primary outcome measured was treatment-related adverse events within 3 months.
  • Independent predictors analyzed using multivariable logistic regression.
  • Longitudinal changes in OAB symptoms assessed with linear mixed-effects models.
  • Adverse events occurred in 52 patients (42.6%), with rates higher in frail groups: 4.7% robust, 40.0% prefrail, and 57.3% frail (p < 0.01 for trend).
  • Frailty was independently associated with adverse events (OR 2.97 per status increase, p < 0.01).
  • Anticholinergic use and baseline post-void residual volume also linked to adverse events.
  • Chronological age did not show a significant association with adverse events.

Abstract

ABSTRACT Objectives To evaluate whether frailty at treatment initiation is associated with treatment‐related adverse events in patients with newly diagnosed overactive bladder (OAB). Methods This retrospective, single‐center cohort study included 122 patients who initiated pharmacotherapy for OAB between April 2024 and January 2026. Frailty was evaluated using the Frailty Screening Index and classified as robust, prefrail, or frail. The primary outcome was treatment‐related adverse events within 3 months, and independent predictors were identified using multivariable logistic regression. Longitudinal changes in OAB symptoms were examined using linear mixed‐effects models. Results During follow‐up, adverse events occurred in 52 patients (42.6%), rising with frailty (4.7%, 40.0%, and 57.3% in robust, prefrail, and frail groups, respectively; p < 0.01 for trend). In multivariable analysis, frailty (odds ratio OR 2.97 per status increase, 95% confidence interval CI 1.45–6.52; p < 0.01), anticholinergic use (OR 7.96, 95% CI 2.94–24.46; p < 0.01), and baseline post‐void residual volume (OR 1.22 per 10 mL increase, 95% CI 1.01–1.34; p = 0.02) were independently associated with adverse events; chronological age was not. Symptom improvement over time did not differ significantly by frailty status. Conclusions Frailty, rather than chronological age, was associated with short‐term treatment‐related adverse events among patients starting pharmacotherapy for OAB. Frailty assessment may help identify patients at higher risk of adverse events and support individualized, safety‐conscious treatment decisions.

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Cite This Study

Iwagami et al. (2026) studied this question.

synapsesocial.com/papers/69d9e58f78050d08c1b75c1ahttps://doi.org/10.1111/luts.70060
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