Key result
Severe polypharmacy is not associated with increased all-cause mortality in heart failure.
Why the study?
Polypharmacy is highly prevalent in patients with HF, but the prognostic significance of severe polypharmacy regarding all-cause mortality remained uncertain.
Does severe polypharmacy increase all-cause mortality in adults with heart failure?
Meta-Analysis (n=44,213)
Does severe polypharmacy increase all-cause mortality in adults with heart failure?
Answers are grounded in this paper and cite their sources.
Severe polypharmacy as a raw medication count was not significantly associated with all-cause mortality in heart failure patients, suggesting that medication count should be evaluated alongside treatment appropriateness and clinical complexity, though certainty of evidence is very low.
Background: Polypharmacy is highly prevalent in patients with heart failure (HF), but the prognostic significance of severe polypharmacy remains uncertain. This systematic review and meta-analysis evaluated its association with all-cause mortality in adults with HF. Methods: PubMed, MEDLINE, Embase, Scopus and the Cochrane Library were searched from inception through August 2026. Observational studies assessing severe polypharmacy (the highest medication-burden category in each study; ≥9 to ≥15 medications) and all-cause mortality in adults with HF were eligible. Adjusted hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled using a random-effects model. Leave-one-out sensitivity analyses and post hoc threshold-specific analyses were performed. Risk of bias and certainty of evidence were assessed using the Newcastle–Ottawa Scale (NOS) and GRADE, respectively. The protocol was registered in PROSPERO (CRD420261507517). Results: Nine studies included 44,213 patients. Severe polypharmacy was not significantly associated with all-cause mortality (HR 1.04, 95% CI 0.86–1.26; p = 0.67; I2 = 79%). NOS scores ranged from 6 to 9. Leave-one-out HRs ranged from 0.996 to 1.097, with all 95% CIs including 1. In six studies defining severe polypharmacy as ≥10 medications, the pooled HR was 1.15 (95% CI 1.00–1.32; p = 0.054; I2 = 37.8%). Certainty of evidence was very low because of serious inconsistency and imprecision. Conclusions: No statistically significant association was identified, but very low certainty of evidence precludes firm conclusions, and clinically important associations cannot be excluded. Medication count should be interpreted alongside treatment appropriateness and clinical complexity.
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Valcuende‐Rosique et al. (2026) conducted a meta-analysis in Heart failure (n=44,213). Severe polypharmacy (≥9 to ≥15 medications) vs. Lower medication-burden categories was evaluated on All-cause mortality (HR 1.04, 95% CI 0.86-1.26, p=0.67). Severe polypharmacy was not significantly associated with all-cause mortality in adults with heart failure (HR 1.04, 95% CI 0.86–1.26; p = 0.67).
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