Key result
Continuing chronic beta-blockers perioperatively cuts 30-day mortality ~78% vs. discontinuation.
Why the study?
Although guidelines recommend continuing chronic β-blocker therapy during non-cardiac surgery, direct randomized evidence supporting this practice is limited and concerns regarding potential adverse effects persist.
Does perioperative continuation of chronic beta-blocker therapy reduce 30-day all-cause mortality compared to discontinuation in adult patients undergoing elective non-cardiac surgery?
Meta-Analysis (n=16,280)
Randomized controlled trials
Does perioperative continuation of chronic beta-blocker therapy reduce 30-day all-cause mortality compared to discontinuation in adult patients undergoing elective non-cardiac surgery?
Perioperative continuation of chronic beta-blocker therapy in patients undergoing elective non-cardiac surgery is associated with a significant reduction in nonfatal myocardial infarction and 30-day all-cause mortality, supporting current guideline recommendations.
Answers are grounded in this paper and cite their sources.
Supports perioperative continuation of chronic beta-blockers; reinforces guidelines despite POISE discordance and high heterogeneity.
Background: Perioperative β-blocker management in patients undergoing non-cardiac surgery remains controversial. While guidelines recommend continuation of chronic β-blocker therapy, direct randomized evidence supporting this practice is limited, and concerns persist regarding potential adverse effects. Objectives: To evaluate the impact of perioperative continuation versus discontinuation of chronic β-blocker therapy on postoperative outcomes in patients undergoing elective non-cardiac surgery. Methods: A systematic review and meta-analysis of randomized controlled trials was conducted. Studies including adult patients on chronic β-blocker therapy undergoing elective non-cardiac surgery were identified. The primary outcome was 30-day all-cause mortality. The secondary outcome was nonfatal myocardial infarction. Pooled effect estimates were calculated using a random-effects inverse-variance model and reported as odds ratios (ORs) or risk ratios (RRs) with 95% confidence intervals (CIs). Results: Six randomized controlled trials including 16,280 patients were analyzed for 30-day all-cause mortality. β-blocker continuation was associated with a significant reduction in mortality compared with discontinuation (OR 0.22, 95% CI 0.06-0.82; P = 0.02), although substantial heterogeneity was observed (I 2 = 96%). This variability was largely driven by discordant findings from the POISE trial.Three randomized controlled trials including 11,853 patients were analyzed for nonfatal myocardial infarction. β-blocker therapy was associated with a significant reduction in myocardial infarction (RR 0.60, 95% CI 0.43-0.84; P = 0.003), with moderate heterogeneity (I 2 = 52%) and consistent directionality across studies. Conclusions: Continuation of chronic β-blocker therapy in the perioperative period is associated with reduced nonfatal myocardial infarction and may also reduce 30-day mortality, although the latter finding is limited by substantial heterogeneity. These results support guideline recommendations while emphasizing the need for individualized perioperative management and further research to define optimal patient selection and treatment strategies.
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Weber et al. (2026) conducted a meta-analysis in Elective non-cardiac surgery in patients on chronic beta-blocker therapy (n=16,280). Perioperative continuation of chronic beta-blocker therapy vs. Perioperative discontinuation of chronic beta-blocker therapy was evaluated on 30-day all-cause mortality (OR 0.22, 95% CI 0.06-0.82, p=0.02). Perioperative continuation of chronic beta-blockers reduced 30-day all-cause mortality compared with discontinuation (OR 0.22; 95% CI 0.06-0.82; P=0.02), though with high heterogeneity.
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