Key result
Beta-blocker therapy was associated with a 72% relative risk reduction in 30-day all-cause mortality (IRR 0.28) compared to non-users in patients undergoing emergency hip fracture surgery.
Why the study?
Hip fracture surgery has high postoperative mortality, and whether mitigating the trauma-induced hyper-adrenergic state with beta-blockers improves survival in this population had not been studied.
Does ongoing beta-blocker therapy reduce 30-day all-cause mortality in adults undergoing emergency hip fracture surgery?
Cohort (n=134,915)
Yes
Does ongoing beta-blocker therapy reduce 30-day all-cause mortality in adults undergoing emergency hip fracture surgery?
Relative Risk: 0.28 (95% CI 0.26–0.29)
Absolute Event Rate: 3.7% vs 10%
Absolute Risk Reduction: 6.3%
Number Needed to Treat: 16
p-value: p=<0.001
Ongoing beta-blocker therapy is associated with a significant 72% relative risk reduction in 30-day all-cause mortality among patients undergoing emergency hip fracture surgery.
PURPOSE: Despite advances in the care of hip fractures, this area of surgery is associated with high postoperative mortality. Downregulating circulating catecholamines, released as a response to traumatic injury and surgical trauma, is believed to reduce the risk of death in noncardiac surgical patients. This effect has not been studied in hip fractures. This study aims to assess whether survival benefits are gained by reducing the effects of the hyper-adrenergic state with beta-blocker therapy in patients undergoing emergency hip fracture surgery. METHODS: This is a retrospective nationwide observational cohort study. All adults [Formula: see text] 18 years were identified from the prospectively collected national quality register for hip fractures in Sweden during a 10-year period. Pathological fractures were excluded. The cohort was subdivided into beta-blocker users and non-users. Poisson regression with robust standard errors and adjustments for confounders was used to evaluate 30-day mortality. RESULTS: 134,915 patients were included of whom 38.9% had ongoing beta-blocker therapy at the time of surgery. Beta-blocker users were significantly older and less fit for surgery. Crude 30-day all-cause mortality was significantly increased in non-users (10.0% versus 3.7%, p < 0.001). Beta-blocker therapy resulted in a 72% relative risk reduction in 30-day all-cause mortality (incidence rate ratio 0.28, 95% CI 0.26-0.29, p < 0.001) and was independently associated with a reduction in deaths of cardiovascular, respiratory, and cerebrovascular origin and deaths due to sepsis or multiorgan failure. CONCLUSIONS: Beta-blockers are associated with significant survival benefits when undergoing emergency hip fracture surgery. Outlined results strongly encourage an interventional design to validate the observed relationship.
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Ahl et al. (2021) conducted a cohort in Hip fracture (n=134,915). Beta-blocker therapy vs. Beta-blocker non-users was evaluated on 30-day all-cause mortality (IRR 0.28, 95% CI 0.26-0.29, p=<0.001). Beta-blocker therapy was associated with a 72% relative risk reduction in 30-day all-cause mortality (IRR 0.28) compared to non-users in patients undergoing emergency hip fracture surgery.
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