Key result
Beta-blocker exposure during fracture care is linked to a ~13% increase in fracture nonunion.
Why the study?
While animal studies showed positive skeletal effects from beta-blockers, population studies showed mixed effects on bone mineral density and fracture risk, leaving their association with fracture nonunion unclear.
Does beta-blocker exposure increase the risk of fracture nonunion in geriatric patients with extremity fractures?
Cohort (n=253,266)
Does beta-blocker exposure increase the risk of fracture nonunion in geriatric patients with extremity fractures?
In a large geriatric cohort, beta-blocker exposure was associated with a significantly increased risk of fracture nonunion, contradicting previous animal models that suggested a positive effect on bone healing.
Answers are grounded in this paper and cite their sources.
Should not change beta-blocker prescribing in fracture care; leaves open causality and requires prospective validation.
Previously published animal studies have shown positive skeletal effects with local or systemic administration of beta blockers (BBs). However, population studies have shown mixed effects on bone mineral density (BMD) and fracture risk with BB use. The goal of this study was to evaluate whether exposure to BB is associated with fracture nonunion. Fee-for-service Medicare beneficiaries with an extremity fracture were identified by International Classification of Diseases (ICD)-10 and current procedural terminology (CPT) codes from 2016-2019. Charlson Comorbidity Index (CCI) was assigned using diagnoses prior to index fracture and nonunion identified by ICD-10 or CPT codes within one year from index fracture diagnosis. Patients were classified by BB exposure based on Part D (Pharmacy) claims between 90 days prior to and one year following index fracture. Chi square and Student’s T-tests were performed on categorical and continuous variables, respectively. Logistic regression was performed to evaluate the association between BB use and nonunion, controlling for age, sex, race, and comorbidity. Total number of fractures meeting inclusion criteria was 253,266 with 45% of patients having used a BB during the study period. The incidence of nonunion was 3.9% overall. BBs were associated with a 13% increase in non-union for all fracture types, after controlling for age, sex, fracture location, and CCI (OR 1.13 [CI 1.06-1.20], p<.001). Results of this study suggest a negative influence of BB on bone healing, contrary to results of previously published animal models and epidemiologic observations, and demonstrate that BB use during fracture care is associated with significant increase in incidence of nonunion.
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Steffenson et al. (2023) conducted a cohort in Extremity fractures (n=253,266). Beta blockers vs. Non-users was evaluated on Fracture nonunion at 1 year (OR 1.13, 95% CI 1.06-1.20, p=<0.001). Beta-blocker exposure during fracture care was associated with a 13% increase in the incidence of fracture nonunion (OR 1.13) in a geriatric cohort.
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