Key result
An expedited surgical protocol for hip fracture patients on DOACs achieved a median time to theatre of 26.0 hours, showing no significant difference compared to non-anticoagulated controls (p=0.133).
Why the study?
Patients who sustain a hip fracture while taking DOACs experience surgical delays that increase morbidity and mortality, often missing the 36-hour surgery target for best practice tariff.
Does an expedited surgery protocol achieve surgery within 36 hours in hip fracture patients on DOACs without increasing complications compared to non-anticoagulated controls?
Cohort (n=160)
No
Does an expedited surgery protocol achieve surgery within 36 hours in hip fracture patients on DOACs without increasing complications compared to non-anticoagulated controls?
Mean Difference: 3.3 (95% CI -0.935–7.52)
Absolute Event Rate: 26% vs 22.4%
p-value: p=0.133
An expedited surgical protocol for hip fracture patients on DOACs can achieve surgery within 36 hours without increasing peri-operative complications compared to non-anticoagulated patients.
May enable more DOAC-treated hip fracture patients to meet 36-h surgery targets; leaves open effects on morbidity, mortality, and need for randomized confirmation.
Background Patients who sustain a hip fracture whilst taking direct oral anticoagulants (DOACs) experience delays to surgery, which can increase morbidity and mortality. Achievement of the prompt surgery aspect of the National Hip Fracture Database (NHFD) best practice tariff (BPT) stipulates surgery within 36 h, which these patients often fail to meet. Patients and methods Our protocol for expedited hip fracture surgery in patients taking DOACs was implemented. We compared surgery within 36 h (primary outcome) and peri-operative blood transfusions, 30-day mortality, wound leakage, return to theatre and length of hospital stay (secondary outcomes) with standard care of 80 matched non-anticoagulated controls. Results Median times to theatre were 26.0 h (IQR 16.2 h) in DOAC patients and 22.4 h (IQR 16.9 h) in controls: bootstrapped 95% CI for the difference (−0.935, 7.52). Bias-corrected related samples bootstrapped t-test revealed no evidence for a group difference on the primary outcome ( p = 0.133) or any secondary outcome, including post-operative transfusions (χ 2 (1) = 0.533; p = 0.465, 95% CI for the difference −18.3% to 8.37%); death within 30 days (χ 2 (1) = 0.667; p = 0.414, 95% CI for the difference −3.48% to 8.48%); wound leakage (χ 2 (1) = 0.571; p = 0.450, 95% CI −1.79% to 0.792%); return to theatre (χ 2 (1) = 0.00; p = 1.00); and median length of hospital stay ( p = 0.678, bias-corrected bootstrapped 95% CI for the difference −4.47 to 6.68). Discussion Our protocol is simple, does not require plasma DOAC level testing and can be used to achieve the NHFD recommendation of surgery within 36 h without increasing peri-operative transfusions, wound leakage, return to theatre, length of stay or mortality.
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Mayor et al. (2023) conducted a cohort in Hip fracture in patients taking direct oral anticoagulants (n=160). Expedited hip fracture surgery protocol based on DOAC elimination half-life vs. Standard care in matched non-anticoagulated controls was evaluated on Time to theatre (hours) (MD 3.3, 95% CI -0.935 to 7.52, p=0.133). An expedited surgical protocol for hip fracture patients on DOACs achieved a median time to theatre of 26.0 hours, showing no significant difference compared to non-anticoagulated controls (p=0.133).
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