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Delayed Surgery Does Not Reduce Transfusion Rates in Low-Energy Hip Fractures on Direct Oral Anticoagulants
Ashley E Levack1, Harold G Moore1, Stephen Stephan2
1Orthopaedic Trauma Service, Hospital for Special Surgery, New York, NY.
Direct oral anticoagulants (DOACs) do not increase transfusion rates in hip fracture surgery patients. DOAC use should not delay surgery for hip fracture patients when medically optimized.
Area of Science:
- Orthopedic Surgery
- Geriatric Medicine
- Pharmacology
Background:
- Hip fractures are common in elderly patients, often requiring surgery.
- Anticoagulation therapy is frequently used in this population for various indications.
- The management of anticoagulated patients undergoing hip fracture surgery presents clinical challenges regarding surgical timing and outcomes.
Purpose of the Study:
- To compare perioperative transfusion rates in hip fracture patients on direct oral anticoagulants (DOACs) versus nonanticoagulated patients.
- To assess differences in time to surgery and 90-day complications between these groups.
Main Methods:
- Multicenter retrospective cohort study involving three academic Level I trauma centers.
- Included patients aged 55 years and older with acute, operatively treated hip fractures.
- Propensity score matching was used to compare 132 DOAC patients with 262 nonanticoagulated controls.
Main Results:
- No significant difference in overall perioperative transfusion rates between DOAC and control groups (43.2% vs. 39.7%).
- DOAC patients experienced a longer median time to surgery (41.7 hours vs. 26.0 hours, P < 0.001).
- No significant differences in 90-day complications, readmissions, reoperations, or mortality were observed between groups.
Conclusions:
- DOAC use is not associated with increased transfusion rates in hip fracture surgery.
- Surgery for hip fracture patients on DOACs should not be delayed solely due to anticoagulation status if medically optimized.
- Findings support current evidence suggesting safe surgical management of hip fracture patients on DOACs.
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