Autologous Breast Reconstruction Success Rates in Hypercoagulable Patients

Hypercoagulable disorders may adversely affect microsurgical outcomes, including increased flap failure and complication rates. Outcomes specific to autologous breast reconstruction are not well described. A retrospective review was performed of autologous breast reconstructions between 2009 and 202...

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Bibliographic Details
Published in:Plastic and reconstructive surgery (1963) Vol. 153; no. 3; pp. 516e - 522e
Main Authors: Egan, Katie G, Elver, Ashlie A, Birney, Jalee M, Nazir, Niaman, Butterworth, James A, Lai, Eric C
Format: Journal Article
Language:English
Published: United States Lippincott Williams & Wilkins 01-03-2024
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Summary:Hypercoagulable disorders may adversely affect microsurgical outcomes, including increased flap failure and complication rates. Outcomes specific to autologous breast reconstruction are not well described. A retrospective review was performed of autologous breast reconstructions between 2009 and 2020. Patients with either a thrombophilic disorder (TD) diagnosis or a previous thrombotic event (TE) were identified. The analysis compared perioperative complications and flap success rates. In this series, 23 patients with a TD underwent 39 flaps, and 78 patients who had experienced a TE underwent 126 flaps, compared with 815 control patients, who underwent 1300 flaps. In logistic regression models, a TD diagnosis was an independent predictor of early total flap loss [OR, 8.42 (95% CI, 1.59 to 44.47); P = 0.01], late partial flap loss [OR, 3.9 (95% CI, 1.0 to 15.22); P = 0.05], and delayed healing [OR, 2.26 (95% CI, 1.02 to 5.04); P = 0.04]. TE history trended toward an association only with late partial flap loss ( P = 0.057). Flap salvage rates (25%) and flap success rates (92.3%) were statistically lower in patients with a TD but normal in patients who had experienced a TE. Microsurgical breast reconstruction is a reasonable option for patients with hypercoagulation disorders. No increased risk of flap complications was associated with a previous TE; however, TDs carried increased risk. Risk, II.
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ISSN:0032-1052
1529-4242
DOI:10.1097/PRS.0000000000010708