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Incidence and significance of microscopic pathological lesions found in pedicle and recipient vessels used in microsurgical breast reconstruction

Lookup NU author(s): Neil McLean, Peter Hodgkinson

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Abstract

The purpose of this study was to assess the incidence of abnormal vascular histology and to determine whether or not this was correlated with the incidence of postoperative microvascular problems. The microvascular histology of both donor and recipient vessels was studied in 38 patients (40 flaps) undergoing breast reconstruction with free TRAM flaps. Preoperative risk factors were assessed and correlated with histological changes in vessels, and both were tested against anastomotic complications. Thrombosis of either the artery or the vein of the flap was seen in 6 cases (15%), and of these, two flaps failed completely and one suffered partial necrosis. The occlusion affected the arterial anastomosis in 3 patients, and the venous anastomosis in 2 patients, while both the artery and the vein were thrombosed in one case. Preoperative risk factors such as smoking, obesity, radio-therapy, and chemotherapy were not associated with a significantly higher incidence of thrombosis or with significant histological abnormalities in vessels (P value varied between 0.3-0.06). Microvascular histology showed variable degrees of pathological changes in six flaps (15%); nevertheless, in this group, only one flap suffered a venous thrombosis, which ended in total flap loss. Among those with one or more risk factors (24 patients), only 2 had some evidence of histological abnormality of the blood vessels used for the microvascular anastomosis (P = 0.2).


Publication metadata

Author(s): El-Mrakby HH, McLean NR, Hodgkinson PD, Soames JV

Publication type: Article

Publication status: Published

Journal: Microsurgery

Year: 2003

Volume: 23

Issue: 1

Pages: 6-9

Print publication date: 26/02/2003

ISSN (print): 0738-1085

ISSN (electronic): 1098-2752

Publisher: Wiley-Blackwell Publishing

URL: http://dx.doi.org/10.1002/micr.10085

DOI: 10.1002/micr.10085

PubMed id: 12616511


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