Activation of coagulation and fibrinolysis during reconstructive microsurgery in patients with cancer

Cancer patients are subjected to increased systemic risk of thrombotic events and may therefore be at higher risk of even local thrombosis compromising the outcome of reconstructive microsurgery. Coagulation and fibrinolysis activities were studied serially during and after reconstructive microsurge...

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Published inMicrosurgery Vol. 21; no. 5; pp. 208 - 213
Main Authors Olsson, Eija, Svartling, Nils, Asko-Seljavaara, Sirpa, Lassila, Riitta
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 2001
Wiley-Liss
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Summary:Cancer patients are subjected to increased systemic risk of thrombotic events and may therefore be at higher risk of even local thrombosis compromising the outcome of reconstructive microsurgery. Coagulation and fibrinolysis activities were studied serially during and after reconstructive microsurgery in seven patients with oropharyngeal cancer or sarcoma in the extremities. A preoperative hypercoagulable state was found in four patients (elevated fibrinogen, TAT, F1+2, or D‐dimer); two of these patients also had a local thrombotic event. In all patients, the plasma markers generally varied perioperatively: fibrinogen decreased, whereas TAT and subsequently D‐dimer increased at the end of the operation. However, tPA and PAI‐1 remained unaltered, except in the patients with thrombosis in whom PAI‐1 activity increased progressively during the operation. F1+2 was also clearly elevated in these two patients at the time of thrombosis. Preoperative assessment of hypercoagulability for this group of patients could be helpful in targeting meticulous antithrombotic protection. © 2001 Wiley‐Liss, Inc. Microsurgery 21:208–213 2001
Bibliography:Helsinki University Central Hospital, Helsinki, Finland
istex:F6D3D74D5EB8D61A5C421CCEFC47FEF87C2F7B9D
ark:/67375/WNG-QCXZLKMZ-C
ArticleID:MICR1040
Landstinget Gävleborg, Sweden
Instrumentarium Foundation
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0738-1085
1098-2752
DOI:10.1002/micr.1040