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The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency

The effect of recombinant hirudin, which is the most powerful antithrombotic agent, on flaps with venous insufficiency was investigated. Oedema and congestion are frequent on flaps, causing necrosis unpredictably. Venous insufficiency and thrombosis are experimentally and clinically more frequent th...

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Autores principales: Duzgun, Serdar, Nisanci, Mustafa, Unlu, Erkin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075196/
https://www.ncbi.nlm.nih.gov/pubmed/24987213
http://dx.doi.org/10.4103/0970-0358.129633
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author Duzgun, Serdar
Nisanci, Mustafa
Unlu, Erkin
author_facet Duzgun, Serdar
Nisanci, Mustafa
Unlu, Erkin
author_sort Duzgun, Serdar
collection PubMed
description The effect of recombinant hirudin, which is the most powerful antithrombotic agent, on flaps with venous insufficiency was investigated. Oedema and congestion are frequent on flaps, causing necrosis unpredictably. Venous insufficiency and thrombosis are experimentally and clinically more frequent than arterial occlusion. Twenty-one adult New Zealand rabbits were used in this study. Skin flaps (3 × 6 cm) were elevated on a 1-cm-wide pedicle on rabbit ears. The artery, nerve, and vein were exposed and examined with the aid of a surgical microscope. Venous insufficiency was established by cutting the vein and nerve. In the control group, no additional surgical or medical procedures were performed and the ear flap was inset to its original location. Subcutaneous low molecular weight heparin (LMWH; 320 IU/kg) was administered to a second group of rabbits after the same surgery, and recombinant hirudin (2 μg) was administered via the pedicle artery 5 minutes after the vein and nerve were bound and cut in a third group of rabbits. Compared with control and LMWH groups on day 3 and 7, the hirudin-treated group had less hair loss, lower oedema scores and less haematoma formation. Furthermore, a lower size of necrotic areas and an increase in the circulating area on day 7 was found in the hirudin-treated group. In addition, angiography revealed new vessel development (neovascularisation) only in the hirudin group. On histologic sections, hirudin-treated animals had lower oedema, inflammation and congestion scores than animals in the other two groups. Thus, when administered into the ear flap through the pedicle as a pure recombinant preparation, hirudin increased flap survival by its antithrombotic effects and by accelerating neoangiogenesis. Recombinant hirudin may be used in clinical practice to treat flaps with venous problems and to increase survival rates.
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spelling pubmed-40751962014-07-01 The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency Duzgun, Serdar Nisanci, Mustafa Unlu, Erkin Indian J Plast Surg Original Article The effect of recombinant hirudin, which is the most powerful antithrombotic agent, on flaps with venous insufficiency was investigated. Oedema and congestion are frequent on flaps, causing necrosis unpredictably. Venous insufficiency and thrombosis are experimentally and clinically more frequent than arterial occlusion. Twenty-one adult New Zealand rabbits were used in this study. Skin flaps (3 × 6 cm) were elevated on a 1-cm-wide pedicle on rabbit ears. The artery, nerve, and vein were exposed and examined with the aid of a surgical microscope. Venous insufficiency was established by cutting the vein and nerve. In the control group, no additional surgical or medical procedures were performed and the ear flap was inset to its original location. Subcutaneous low molecular weight heparin (LMWH; 320 IU/kg) was administered to a second group of rabbits after the same surgery, and recombinant hirudin (2 μg) was administered via the pedicle artery 5 minutes after the vein and nerve were bound and cut in a third group of rabbits. Compared with control and LMWH groups on day 3 and 7, the hirudin-treated group had less hair loss, lower oedema scores and less haematoma formation. Furthermore, a lower size of necrotic areas and an increase in the circulating area on day 7 was found in the hirudin-treated group. In addition, angiography revealed new vessel development (neovascularisation) only in the hirudin group. On histologic sections, hirudin-treated animals had lower oedema, inflammation and congestion scores than animals in the other two groups. Thus, when administered into the ear flap through the pedicle as a pure recombinant preparation, hirudin increased flap survival by its antithrombotic effects and by accelerating neoangiogenesis. Recombinant hirudin may be used in clinical practice to treat flaps with venous problems and to increase survival rates. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4075196/ /pubmed/24987213 http://dx.doi.org/10.4103/0970-0358.129633 Text en Copyright: © Indian Journal of Plastic Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Duzgun, Serdar
Nisanci, Mustafa
Unlu, Erkin
The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title_full The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title_fullStr The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title_full_unstemmed The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title_short The effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
title_sort effect of recombinant hirudin on rabbit ear flaps with venous insufficiency
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075196/
https://www.ncbi.nlm.nih.gov/pubmed/24987213
http://dx.doi.org/10.4103/0970-0358.129633
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