Literature DB >> 18068562

Primary chronic venous disorders.

Mark H Meissner1, Peter Gloviczki, John Bergan, Robert L Kistner, Nick Morrison, Felizitas Pannier, Peter J Pappas, Eberhard Rabe, Seshadri Raju, J Leonel Villavicencio.   

Abstract

Primary chronic venous disorders, which according to the CEAP classification are those not associated with an identifiable mechanism of venous dysfunction, are among the most common in Western populations. Varicose veins without skin changes are present in about 20% of the population while active ulcers may be present in as many as 0.5%. Primary venous disorders are thought to arise from intrinsic structural and biochemical abnormalities of the vein wall. Advanced cases may be associated with skin changes and ulceration arising from extravasation of macromolecules and red blood cells leading to endothelial cell activation, leukocyte diapedesis, and altered tissue remodeling with intense collagen deposition. Laboratory evaluation of patients with primary venous disorders includes venous duplex ultrasonography performed in the upright position, occasionally supplemented with plethysmography and, when deep venous reconstruction is contemplated, ascending and descending venography. Primary venous disease is most often associated with truncal saphenous insufficiency. Although historically treated with stripping of the saphenous vein and interruption and removal of major tributary and perforating veins, a variety of endovenous techniques are now available to ablate the saphenous veins and have generally been demonstrated to be safe and less morbid than traditional procedures. Sclerotherapy also has an important role in the management of telangiectasias; primary, residual, or recurrent varicosities without connection to incompetent venous trunks; and congenital venous malformations. The introduction of ultrasound guided foam sclerotherapy has broadened potential indications to include treatment of the main saphenous trunks, varicose tributaries, and perforating veins. Surgical repair of incompetent deep venous valves has been reported to be an effective procedure in nonrandomized series, but appropriate case selection is critical to successful outcomes.

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Year:  2007        PMID: 18068562     DOI: 10.1016/j.jvs.2007.08.038

Source DB:  PubMed          Journal:  J Vasc Surg        ISSN: 0741-5214            Impact factor:   4.268


  25 in total

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Authors:  Orhan Bozoglan; Bulent Mese; Mehmet Fatih Inci; Erdinc Eroglu
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Review 2.  Role of interventional radiologists in the management of lower extremity venous insufficiency.

Authors:  Rulon L Hardman; Paul J Rochon
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Review 3.  Evaluation and Management of Chronic Venous Disease Using the Foundation of CEAP.

Authors:  Teresa L Carman; Ali Al-Omari
Journal:  Curr Cardiol Rep       Date:  2019-08-30       Impact factor: 2.931

4.  Absence of venous valves in mice lacking Connexin37.

Authors:  Stephanie J Munger; John D Kanady; Alexander M Simon
Journal:  Dev Biol       Date:  2012-11-07       Impact factor: 3.582

5.  Matrix metalloproteinase activity and glycosaminoglycans in chronic venous disease: the linkage among cell biology, pathology and translational research.

Authors:  Ferdinando Mannello; Joseph D Raffetto
Journal:  Am J Transl Res       Date:  2010-11-23       Impact factor: 4.060

6.  Endovascular laser therapy for varicose veins: an evidence-based analysis.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2010-04-01

7.  A novel role for relaxin-2 in the pathogenesis of primary varicosis.

Authors:  Julia Adams; Sarah Schott; Arno Bern; Matthias Renz; Kristian Ikenberg; Claus Garbe; Christian Busch
Journal:  PLoS One       Date:  2012-06-21       Impact factor: 3.240

8.  The design, development, and evaluation of a prototypic, prosthetic venous valve.

Authors:  Matt T Oberdier; Stanley E Rittgers
Journal:  Biomed Eng Online       Date:  2008-09-19       Impact factor: 2.819

9.  Nonthermal Endovenous Procedures for Varicose Veins: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2021-06-04

10.  RASA1-driven cellular export of collagen IV is required for the development of lymphovenous and venous valves in mice.

Authors:  Di Chen; Xin Geng; Philip E Lapinski; Michael J Davis; R Sathish Srinivasan; Philip D King
Journal:  Development       Date:  2020-12-07       Impact factor: 6.862

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