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Başlık: Early-term outcomes for treatment of saphenous vein insufficiency with N-butyl cyanoacrylate: A novel, non-thermal, and non-tumescent percutaneous embolization technique
Yazarlar: Tüydeş, Oktay
Yüksel, Ahmet
Şenol, Sefa
Akarsu, Serkan
Uludağ Üniversitesi/Tıp Fakültesi/Kalp Damar Cerrahisi Anabilim Dalı.
Tok, Mustafa
6506976035
Anahtar kelimeler: Cardiovascular system & cardiology
Surgery
Thermal ablation
Varicose-veins
Follow-up
Polidocanol foam
Great
Sclerotherapy
Multicenter
Trial
Adhesive
Reflux
Yayın Tarihi: Haz-2016
Yayıncı: Forum Multimedia Publishing
Atıf: Tok, M. vd. (2016). "Early-term outcomes for treatment of saphenous vein insufficiency with N-butyl cyanoacrylate: A novel, non-thermal, and non-tumescent percutaneous embolization technique". Heart Surgery Forum, 19(3), E118-E122.
Özet: Background: The purpose of this study was to present early-term outcomes of VariClose r Vein Sealing System, which is a novel, non-thermal, and non-tumescent percutaneous embolization technique for treatment of saphenous vein insufficiency. Methods: Between March 2014 and July 2015, 189 saphenous veins in 141 patients were treated with Variclose Vein Sealing System containing n-butyl cyanoacrylate. Pre-, intra-, post-procedural, and follow-up data of patients were collected and retrospectively reviewed. Results: Mean age of patients was 42.5 +/- 14.0 years, of which 53% were female. Technical success rate of intervention was 98.9%. Mean procedure time was 14.3 +/- 7.5 minutes. Eighty-nine percent of patients (n = 126/ 141) were available at mean follow-up time of 6.7 months. Mean Venous Clinical Severity Score was significantly improved from 8.3 +/- 2.2 at pre-procedure period to 3.3 +/- 1.8 at follow-up. No complete recanalization was observed, but 2 patients were presented with partial recanalization during follow-up. The complete occlusion rate was 98.4%. No serious adverse event related to procedure was observed. Conclusion: Variclose Vein Sealing System appears to be safe and effective in treatment of saphenous vein insufficiency. Further randomized studies with long-term outcomes are required for determining optimal treatment modality in patients with saphenous vein insufficiency.
URI: https://doi.org/10.1532/hsf.1496
https://journal.hsforum.com/index.php/HSF/article/view/1496
http://hdl.handle.net/11452/29235
ISSN: 1098-3511
1522-6662
Koleksiyonlarda Görünür:Scopus
Web of Science

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