Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator
Abstract Objective To explore the feasibility and safety of using tissue-type plasminogen activator (t-PA) to prevent graft restenosis after coronary artery bypass grafting (CABG). Methods In this prospective observational study, 37 patients underwent CABG between June 2009 and May 2013. These patie...
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doaj-b3c24c0c78b2438d9f54af873343e0192020-11-25T00:20:51ZengBMCEuropean Journal of Medical Research2047-783X2017-06-012211510.1186/s40001-017-0259-8Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activatorRuixiong Li0Bin Lan1Tianxiang Zhu2Yanlong Yang3Muyan Cai4Zhongmin Fang5Chensheng Ma6Shu Chen7Cardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityCardiothoracic Surgery, Shantou Central Hospital and Affiliated Shantou Hospital of Sun Yat-sen UniversityAbstract Objective To explore the feasibility and safety of using tissue-type plasminogen activator (t-PA) to prevent graft restenosis after coronary artery bypass grafting (CABG). Methods In this prospective observational study, 37 patients underwent CABG between June 2009 and May 2013. These patients were grouped according to the anti-coagulation strategy after surgery: t-PA (n = 12) and conventional treatments (n = 25). In the t-PA group, the patients received acetylsalicylic acid (ASA) and clopidogrel plus intravenous infusion of t-PA (0.25 mg/kg/day) starting at 24 h after surgery and that lasted for 3 days. In the conventional group, the patients received only ASA and clopidogrel. 64-row spiral computed tomographic coronary angiography was performed at 1 week, 1, and 3 months after surgery to evaluate the patency of the graft vessel. Results The mean stenosis severity of the saphenous vein grafts was lower in the t-PA group compared with the conventional group at 3 months after surgery (p < 0.05), but there was no significant difference at 1 week and 1 month (p > 0.05). The patency rate of the grafts was not significantly different between the two groups at 1 week, 1, and 3 months after surgery (p > 0.05). Conclusion Early application of t-PA after CABG was feasible and safe, and might help prevent early restenosis of SV grafts. Additional clinical randomized trials are necessary to address this issue.http://link.springer.com/article/10.1186/s40001-017-0259-8Coronary artery bypass graftingRestenosisTissue-type plasminogen activator |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ruixiong Li Bin Lan Tianxiang Zhu Yanlong Yang Muyan Cai Zhongmin Fang Chensheng Ma Shu Chen |
spellingShingle |
Ruixiong Li Bin Lan Tianxiang Zhu Yanlong Yang Muyan Cai Zhongmin Fang Chensheng Ma Shu Chen Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator European Journal of Medical Research Coronary artery bypass grafting Restenosis Tissue-type plasminogen activator |
author_facet |
Ruixiong Li Bin Lan Tianxiang Zhu Yanlong Yang Muyan Cai Zhongmin Fang Chensheng Ma Shu Chen |
author_sort |
Ruixiong Li |
title |
Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
title_short |
Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
title_full |
Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
title_fullStr |
Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
title_full_unstemmed |
Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
title_sort |
preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator |
publisher |
BMC |
series |
European Journal of Medical Research |
issn |
2047-783X |
publishDate |
2017-06-01 |
description |
Abstract Objective To explore the feasibility and safety of using tissue-type plasminogen activator (t-PA) to prevent graft restenosis after coronary artery bypass grafting (CABG). Methods In this prospective observational study, 37 patients underwent CABG between June 2009 and May 2013. These patients were grouped according to the anti-coagulation strategy after surgery: t-PA (n = 12) and conventional treatments (n = 25). In the t-PA group, the patients received acetylsalicylic acid (ASA) and clopidogrel plus intravenous infusion of t-PA (0.25 mg/kg/day) starting at 24 h after surgery and that lasted for 3 days. In the conventional group, the patients received only ASA and clopidogrel. 64-row spiral computed tomographic coronary angiography was performed at 1 week, 1, and 3 months after surgery to evaluate the patency of the graft vessel. Results The mean stenosis severity of the saphenous vein grafts was lower in the t-PA group compared with the conventional group at 3 months after surgery (p < 0.05), but there was no significant difference at 1 week and 1 month (p > 0.05). The patency rate of the grafts was not significantly different between the two groups at 1 week, 1, and 3 months after surgery (p > 0.05). Conclusion Early application of t-PA after CABG was feasible and safe, and might help prevent early restenosis of SV grafts. Additional clinical randomized trials are necessary to address this issue. |
topic |
Coronary artery bypass grafting Restenosis Tissue-type plasminogen activator |
url |
http://link.springer.com/article/10.1186/s40001-017-0259-8 |
work_keys_str_mv |
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