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Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease

Dual antiplatelet therapy (DAPT) after percutaneous coronary intervention increases the risk of bleeding. We studied the safety and clinical outcomes of switching from DAPT to aspirin monotherapy at 3 months after ZES implantation. We retrospectively evaluated 168 consecutive patients with coronary...

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Autores principales: Wada, Tadashi, Nakahama, Makoto, Toda, Hironobu, Watanabe, Atsuyuki, Hashimoto, Katsushi, Terasaka, Ritsuko, Nakamura, Kazufumi, Yamada, Nobuyuki, Ito, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649238/
https://www.ncbi.nlm.nih.gov/pubmed/23762606
http://dx.doi.org/10.1155/2013/518968
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author Wada, Tadashi
Nakahama, Makoto
Toda, Hironobu
Watanabe, Atsuyuki
Hashimoto, Katsushi
Terasaka, Ritsuko
Nakamura, Kazufumi
Yamada, Nobuyuki
Ito, Hiroshi
author_facet Wada, Tadashi
Nakahama, Makoto
Toda, Hironobu
Watanabe, Atsuyuki
Hashimoto, Katsushi
Terasaka, Ritsuko
Nakamura, Kazufumi
Yamada, Nobuyuki
Ito, Hiroshi
author_sort Wada, Tadashi
collection PubMed
description Dual antiplatelet therapy (DAPT) after percutaneous coronary intervention increases the risk of bleeding. We studied the safety and clinical outcomes of switching from DAPT to aspirin monotherapy at 3 months after ZES implantation. We retrospectively evaluated 168 consecutive patients with coronary artery disease who had been implanted with a ZES from June 2009 through March 2010. After excluding 40 patients according to exclusion criteria such as myocardial infarction, 128 patients were divided into a 3-month DAPT group (67 patients, 88 lesions) and a 12-month conventional DAPT group (61 patients, 81 lesions). Coronary angiographic followup and clinical followup were conducted at more than 8 months and at 12 months after ZES implantation, respectively. Minor and major bleeding events, stent thrombosis (ST), and major adverse cardiac events (MACE) (death, myocardial infarction, cerebrovascular accident, target lesion revascularization, and target vessel revascularization) were evaluated. There were no statistically significant differences in the incidences of ST and MACE between the two groups. The incidence of bleeding events was significantly lower in the 3-month group than in the 12-month group (1.5% versus 11.5%, P < 0.05). DAPT can be safely discontinued at 3 months after ZES implantation, which reduces bleeding risk.
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spelling pubmed-36492382013-06-12 Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease Wada, Tadashi Nakahama, Makoto Toda, Hironobu Watanabe, Atsuyuki Hashimoto, Katsushi Terasaka, Ritsuko Nakamura, Kazufumi Yamada, Nobuyuki Ito, Hiroshi ISRN Cardiol Clinical Study Dual antiplatelet therapy (DAPT) after percutaneous coronary intervention increases the risk of bleeding. We studied the safety and clinical outcomes of switching from DAPT to aspirin monotherapy at 3 months after ZES implantation. We retrospectively evaluated 168 consecutive patients with coronary artery disease who had been implanted with a ZES from June 2009 through March 2010. After excluding 40 patients according to exclusion criteria such as myocardial infarction, 128 patients were divided into a 3-month DAPT group (67 patients, 88 lesions) and a 12-month conventional DAPT group (61 patients, 81 lesions). Coronary angiographic followup and clinical followup were conducted at more than 8 months and at 12 months after ZES implantation, respectively. Minor and major bleeding events, stent thrombosis (ST), and major adverse cardiac events (MACE) (death, myocardial infarction, cerebrovascular accident, target lesion revascularization, and target vessel revascularization) were evaluated. There were no statistically significant differences in the incidences of ST and MACE between the two groups. The incidence of bleeding events was significantly lower in the 3-month group than in the 12-month group (1.5% versus 11.5%, P < 0.05). DAPT can be safely discontinued at 3 months after ZES implantation, which reduces bleeding risk. Hindawi Publishing Corporation 2013-04-04 /pmc/articles/PMC3649238/ /pubmed/23762606 http://dx.doi.org/10.1155/2013/518968 Text en Copyright © 2013 Tadashi Wada et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Wada, Tadashi
Nakahama, Makoto
Toda, Hironobu
Watanabe, Atsuyuki
Hashimoto, Katsushi
Terasaka, Ritsuko
Nakamura, Kazufumi
Yamada, Nobuyuki
Ito, Hiroshi
Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title_full Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title_fullStr Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title_full_unstemmed Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title_short Dual Antiplatelet Therapy Can Be Discontinued at Three Months after Implantation of Zotarolimus-Eluting Stent in Patients with Coronary Artery Disease
title_sort dual antiplatelet therapy can be discontinued at three months after implantation of zotarolimus-eluting stent in patients with coronary artery disease
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649238/
https://www.ncbi.nlm.nih.gov/pubmed/23762606
http://dx.doi.org/10.1155/2013/518968
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