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Preferred monotherapy after short-term dual antiplatelet therapy: Systematic review and network meta-analysis of randomized trials.
Shoji, Satoshi; Kuno, Toshiki; Ueyama, Hiroki; Takagi, Hisato; Briasoulis, Alexandros; Kim, Hyo-Soo; Koo, Bon-Kwon; Kang, Jeehoon; Watanabe, Hirotoshi; Kimura, Takeshi; Kohsaka, Shun.
Afiliação
  • Shoji S; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan; Duke Clinical Research Institute, Durham, NC, USA.
  • Kuno T; Division of Cardiology, Montefiore Medical Center, Albert Einstein College of Medicine, New York, NY, USA; Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York, NY, USA. Electronic address: tkuno@montefiore.org.
  • Ueyama H; Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York, NY, USA; Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Takagi H; Department of Cardiovascular Surgery, Shizuoka Medical Center, Shizuoka, Japan.
  • Briasoulis A; Division of Cardiology, Heart Failure and Transplantation, University of Iowa, Iowa City, IA, USA.
  • Kim HS; Cardiovascular Center, Seoul National University Hospital, Seoul, South Korea.
  • Koo BK; Cardiovascular Center, Seoul National University Hospital, Seoul, South Korea.
  • Kang J; Cardiovascular Center, Seoul National University Hospital, Seoul, South Korea.
  • Watanabe H; Department of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.
  • Kimura T; Department of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.
  • Kohsaka S; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
J Cardiol ; 83(5): 338-347, 2024 May.
Article em En | MEDLINE | ID: mdl-37562542
ABSTRACT

BACKGROUND:

Randomized controlled trials (RCTs) have demonstrated the efficacy and safety of P2Y12 inhibitor monotherapy following short-term dual antiplatelet therapy (DAPT) in patients undergoing percutaneous coronary intervention (PCI). However, no studies have compared P2Y12 inhibitor and aspirin monotherapy following short-term DAPT. We aimed to compare available strategies for DAPT duration and post-DAPT antiplatelet monotherapy following PCI.

METHODS:

Seven DAPT strategies [ticagrelor or clopidogrel following 1-month DAPT, ticagrelor following 3-month DAPT, aspirin following 3-6 months of DAPT (reference strategy), aspirin or P2Y12 inhibitor following 6-18-months of DAPT, and DAPT for ≥18 months] were compared using a network meta-analysis. The primary efficacy outcome was defined as a composite of all-cause death, myocardial infarction, and stroke. The primary bleeding outcome was trial-defined major or minor bleeding.

RESULTS:

Our analysis identified 25 eligible RCTs, including 89,371 patients who underwent PCI. Overall, none of the strategies negatively affected the primary efficacy outcomes. For primary bleeding outcomes, ticagrelor following 3-month DAPT was associated with a reduced risk of primary bleeding outcomes (HR 0.73; 95 % CI 0.57-0.95). Clopidogrel following 1-month DAPT was also associated with a reduced risk of primary bleeding outcomes (HR 0.54; 95 % CI 0.34-0.85), however, the strategy was associated with an increased risk of myocardial infarction or stent thrombosis. Similar trends were observed among patients with acute coronary syndrome and high bleeding risk.

CONCLUSIONS:

Compared with aspirin monotherapy following short-term DAPT, ticagrelor following 3-month DAPT was associated with a reduced risk of primary bleeding outcomes without increasing any ischemic outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Intervenção Coronária Percutânea / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Intervenção Coronária Percutânea / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article