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Factor XI as a new target for prevention of thromboembolism in cardiovascular disease: a meta-analysis of randomized controlled trials.
Ali, Ahmed E; Awad, Mohamed K; Ali, Karim; Abouzid, Mohamed Riad; Ahmed, Marwan H; Mazroua, Muhammad S.
Afiliação
  • Ali AE; Department of Medicine, Mayo Clinic, Rochester, MN, USA.
  • Awad MK; Faculty of Medicine, Mansoura University, Mansoura, Egypt.
  • Ali K; Department of Anesthesia and Critical Care, Faculty of Medicine, Ain Shams University, Cairo, Egypt. Mohamed.kheder@med.asu.edu.eg.
  • Abouzid MR; Department of Medicine, Hennepin Healthcare, Minneapolis, MN, USA.
  • Ahmed MH; Faculty of Medicine, Mansoura University, Mansoura, Egypt.
  • Mazroua MS; Department of Medicine, Baptist Hospitals of Southeast Texas, Beaumont, TX, USA.
Article em En | MEDLINE | ID: mdl-38762711
ABSTRACT
Anticoagulant therapy is a mainstay in the management of patients with cardiovascular disease. The use of conventional anticoagulants carries potential side effects, mainly bleeding. Drugs targeting Factor XI (FXI) have been investigated in randomized controlled trials as a new option with more favorable outcomes. A comprehensive literature search was conducted to identify relevant studies comparing FXI inhibitors to placebo or standard therapy. The primary outcomes were incidence of all bleeding events, major bleeding, and thromboembolism. Secondary outcomes included incidence of all adverse events (AE), serious AE, and all-cause mortality. A total of 11 studies involving 10,536 patients were included. FXI inhibitors were associated with a trend toward reduction of bleeding events and incidence of thromboembolism compared to the control group (placebo/standard therapy). There was no statistically significant difference between both groups in terms of adverse events and all-cause mortality. When compared to enoxaparin, FXI inhibitors significantly reduced the risk of bleeding events (RR = 0.42, 95% CI 0.23-0.76, P = 0.004) and thromboembolism (RR = 0.59, 95% CI 0.44-0.77, P = 0.001). On the other hand, when compared to DOACs, FXI inhibitors were associated with a significant reduction in bleeding events but not thromboembolism. Whereas, compared to placebo, FXI inhibitors did not increase the risk of bleeding events, adverse events, or all-cause mortality (P > 0.05). FXI inhibitors could be a safer and more potent option for prevention of thromboembolism than conventional therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Thromb Thrombolysis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Thromb Thrombolysis Ano de publicação: 2024 Tipo de documento: Article