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Prospective observational cohort study of the association between antiplatelet therapy, bleeding and thrombosis in patients with coronary stents undergoing noncardiac surgery.
Howell, S J; Hoeks, S E; West, R M; Wheatcroft, S B; Hoeft, A.
Afiliación
  • Howell SJ; Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, UK. Electronic address: s.howell@leeds.ac.uk.
  • Hoeks SE; Department of Anaesthesiology, Erasmus University Medical Centre, Rotterdam, the Netherlands.
  • West RM; Faculty of Medicine and Health, Leeds Institute of Health Sciences, Leeds, UK.
  • Wheatcroft SB; Division of Cardiovascular and Diabetes Research, Leeds Institute for Cardiovascular and Metabolic Research, University of Leeds, Leeds, UK.
  • Hoeft A; Department of Anaesthesiology and Intensive Care Medicine, University of Bonn, Bonn, Germany.
Br J Anaesth ; 122(2): 170-179, 2019 Feb.
Article en En | MEDLINE | ID: mdl-30686302
ABSTRACT

BACKGROUND:

The perioperative management of antiplatelet therapy in noncardiac surgery patients who have undergone previous percutaneous coronary intervention (PCI) remains a dilemma. Continuing dual antiplatelet therapy (DAPT) may carry a risk of bleeding, while stopping antiplatelet therapy may increase the risk of perioperative major adverse cardiovascular events (MACE).

METHODS:

Occurrence of Bleeding and Thrombosis during Antiplatelet Therapy In Non-Cardiac Surgery (OBTAIN) was an international prospective multicentre cohort study of perioperative antiplatelet treatment, MACE, and serious bleeding in noncardiac surgery. The incidences of MACE and bleeding were compared in patients receiving DAPT, monotherapy, and no antiplatelet therapy before surgery. Unadjusted risk ratios were calculated taking monotherapy as the baseline. The adjusted risks of bleeding and MACE were compared in patients receiving monotherapy and DAPT using propensity score matching.

RESULTS:

A total of 917 patients were recruited and 847 were eligible for inclusion. Ninety-six patients received no antiplatelet therapy, 526 received monotherapy with aspirin, and 225 received DAPT. Thirty-two patients suffered MACE and 22 had bleeding. The unadjusted risk ratio for MACE in patients receiving DAPT compared with monotherapy was 1.9 (0.93-3.88), P=0.08. There was no difference in MACE between no antiplatelet treatment and monotherapy 1.03 (0.31-3.46), P=0.96. Bleeding was more frequent with DAPT 6.55 (2.3-17.96) P=0.0002. In a propensity matched analysis of 177 patients who received DAPT and 177 monotherapy patients, the risk ratio for MACE with DAPT was 1.83 (0.69-4.85), P=0.32. The risk of bleeding was significantly greater in the DAPT group 4.00 (1.15-13.93), P=0.031.

CONCLUSIONS:

OBTAIN showed an increased risk of bleeding with DAPT and found no evidence for protective effects of DAPT from perioperative MACE in patients who have undergone previous PCI.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Operativos / Trombosis / Inhibidores de Agregación Plaquetaria / Stents / Hemorragia Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Anaesth Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Operativos / Trombosis / Inhibidores de Agregación Plaquetaria / Stents / Hemorragia Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Anaesth Año: 2019 Tipo del documento: Article