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Balancing the risk of spontaneous ischemic and major bleeding events in acute coronary syndromes.
Ducrocq, Gregory; Schulte, Phillip J; Budaj, Andrzej; Cornel, Jan H; Held, Claes; Himmelmann, Anders; Husted, Steen; Storey, Robert F; Cannon, Christopher P; Becker, Richard C; James, Stefan K; Katus, Hugo A; Lopes, Renato D; Sorbets, Emmanuel; Wallentin, Lars; Steg, Philippe Gabriel.
Afiliação
  • Ducrocq G; FACT (French Alliance for Cardiovascular Trials), Paris, France; Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat, Paris, France; Université Paris-Diderot, Sorbonne-Paris Cité, Paris, France; INSERM-Unité 1148, Paris, France. Electronic address: gregory
  • Schulte PJ; Duke Clinical Research Institute, Duke University, Medical Center, Durham, NC; Department of Health Sciences Research, Mayo Clinic, Rochester, MN.
  • Budaj A; Postgraduate Medical School, Grochowski Hospital, Warsaw, Poland.
  • Cornel JH; Department of Cardiology, Noordwest Ziekenhuisgroep, Alkmaar, The Netherlands.
  • Held C; Department of Medical Sciences, Cardiology, and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
  • Himmelmann A; AstraZeneca Research and Development, Gothenburg, Sweden.
  • Husted S; Medical Department, Hospital Unit West, Herning/Holstebro, Denmark.
  • Storey RF; Department of Cardiovascular Science, University of Sheffield, Sheffield, UK.
  • Cannon CP; Cardiovascular Division, Brigham and Women's Hospital, and Baim Institute for Clinical Research Boston, MA.
  • Becker RC; Division of Cardiovascular Health and Disease, Heart, Lung and Vascular Institute, University of Cincinnati College of Medicine, Cincinnati, OH.
  • James SK; Department of Medical Sciences, Cardiology, and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
  • Katus HA; Medizinishe Klinik, Universitätsklinikum Heidelberg, Heidelberg, Germany.
  • Lopes RD; Duke Clinical Research Institute, Duke University, Medical Center, Durham, NC.
  • Sorbets E; FACT (French Alliance for Cardiovascular Trials), Paris, France; Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat, Paris, France; INSERM-Unité 1148, Paris, France; Hôpital Avicenne (Assistance Publique-Hôpitaux de Paris), and Université Paris 13, Bobign
  • Wallentin L; Department of Medical Sciences, Cardiology, and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
  • Steg PG; FACT (French Alliance for Cardiovascular Trials), Paris, France; Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat, Paris, France; Université Paris-Diderot, Sorbonne-Paris Cité, Paris, France; INSERM-Unité 1148, Paris, France; NHLI Imperial College, ICMS
Am Heart J ; 186: 91-99, 2017 Apr.
Article em En | MEDLINE | ID: mdl-28454837
Evaluation of antithrombotic treatments for acute coronary syndromes (ACS) requires balancing ischemic and bleeding risks to assess net benefit. We sought to compare the relative effects of ischemic and bleeding events on mortality. METHODS: In the PLATelet inhibition and patient Outcomes (PLATO) trial, we compared spontaneous ischemic events (myocardial infarction or stroke) with spontaneous major bleeding events (PLATO major, Thrombolysis In Myocardial Infarction [TIMI] major, Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries [GUSTO] severe) with respect to risk of mortality using time-dependent Cox proportional hazards models. The comparison was performed using ratio of hazard ratios for mortality increase after ischemic vs bleeding events. RESULTS: A total of 822 patients (4.4%) had ≥1 spontaneous ischemic event; 485 patients (2.6%), ≥1 spontaneous PLATO major bleed, 282 (1.5%), ≥1 spontaneous TIMI major bleed; and 207 (1.1%), ≥1 spontaneous severe GUSTO bleed. In patients who had both events, bleeding occurred first in most patients. Regardless of classification, major bleeding events were associated with increased short- and long-term mortality that were not significantly different from the increase associated with spontaneous ischemic events: ratio of hazard ratios (95% CIs) for short- and long-term mortality after spontaneous ischemic vs bleeding events: 1.46 (0.98-2.19) and 0.92 (0.52-1.62) (PLATO major); 1.26 (0.80-1.96) and 1.19 (0.58-2.24) (TIMI major), 0.72 (0.47-1.10) and 0.83 (0.38-1.79) (GUSTO severe) (all P>0.05) CONCLUSIONS: In patients with ACS on dual antiplatelet therapy, spontaneous major bleeding events seem "prognostically equivalent" to spontaneous ischemic complications. This result allows quantitative comparisons between both actual and predicted bleeding and ischemic risks. Our findings help to better define net clinical benefit of antithrombotic treatments and more accurately estimate mortality after ischemic and bleeding events in patients with ACS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores da Agregação Plaquetária / Acidente Vascular Cerebral / Síndrome Coronariana Aguda / Fibrinolíticos / Hemorragia / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am Heart J Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores da Agregação Plaquetária / Acidente Vascular Cerebral / Síndrome Coronariana Aguda / Fibrinolíticos / Hemorragia / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am Heart J Ano de publicação: 2017 Tipo de documento: Article