Clinical Impact of Gastrointestinal Bleeding in Patients Undergoing Percutaneous Coronary Interventions

Author:

Koskinas Konstantinos C.1,Räber Lorenz1,Zanchin Thomas1,Wenaweser Peter1,Stortecky Stefan1,Moschovitis Aris1,Khattab Ahmed A.1,Pilgrim Thomas1,Blöchlinger Stefan1,Moro Christina1,Jüni Peter1,Meier Bernhard1,Heg Dik1,Windecker Stephan1

Affiliation:

1. From the Department of Cardiology, Bern University Hospital, Bern, Switzerland (K.C.K., L.R., T.Z., P.W., S.S., A.M., A.A.K., T.P., S.B., C.M., B.M., S.W.); and Institute of Primary Health Care (P.J.), Institute of Social and Preventive Medicine (D.H.), and Clinical Trials Unit, Department of Clinical Research (S.W.), University of Bern, Bern, Switzerland.

Abstract

Background— The risk factors and clinical sequelae of gastrointestinal bleeding (GIB) in the current era of drug-eluting stents, prolonged dual antiplatelet therapy, and potent P2Y 12 inhibitors are not well established. We determined the frequency, predictors, and clinical impact of GIB after percutaneous coronary interventions (PCIs) in a contemporary cohort of consecutive patients treated with unrestricted use of drug-eluting stents. Methods and Results— Between 2009 and 2012, all consecutive patients undergoing PCI were prospectively included in the Bern PCI Registry. Bleeding Academic Research Consortium (BARC) GIB and cardiovascular outcomes were recorded within 1 year of follow-up. Among 6212 patients, 84.1% received new-generation drug-eluting stents and 19.5% received prasugrel. At 1 year, GIB had occurred in 65 patients (1.04%); 70.8% of all events and 84.4% of BARC ≥3B events were recorded >30 days after PCI. The majority of events (64.4%) were related to upper GIB with a more delayed time course compared with lower GIB. Increasing age, previous GIB, history of malignancy, smoking, and triple antithrombotic therapy (ie, oral anticoagulation plus dual antiplatelet therapy) were independent predictors of GIB in multivariable analysis. GIB was associated with increased all-cause mortality (adjusted hazard ratio, 3.40; 95% confidence interval, 1.67–6.92; P =0.001) and the composite of death, myocardial infarction, or stroke (adjusted hazard ratio, 3.75; 95% confidence interval, 1.99–7.07; P <0.001) and was an independent predictor of all-cause mortality during 1 year. Conclusions— Among unselected patients undergoing PCI, GIB has a profound effect on prognosis. Triple antithrombotic therapy emerged as the single drug-related predictor of GIB in addition to patient-related risk factors within 1 year of PCI. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT02241291.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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