Association of Proton Pump Inhibitor Use on Cardiovascular Outcomes With Clopidogrel and Ticagrelor Insights From the Platelet Inhibition and Patient Outcomes Trial


Autoria(s): Goodman, Shaun G.; Clare, Robert; Pieper, Karen S.; Nicolau, José C.; Storey, Robert F.; Cantor, Warren J.; Mahaffey, Kenneth W.; Angiolillo, Dominick J.; Husted, Steen; Cannon, Christopher P.; James, Stefan K.; Kilhamn, Jan; Steg, P. Gabriel; Harrington, Robert A.; Wallentin, Lars
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Background-The clinical significance of the interaction between clopidogrel and proton pump inhibitors (PPIs) remains unclear. Methods and Results-We examined the relationship between PPI use and 1-year cardiovascular events (cardiovascular death, myocardial infarction, or stroke) in patients with acute coronary syndrome randomized to clopidogrel or ticagrelor in a prespecified, nonrandomized subgroup analysis of the Platelet Inhibition and Patient Outcomes (PLATO) trial. The primary end point rates were higher for individuals on a PPI (n = 6539) compared with those not on a PPI (n = 12 060) at randomization in both the clopidogrel (13.0% versus 10.9%; adjusted hazard ratio [HR], 1.20; 95% confidence interval [CI], 1.04 -1.38) and ticagrelor (11.0% versus 9.2%; HR, 1.24; 95% CI, 1.07-1.45) groups. Patients on non-PPI gastrointestinal drugs had similar primary end point rates compared with those on a PPI (PPI versus non-PPI gastrointestinal treatment: clopidogrel, HR, 0.98; 95% CI, 0.79-1.23; ticagrelor, HR, 0.89; 95% CI, 0.73-1.10). In contrast, patients on no gastric therapy had a significantly lower primary end point rate (PPI versus no gastrointestinal treatment: clopidogrel, HR, 1.29; 95% CI, 1.12-1.49; ticagrelor, HR, 1.30; 95% CI, 1.14-1.49). Conclusions-The use of a PPI was independently associated with a higher rate of cardiovascular events in patients with acute coronary syndrome receiving clopidogrel. However, a similar association was observed between cardiovascular events and PPI use during ticagrelor treatment and with other non-PPI gastrointestinal treatment. Therefore, in the PLATO trial, the association between PPI use and adverse events may be due to confounding, with PPI use more of a marker for, than a cause of, higher rates of cardiovascular events.

AstraZeneca

BristolMyers Squibb

Daiichi

Eisai

Eli Lilly

Merck

Sanofiaventis

SanofiAventis

Medicines Company

Schering-Plough

MSD

Accumetrics

Eli Lilly/Daiichi Sankyo

Dynabyte

GlaxoSmithKline

Otsuka

Portola

Johnson & Johnson

Pfizer

Bayer

Boehringer Ingelheim

Intekrin Therapeutics

Takeda

Servier

Identificador

Circulation, Philadelphia, v. 125, n. 8, pp. 978-986, Feb, 2012

0009-7322

http://www.producao.usp.br/handle/BDPI/42630

10.1161/CIRCULATIONAHA.111.032912

http://dx.doi.org/10.1161/CIRCULATIONAHA.111.032912

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

PHILADELPHIA

Relação

CIRCULATION

Direitos

closedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #ACUTE CORONARY SYNDROME #CLOPIDOGREL #MORTALITY #MYOCARDIAL INFARCTION #TICAGRELOR #ACUTE CORONARY SYNDROMES #P2Y(12) RECEPTOR ANTAGONIST #RANDOMIZED CROSSOVER #ANTIPLATELET ACTION #CONCOMITANT USE #PLATO TRIAL #OMEPRAZOLE #PANTOPRAZOLE #ASPIRIN #RISK #CARDIAC & CARDIOVASCULAR SYSTEMS #PERIPHERAL VASCULAR DISEASE
Tipo

article

original article

publishedVersion