Combined use of antiplatelet and proton pump inhibitor following myocardial infarction or angina associated with increased risk of death, hospitalization
Following an acute coronary syndrome such as a myocardial
infarction or unstable angina, patients who receive a medication to reduce the
risk of gastrointestinal bleeding that may be associated with the use of the antiplatelet
drug clopidogrel and aspirin have an increased risk of subsequent hospitalization
for acute coronary syndrome or death, according to a study in the March 4 issue
of JAMA.
Treatment with clopidogrel in addition to aspirin reduces
recurrent cardiovascular events following hospitalization for acute coronary syndrome
(ACS) for patients treated either medically or with angioplasty or stent placement.
Proton pump inhibitor (PPI) medications are often prescribed at the start of treatment
with clopidogrel, with the goal of reducing the risk of gastrointestinal tract
bleeding while patients are taking dual-antiplatelet therapy. Recent studies,
however, suggest that PPIs may reduce the effectiveness of clopidogrel, but the
clinical significance of these findings to patients is not clear, according to
background information in the article.
P. Michael Ho, M.D., Ph.D., of the Denver VA Medical
Center, and colleagues evaluated the use of clopidogrel plus PPI following hospital
discharge for ACS and compared rates of all-cause death and rehospitalization
for ACS, between patients taking clopidogrel plus PPI vs. clopidogrel without
PPI. The study included patients from 127 Veterans Affairs hospitals. Vital status
information was available for all patients through September 30, 2006.
Of 8,205 patients with ACS taking clopidogrel after hospital
discharge, 63.9 percent (n = 5,244) were prescribed PPI at discharge or during
follow-up. Death or rehospitalization for ACS occurred in 29.8 percent of patients
prescribed clopidogrel plus PPI and 20.8 percent of patients prescribed clopidogrel
without PPI. Use of clopidogrel plus PPI at any point in time was associated with
a 25 percent increased odds of death or rehospitalization for ACS compared with
use of clopidogrel without PPI.
For the individual outcomes, the rates of recurrent hospitalization
for ACS (14.6 percent vs. 6.9 percent) and revascularization procedures (15.5
percent vs. 11.9 percent) were higher among patients taking clopidogrel plus PPI
compared with those taking clopidogrel without PPI. However, the risk of death
was similar between the two groups.
"When patients were not taking clopidogrel after hospital
discharge, a prescription for PPI was not associated with death or rehospitalization
for ACS, supporting the hypothesis that the interaction of PPI and clopidogrel,
rather than PPI itself, was associated with increased adverse outcomes," the authors
write.
"… this study raises some concern about concomitant [accompanying]
use of PPI medications and clopidogrel following hospitalization for ACS. While
the risk estimates associated with clopidogrel plus PPI vs. clopidogrel without
PPI were modest, the absolute number of adverse events attributable to this potential
drug interaction is considerable when extrapolated to a population level, given
how frequently PPI medications are prescribed to patients receiving dual-antiplatelet
therapy," the researchers write. "Pending additional evidence, however, the results
of this study may suggest that PPIs should be used for patients with a clear indication
for the medication, such as history of gastrointestinal tract bleeding, consistent
with current guideline recommendations, rather than routine prophylactic prescription.
Alternative gastrointestinal tract medication regimens also may be considered
until additional data regarding concomitant use of PPI and clopidogrel becomes
available."
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