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Common
drug-releasing Coronary stents appear to
have similar clinical outcomes
Newswise — A comparison
of use of the first two commercially
available drug-releasing coronary stents
(for the medications sirolimus and
paclitaxel) among patients in “everyday
clinical practice” indicates no significant
differences for outcomes such as heart
attack or cardiac death, according to a
study in the January 30 issue of JAMA.
Drug-releasing
(eluting) stents are used for percutaneous
coronary interventions (PCI) to help reduce
the rate of re-narrowing of a coronary
artery, according to background information
in the article.
Approval of
drug-eluting coronary stents was based on
results of relatively small trials of
selected patients; however, in routine
practice, stents are used in a broader
spectrum of patients.
Anders M. Galløe, M.D.,
of the University of Copenhagen, Denmark,
and colleagues compared the efficacy and
safety of sirolimus-eluting and paclitaxel-eluting
stents in a study designed to reflect
everyday clinical practice.
The SORT OUT II
trial included 2,098 men and women treated
with PCI and randomized to receive either
sirolimus-eluting (n = 1,065) or paclitaxel-eluting
(n = 1,033) stents at five university
hospitals in Denmark.
The patients were
initially treated for ST-segment elevation
myocardial infarction (STEMI; a certain
pattern on an electrocardiogram following a
heart attack), non-STEMI or unstable angina
pectoris, and stable angina.
The researchers found
that the proportion of patients experiencing
major adverse cardiac events, such as
cardiac death, heart attack, target lesion
revascularization, or target vessel
revascularization, were 98 (9.3 percent) for
the sirolimus-eluting stent group and 114
(11.2 percent) for the paclitaxel-eluting
stent group.
The stent thrombosis
rates were 27 (2.5 percent) in the sirolimus-eluting
stent group and 30 (2.9 percent) in the
paclitaxel-eluting stent group.
“In conclusion, the
SORT OUT II trial found no statistical
significant differences in the primary or
secondary end points between the sirolimus-eluting
stent and paclitaxel-eluting stent in
everyday clinical practice among patients
undergoing PCI for ST-segment elevation
myocardial infarction, non–ST-segment
elevation myocardial infarction or unstable
angina pectoris, and stable angina.
"The
rates of serious adverse events, cardiac
death, acute myocardial infarction, and
stent thrombosis were low, suggesting that,
at least when considering 18 months of
follow-up, the use of drug-eluting stents in
the general population may be safe,” the
authors write.
Editorial: Effectiveness of Drug-Eluting
Stents in Real-World Patients
In an accompanying
editorial, Debabrata Mukherjee, M.D., and
David J. Moliterno, M.D., of the University
of Kentucky, Lexington, comment on the
findings of Galløe and colleagues regarding
the comparison of stents.
“In 2008, clinicians
will have additional choices of drug-eluting
stents with the availability of
second-generation devices—namely, the
everolimus-eluting stent, which yielded
similar or fewer major adverse cardiac
events among patients as compared with the
paclitaxel-eluting stent, and the
zotarolimus-eluting stent, which was shown
to be noninferior to the paclitaxel-eluting
stent.
"The
ongoing choice of a drug-eluting stent will
likely depend on multiple factors that will
include safety, effectiveness,
deliverability, and—given recent cuts in
reimbursement—cost of the device.”
“The current literature
for drug-eluting stents can be challenging
to interpret because of differing criteria
for study enrollment, definitions for acute
stent thrombosis and other clinical end
points, and varied intervals of dual
antiplatelet therapy and follow-up after
stent implantation.
"Similarly, current real-world registries
are usually limited by lack of valid control
groups and often use historical controls. A
large longitudinal database for patients
receiving these various drug-eluting stents
with open entry to fully capture all
procedures may help determine the safest and
most effective revascularization practice
possible and should help guide future
recommendations,” they write.