The San
Francisco Chronicle (8/29, Allday, Lee, Colliver) reports, "Patients
who are asymptomatic but have at least one narrowed blood vessel that severely
lowers blood flow to the heart are better off being treated with drugs and a
stent placed in the artery than with drug therapy alone, according to results
of a large trial" published online Aug. 28 in the New England Journal of
Medicine.
HealthDay (8/29, Mann) reports that for "the new study, researchers
used a diagnostic tool called fractional flow reserve (FFR) to help determine
the best course of treatment among more than 1,200 people with stable heart
disease." The research "was stopped early due to high rates of
hospitalization and urgent need for stenting seen among people who only
received drug therapy...initially."
The Minneapolis Star Tribune (8/29, Walsh) reports that Dr. Bernard De
Bruyne, the coordinating clinical investigator of the FAME II Trial, said,
"With this new knowledge, I believe that FFR should become the standard of
care for treating patients with stable coronary artery disease and significant
coronary narrowings."
On its website, ABC (8/29) reports, "However, the new study is
unlikely to end the debate over the use of stents, which has raged since a
landmark study in 2007 known as the COURAGE trial."
MedPage Today (8/29, Neale) reports, "Spencer King III, MD,
professor emeritus at Emory University and a past president of the American
College of Cardiology, said that there would be some criticisms about the study
regarding the inclusion of urgent revascularization - often considered a 'soft'
outcome - in the primary composite endpoint with the hard outcomes of death and
MI."
WebMD (8/29, Laino) reports, "Fractional flow reserve is available
at most medical centers. And It's being used more and more to help determine
the best course of treatment for opening narrowed arteries, says American
College of Cardiology immediate past president David Holmes, MD."
CardioSource (8/29) reports "A couple of limitations warrant
mention. The mean follow-up was very short-approximately 7 months. Thus, it was
too short to study meaningful differences in hard endpoints such as death or
MI, and also for assessing the impact of restenosis in the PCI arm. Thus, it
will remain a point of discussion that the Data Safety Monitoring Board
terminated this trial early based on differences in unplanned revascularization
between the two arms, since rates of death and MI were similar. The
practicality and cost-effectiveness of FFR-guided PCI for every stable angina
lesion will need to be further studied.
Steven
Almany M.D.
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