Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease

Bernard De Bruyne(Onze Lieve Vrouwziekenhuis Hospital), Nico H.J. Pijls(Catharina Ziekenhuis), Bindu Kalesan(Institute of Social and Preventive Medicine), Emanuele Barbato(Onze Lieve Vrouwziekenhuis Hospital), Pim A.L. Tonino(Catharina Ziekenhuis), Zsolt Piróth(Gottsegen National Cardiovascular Center), Nikola Jagić(Clinical Centre of Kragujevac), Sven Möbius‐Winkler(Leipzig Heart Institute), Gilles Rioufol, Nils Witt(Karolinska Institutet), Petr Kala(University Hospital Brno), Philip MacCarthy(King's College Hospital), Thomas Engström(Rigshospitalet), Keith G. Oldroyd(Golden Jubilee National Hospital), Kreton Mavromatis(Veterans Health Administration), Ganesh Manoharan(University of Ulster), Peter VerLee, Ole Fröbert(Örebro University Hospital), Nick Curzen(University Hospital Southampton NHS Foundation Trust), Jane B. Johnson(St. Jude Medical Center), Peter Jüni(Institute of Social and Preventive Medicine), William F. Fearon(Stanford University)
New England Journal of Medicine
August 28, 2012
Cited by 2,725Open Access
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Abstract

BACKGROUND: The preferred initial treatment for patients with stable coronary artery disease is the best available medical therapy. We hypothesized that in patients with functionally significant stenoses, as determined by measurement of fractional flow reserve (FFR), percutaneous coronary intervention (PCI) plus the best available medical therapy would be superior to the best available medical therapy alone. METHODS: In patients with stable coronary artery disease for whom PCI was being considered, we assessed all stenoses by measuring FFR. Patients in whom at least one stenosis was functionally significant (FFR, ≤0.80) were randomly assigned to FFR-guided PCI plus the best available medical therapy (PCI group) or the best available medical therapy alone (medical-therapy group). Patients in whom all stenoses had an FFR of more than 0.80 were entered into a registry and received the best available medical therapy. The primary end point was a composite of death, myocardial infarction, or urgent revascularization. RESULTS: Recruitment was halted prematurely after enrollment of 1220 patients (888 who underwent randomization and 332 enrolled in the registry) because of a significant between-group difference in the percentage of patients who had a primary end-point event: 4.3% in the PCI group and 12.7% in the medical-therapy group (hazard ratio with PCI, 0.32; 95% confidence interval [CI], 0.19 to 0.53; P<0.001). The difference was driven by a lower rate of urgent revascularization in the PCI group than in the medical-therapy group (1.6% vs. 11.1%; hazard ratio, 0.13; 95% CI, 0.06 to 0.30; P<0.001); in particular, in the PCI group, fewer urgent revascularizations were triggered by a myocardial infarction or evidence of ischemia on electrocardiography (hazard ratio, 0.13; 95% CI, 0.04 to 0.43; P<0.001). Among patients in the registry, 3.0% had a primary end-point event. CONCLUSIONS: In patients with stable coronary artery disease and functionally significant stenoses, FFR-guided PCI plus the best available medical therapy, as compared with the best available medical therapy alone, decreased the need for urgent revascularization. In patients without ischemia, the outcome appeared to be favorable with the best available medical therapy alone. (Funded by St. Jude Medical; ClinicalTrials.gov number, NCT01132495.).


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