Gray zone fractional flow reserve 0.81–0.85 is associated with an increased risk of cardio-vascular events

Fractional Flow Reserve (FFR) is a widely accepted prognostic tool to estimate the risk of myocardial ischemia in coronary stenosis. Values above 0.80 are considered as an indication for medical therapy only. Whether intermediate values ranging from 0.81 to 0.85 are associated with an increase cardi...

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Published inArchives of Cardiovascular Diseases Supplements Vol. 11; no. 1; p. e287
Main Authors Cador, R., Durand, P.H., Kamtchueng, P., Schoukroun, G., Komajda, M., Azzaz, S.
Format Journal Article
LanguageEnglish
Published Elsevier Masson SAS 01.04.2019
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Summary:Fractional Flow Reserve (FFR) is a widely accepted prognostic tool to estimate the risk of myocardial ischemia in coronary stenosis. Values above 0.80 are considered as an indication for medical therapy only. Whether intermediate values ranging from 0.81 to 0.85 are associated with an increase cardio-vascular (CV) risk is unknown. In a prospective study, 91 patients with FFR>0.80 were enrolled and followed up for at least 1 year. Clinical outcomes of the subgroup with FFR>0.85 (N=67) were compared with those of the subgroup with intermediate values of 0.81–0.85 (N=24). The outcome was a composite of cardio-vascular death/myocardial infarction/CV hospitalization/target lesion revascularization. There was significant difference in baseline demographic data or medical therapy between the two groups (Table 1). The average follow-up is 2.505±0.6 years. We observed a significantly higher number of events in patients with FFR between 0.81 and 0.85 than in those with FFR>0.85. These events occurred respectively in 45.9% and 13.4% of patients (P=0.01) and were mostly the result of revascularizations and CV hospitalizations (Fig. 1). FFR values in the gray zone of 0.81–0.85 are correlated with an increased CV risk compared to FFR values>0.85. Appropriately powered trials are needed to assess the potential benefit of revascularization in this subset of patients.
ISSN:1878-6480
DOI:10.1016/j.acvdsp.2019.01.012