Accuracy of Fractional Flow Reserve Derived From Coronary Angiography

BACKGROUND:Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFRangio) eliminates both of these requirements and displays FFR valu...

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Published inCirculation (New York, N.Y.) Vol. 139; no. 4; pp. 477 - 484
Main Authors Fearon, William F., Achenbach, Stephan, Engstrom, Thomas, Assali, Abid, Shlofmitz, Richard, Jeremias, Allen, Fournier, Stephane, Kirtane, Ajay J., Kornowski, Ran, Greenberg, Gabriel, Jubeh, Rami, Kolansky, Daniel M., McAndrew, Thomas, Dressler, Ovidiu, Maehara, Akiko, Matsumura, Mitsuaki, Leon, Martin B., De Bruyne, Bernard
Format Journal Article
LanguageEnglish
Published United States by the American College of Cardiology Foundation and the American Heart Association, Inc 22.01.2019
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Abstract BACKGROUND:Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFRangio) eliminates both of these requirements and displays FFR values of the entire coronary tree. The FFRangio Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, international trial with the primary goal of determining the accuracy of FFRangio. METHODS:Coronary angiography was performed in a routine fashion in patients with suspected coronary artery disease. FFR was measured in vessels with coronary lesions of varying severity using a coronary pressure wire and hyperemic stimulus. Based on angiograms of the respective arteries acquired in ≥2 different projections, on-site operators blinded to FFR then calculated FFRangio using proprietary software. Coprimary end points were the sensitivity and specificity of the dichotomously scored FFRangio for predicting pressure wire–derived FFR using a cutoff value of 0.80. The study was powered to meet prespecified performance goals for sensitivity and specificity. RESULTS:Ten centers in the United States, Europe, and Israel enrolled a total of 301 subjects and 319 vessels meeting inclusion/exclusion criteria which were included in the final analysis. The mean FFR was 0.81 and 43% of vessels had an FFR≤0.80. The per-vessel sensitivity and specificity were 94% (95% CI, 88% to 97%) and 91% (86% to 95%), respectively, both of which exceeded the prespecified performance goals. The diagnostic accuracy of FFRangio was 92% overall and remained high when only considering FFR values between 0.75 to 0.85 (87%). FFRangio values correlated well with FFR measurements (r=0.80, P<0.001) and the Bland–Altman 95% confidence limits were between −0.14 and 0.12. The device success rate for FFRangio was 99%. CONCLUSIONS:FFRangio measured from the coronary angiogram alone has a high sensitivity, specificity, and accuracy compared with pressure wire–derived FFR. FFRangio has the promise to substantially increase physiological coronary lesion assessment in the catheterization laboratory, thereby potentially leading to improved patient outcomes. CLINICAL TRIAL REGISTRATION:URLhttps://www.clinicaltrials.gov. Unique IdentifierNCT03226262.
AbstractList BACKGROUND:Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFRangio) eliminates both of these requirements and displays FFR values of the entire coronary tree. The FFRangio Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, international trial with the primary goal of determining the accuracy of FFRangio. METHODS:Coronary angiography was performed in a routine fashion in patients with suspected coronary artery disease. FFR was measured in vessels with coronary lesions of varying severity using a coronary pressure wire and hyperemic stimulus. Based on angiograms of the respective arteries acquired in ≥2 different projections, on-site operators blinded to FFR then calculated FFRangio using proprietary software. Coprimary end points were the sensitivity and specificity of the dichotomously scored FFRangio for predicting pressure wire–derived FFR using a cutoff value of 0.80. The study was powered to meet prespecified performance goals for sensitivity and specificity. RESULTS:Ten centers in the United States, Europe, and Israel enrolled a total of 301 subjects and 319 vessels meeting inclusion/exclusion criteria which were included in the final analysis. The mean FFR was 0.81 and 43% of vessels had an FFR≤0.80. The per-vessel sensitivity and specificity were 94% (95% CI, 88% to 97%) and 91% (86% to 95%), respectively, both of which exceeded the prespecified performance goals. The diagnostic accuracy of FFRangio was 92% overall and remained high when only considering FFR values between 0.75 to 0.85 (87%). FFRangio values correlated well with FFR measurements (r=0.80, P<0.001) and the Bland–Altman 95% confidence limits were between −0.14 and 0.12. The device success rate for FFRangio was 99%. CONCLUSIONS:FFRangio measured from the coronary angiogram alone has a high sensitivity, specificity, and accuracy compared with pressure wire–derived FFR. FFRangio has the promise to substantially increase physiological coronary lesion assessment in the catheterization laboratory, thereby potentially leading to improved patient outcomes. CLINICAL TRIAL REGISTRATION:URLhttps://www.clinicaltrials.gov. Unique IdentifierNCT03226262.
Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFR ) eliminates both of these requirements and displays FFR values of the entire coronary tree. The FFR Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, international trial with the primary goal of determining the accuracy of FFR . Coronary angiography was performed in a routine fashion in patients with suspected coronary artery disease. FFR was measured in vessels with coronary lesions of varying severity using a coronary pressure wire and hyperemic stimulus. Based on angiograms of the respective arteries acquired in ≥2 different projections, on-site operators blinded to FFR then calculated FFR using proprietary software. Coprimary end points were the sensitivity and specificity of the dichotomously scored FFR for predicting pressure wire-derived FFR using a cutoff value of 0.80. The study was powered to meet prespecified performance goals for sensitivity and specificity. Ten centers in the United States, Europe, and Israel enrolled a total of 301 subjects and 319 vessels meeting inclusion/exclusion criteria which were included in the final analysis. The mean FFR was 0.81 and 43% of vessels had an FFR≤0.80. The per-vessel sensitivity and specificity were 94% (95% CI, 88% to 97%) and 91% (86% to 95%), respectively, both of which exceeded the prespecified performance goals. The diagnostic accuracy of FFR was 92% overall and remained high when only considering FFR values between 0.75 to 0.85 (87%). FFR values correlated well with FFR measurements ( r=0.80, P<0.001) and the Bland-Altman 95% confidence limits were between -0.14 and 0.12. The device success rate for FFR was 99%. FFR measured from the coronary angiogram alone has a high sensitivity, specificity, and accuracy compared with pressure wire-derived FFR. FFR has the promise to substantially increase physiological coronary lesion assessment in the catheterization laboratory, thereby potentially leading to improved patient outcomes. URL: https://www.clinicaltrials.gov . Unique Identifier: NCT03226262.
Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFRangio) eliminates both of these requirements and displays FFR values of the entire coronary tree. The FFRangio Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, international trial with the primary goal of determining the accuracy of FFRangio.BACKGROUNDMeasuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a hyperemic stimulus. FFR derived from routine coronary angiography (FFRangio) eliminates both of these requirements and displays FFR values of the entire coronary tree. The FFRangio Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, international trial with the primary goal of determining the accuracy of FFRangio.Coronary angiography was performed in a routine fashion in patients with suspected coronary artery disease. FFR was measured in vessels with coronary lesions of varying severity using a coronary pressure wire and hyperemic stimulus. Based on angiograms of the respective arteries acquired in ≥2 different projections, on-site operators blinded to FFR then calculated FFRangio using proprietary software. Coprimary end points were the sensitivity and specificity of the dichotomously scored FFRangio for predicting pressure wire-derived FFR using a cutoff value of 0.80. The study was powered to meet prespecified performance goals for sensitivity and specificity.METHODSCoronary angiography was performed in a routine fashion in patients with suspected coronary artery disease. FFR was measured in vessels with coronary lesions of varying severity using a coronary pressure wire and hyperemic stimulus. Based on angiograms of the respective arteries acquired in ≥2 different projections, on-site operators blinded to FFR then calculated FFRangio using proprietary software. Coprimary end points were the sensitivity and specificity of the dichotomously scored FFRangio for predicting pressure wire-derived FFR using a cutoff value of 0.80. The study was powered to meet prespecified performance goals for sensitivity and specificity.Ten centers in the United States, Europe, and Israel enrolled a total of 301 subjects and 319 vessels meeting inclusion/exclusion criteria which were included in the final analysis. The mean FFR was 0.81 and 43% of vessels had an FFR≤0.80. The per-vessel sensitivity and specificity were 94% (95% CI, 88% to 97%) and 91% (86% to 95%), respectively, both of which exceeded the prespecified performance goals. The diagnostic accuracy of FFRangio was 92% overall and remained high when only considering FFR values between 0.75 to 0.85 (87%). FFRangio values correlated well with FFR measurements ( r=0.80, P<0.001) and the Bland-Altman 95% confidence limits were between -0.14 and 0.12. The device success rate for FFRangio was 99%.RESULTSTen centers in the United States, Europe, and Israel enrolled a total of 301 subjects and 319 vessels meeting inclusion/exclusion criteria which were included in the final analysis. The mean FFR was 0.81 and 43% of vessels had an FFR≤0.80. The per-vessel sensitivity and specificity were 94% (95% CI, 88% to 97%) and 91% (86% to 95%), respectively, both of which exceeded the prespecified performance goals. The diagnostic accuracy of FFRangio was 92% overall and remained high when only considering FFR values between 0.75 to 0.85 (87%). FFRangio values correlated well with FFR measurements ( r=0.80, P<0.001) and the Bland-Altman 95% confidence limits were between -0.14 and 0.12. The device success rate for FFRangio was 99%.FFRangio measured from the coronary angiogram alone has a high sensitivity, specificity, and accuracy compared with pressure wire-derived FFR. FFRangio has the promise to substantially increase physiological coronary lesion assessment in the catheterization laboratory, thereby potentially leading to improved patient outcomes.CONCLUSIONSFFRangio measured from the coronary angiogram alone has a high sensitivity, specificity, and accuracy compared with pressure wire-derived FFR. FFRangio has the promise to substantially increase physiological coronary lesion assessment in the catheterization laboratory, thereby potentially leading to improved patient outcomes.URL: https://www.clinicaltrials.gov . Unique Identifier: NCT03226262.CLINICAL TRIAL REGISTRATIONURL: https://www.clinicaltrials.gov . Unique Identifier: NCT03226262.
Author Dressler, Ovidiu
Jubeh, Rami
Matsumura, Mitsuaki
Fournier, Stephane
McAndrew, Thomas
Assali, Abid
Shlofmitz, Richard
Engstrom, Thomas
Kirtane, Ajay J.
De Bruyne, Bernard
Kolansky, Daniel M.
Maehara, Akiko
Leon, Martin B.
Achenbach, Stephan
Greenberg, Gabriel
Fearon, William F.
Kornowski, Ran
Jeremias, Allen
AuthorAffiliation Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University School of Medicine, CA (W.F.F.). Department of Cardiology, Friedrich-Alexander University Erlangen-Nürnberg, Germany (S.A.). The Heart Center, Rigs Hospital, University of Copenhagen, Denmark (T.E.). Department of Cardiology, Rabin Medical Center, Petach Tikva, Israel (A.A., R.K.). Department of Cardiology, St. Francis Hospital, Roslyn, NY (R.S., A.J.). Department of Cardiology, Cardiovascular Center Aalst OLV Hospital, Belgium (S.F., B.D.B.). Columbia University Medical Center (A.J.K., A.M., M.B.L.), New York, NY. Cardiovascular Research Foundation (A.J.K., A.M., M.B.L., T.M., O.D., M.M.), New York, NY. Department of Cardiology, HaSharon Medical Center, Petach Tikva, Israel (G.G.). Department of Cardiology, Shaare Zedek Medical Center, Jerusalem, Israel (R.J.). Division of Cardiovascular Medicine, University of Pennsylvania School of Medicine, Philadelphia (D.M.K.)
AuthorAffiliation_xml – name: Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University School of Medicine, CA (W.F.F.). Department of Cardiology, Friedrich-Alexander University Erlangen-Nürnberg, Germany (S.A.). The Heart Center, Rigs Hospital, University of Copenhagen, Denmark (T.E.). Department of Cardiology, Rabin Medical Center, Petach Tikva, Israel (A.A., R.K.). Department of Cardiology, St. Francis Hospital, Roslyn, NY (R.S., A.J.). Department of Cardiology, Cardiovascular Center Aalst OLV Hospital, Belgium (S.F., B.D.B.). Columbia University Medical Center (A.J.K., A.M., M.B.L.), New York, NY. Cardiovascular Research Foundation (A.J.K., A.M., M.B.L., T.M., O.D., M.M.), New York, NY. Department of Cardiology, HaSharon Medical Center, Petach Tikva, Israel (G.G.). Department of Cardiology, Shaare Zedek Medical Center, Jerusalem, Israel (R.J.). Division of Cardiovascular Medicine, University of Pennsylvania School of Medicine, Philadelphia (D.M.K.)
Author_xml – sequence: 1
  givenname: William
  surname: Fearon
  middlename: F.
  fullname: Fearon, William F.
  organization: Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University School of Medicine, CA (W.F.F.). Department of Cardiology, Friedrich-Alexander University Erlangen-Nürnberg, Germany (S.A.). The Heart Center, Rigs Hospital, University of Copenhagen, Denmark (T.E.). Department of Cardiology, Rabin Medical Center, Petach Tikva, Israel (A.A., R.K.). Department of Cardiology, St. Francis Hospital, Roslyn, NY (R.S., A.J.). Department of Cardiology, Cardiovascular Center Aalst OLV Hospital, Belgium (S.F., B.D.B.). Columbia University Medical Center (A.J.K., A.M., M.B.L.), New York, NY. Cardiovascular Research Foundation (A.J.K., A.M., M.B.L., T.M., O.D., M.M.), New York, NY. Department of Cardiology, HaSharon Medical Center, Petach Tikva, Israel (G.G.). Department of Cardiology, Shaare Zedek Medical Center, Jerusalem, Israel (R.J.). Division of Cardiovascular Medicine, University of Pennsylvania School of Medicine, Philadelphia (D.M.K.)
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  fullname: Kirtane, Ajay J.
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  fullname: Kornowski, Ran
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  givenname: Daniel
  surname: Kolansky
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  fullname: Kolansky, Daniel M.
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  givenname: Thomas
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  fullname: McAndrew, Thomas
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  givenname: Ovidiu
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  givenname: Akiko
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  givenname: Bernard
  surname: De Bruyne
  fullname: De Bruyne, Bernard
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30586699$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1056/NEJMoa0807611
10.1016/j.jcin.2016.07.013
10.1016/j.jacbts.2017.04.003
10.1016/j.ijcard.2018.06.080
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10.1016/j.jacbts.2017.07.005
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31283372 - Circulation. 2019 Jul 9;140(2):e96-e97. doi: 10.1161/CIRCULATIONAHA.119.040942.
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Snippet BACKGROUND:Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need...
Measuring fractional flow reserve (FFR) with a pressure wire remains underutilized because of the invasiveness of guide wire placement or the need for a...
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SubjectTerms Aged
Cardiac Catheterization
Coronary Angiography - methods
Coronary Artery Disease - diagnostic imaging
Coronary Artery Disease - physiopathology
Coronary Stenosis - diagnostic imaging
Coronary Stenosis - physiopathology
Coronary Vessels - diagnostic imaging
Coronary Vessels - physiopathology
Europe
Female
Fractional Flow Reserve, Myocardial
Humans
Imaging, Three-Dimensional - methods
Israel
Male
Middle Aged
Predictive Value of Tests
Prospective Studies
Radiographic Image Interpretation, Computer-Assisted - methods
Reproducibility of Results
Severity of Illness Index
United States
Title Accuracy of Fractional Flow Reserve Derived From Coronary Angiography
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