Impact of the Presence and Extent of Incomplete Angiographic Revascularization After Percutaneous Coronary Intervention in Acute Coronary Syndromes

  • Gregg F. Rosner
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Ajay J. Kirtane
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Philippe Genereux
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Alexandra J. Lansky
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Ecaterina Cristea
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Bernard J. Gersh
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Giora Weisz
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Helen Parise
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Martin Fahy
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Roxana Mehran
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).
  • Gregg W. Stone
    From the New York–Presbyterian Hospital, Columbia University Medical Center and Cardiovascular Research Foundation, New York, NY (G.F.R., A.J.K., P.G., A.J.L., E.C., G.W., H.P., M.F., R.M., G.W.S.), and Mayo Clinic, Rochester, MN (B.J.G.).

Bibliographic Information

Other Title
  • The Acute Catheterization and Urgent Intervention Triage Strategy (ACUITY) Trial

Description

<jats:sec> <jats:title>Background—</jats:title> <jats:p>The clinical significance of incomplete coronary revascularization (ICR) after percutaneous coronary intervention in patients with acute coronary syndromes is unknown.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods and Results—</jats:title> <jats:p> We performed quantitative angiography of the entire coronary tree in 2954 patients with acute coronary syndromes in the Acute Catheterization and Urgent Intervention Triage Strategy (ACUITY) trial. ICR was variably defined if any lesion with diameter stenosis (DS) cutoffs ranging from ≥30% to ≥70% with reference vessel diameter ≥2.0 mm remained after percutaneous coronary intervention. The primary outcome was 1-year composite rate of major adverse cardiac events (death, myocardial infarction, or ischemia-driven unplanned revascularization). With the use of DS cutoffs ≥30%, ≥40%, ≥50%, ≥60%, and ≥70%, the prevalence of ICR after percutaneous coronary intervention was 75%, 55%, 37%, 25%, and 17%, respectively. The 1-year major adverse cardiac event rate was increased among patients with ICR using all of the DS cutoffs. ICR (≥50% DS) was associated with higher 1-year rates of myocardial infarction (12.0% versus 8.2%; hazard ratio, 1.50; 95% confidence interval, 1.18–1.89; <jats:italic>P</jats:italic> =0.0007) and ischemia-driven unplanned revascularization (15.7% versus 10.2%; hazard ratio, 1.58; 95% confidence interval, 1.28–1.96; <jats:italic>P</jats:italic> <0.0001), with a trend toward increased mortality (3.1% versus 2.2%; hazard ratio, 1.43; 95% confidence interval, 0.90–2.27; <jats:italic>P</jats:italic> =0.13). By multivariable analysis, ICR (≥50% DS) was an independent predictor of 1-year major adverse cardiac events (hazard ratio, 1.36; 95% confidence interval, 1.12–1.64; <jats:italic>P</jats:italic> =0.002). The impact of ICR on major adverse cardiac events was similar regardless of chronic total occlusion presence, but it was more pronounced with a greater number of nonrevascularized lesions. </jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions—</jats:title> <jats:p>Depending on the threshold of percent DS, ICR was present in 17% to 75% of patients with acute coronary syndromes after percutaneous coronary intervention. Regardless of the threshold, ICR was strongly associated with 1-year myocardial infarction, ischemia-driven unplanned revascularization, and major adverse cardiac events.</jats:p> </jats:sec> <jats:sec> <jats:title>Clinical Trial Registration—</jats:title> <jats:p> URL: <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.clinicaltrials.gov">http://www.clinicaltrials.gov</jats:ext-link> . Unique identifier: NCT00093158. </jats:p> </jats:sec>

Journal

  • Circulation

    Circulation 125 (21), 2613-2620, 2012-05-29

    Ovid Technologies (Wolters Kluwer Health)

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