Zero-Flow Pressure Measured Immediately After Primary Percutaneous Coronary Intervention for ST-Segment Elevation Myocardial Infarction Provides the Best Invasive Index for Predicting the Extent of Myocardial Infarction at 6 Months: An OxAMI Study (Oxford Acute Myocardial Infarction)
- PMID: 26404192
- DOI: 10.1016/j.jcin.2015.04.029
Zero-Flow Pressure Measured Immediately After Primary Percutaneous Coronary Intervention for ST-Segment Elevation Myocardial Infarction Provides the Best Invasive Index for Predicting the Extent of Myocardial Infarction at 6 Months: An OxAMI Study (Oxford Acute Myocardial Infarction)
Abstract
Objectives: The aim of this study was to define which measure of microvascular best predicts the extent of left ventricular (LV) infarction.
Background: Microvascular injury after ST-segment elevation myocardial infarction (STEMI) is an important determinant of outcome. Several invasive measures of the microcirculation at primary percutaneous coronary intervention (PPCI) have been described. One such measure is zero-flow pressure (Pzf), the calculated pressure at which coronary flow would cease.
Methods: In 34 STEMI patients, Pzf, hyperemic microvascular resistance (hMR), and index of microcirculatory resistance (IMR) were derived using thermodilution flow/pressure and Doppler flow/pressure wire assessment of the infarct-related artery following PPCI. The extent of infarction was determined by blinded late gadolinium enhancement on cardiac magnetic resonance at 6 months post-PPCI. Infarction of ≥24% total LV mass was used as a categorical cutoff in receiver-operating characteristic curve analysis.
Results: Pzf was superior to both hMR and IMR for predicting ≥24% infarction area under the curve: 0.94 for Pzf versus 0.74 for hMR (p = 0.04) and 0.54 for IMR (p = 0.003). Pzf ≥42 mm Hg was the optimal cutoff value, offering 100% sensitivity and 73% specificity. Patients with Pzf ≥42 mm Hg also had a lower salvage index (61.3 ± 8.1 vs. 44.4 ± 16.8, p = 0.006) and 6-month ejection fraction (62.4 ± 3.6 vs. 49.9 ± 9.6, p = 0.002). In addition, there were significant direct relationships between Pzf and troponin area under the curve (rho = 0.55, p = 0.002), final infarct mass (rho = 0.75, p < 0.0001), percentage of LV infarction and percent transmurality of infarction (rho = 0.77 and 0.74, respectively, p < 0.0001), and inverse relationships with myocardial salvage index (rho = -0.53, p = 0.01) and 6-month ejection fraction (rho = -0.73, p = 0.0001).
Conclusions: Pzf measured at the time of PPCI is a better predictor of the extent of myocardial infarction than hMR or IMR. Pzf may provide important prognostic information at the time of PPCI and merits further investigation in clinical studies with relevant outcome measures.
Keywords: angioplasty; magnetic resonance imaging; microcirculation; myocardial infarction; physiology.
Copyright © 2015 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Comment in
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Is Coronary Wedge Pressure a Technique to Identify High-Risk Patients Who May Benefit From Alternative Treatment in Acute Myocardial Infarction?: Is This The Next Step?JACC Cardiovasc Interv. 2016 Jan 11;9(1):104-105. doi: 10.1016/j.jcin.2015.10.018. JACC Cardiovasc Interv. 2016. PMID: 26762918 No abstract available.
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Reply: Is Coronary Wedge Pressure a Technique to Identify High-Risk Patients Who May Benefit From Alternative Treatment in Acute Myocardial Infarction?: Is This The Next Step?JACC Cardiovasc Interv. 2016 Jan 11;9(1):105. doi: 10.1016/j.jcin.2015.10.016. JACC Cardiovasc Interv. 2016. PMID: 26762920 No abstract available.
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Microvascular Function in Ischemic Heart Disease: There May Be Room for Improvement.JACC Cardiovasc Interv. 2016 Feb 22;9(4):392-393. doi: 10.1016/j.jcin.2015.10.041. Epub 2016 Jan 6. JACC Cardiovasc Interv. 2016. PMID: 26777333 No abstract available.
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Reply: Microvascular Function in Ischemic Heart Disease: There May Be Room for Improvement.JACC Cardiovasc Interv. 2016 Feb 22;9(4):394-395. doi: 10.1016/j.jcin.2015.11.026. JACC Cardiovasc Interv. 2016. PMID: 26892089 No abstract available.
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