Comparative Prognostic Utility of Indexes of Microvascular Function Alone or in Combination in Patients With an Acute ST-Segment-Elevation Myocardial Infarction

被引:157
作者
Carrick, David [1 ,3 ]
Haig, Caroline [2 ]
Ahmed, Nadeem [1 ,3 ]
Carberry, Jaclyn [1 ]
May, Vannesa Teng Yue [1 ,3 ]
McEntegart, Margaret [1 ,3 ]
Petrie, Mark C. [1 ,3 ]
Eteiba, Hany [3 ]
Lindsay, Mitchell [3 ]
Hood, Stuart [3 ]
Watkins, Stuart [3 ]
Davie, Andrew [3 ]
Mahrous, Ahmed [3 ]
Mordi, Ify [1 ,3 ]
Ford, Ian [2 ]
Radjenovic, Aleksandra [1 ]
Oldroyd, Keith G. [1 ,3 ]
Berry, Colin [1 ,3 ]
机构
[1] Univ Glasgow, BHF Glasgow Cardiovasc Res Ctr, Inst Cardiovasc & Med Sci, 126 Univ Pl, Glasgow G12 8TA, Lanark, Scotland
[2] Univ Glasgow, Robertson Ctr Biostat, Glasgow, Lanark, Scotland
[3] Golden Jubilee Natl Hosp, West Scotland Heart & Lung Ctr, Clydebank, Scotland
关键词
magnetic resonance imaging; microcirculation; myocardial infarction; prognosis; PERCUTANEOUS CORONARY INTERVENTION; FRACTIONAL FLOW RESERVE; THERMODILUTION-DERIVED INDEX; ASSOCIATION TASK-FORCE; MICROCIRCULATORY RESISTANCE; MAGNETIC-RESONANCE; SUCCESSFUL REPERFUSION; PRIMARY ANGIOPLASTY; INVERSION-RECOVERY; AMERICAN-COLLEGE;
D O I
10.1161/CIRCULATIONAHA.116.022603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Primary percutaneous coronary intervention is frequently successful at restoring coronary artery blood flow in patients with acute ST-segment-elevation myocardial infarction; however, failed myocardial reperfusion commonly passes undetected in up to half of these patients. The index of microvascular resistance (IMR) is a novel invasive measure of coronary microvascular function. We aimed to investigate the pathological and prognostic significance of an IMR>40, alone or in combination with a coronary flow reserve (CFR2.0), in the culprit artery after emergency percutaneous coronary intervention for acute ST-segment-elevation myocardial infarction. Methods: Patients with acute ST-segment-elevation myocardial infarction were prospectively enrolled during emergency percutaneous coronary intervention and categorized according to IMR (40 or >40) and CFR (2.0 or >2.0). Cardiac magnetic resonance imaging was acquired 2 days and 6 months after myocardial infarction. All-cause death or first heart failure hospitalization was a prespecified outcome (median follow-up, 845 days). Results: IMR and CFR were measured in the culprit artery at the end of percutaneous coronary intervention in 283 patients with ST-segment-elevation myocardial infarction (meanSD age, 6012 years; 73% male). The median IMR and CFR were 25 (interquartile range, 15-48) and 1.6 (interquartile range, 1.1-2.1), respectively. An IMR>40 was a multivariable associate of myocardial hemorrhage (odds ratio, 2.10; 95% confidence interval, 1.03-4.27; P=0.042). An IMR>40 was closely associated with microvascular obstruction. Symptom-to-reperfusion time, TIMI (Thrombolysis in Myocardial Infarction) blush grade, and no (30%) ST-segment resolution were not associated with these pathologies. An IMR>40 was a multivariable associate of the changes in left ventricular ejection fraction (coefficient, -2.12; 95% confidence interval, -4.02 to -0.23; P=0.028) and left ventricular end-diastolic volume (coefficient, 7.85; 95% confidence interval, 0.41-15.29; P=0.039) at 6 months independently of infarct size. An IMR>40 (odds ratio, 4.36; 95% confidence interval, 2.10-9.06; P<0.001) was a multivariable associate of all-cause death or heart failure. Compared with an IMR>40, the combination of IMR>40 and CFR2.0 did not have incremental prognostic value. Conclusions: An IMR>40 is a multivariable associate of left ventricular and clinical outcomes after ST-segment-elevation myocardial infarction independently of the infarction size. Compared with standard clinical measures of the efficacy of myocardial reperfusion, including the ischemic time, ST-segment elevation, angiographic blush grade, and CFR, IMR has superior clinical value for risk stratification and may be considered a reference test for failed myocardial reperfusion. Clinical Trial Registration: URL: https//www.clinicaltrials.gov. Unique identifier: NCT02072850.
引用
收藏
页码:1833 / 1847
页数:15
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