Predictors of cardiovascular magnetic resonance-derived microvascular obstruction on patient admission in STEMI

被引:19
作者
Husser, Oliver [1 ,2 ]
Bodi, Vicente [1 ]
Sanchis, Juan [1 ]
Nunez, Julio [1 ]
Lopez-Lereu, Maria P. [3 ]
Monmeneu, Jose V. [3 ]
Gomez, Cristina [1 ]
Rumiz, Eva [1 ]
Merlos, Pilar [1 ]
Bonanad, Clara [1 ]
Minana, Gema [1 ]
Valero, Ernesto [1 ]
Chaustre, Fabian [1 ]
Forteza, Maria J. [1 ]
Riegger, Guenter A. J. [2 ]
Chorro, Francisco J. [1 ]
Llacer, Angel [1 ]
机构
[1] Univ Valencia, Dept Cardiol, Hosp Clin Univ, INCLIVA, Valencia 46010, Spain
[2] Univ Regensburg, Med Ctr, Klin & Poliklin Innere Med 2, D-93053 Regensburg, Germany
[3] ERESA, Unit Cardiovasc Magnet Resonance Imaging, Valencia, Spain
关键词
Cardiovascular magnetic resonance; ST-elevation myocardial infarction; Microvascular obstruction; ACUTE MYOCARDIAL-INFARCTION; ST-SEGMENT ELEVATION; PRIMARY ANGIOPLASTY; PROGNOSTIC-SIGNIFICANCE; NO-REFLOW; REPERFUSION; RECOVERY; ECHOCARDIOGRAPHY; THROMBOLYSIS; ISCHEMIA;
D O I
10.1016/j.ijcard.2011.09.083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Early stratification of patients according to the risk for developing microvascular obstruction (MVO) after ST-segment elevation myocardial infarction (STEMI) is desirable. We aimed to identify predictors of cardiovascular magnetic resonance (CMR)-derived MVO from clinical + ECG, laboratory and angiographic parameters available on admission. Methods: Characteristics available on admission were documented in 97 STEMI patients referred for primary angioplasty. MVO was determined using contrast-enhanced CMR. Results: MVO was present in 44 patients (45%). The C-statistic for predicting MVO was: clinical + ECG (.832), laboratory (.743), and angiographic parameters (.669). Adding laboratory to clinical + ECG information did not improve the C-statistic (.873 vs. .832, p = .2). Further addition of angiographic data (.904) improved the C-statistic of clinical + ECG (p =. 04) but not of clinical + ECG and laboratory (p = .2). Independent predictors of MVO using clinical and ECG parameters were: Killip class >1 (OR 15.97 95%CI [1.37-186.76], p = .03), diabetes (OR 6.15 95%CI [1.49-25.39], p = .01), age <55 years (OR 4.70 95%CI [1.56-14.17], p = .006), sum of ST-segment elevation >10 mm (OR 4.5 95%CI [1.58-12.69], p = .005) and delayed presentation >3 h (OR 3.80 95%CI [1.19-12.1], p = .02). A score was constructed assigning Killip class >1 2 points and the remaining indexes 1 point. The incidence of MVO increased with the score: 0 point: 8.7%; 1 point: 28.1%; 2 points: 71.4%; and 3+ points: 93% (p < .0001). Conclusions: MVO can be predicted using parameters already available on patient admission. We developed a clinical-ECG score allowing for early and reliable classification of STEMI patients according to the risk of MVO. (c) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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