6533b820fe1ef96bd127a52d

RESEARCH PRODUCT

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

Cristina GomezErnesto ValeroMaria Pilar López‐lereuJose V. MonmeneuClara BonanadPilar MerlosJuan SanchisFabian ChaustreGema MiñanaJulio NúñezMaria J. FortezaOliver HusserÀNgel LlàcerFrancisco J. ChorroGünter A.j. RieggerEva RumizVicente Bodi

subject

AdultMalemedicine.medical_specialtyMyocardial InfarctionMagnetic Resonance Imaging CineCoronary Artery DiseaseDelayed presentationPatient AdmissionPredictive Value of TestsCoronary CirculationDiabetes mellitusInternal medicineHumansMedicineProspective Studiescardiovascular diseasesMyocardial infarctionProspective cohort studyAgedKillip classmedicine.diagnostic_testbusiness.industryMicrocirculationMagnetic resonance imagingMiddle Agedmedicine.diseaseSurgeryPredictive value of testsCardiologyFemaleMyocardial infarction diagnosisCardiology and Cardiovascular Medicinebusinesshuman activities

description

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.Characteristics available on admission were documented in 97 STEMI patients referred for primary angioplasty. MVO was determined using contrast-enhanced CMR.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 class1 (OR 15.97 95%CI [1.37-186.76], p=.03), diabetes (OR 6.15 95%CI [1.49-25.39], p=.01), age55years (OR 4.70 95%CI [1.56-14.17], p=.006), sum of ST-segment elevation10mm (OR 4.5 95%CI [1.58-12.69], p=.005) and delayed presentation3h (OR 3.80 95%CI [1.19-12.1], p=.02). A score was constructed assigning Killip class1 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).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.

https://doi.org/10.1016/j.ijcard.2011.09.083