TY - JOUR
T1 - Impact of early vs. late microvascular obstruction assessed by magnetic resonance imaging on long-term outcome after ST-elevation myocardial infarction: A comparison with traditional prognostic markers
AU - De Waha, Suzanne
AU - Desch, Steffen
AU - Eitel, Ingo
AU - Fuernau, Georg
AU - Zachrau, Johannes
AU - Leuschner, Anja
AU - Gutberlet, Matthias
AU - Schuler, Gerhard
AU - Thiele, Holger
PY - 2010/11/1
Y1 - 2010/11/1
N2 - Aims Early and late microvascular obstruction (MO) assessed by magnetic resonance imaging (MRI) are prognostic markers for combined clinical endpoints after ST-elevation myocardial infarction (STEMI). However, there are only limited data for hard endpoints and no consensus exists which of the two best predicts clinical outcome. Furthermore, it is unclear whether the assessment of MO by MRI adds incremental prognostic information independent of traditional outcome markers. Methods and resultsSTEMI patients reperfused by primary angioplasty (n = 438) <12 h after symptom onset underwent MRI at a median of 3 days after the index event. Microvascular obstruction was measured 1 and 15 min after gadolinium injection (early and late MO). Clinical follow-up was conducted after a median of 19 months. The primary endpoint was defined as a composite of death, non-fatal myocardial re-infarction, and congestive heart failure. In contrast to the presence and extent of early MO, the presence and extent of late MO were independently associated with the composite primary endpoint in the multivariable Cox regression analysis adjusting for post-percutaneous coronary intervention TIMI-flow, ST-resolution, TIMI-risk score, ejection fraction, and infarct size. The presence of late MO was identified as the strongest independent predictor for the occurrence of the composite endpoint (hazard ratio 4.23, 95CI 1.73-10.34, P = 0.002). Furthermore, the presence and extent of late MO provided an incremental prognostic value above the traditional prognostic markers. Conclusion In contrast to early MO, the presence and extent of late MO are strong independent prognosticators after STEMI.www.ClinicalTrials.gov: NCT00299377.
AB - Aims Early and late microvascular obstruction (MO) assessed by magnetic resonance imaging (MRI) are prognostic markers for combined clinical endpoints after ST-elevation myocardial infarction (STEMI). However, there are only limited data for hard endpoints and no consensus exists which of the two best predicts clinical outcome. Furthermore, it is unclear whether the assessment of MO by MRI adds incremental prognostic information independent of traditional outcome markers. Methods and resultsSTEMI patients reperfused by primary angioplasty (n = 438) <12 h after symptom onset underwent MRI at a median of 3 days after the index event. Microvascular obstruction was measured 1 and 15 min after gadolinium injection (early and late MO). Clinical follow-up was conducted after a median of 19 months. The primary endpoint was defined as a composite of death, non-fatal myocardial re-infarction, and congestive heart failure. In contrast to the presence and extent of early MO, the presence and extent of late MO were independently associated with the composite primary endpoint in the multivariable Cox regression analysis adjusting for post-percutaneous coronary intervention TIMI-flow, ST-resolution, TIMI-risk score, ejection fraction, and infarct size. The presence of late MO was identified as the strongest independent predictor for the occurrence of the composite endpoint (hazard ratio 4.23, 95CI 1.73-10.34, P = 0.002). Furthermore, the presence and extent of late MO provided an incremental prognostic value above the traditional prognostic markers. Conclusion In contrast to early MO, the presence and extent of late MO are strong independent prognosticators after STEMI.www.ClinicalTrials.gov: NCT00299377.
UR - http://www.scopus.com/inward/record.url?scp=78149337886&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehq247
DO - 10.1093/eurheartj/ehq247
M3 - Journal articles
C2 - 20675660
AN - SCOPUS:78149337886
SN - 0195-668X
VL - 31
SP - 2660
EP - 2668
JO - European Heart Journal
JF - European Heart Journal
IS - 21
ER -