Clinical implications of serial changes in ST-segment elevation after reperfusion in patients with anterior acute myocardial infarction

Circ J. 2008 Mar;72(3):409-14. doi: 10.1253/circj.72.409.

Abstract

Background: In patients with acute myocardial infarction (AMI), the relationship of serial changes in ST-segment elevation after reperfusion to left ventricular (LV) function remains unclear.

Methods and results: The study group comprised 164 patients with reperfused anterior AMI within 6 h of symptom onset. The sum of ST-segment deviation was calculated on admission (SigmaST-admission), and 1 h (SigmaST-1 h) and 24 h (SigmaST-24 h) after reperfusion. ST resolution was defined as a reduction in SigmaST-1 h of > or =50% as compared with SigmaST-admission. Patients were classified into 3 groups: group A, 82 patients with ST resolution in whom SigmaST-1 h > or = SigmaST-24 h; group B, 37 patients with ST resolution in whom SigmaST-1 h < SigmaST-24 h; group C, 45 patients without ST resolution. Peak creatine kinase were higher in groups B and C than in group A (4,578+/-2,176, 4,236+/-2,638, 2,222+/-1,926 mU/ml, p<0.01). At 6 months follow-up, the LV ejection fraction were lower in groups B and C than in group A (53+/-8, 54+/-12, 62+/-9%, p<0.01).

Conclusions: An increase in ST-segment elevation 1-24 h after reperfusion, despite ST resolution, is associated with a larger infarction and poorer LV function in patients with reperfused anterior AMI.

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Aged, 80 and over
  • C-Reactive Protein / metabolism
  • Creatine Kinase / blood
  • Electrocardiography*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Myocardial Infarction / diagnosis
  • Myocardial Infarction / pathology*
  • Myocardial Infarction / physiopathology*
  • Myocardial Reperfusion*
  • Predictive Value of Tests
  • Prognosis
  • Stroke Volume / physiology
  • Time Factors
  • Ventricular Dysfunction, Left / physiopathology*

Substances

  • C-Reactive Protein
  • Creatine Kinase