What is the Optimal Evaluation Time of the QT Dispersion After Acute Myocardial Infarction for the Risk Stratification?

• Published in: Angiology Vol. 52; no. 7; pp. 463 - 468
• Main Authors: Kabakci, G., Önalan, O., Kemal Batur, M., Yildirir, A., Çağrikul, R., Açil, T., Tokgözoğlu, L., Oto, A., Özmen, F., Kes, S.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Thousand Oaks, CA SAGE Publications 01.07.2001; Westminster; Sage Publications, Inc; SAGE PUBLICATIONS, INC
• Subjects: Biological and medical sciences; Death; Electrocardiography; Electrocardiography. Vectocardiography; Electrodiagnosis. Electric activity recording; Evaluation; Female; Heart attack; Humans; Investigative techniques, diagnostic techniques (general aspects); Male; Medical sciences; Middle Aged; Myocardial Infarction - drug therapy; Myocardial Infarction - mortality; Myocardial Infarction - physiopathology; Reproducibility of Results; Risk assessment; Risk Factors; Tachycardia, Ventricular - diagnosis; Thrombolytic Therapy; Time Factors; Ventricular Fibrillation - diagnosis; United States; Human; QT interval; Prognosis; Infarct; Arrhythmia; Acute; Treatment efficiency; Cardiovascular disease; Exploration; Risk analysis; Coronary heart disease; Myocardial disease; Fibrinolysis; Dispersion; Electrodiagnosis; Treatment; Heart disease; Electrocardiography; Myocardium; Complication; Timing
• ISSN: 0003-3197; 1940-1574
• DOI: 10.1177/000331970105200704

The sequential changes of the corrected QT dispersion (QTcD) were studied in 136 patients 1 day to 30 days after a transmural acute myocardial infarction (AMI) to investigate the optimal measurement time of QT dispersion for risk stratification. The study group included 136 patients (89 men; mean age, 57 ±10 years) with transmural AMI who were treated with throm bolytics (Tr+ group, n = 73) or not (Tr- group, n = 63) and 65 healthy controls (43 men; mean age, 56 ±7 years). Fourteen patients in whom ventricular tachycardia (VT), ventricular fibrilla tion (VF), or sudden cardiac death developed during the 30-day period were also evaluated as major cardiac arrhythmia (MCA) group. ECGs were obtained for each patient on days 1, 3, 5, 10, 15, and 30 after AMI. QTc dispersion in patients with AMI (for every period of QTcD after MI) was significantly more prolonged than in normal controls (49.3 ± 16.3 ms) (p < 0.001). QTcD was significantly greater in patients without thrombolytics than in patients with thrombolytics for every period (days 1, 3, 5, 10, 15, and 30) of QTcD after MI (p < 0.001). The mean of QTcD was significantly greater in patients with MCA than in patients without MCA group for every period (days 1, 3, 5, 10, 15, and 30) of QTcD after MI (p < 0.05). Maximal QTcD was seen on day 10 (p < 0.05 1st vs day 10 for each group) after myocardial infarction, and then reached a plateau for an each group. The ideal time to measure the QTD for risk stratification is at least 10 days after AMI.