Time-frequency mapping of the QRS complex in normal subjects and in postmyocardial infarction patients

Journal of Electrocardiology(1994)

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摘要
The effect of myocardial infarction upon the frequency content of the QRS complex was analyzed. Three bipolar signal-averaged surface electrograms, recorded during the early (10–15 days) and late (6 months) chronic phases of myocardial infarction, were analyzed in 61 patients and 11 healthy subjects. All patients were free of ventricular arrhythmia during 6 months of follow-up examinations. Time-frequency analysis of the QRS complex was based on the modified Wigner distribution, which is well suited to examine nonstationary character of data. Standard time-domain analysis for the presence of late potentials was used for comparison. High-frequency (≥90 Hz) components, separable from the dominant low-frequency components (<90 Hz), were found in all groups. They were present throughout the QRS complex and were peaking in its middle portion. The high-frequency components were found significantly higher in postinfarction patients in both early (P < .007) and late chronic stage myocardial infarction (P < .05) compared to healthy subjects. Patients who tested positive for late potentials (24%) also had elevated high-frequency components; however, a comparable increase was also observed in late potential negative patients. Furthermore, the high-frequency component increase occurred in all patients earlier in the QRS than in its terminal 40 ms, where late potentials are traditionally evaluated. It is concluded that high-frequency components are an integral part of the QRS complex under physiologic conditions and persist in variable amount throughout its duration. The high-frequency components are increased in patients after myocardial infarction not associated with ventricular arrhythmia, and their elevation is not limited to the terminal QRS complex.
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关键词
electrocardiography,myocardial infarction,ventricular activation,time-frequency mapping,Wigner distribution,late ventricular potentials
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