Why the study?
Does automatic measurement of Tp-Te dispersion differentiate normal subjects from patients with hypertrophic cardiomyopathy, and is it reproducible?
Does automatic measurement of Tp-Te dispersion differentiate normal subjects from patients with hypertrophic cardiomyopathy, and is it reproducible?
Automatic measurement of Tp-Te dispersion fails to differentiate normal subjects from HC patients and has low reproducibility, limiting its clinical utility for risk stratification.
Tp-Te dispersion should not guide hypertrophic cardiomyopathy evaluation; leaves open QT dispersion's prognostic value in prospective studies.
Background Prolonged QT interval and QT dispersion have been reported to be associated with arrhythmogenesis in patients with cardiac disorders. However, the use of QT dispersion for risk stratification is limited by its low reproducibility. Recently, measurement of the interval between the peak and the end of the T wave (T p ‐T e interval) has been suggested for detection of repolarization abnormalities, but its clinical utility has not been studied in a systematic fashion. Methods This study assessed the intrasubject reproducibility of automatic measurements of QT end , QT peak , and T p ‐T e interval dispersion in 71 normal subjects and 37 patients with hypertrophic Cardiomyopathy (HC). A set of 20 ECGs (10 in supine and 10 in standing position) was evaluated in each subject. Measurements were performed automatically using an advanced commercial computer system. Results HC patients showed significantly higher values of QT tend , QT peak , T p ‐T e intervals, and QT end , QT peak dispersion compared to normal subjects (42 ± 20 vs 20 ± 12 ms and 45 ± 24 vs 33 ± 12 ms, respectively; P < 0.04), but no significant difference was observed in T p ‐T e dispersion between both groups (32 ± 16 vs 29 ± 8 ms; NS). The reproducibility of QT end , QT peak , and T p ‐T e dispersion, expressed as coefficients of variation, was poor in both groups (14%‐28% in normal subjects and 18% to 37% in HC patients). Conclusion Despite higher values of QT end , QT peak T p ‐T e intervals and QT end , QT peak dispersion in HC patients than in normal subjects, T p ‐T e dispersion was similar in both groups. The reproducibility of QT end , QT peak , and T p ‐T e dispersion was low. Automatic measurement of Tp‐Tp dispersion failed to differentiate normal subjects and HC patients.
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Savelieva et al. (1998) studied this question.
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