Dispersion in ventricular repolarization in patients with severe intraventricular conduction disturbances

Citation
A. Englund et al., Dispersion in ventricular repolarization in patients with severe intraventricular conduction disturbances, PACE, 24(7), 2001, pp. 1067-1075
Citations number
49
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
ISSN journal
01478389 → ACNP
Volume
24
Issue
7
Year of publication
2001
Pages
1067 - 1075
Database
ISI
SICI code
0147-8389(200107)24:7<1067:DIVRIP>2.0.ZU;2-C
Abstract
Increased dispersion of repolarization, measured invasively or by QT interv al measurements, is associated with an increased risk for ventricular arrhy thmias and sudden death. Most studies on this issue have included patients with normal intraventricular conduction, and it is not known if this findin g has a predictive value also in patients with intraventricular conduction disorders. An invasive electrophysiological study, including programmed ven tricular stimulation and assessment of effective refractory periods at two RV sites, was performed in 103 patients with bifascicular block (mean age 6 7 +/- 12 years). QT dispersion was measured from standard 12-lead ECGs. In patients with inducible sustained polymorphic VT or VF the dispersion in re fractoriness between the two RV sites was significantly greater (46 +/- 11 ms, n = 13) than in noninducible patients (14 +/- 14 ms, n = 84) and in pat ients with inducible sustained monomorphic VT (16 +/- 5 ms, n = 6) (P < 0.0 1). Similarly, QT dispersion was 104 +/- 46 ms, 66 +/- 31 ms, and 77 +/- 33 ms, respectively, in the three groups (P < 0.05). Dispersion in repolariza tion, neither measured invasively nor by QT interval measurements, predicte d sudden death, all cause mortality or ventricular arrhythmia during a mean follow-up period of 3 years. In patients with bifascicular block, there is a relation between the degree of dispersion of ventricular repolarization and the inducibility of polymorphic ventricular arrhythmia, but this outcom e did not occur during follow-up.