Short QT Syndrome

Fiorenzo Gaïta(Heidelberg University), Carla Giustetto(Heidelberg University), Francesca Bianchi(Heidelberg University), Christian Wolpert(Heidelberg University), Rainer Schimpf(Heidelberg University), Riccardo Riccardi(Heidelberg University), Stefano Grossi(Heidelberg University), Elena Richiardi(Heidelberg University), Martin Borggrefe(Heidelberg University)
Circulation
August 19, 2003
Cited by 708

Abstract

BACKGROUND: A prolonged QT interval is associated with a risk for life-threatening events. However, little is known about prognostic implications of the reverse-a short QT interval. Several members of 2 different families were referred for syncope, palpitations, and resuscitated cardiac arrest in the presence of a positive family history for sudden cardiac death. Autopsy did not reveal any structural heart disease. All patients had a constantly and uniformly short QT interval at ECG. METHODS AND RESULTS: Six patients from both families were submitted to extensive noninvasive and invasive work-up, including serial resting ECGs, echocardiogram, cardiac MRI, exercise testing, Holter ECG, and signal-averaged ECG. Four of 6 patients underwent electrophysiological evaluation including programmed ventricular stimulation. In all subjects, a structural heart disease was excluded. At baseline ECG, all patients exhibited a QT interval <or=280 ms (QTc <or=300 ms). During electrophysiological study, short atrial and ventricular refractory periods were documented in all and increased ventricular vulnerability to fibrillation in 3 of 4 patients. CONCLUSIONS: The short QT syndrome is characterized by familial sudden death, short refractory periods, and inducible ventricular fibrillation. It is important to recognize this ECG pattern because it is related to a high risk of sudden death in young, otherwise healthy subjects.


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