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Selected Publication:

Mache, CJ; Beitzke, A; Haidvogl, M; Gamillscheg, A; Suppan, C; Stein, JI.
Perinatal manifestations of idiopathic long QT syndrome.
Pediatr Cardiol. 1996; 17(2):118-121 Doi: 10.1007%2Fs002469900026 (- Case Report)
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Leading authors Med Uni Graz
Mache Christoph
Co-authors Med Uni Graz
Beitzke Albrecht
Gamillscheg Andreas
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Abstract:
A neonate who had presented with sustained irregular heart rate during labor was found to have QT prolongation and repetitive polymorphic ventricular tachycardia (torsades de pointes) postnatally. Propranolol and propafenone successfully controlled the ventricular arrhythmias. Follow-up electrocardiograms and Holter records show persistent QT prolongation, bizarre T waves, and intermittent episodes of T wave alternans. On propranolol monotherapy the boy is thriving and completely free of ventricular arrhythmias. In the rare case of long QT syndrome in the neonate, early detection and therapy are mandatory to prevent ventricular arrhythmias and sudden death.
Find related publications in this database (using NLM MeSH Indexing)
Anti-Arrhythmia Agents - administration and dosage
Electrocardiography - administration and dosage
Electrocardiography, Ambulatory - administration and dosage
Fetal Diseases - diagnosis
Humans - diagnosis
Infant, Newborn - diagnosis
Long QT Syndrome - complications
Male - complications
Prenatal Diagnosis - complications
Propafenone - administration and dosage
Propranolol - administration and dosage
Tachycardia, Ventricular - diagnosis

Find related publications in this database (Keywords)
Long QT Syndrome
Neonatal Presentation
Syncope
Ventricular Arrhythmias
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