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)
Web of Science
PubMed
FullText
FullText_MUG
- Leading authors Med Uni Graz
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Mache Christoph
- Co-authors Med Uni Graz
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Beitzke Albrecht
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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)
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Anti-Arrhythmia Agents - administration and dosage
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Electrocardiography - administration and dosage
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Electrocardiography, Ambulatory - administration and dosage
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Fetal Diseases - diagnosis
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Humans - diagnosis
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Infant, Newborn - diagnosis
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Long QT Syndrome - complications
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Male - complications
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Prenatal Diagnosis - complications
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Propafenone - administration and dosage
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Propranolol - administration and dosage
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Tachycardia, Ventricular - diagnosis
- Find related publications in this database (Keywords)
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Long QT Syndrome
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Neonatal Presentation
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Syncope
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Ventricular Arrhythmias