Literature DB >> 7365362

Permanent overdrive pacing for the suppression of recurrent ventricular tachycardia in a newborn with long QT syndrome.

E Di Segni, D David, M Katzenstein, H O Klein, E Kaplinsky, M J Levy.   

Abstract

A newborn with long QT interval and repetitive ventricular tachycardia of the "torsade de pointes" type was seen at the age of one day. The arrhythmia was resistant to lidocaine, propranolol and atropine, but was controlled by isoproterenol infusion. A transvenous pacemaker, inserted at three days of age, suppressed the ventricular tachycardia at stimulation rates above 100/minute. At 19 days of age a permanent pacemaker at pulse rate of 119 beats/minute was implanted. At one year of age the infant was thriving and was completely free of ventricular arrhythmia.

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Year:  1980        PMID: 7365362     DOI: 10.1016/s0022-0736(80)80053-7

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  4 in total

Review 1.  Arrhythmias in the congenital long QT syndrome: how often is torsade de pointes pause dependent?

Authors:  S Viskin; R Fish; D Zeltser; B Belhassen; K Heller; D Brosh; S Laniado; H V Barron
Journal:  Heart       Date:  2000-06       Impact factor: 5.994

2.  Prenatal findings in patients with prolonged QT interval in the neonatal period.

Authors:  M Hofbeck; H Ulmer; E Beinder; E Sieber; H Singer
Journal:  Heart       Date:  1997-03       Impact factor: 5.994

3.  Congenital and drug-induced long-QT syndrome: an update.

Authors:  X H T Wehrens; P A Doevendans
Journal:  Neth Heart J       Date:  2004-04       Impact factor: 2.380

4.  Revisiting atrial pacing in the long QT genotype era.

Authors:  Gregory Webster
Journal:  J Cardiovasc Electrophysiol       Date:  2021-02-10
  4 in total

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