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Manifestation of Long QT syndrome with normal QTc interval under anesthesia: a case report.

Abstract
Patients with congenital Long QT are known to have normal QT interval in symptom-free period and in the early years of life. Precipitating factors like surgical stress, interactions with anesthetic agents prolonging QT interval, and electrolyte imbalances can manifest with life threatening arrhythmias in congenital or acquired Long QT syndrome. We report a case of concealed LQTS manifesting under anesthesia and its subsequent perioperative course.
AuthorsBanashree Mandal, Gurpreet Kaur, Yatindra K Batra, Sachin Mahajan
JournalPaediatric anaesthesia (Paediatr Anaesth) Vol. 21 Issue 12 Pg. 1265-7 (Dec 2011) ISSN: 1460-9592 [Electronic] France
PMID21824216 (Publication Type: Case Reports, Journal Article)
Copyright© 2011 Blackwell Publishing Ltd.
Chemical References
  • Adrenergic alpha-Agonists
  • Anti-Arrhythmia Agents
  • Atracurium
  • Potassium Chloride
  • Atropine
  • Fentanyl
  • Propofol
  • Epinephrine
Topics
  • Adrenergic alpha-Agonists
  • Anesthesia (methods)
  • Anti-Arrhythmia Agents
  • Atracurium
  • Atropine
  • Cardiopulmonary Resuscitation
  • Ductus Arteriosus, Patent (complications, surgery)
  • Electric Countershock
  • Electrocardiography (methods)
  • Epinephrine
  • Fentanyl
  • Humans
  • Hypocalcemia (complications, drug therapy)
  • Infant
  • Long QT Syndrome (complications, diagnosis, therapy)
  • Male
  • Potassium Chloride (administration & dosage)
  • Propofol
  • Ventricular Fibrillation (diagnosis, etiology, therapy)

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