Concealed congenital long QT syndrome during velopharyngeal dysfunction correction: a case report.
Electrocardiogram
Long QT Syndrome
Torsades de Pointes
Journal
Journal of dental anesthesia and pain medicine
ISSN: 2383-9309
Titre abrégé: J Dent Anesth Pain Med
Pays: Korea (South)
ID NLM: 101690691
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
08
04
2020
revised:
07
05
2020
accepted:
12
05
2020
entrez:
4
7
2020
pubmed:
4
7
2020
medline:
4
7
2020
Statut:
ppublish
Résumé
The congenital long QT syndrome (LQTS) is an inherited cardiac disorder characterized by increased QT intervals and a tendency to experience ventricular tachycardia, which can cause fainting, heart failure, or sudden death. A 4-year-old female patient undergoing velopharyngeal correction surgery under general anesthesia suddenly developed Torsades de pointes. Although the patient spontaneously resolved to sinus rhythm without treatment, subsequent QT prolongation persisted. Here, we report a case of concealed LQTS with a literature review.
Identifiants
pubmed: 32617412
doi: 10.17245/jdapm.2020.20.3.165
pmc: PMC7321742
doi:
Types de publication
Case Reports
Langues
eng
Pagination
165-171Informations de copyright
Copyright © 2020 Journal of Dental Anesthesia and Pain Medicine.
Déclaration de conflit d'intérêts
DECLARATION OF INTERESTS: All authors declare that they have no competing interests.
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