Abstract
Torsades de Pointes (TdP) is a life-threatening ventricular arrhythmia that can be associated with metabolic abnormalities, exposure to arrhythmogenic medications, and congenital long-QT syndrome. This report describes a patient with ALL and multiple complications of therapy who developed TdP. The patient had no evidence of congenital long-QT syndrome, but a constellation of factors appears to have led to QT prolongation, ventricular ectopy, and TdP. Although the patient suffered cardiac arrest, rapid recognition of TdP and prompt defibrillation resulted in an excellent outcome.
Original language | English (US) |
---|---|
Pages (from-to) | 996-999 |
Number of pages | 4 |
Journal | Pediatric Blood and Cancer |
Volume | 49 |
Issue number | 7 |
DOIs | |
State | Published - Dec 2007 |
Keywords
- Acute lymphocytic leukemia
- Cardiac arrest
- Torsades de Pointes
- Ventricular arrhythmia
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Hematology
- Oncology