Key result
Administration of mexiletine successfully controlled fatal ventricular arrhythmia (Torsades de Pointes) in a postpartum patient with long QT syndrome and peripartum cardiomyopathy.
Why the study?
Although rare, long QT syndrome and peripartum cardiomyopathy are major causes of maternal cardiovascular death.
Case Report (n=1)
No
Answers are grounded in this paper and cite their sources.
In patients with Long-QT syndrome and peripartum cardiomyopathy, careful management of electrolyte balance and circulating volume is crucial to prevent life-threatening ventricular arrhythmias triggered by diuretic use.
Although rare, long QT syndrome (LQTS) and peripartum cardiomyopathy (PPCM) are the major causes of maternal cardiovascular death. We herein present a case study of a 23-year-old woman with LQTS, pregnancy-induced hypertension, and PPCM. During the postpartum period, her left ventricular systolic function had severely decreased, requiring the administration of loop diuretics. Diuretics cause several changes in the circulating blood volume, electrolyte balance, and hormonal status during pregnancy, delivery, and the peripartum period. Extreme QTc prolongation and fatal ventricular arrhythmia require frequent defibrillation. For the patient in this study, we corrected her electrolyte abnormality, and eventually, we controlled the arrhythmia by administering a β-blocker and Na-channel blocker. Although the arrhythmia subsided, she continued on medication after discharge to prevent the recurrence of fatal arrhythmia. In conclusion, close attention should be paid to patients with LQTS, especially when some changes that may lead to QTc prolongation could occur during the peripartum period.
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Nakatsukasa et al. (2023) conducted a case report in Long-QT Syndrome and Peripartum Cardiomyopathy (n=1). Mexiletine was evaluated on Suppression of ventricular arrhythmia (Torsades de Pointes). Administration of mexiletine successfully controlled fatal ventricular arrhythmia (Torsades de Pointes) in a postpartum patient with long QT syndrome and peripartum cardiomyopathy.
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