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Sleep-Associated Torsades de Pointes: A Case Report
1SUNY Downstate University Hospital of Brooklyn, Kings County Hospital Center, Department of Emergency Medicine, Brooklyn, New York.
Clinical Practice and Cases in Emergency Medicine
|June 1, 2018
Summary
Torsades de Pointes (TdP) is a rare heart rhythm. This case study highlights a patient with acquired Long QT Syndrome (LQTS) who experienced TdP episodes due to methadone and renal disease.
Area of Science:
- Cardiology
- Clinical Electrophysiology
- Pharmacology
Background:
- Torsades de Pointes (TdP) is a life-threatening ventricular arrhythmia associated with Long QT Syndrome (LQTS).
- Acquired LQTS can result from various factors, including medications and electrolyte imbalances, particularly in patients with chronic conditions.
Observation:
- A 57-year-old male with end-stage renal disease on methadone maintenance therapy presented with recurrent TdP episodes during sleep.
- Electrocardiogram revealed a significantly prolonged QTc interval (548 milliseconds), indicative of QT prolongation.
Findings:
- The patient's TdP was successfully managed by discontinuing methadone and initiating isoproterenol infusion.
- A multifactorial acquired LQTS, exacerbated by somnolence, was identified as the likely cause of the TdP episodes.
Implications:
- This case underscores the critical need to monitor QTc intervals in patients with risk factors for acquired LQTS, especially those on methadone.
- Management strategies involving medication adjustment and targeted therapies like isoproterenol can effectively treat TdP in susceptible individuals.
- Understanding the interplay of renal disease, methadone, and QT prolongation is crucial for preventing TdP in complex patient populations.
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