Endoscopic thoracic sympathectomy for long QT syndrome
1Department of Vascular Surgery, St Vincent's University Hospital, Dublin 4, Ireland. iangmurphy@gmail.com
Irish Journal of Medical Science
|February 26, 2008
Summary
A minimally invasive cardiac sympathectomy effectively treated a patient with drug-resistant ventricular arrhythmias from familial long-QT syndrome. This endoscopic procedure provided significant relief from recurrent defibrillator shocks.
Area of Science:
- Cardiology
- Thoracic Surgery
- Clinical Electrophysiology
Background:
- Patient presented with intractable ventricular arrhythmias due to familial long-QT syndrome.
- Previous treatment included an Automatic Implantable Cardioverter Defibrillator (AICD) and sympathetic blockers.
- Ongoing tachyarrhythmias and AICD shocks caused significant patient distress.
Observation:
- The patient underwent a left transthoracic endoscopic cardiac sympathectomy.
- The procedure was technically successful with a good postoperative recovery.
Findings:
- The patient remained asymptomatic at four months post-procedure.
- Endoscopic cardiac sympathectomy demonstrated efficacy in managing refractory ventricular arrhythmias.
Implications:
- Thoracoscopic sympathetic cardiac denervation offers a less invasive alternative to open sympathectomy.
- This case highlights the potential of minimally invasive techniques for managing complex arrhythmias.
- Further research into thoracoscopic sympathetic denervation for long-QT syndrome is warranted.
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