Register for email alerts and news feeds:
This journal | BMJ Group
rss
Heart 2005;91:15-17; doi:10.1136/hrt.2004.039271
Copyright © 2005 BMJ Publishing Group Ltd & British Cardiovascular Society
Heart 2005;91:15-17
© 2005 by BMJ Publishing Group & British Cardiac Society

FEATURED CASE REPORT

Bilateral thoracoscopic cervical sympathectomy for the treatment of recurrent polymorphic ventricular tachycardia

A J Turley, J Thambyrajah, A A Harcombe

Cardiothoracic Division, The James Cook University Hospital, Middlesbrough, UK

Correspondence to:
Correspondence to:
Dr Andrew J Turley
Cardiothoracic Division, The James Cook University Hospital, Marton Road, Middlesbrough TS4 3BW, UK; andrew.turley{at}stees.nhs.uk

ABSTRACT

Congenital long QT syndrome (LQTS) is a disorder of prolonged cardiac repolarisation, manifest by a prolonged QT interval and characterised by recurrent presyncope/syncope, polymorphic ventricular tachycardia (PMVT), or sudden cardiac death. A 46 year old woman with no family history of sudden death or deafness presented with recurrent syncope. Physical examination and electrolytes were normal and a 12 lead ECG showed a corrected QT interval of 458 ms. A monitored syncopal episode documented PMVT. Despite potassium and magnesium supplements, ß blockade, implantation of a single then dual chamber implantable cardioverter defibrillator (ICD), amiodarone, nicorandil, and mexiletine, the patient continued to experience arrhythmia storms, receiving more than 700 ICD discharges over seven months. She was ultimately treated successfully with bilateral thoracoscopic cervicothoracic sympathectomies. This is the first reported bilateral thoracoscopic treatment of a patient with LQTS and symptomatic life threatening ventricular tachyarrhythmias refractory to current pharmacological and pacing techniques.

Abbreviations: ICD, implantable cardioverter defibrillator; LQTS, long QT syndrome; PMVT, polymorphic ventricular tachycardia

Keywords: long QT syndrome; polymorphic ventricular tachycardia; stellate ganglion blockade; thoracoscopic sympathectomy


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Vincent, G. M. (2008). Genotyping Has a Minor Role in Selecting Therapy for Congenital Long-QT Syndromes at Present. Circ Arrhythm Electrophysiol 1: 227-233 [Full Text]  

eLetters:

Read all eLetters

Bilateral thoracoscopic cervical sympathectomy for the treatment of recurrent polymorphic ventricula
Andrew J Turley, et al.
Online, 2 Aug 2005 [Full text]

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.