Video-Assisted Thoracoscopic Cardiac Denervation: A Potential Novel Therapeutic Option for Children With Intractable Ventricular Arrhythmias

被引:65
作者
Atallah, Joseph
Fynn-Thompson, Francis
Cecchin, Frank
DiBardino, Daniel J.
Walsh, Edward P.
Berul, Charles I. [1 ]
机构
[1] Harvard Univ, Sch Med, Childrens Hosp Boston, Dept Cardiol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.athoracsur.2008.07.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Left cardiac sympathetic denervation is one of the therapeutic modalities used in the management of patients with medically refractory long QT syndrome. Traditionally, a thoracotomy or cervical incision has been used as the standard surgical approach for performing left cardiac sympathetic denervation. Video-assisted thoracoscopic surgery allows a minimally invasive technique. There is only one published series on the use of video-assisted thoracoscopic surgery for left cardiac sympathetic denervation in patients with long QT syndrome. Methods. We performed a retrospective clinical review of pertinent medical records and report a series including 9 pediatric patients (4 long QT syndrome, 4 catecholaminergic polymorphic ventricular tachycardia, and 1 idiopathic ventricular tachycardia) who underwent a left cardiac sympathetic denervation by means of video-assisted thoracoscopic surgery. Results. There were no severe complications, and 6 of 7 symptomatic patients with available follow-up experienced marked improvement in the first month after sympathectomy. Conclusions. This minimally invasive procedure provides a safe novel therapeutic option for children with drug-refractory catecholaminergic polymorphic ventricular tachycardia and other catecholamine-triggered arrhythmias.
引用
收藏
页码:1620 / 1625
页数:6
相关论文
共 25 条
[1]   Long QT syndrome in children in the era of implantable defibrillators [J].
Etheridge, Susan P. ;
Sanatani, Shubhayan ;
Cohen, Mitchell I. ;
Albaro, Cecilia A. ;
Saarel, Elizabeth V. ;
Bradley, David J. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 50 (14) :1335-1340
[2]   Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome [J].
Goldenberg, Ilan ;
Moss, Arthur J. ;
Zareba, Wojciech ;
Mcnitt, Scott ;
Robinson, Jennifer L. ;
Qi, Ming ;
Towbin, Jeffrey A. ;
Ackerman, Michael J. ;
Murphy, Laura .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2006, 17 (11) :1161-1168
[3]   Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome [J].
Hobbs, Jenny B. ;
Peterson, Derick R. ;
Moss, Arthur J. ;
McNitt, Scott ;
Zareba, Wojciech ;
Goldenberg, Ilan ;
Qi, Ming ;
Robinson, Jennifer L. ;
Sauer, Andrew J. ;
Ackerman, Michael J. ;
Benhorin, Jesaia ;
Kaufman, Elizabeth S. ;
Locati, Emanuela H. ;
Napolitano, Carlo ;
Priori, Silvia G. ;
Towbin, Jeffrey A. ;
Vincent, G. Michael ;
Zhang, Li .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 296 (10) :1249-1254
[4]   Catecholaminergic polymorphic ventricular tachycardia: Recent mechanistic insights [J].
Kontula, K ;
Laitinen, PJ ;
Lehtonen, A ;
Toivonen, L ;
Viitasalo, M ;
Swan, H .
CARDIOVASCULAR RESEARCH, 2005, 67 (03) :379-387
[5]   A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel [J].
Lahat, H ;
Pras, E ;
Olender, T ;
Avidan, N ;
Ben-Asher, E ;
Man, O ;
Levy-Nissenbaum, E ;
Khoury, A ;
Lorber, A ;
Goldman, B ;
Lancet, D ;
Eldar, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) :1378-1384
[6]  
Lahat H, 2001, CIRCULATION, V103, P2822
[7]   Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia [J].
Laitinen, PJ ;
Brown, KM ;
Piippo, K ;
Swam, H ;
Devaney, JM ;
Brahmbhatt, B ;
Donarum, EA ;
Marino, M ;
Tiso, N ;
Viitasalo, M ;
Toivonen, L ;
Stephan, DA ;
Kontula, K .
CIRCULATION, 2001, 103 (04) :485-490
[8]   Video-assisted thoracoscopic sympathectomy for congenital long QT syndromes [J].
Li, JF ;
Wang, LX ;
Wang, J .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2003, 26 (04) :870-873
[9]   Sudden cardiac death despite an implantable cardioverter-defibrillator in a young female with catecholaminergic ventricular tachycardia [J].
Mohamed, Uwais ;
Gollob, Michael H. ;
Gow, Robert M. ;
Krahn, Andrew D. .
HEART RHYTHM, 2006, 3 (12) :1486-1489
[10]   A cardiac arrhythmia syndrome caused by loss of ankyrin-B function [J].
Mohler, PJ ;
Splawski, I ;
Napolitano, C ;
Bottelli, G ;
Sharpe, L ;
Timothy, K ;
Priori, SG ;
Keating, MT ;
Bennett, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (24) :9137-9142