ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Takuro Misaki
Go Watanabe
Takashi Iwa
Hiroshi Ohtake
Yoh Watanabe
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Misaki, T.
Right arrow Articles by Watanabe, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Misaki, T.
Right arrow Articles by Watanabe, Y.

Ann Thorac Surg 1994;58:1380-1385
© 1994 The Society of Thoracic Surgeons


Articles

Surgical treatment of arrhythmogenic right ventricular dysplasia: Long-term outcome

Takuro Misaki, MD, Go Watanabe, MD*, Takashi Iwa, MD, Makoto Tsubota, MD, Hiroshi Ohtake, MD, Keiichi Yamamoto, MD, Yoh Watanabe, MD

Departments of Surgery (1), Toyama Medical and Pharmaceutical University, Toyama, and Kanazawa University School of Medicine, Kanazawa, Japan

Accepted for publication March 29, 1994.

* Address reprint requests to Dr Watanabe, Department of Surgery (1), Toyama Medical and Pharmaceutical University, Sugitani Toyama 2630, Toyama, Japan 930-01.

Eight male patients ranging from 15 to 51 years old (mean age, 36.3 years) underwent surgical treatment of ventricular tachycardia (VT) associated with arrhythmogenic right ventricular dysplasia. One patient had an associated left ventricular aneurysm. The earliest activation site was detected for 15 lesions, and delayed potentials were recorded during sinus rhythm in all patients. On the basis of the epicardial mapping, the origins of the VT foci in the right ventricle were resected. Cryoablation on the surrounding myocardium was performed. There were no surgical deaths or postoperative fatal complications. During long-term follow-up, there has been no recurrence of VT and no congestive heart failure in the 6 patients without left ventricular involvement. The 2 patients with LV involvement died late of either congestive heart failure or development of VT originating from the left ventricle. In conclusion, a surgical approach consisting of myocardial excision and cryocoagulation offers a curative treatment of VT associated with arrhythmogenic right ventricular dysplasia and yields excellent long-term results when the VT origin is well identified in the right ventricle.




This article has been cited by other articles:


Home page
J. Thorac. Cardiovasc. Surg.Home page
S. Kanaan, K. Shamsuddin, M. Silka, and W. Wells
Right ventricular outflow tract resection for treatment of refractory ventricular tachycardia in a 2-year-old child
J. Thorac. Cardiovasc. Surg., September 1, 2005; 130(3): 948 - 949.
[Full Text] [PDF]


Home page
Anesth. Analg.Home page
P. Motta, E. Mossad, and R. Savage
Right Ventricular Exclusion Surgery for Arrhythmogenic Right Ventricular Dysplasia with Cardiomyopathy
Anesth. Analg., June 1, 2003; 96(6): 1598 - 1602.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
S. Sano, K. Ishino, M. Kawada, S. Kasahara, T. Kohmoto, M. Takeuchi, and S.-i. Ohtsuki
Total right ventricular exclusion procedure: An operation for isolated congestive right ventricular failure
J. Thorac. Cardiovasc. Surg., April 1, 2002; 123(4): 640 - 647.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS
Copyright © 1994 by The Society of Thoracic Surgeons.