|
|
||||||||
American Journal of Roentgenology, Vol 165, 275-279, Copyright © 1995 by American Roentgen Ray Society
ARTICLES |
EA Drucker, R Brooks, H Garan, MO Sweeney, JM Ruskin, BA McGovern and SW Miller
Department of Radiology, Massachusetts General Hospital, Boston, MA 02114, USA.
OBJECTIVE. The purpose of this study was to determine the frequency of system malfunction in patients with nonthoracotomy implantable cardioverter defibrillators and to assess the role of chest radiography in detecting and determining the cause of malfunction. MATERIALS AND METHODS. The study population consisted of 300 consecutive patients in whom implantable cardioverter defibrillators were implanted using an initial nonthoracotomy approach between September 1990 and October 1994. Transvenous electrodes were placed via the subclavian or cephalic vein under local anesthetic. Intraoperative testing, pulse generator implantation, and, if necessary, subcutaneous patch or extrapericardial patch placement via thoracotomy were done in the operating room under general anesthetic. Follow-up consisted of routine device interrogation every 2-3 months and annual chest radiography. Chest radiographs were obtained more often if patients were symptomatic or if results of device interrogation were abnormal. RESULTS. Patients were followed up for a mean +/- SD of 19 +/- 14 months following implantation. Implantable cardioverter-defibrillator malfunction occurred in 17 patients (6%) during the follow-up period. Of these, 12 (71%) had component abnormalities on chest radiographs. Patients with radiographically apparent implantable cardioverter-defibrillator abnormalities presented in two discrete time periods after device implantation, early (mean, 35 +/- 14 days) and late (mean, 18 +/- 5 months). CONCLUSION. Malfunction of nonthoracotomy implantable cardioverter-defibrillator systems develops infrequently after device implantation. In most cases, the cause can be identified on chest radiographs.
This article has been cited by other articles:
![]() |
A. Goette, F. Cantu, L. van Erven, P. Geelen, F. Halimi, J. L. Merino, J. M. Morgan, and on behalf of the Scientific Initiative Committee o Performance and survival of transvenous defibrillation leads: need for a European data registry Europace, November 11, 2008; (2008) eun301v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. B. Hunter, M. S. Taljanovic, P. H. Tsau, W. G. Berger, and J. R. Standen Medical Devices of the Chest RadioGraphics, November 1, 2004; 24(6): 1725 - 1746. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. A. L. E. Bracke, A. Meijer, and L. M. van Gelder Malfunction of endocardial defibrillator leads and lead extraction: where do they meet? Europace, January 1, 2002; 4(1): 19 - 24. [Full Text] [PDF] |
||||
![]() |
A. Oto, A. Yildirir, G. Kabakci, and E. Atalar Inappropriate Shocks Diagnosed by Stored Electrograms of Implantable Cardioverter Defibrillators: Two Case Reports Angiology, May 1, 2000; 51(5): 425 - 430. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |