Skip Navigation

Europace 1999 1(2):96-102; doi:10.1053/eupc.1998.0023
© 1999 by European Society of Cardiology
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (14)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sticherling, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sticherling, C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

First worldwide clinical experience with a new dual chamber implantable cardioverter defibrillator

Advantages and complications

C. Sticherling, A. Schaumann*, T. Klingenheben, S. H. Hohnloser for the Ventak AV II DR investigators

Department of Cardiology, J.W. Goethe University Frankfurt, Germany; *Department of Cardiology, Georg-August University Göttingen, Germany

AIMS: The need for physiological pacing and for improving the ability to discriminate atrial from ventricular tachy-arrhythmias has prompted the development of dual chamber implantable cardioverter/defibrillators (ICDs).

METHODS: Fifty-two patients were implanted with a newly developed dual-chamber ICD providing rate-responsive physiological pacing (Ventak AV II DR). The device possesses two new arrhythmia detection algorithms (‘atrial fibrillation rate threshold’ and ‘ventricular to atrial rate relationship’) in addition to commonly used features such as ‘onset’ and ‘stability’. During implantation, the atrial and ventricular lead impedances and pacing thresholds were determined together with the defibrillation threshold. Prior to discharge, attempts were made to induce both atrial and ventricular tachyarrhythmias in order to test those new detection criteria. All patients were followed for at least 3 months.

RESULTS: The device was successfully implanted in all 52 patients. Placement of the atrial lead was successful in 50/52 patients (96%; P-wave 3·2±1·4 mV; impedance 576±123 |gQ; atrial pacing threshold 1·2±0·9 V). Prior to discharge, 32 episodes of atrial fibrillation (AF) alone, 38 episodes of AF with ventricular fibrillation and 10 episodes of AF with monomorphic ventricular tachycardia were induced in 33/50 patients (66%) and all were appropriately classified by the detection algorithm. During the 3 months follow-up, 12 patients (23%) had appropriate and successful therapies for ventricular arrhythmias, while four patients (8%) experienced inappropriate ICD therapies. Although all these episodes were detected correctly as supraventricular arrhythmias by the device, therapy was delivered because of incorrect or incomplete programming. In all cases reprogramming of the device resolved the problem.

CONCLUSION: Implantation of dual chamber ICDs is feasible and appears to improve discrimination of supraventricular from ventricular tachyarrhythmias. In addition, patients with tachyarrhythmias and concomitant bradyarrhythmias may benefit from simultaneous physiological pacing. However, implantation and follow-up of such patients should be performed at experienced centres since both surgical handling and programming of these devices is more difficult and complex than conventional ICDs.

Key Words: Implantable cardioverter/defibrillator, sudden cardiac death, dual chamber pacing, atrial fibrillation, discrimination of atrial and ventricular arrhythmias, inappropriate ICD shock


Correspondence: Stefan H. Hohnloser, MD, FACC, FESC, J.W. Goethe University, Department of Internal Medicine, Division of Cardiology, Theodor-Stern-Kai 7, D-60596 Frankfurt, Germany.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
CirculationHome page
S. Saba, K. Volosin, R. Yee, C. Swerdlow, M. Brown, and for the Dynamic Discrimination Investigators
Combined Atrial and Ventricular Antitachycardia Pacing as a Novel Method of Rhythm Discrimination: The Dynamic Discrimination Download Study
Circulation, February 2, 2010; 121(4): 487 - 497.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
D. A.M.J. Theuns, A. P. J. Klootwijk, D. M. Goedhart, and L. J.L.M. Jordaens
Prevention of inappropriate therapy in implantable cardioverter-defibrillators: Results of a prospective, randomized study of tachyarrhythmia detection algorithms
J. Am. Coll. Cardiol., December 21, 2004; 44(12): 2362 - 2367.
[Abstract] [Full Text] [PDF]


Home page
EuropaceHome page
A. Quesada, J.ús Almendral, F. Arribas, R. Ricci, C. Wolpert, P. Adragao, E. Cobo, X. Navarro, and on behalf DATAS investigators
The DATAS rationale and design: a controlled, randomized trial to assess the clinical benefit of dual chamber (DDED) defibrillator
Europace, January 1, 2004; 6(2): 142 - 150.
[Abstract] [Full Text] [PDF]


Home page
EuropaceHome page
E. Aliot, Rém. Nitzsché, and A. Ripart
Arrhythmia detection by dual-chamber implantable cardioverter defibrillators: A review of current algorithms
Europace, January 1, 2004; 6(4): 273 - 286.
[Abstract] [Full Text] [PDF]


Home page
EuropaceHome page
D. Theuns, A. P. Klootwijk, G. P. Kimman, T. Szili-Torok, J. R. T. C. Roelandt, and L. Jordaens
Initial clinical experience with a new arrhythmia detection algorithm in dual chamber implantable cardioverter defibrillators
Europace, January 1, 2001; 3(3): 181 - 186.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.