Skip Navigation


European Journal of Heart Failure Advance Access originally published online on November 1, 2009
European Journal of Heart Failure 2009 11(12):1143-1151; doi:10.1093/eurjhf/hfp149
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
11/12/1143    most recent
hfp149v1
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 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 arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by van Veldhuisen, D. J.
Right arrow Articles by Swedberg, K.
PubMed
Right arrow PubMed Citation
Right arrow Articles by van Veldhuisen, D. J.
Right arrow Articles by Swedberg, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org.

Implementation of device therapy (cardiac resynchronization therapy and implantable cardioverter defibrillator) for patients with heart failure in Europe: changes from 2004 to 2008

Dirk J. van Veldhuisen1,*, Alexander H. Maass1, Silvia G. Priori2, Pelle Stolt3, Isabelle C. van Gelder1, Kenneth Dickstein4 and Karl Swedberg5

1 Department of Cardiology, University Medical Center Groningen, University of Groningen, PO Box 30.001, 9700RB Groningen, The Netherlands
2 University of Pavia, Fondazione Salvatore Maugeri, Pavia, Italy
3 Medtronic Europe, Tolchenaz, Switzerland
4 Stavanger University Hospital, University of Bergen, Norway
5 University of Gothenborg, Göteborg, Sweden

* Corresponding author. Tel: +31 50 3612355, Fax: +31 50 3614391, Email: d.j.van.veldhuisen{at}thorax.umcg.nl


   Abstract

Aims: Heart failure (HF) patients increasingly receive device therapy, either an implantable cardioverter defibrillator (ICD) or a biventricular pacemaker, also called cardiac resynchronization therapy (CRT), or a CRT device with an ICD (CRT-D). However, epidemiological data on the use of device therapy in Europe are limited.

Methods and results: Data on implantation rates for conventional pacemakers, ICD, CRT, and CRT-D in 15 Western European countries were obtained from the Eucomed Registry for the 5-year period 2004–2008. Implantation of conventional pacemakers increased by 9% in Europe over the 5 years (reaching 907/million in 2008) and there were significant differences between countries. Implantable cardioverter defibrillator implantations increased by 75% from 80/million in 2004 to 140/million in 2008, and differences between countries were larger than those for conventional pacemakers. Implantation rates for CRT-P alone increased slightly from 2004 to 2006, but remained at 25/million thereafter in Europe overall. The total number of CRT implants (CRT-P and -D) markedly increased from 46/million in 2004 to 99/million in 2008 (115%), but this was mainly due to more CRT-D implants, i.e. an increase in the proportion of CRT-D (from 55% in 2004 to 75% in 2008). Implantation rates for ICD, CRT, and CRT-D remained markedly different throughout the study period between countries.

Conclusion: Implantation rates of devices for HF, in particular ICD and CRT-D, have increased significantly between 2004 and 2008 in Europe, but there remain major differences between countries.

Key Words: Heart failure • Device therapy • ICD • CRT • Implementation • Geographic differences

Received July 21, 2009; Revised September 11, 2009; Accepted September 24, 2009


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




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.