Optimal Implantation Depth and Adherence to Guidelines on Permanent Pacing to Improve the Results of Transcatheter Aortic Valve Replacement With the Medtronic CoreValve System: The CoreValve Prospective, International, Post-Market ADVANCE-II Study
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, multicentrická studie, pozorovací studie, práce podpořená grantem
PubMed
25999108
DOI
10.1016/j.jcin.2015.02.005
PII: S1936-8798(15)00251-4
Knihovny.cz E-zdroje
- Klíčová slova
- aortic stenosis, conduction disturbance, permanent pacemaker implantation, transcatheter aortic valve replacement,
- MeSH
- aortální chlopeň * patofyziologie MeSH
- aortální stenóza diagnóza mortalita patofyziologie terapie MeSH
- časové faktory MeSH
- chirurgická náhrada chlopně škodlivé účinky přístrojové vybavení metody mortalita MeSH
- dodržování směrnic * normy MeSH
- Kaplanův-Meierův odhad MeSH
- kardiostimulace umělá * škodlivé účinky mortalita normy MeSH
- lékařská praxe - způsoby provádění * normy MeSH
- lidé MeSH
- postmarketingový dozor MeSH
- prospektivní studie MeSH
- protézy - design MeSH
- rizikové faktory MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- směrnice pro lékařskou praxi jako téma * normy MeSH
- srdeční arytmie diagnóza etiologie mortalita patofyziologie terapie MeSH
- srdeční chlopně umělé * MeSH
- srdeční katetrizace škodlivé účinky přístrojové vybavení metody mortalita MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Evropa MeSH
OBJECTIVES: The aim of the CoreValve prospective, international, post-market ADVANCE-II study was to define the rates of conduction disturbances and permanent pacemaker implantation (PPI) after transcatheter aortic valve replacement with the Medtronic CoreValve System (Minneapolis, Minnesota) using optimized implantation techniques and application of international guidelines on cardiac pacing. BACKGROUND: Conduction disturbances are a frequent complication of transcatheter aortic valve replacement. The rates of PPI in the published reports vary according to bioprosthesis type and the indications for PPI. METHODS: The primary endpoint was the 30-day incidence of PPI with Class I/II indications when the Medtronic CoreValve System was implanted at an optimal depth (≤6 mm below the aortic annulus). The timing and resolution of all new-onset conduction disturbances were analyzed. RESULTS: A total of 194 patients were treated. The overall rate of PPI for Class I/II indications was 18.2%. An optimal depth was reached in 43.2% of patients, with a nonsignificantly lower incidence of PPI in patients with depths ≤6 mm, compared with those with deeper implants (13.3% vs. 21.1%; p = 0.14). In a paired analysis, new-onset left bundle branch block and first-degree atrioventricular block occurred in 45.4% and 39.0% of patients, respectively, and resolved spontaneously within 30 days in 43.2% and 73.9%, respectively. In patients with new PPI, the rate of intrinsic sinus rhythm increased from 25.9% at 7 days to 59.3% at 30 days (p = 0.004). CONCLUSIONS: Optimal Medtronic CoreValve System deployment and adherence to international guidelines on cardiac pacing are associated with a lower rate of new PPI after transcatheter aortic valve replacement, compared with results reported in previous studies. (CoreValve Advance-II Study: Prospective International Post-Market Study [ADVANCE II]; NCT01624870).
Cardiothoracic and Vascular Department Azienda Ospedaliero Universitaria Pisana Pisa Italy
Department of Biostatistics North American Sciences Associates Inc Minneapolis Minnesota
Department of Cardiology and Angiology Charite Campus Mitte Kardiologie Berlin Germany
Department of Cardiology Cardiocenter Hospital Podlesi Trinec Czech Republic
Department of Cardiology Glenfield Hospital Leicester United Kingdom
Department of Cardiology Istituto Clinico S Ambrogio Milan Italy
Department of Cardiology Thoraxcenter Erasmus Medical Center Rotterdam the Netherlands
Department of Cardiology Universitätsklinikum Heidelberg Heidelberg Germany
Department of Cardiology University Hospital Antwerp Antwerp Belgium
Department of Medicine 2 Universitätsklinikum Bonn Bonn Germany
Department of Structural Heart Clinical Operations Medtronic Inc Mounds View Minnesota
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT01624870