Early and late pace-maker implantation after transcatheter and surgical aortic valve replacement.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
03 2021
Historique:
revised: 06 07 2020
received: 13 06 2020
accepted: 19 07 2020
pubmed: 9 8 2020
medline: 25 9 2021
entrez: 9 8 2020
Statut: ppublish

Résumé

Conduction defects requiring permanent pacemaker (PPM) implantation are frequent complications occurring after surgical (SAVR) and transcatheter aortic valve replacement (TAVR). Patients who underwent TAVR or SAVR with a bioprosthesis from the nationwide FinnValve registry were the subjects of this study. Patients with prior PPM, who received a sutureless prosthesis, or required cardiac resynchronization therapy or implantable cardioverter defibrillator were excluded from this analysis. Four thousand and ten patients underwent SAVR and 1,897 underwent TAVR. TAVR had an increased risk of PPM implantation at 30-day (10.1% vs. 3.5%, unadjusted OR 3.11, 95%CI 2.56-3.87) and 5-year (15.7% vs. 8.6%, unadjusted SHR, 2.12, 95%CI 1.81-2.48) compared to SAVR. PPM implantation within 30 days from the index procedure did not increase the risk of 5-year mortality after either SAVR or TAVR. Among 1,042 propensity score matched pairs, TAVR had an increased risk of PPM implantation at 30-day (9.9% vs. 4.7%, p < .0001) and 5-year (14.7% vs. 11.4%, p = .001), but late (>30 days) PPM implantation at 5-year (4.7% vs. 6.9% SHR 0.72, 95%CI 0.47-1.10) was comparable to SAVR. The types of prosthesis had an impact on 30-day PPM implantation after TAVR, but not on late (>30 days) PPM implantation. Although the risk of 30-day PPM implantation is higher after TAVR compared to SAVR, late (>30 days) PPM implantation was comparable with these treatment methods. PPM implantation within 30 days did not affect late survival.

Sections du résumé

BACKGROUND
Conduction defects requiring permanent pacemaker (PPM) implantation are frequent complications occurring after surgical (SAVR) and transcatheter aortic valve replacement (TAVR).
METHODS
Patients who underwent TAVR or SAVR with a bioprosthesis from the nationwide FinnValve registry were the subjects of this study. Patients with prior PPM, who received a sutureless prosthesis, or required cardiac resynchronization therapy or implantable cardioverter defibrillator were excluded from this analysis.
RESULTS
Four thousand and ten patients underwent SAVR and 1,897 underwent TAVR. TAVR had an increased risk of PPM implantation at 30-day (10.1% vs. 3.5%, unadjusted OR 3.11, 95%CI 2.56-3.87) and 5-year (15.7% vs. 8.6%, unadjusted SHR, 2.12, 95%CI 1.81-2.48) compared to SAVR. PPM implantation within 30 days from the index procedure did not increase the risk of 5-year mortality after either SAVR or TAVR. Among 1,042 propensity score matched pairs, TAVR had an increased risk of PPM implantation at 30-day (9.9% vs. 4.7%, p < .0001) and 5-year (14.7% vs. 11.4%, p = .001), but late (>30 days) PPM implantation at 5-year (4.7% vs. 6.9% SHR 0.72, 95%CI 0.47-1.10) was comparable to SAVR. The types of prosthesis had an impact on 30-day PPM implantation after TAVR, but not on late (>30 days) PPM implantation.
CONCLUSIONS
Although the risk of 30-day PPM implantation is higher after TAVR compared to SAVR, late (>30 days) PPM implantation was comparable with these treatment methods. PPM implantation within 30 days did not affect late survival.

Identifiants

pubmed: 32767643
doi: 10.1002/ccd.29177
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

E560-E568

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

Fausto Biancari (F)

Heart and Lung Center, Helsinki University Hospital, Helsinki, Finland.
Heart Center, Turku University Hospital, and University of Turku, Turku, Finland.
Research Unit of Surgery, Anesthesiology and Critical Care, University of Oulu, Oulu, Finland.

Jouni Pykäri (J)

Heart Center, Turku University Hospital, and University of Turku, Turku, Finland.

Mikko Savontaus (M)

Heart Center, Turku University Hospital, and University of Turku, Turku, Finland.

Mika Laine (M)

Heart and Lung Center, Helsinki University Hospital, Helsinki, Finland.

Annastiina Husso (A)

Heart Center, Kuopio University Hospital, Kuopio, Finland.

Marko Virtanen (M)

Heart Hospital, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Pasi Maaranen (P)

Heart Hospital, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Matti Niemelä (M)

Department of Internal Medicine, Oulu University Hospital, Oulu, Finland.

Timo Mäkikallio (T)

Department of Internal Medicine, Oulu University Hospital, Oulu, Finland.

Tuomas Tauriainen (T)

Research Unit of Surgery, Anesthesiology and Critical Care, University of Oulu, Oulu, Finland.

Markku Eskola (M)

Heart Hospital, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Peter Raivio (P)

Heart and Lung Center, Helsinki University Hospital, Helsinki, Finland.

Antti Valtola (A)

Heart Center, Kuopio University Hospital, Kuopio, Finland.

Tatu Juvonen (T)

Heart and Lung Center, Helsinki University Hospital, Helsinki, Finland.
Research Unit of Surgery, Anesthesiology and Critical Care, University of Oulu, Oulu, Finland.

Juhani Airaksinen (J)

Heart Center, Turku University Hospital, and University of Turku, Turku, Finland.

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