Right ventricular outflow tract prestenting with AndraStent XXL before percutaneous pulmonary valve implantation.


Journal

Archives of cardiovascular diseases
ISSN: 1875-2128
Titre abrégé: Arch Cardiovasc Dis
Pays: Netherlands
ID NLM: 101465655

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 30 06 2019
revised: 03 12 2019
accepted: 12 12 2019
pubmed: 23 2 2020
medline: 23 6 2020
entrez: 22 2 2020
Statut: ppublish

Résumé

The indications for percutaneous pulmonary valve implantation (PPVI) have been extended to include large dysfunctional right ventricular outflow tracts (RVOTs). Prestenting of the RVOT is commonly performed before PPVI in order to ensure a stable landing zone. The AndraStent XXL (AndraMed GmbH, Reutlingen, Germany), a cobalt-chromium stent with semi-open cell design, has unique mechanical properties in this indication but is no longer available in France. To assess the efficiency of AndraStent XXL before PPVI. In this retrospective multicentre cohort study, 86 AndraStents XXL were implanted in 77 patients in 6 centres. PPVI was indicated mainly for pulmonary regurgitation (75.3%) in native or patched RVOT (88.3%). The stents were manually mounted on balloon catheters and delivered through sheaths using a conventional femoral approach. PPVI was performed successfully in 97.4% of patients after successful prestenting, generally during the same procedure (77.9%). There were no deaths associated with stent implantation, and four patients experienced five complications, mainly stent embolization, including one requiring surgery. Neither stent fracture nor dysfunction were observed in any patient during a mean follow-up of 19.2±8.7months. Stent analysis showed an excellent maximal stent expansion (97.1%) regardless of balloon size. A 22.3%±3.4 stent shortening with a 30mm balloon was observed. Implantation of large cobalt-chromium AndraStent XXL stents is efficient for prestenting before PPVI.

Sections du résumé

BACKGROUND BACKGROUND
The indications for percutaneous pulmonary valve implantation (PPVI) have been extended to include large dysfunctional right ventricular outflow tracts (RVOTs). Prestenting of the RVOT is commonly performed before PPVI in order to ensure a stable landing zone. The AndraStent XXL (AndraMed GmbH, Reutlingen, Germany), a cobalt-chromium stent with semi-open cell design, has unique mechanical properties in this indication but is no longer available in France.
AIMS OBJECTIVE
To assess the efficiency of AndraStent XXL before PPVI.
METHODS METHODS
In this retrospective multicentre cohort study, 86 AndraStents XXL were implanted in 77 patients in 6 centres.
RESULTS RESULTS
PPVI was indicated mainly for pulmonary regurgitation (75.3%) in native or patched RVOT (88.3%). The stents were manually mounted on balloon catheters and delivered through sheaths using a conventional femoral approach. PPVI was performed successfully in 97.4% of patients after successful prestenting, generally during the same procedure (77.9%). There were no deaths associated with stent implantation, and four patients experienced five complications, mainly stent embolization, including one requiring surgery. Neither stent fracture nor dysfunction were observed in any patient during a mean follow-up of 19.2±8.7months. Stent analysis showed an excellent maximal stent expansion (97.1%) regardless of balloon size. A 22.3%±3.4 stent shortening with a 30mm balloon was observed.
CONCLUSIONS CONCLUSIONS
Implantation of large cobalt-chromium AndraStent XXL stents is efficient for prestenting before PPVI.

Identifiants

pubmed: 32081640
pii: S1875-2136(20)30020-6
doi: 10.1016/j.acvd.2019.12.004
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-120

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Auteurs

Clement Karsenty (C)

CHU Toulouse, Pediatric and Congenital Cardiology, Children's Hospital, Université de Toulouse, 31300 Toulouse, France; Institut des Maladies Métaboliques et Cardiovasculaires, Université de Toulouse, INSERM U1048, I2MC, 1, Avenue Jean-Poulhès, BP 84225, Toulouse, France. Electronic address: clement.karsenty@hotmail.fr.

Sophie Malekzadeh-Milani (S)

Centre de Référence Malformations Cardiaques Congénitales, Complexes-M3C, Necker Hospital for Sick Children, George-Pompidou European Hospital, Assistance Publique des Hopitaux de Paris (AP-HP), 75015 Paris, France.

Alain Fraisse (A)

Paediatric Cardiology and Cardiac Surgery Services, Royal Brompton and Harefield NHS Foundation Trust, London, UK.

Marc Gewillig (M)

Fetal and Pediatric Cardiology, University Hospitals Leuven, Herestraat 49, 3000 Leuven, Belgium.

Damien Bonnet (D)

Centre de Référence Malformations Cardiaques Congénitales, Complexes-M3C, Necker Hospital for Sick Children, George-Pompidou European Hospital, Assistance Publique des Hopitaux de Paris (AP-HP), 75015 Paris, France.

Philippe Aldebert (P)

Pediatric and Congenital Cardiology, M3C Regional Reference CHD Centre, University Hospital, Marseille, France.

Caroline Ovaert (C)

Pediatric and Congenital Cardiology, M3C Regional Reference CHD Centre, University Hospital, Marseille, France.

Helene Bouvaist (H)

Department of Cardiology, M3C Regional Reference CHD Centre, CHU Grenoble, France.

Aleksander Kempny (A)

Adult Congenital Heart Centre, Royal Brompton Hospital, London, UK.

Ali Houeijeh (A)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France.

Jerome Petit (J)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France.

Sebastien Hascoet (S)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France.

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