Your browser doesn't support javascript.
loading
Transcatheter Closure of Atrial Septal Defect with Carag Bioresorbable Septal Occluder™: First-in-Child Experience with 12-MonthFollow-Up.
Callegari, Alessia; Quandt, Daniel; Nordmeyer, Johannes; Schubert, Stephan; Kramer, Peter; Knirsch, Walter; Kretschmar, Oliver.
Afiliação
  • Callegari A; Division of Pediatric Cardiology, Pediatric Heart Center, and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
  • Quandt D; University of Zürich (UZH), Zurich, Switzerland.
  • Nordmeyer J; Division of Pediatric Cardiology, Pediatric Heart Center, and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
  • Schubert S; University of Zürich (UZH), Zurich, Switzerland.
  • Kramer P; Department for Congenital Heart Disease/Pediatric Cardiology, German Heart Institute, Berlin, Germany.
  • Knirsch W; Department for Congenital Heart Disease/Pediatric Cardiology, German Heart Institute, Berlin, Germany.
  • Kretschmar O; Department of Congenital Heart Disease/Pediatric Cardiology, Heart and Diabetes Center NRW, Ruhr-University Bochum, Bad Oeynhausen, Germany.
J Interv Cardiol ; 2022: 3476398, 2022.
Article em En | MEDLINE | ID: mdl-36684829
ABSTRACT

Background:

Nowadays, transcatheter device closure of an atrial septal defect (ASD) is a standard approach in children. Potential early and long-term side effects or complications related to the metal framework of the devices are a known issue. A bioresorbable device such as the Carag Bioresorbable Septal Occluder™ (CBSO) could resolve such complications. Material and Results. The Carag Bioresorbable Septal Occluder™ (CBSO; Carag AG, Baar, Switzerland) is a self-centering double disk, repositionable, and retractable device with a bioresorbable framework (polylactic-co-glycolic acid), which is almost completely resorbed by 18-24 months postimplantation. This manuscript reports the four first-in-child ASD device closures using a CBSO. The patients' age was median (IQ1-IQ3), 4.5 years (4-7.25). Weight was 21.3 kg (17.6-32.7). We demonstrated procedural feasibility and safety. Effective defect closure with the device was 100%. Echocardiographic measurements of the thickness of the interatrial septum did not show any relevant increase over a 12-monthfollow-up period. There were no residual defects found after the procedure or later during the resorption process. The patients showed no evidence of any local or systemic inflammatory reaction.

Conclusions:

The CBSO device system could offer a new treatment option for transcatheter ASD device closure in the pediatric and adult fields. In our first-in-child experience, it was effectively and safely implanted. During the first 12 months of follow-up, no complications occurred.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Septo Interatrial / Dispositivo para Oclusão Septal / Comunicação Interatrial Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Septo Interatrial / Dispositivo para Oclusão Septal / Comunicação Interatrial Idioma: En Ano de publicação: 2022 Tipo de documento: Article