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Severe scoliosis and percutaneous atrial septal defect closure, a word of caution

Published online by Cambridge University Press:  23 April 2021

Biagio Castaldi*
Affiliation:
Pediatric Cardiology Unit, Department of Women’s and Children’s Health, University of Padua, Padova, Italy
Domenico Sirico
Affiliation:
Pediatric Cardiology Unit, Department of Women’s and Children’s Health, University of Padua, Padova, Italy
Giovanni Di Salvo
Affiliation:
Pediatric Cardiology Unit, Department of Women’s and Children’s Health, University of Padua, Padova, Italy
*
Author for correspondence: Biagio Castaldi, Pediatric Cardiology Unit, Department of Women’s and Children’s Health, University of Padua, Via Giustiniani 3, 35126 Padova, Italy. Tel: +39 0498213558; Fax: +39 0498218089. E-mail: b.castaldi@yahoo.it
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Abstract

In the presence of complex septal morphology or extra-cardiac factors like severe scoliosis or diaphragm paralysis, the procedure may become more challenging, and pre-formed sheaths and devices thought to facilitate the implantation might turn into a problem to address. Similarly to Herron and Kobayashi, we have experienced a similar issue during atrial septal defect closure with Gore Cardioform atrial septal defect device® in a 12-year-old female patient with severe scoliosis. After the conformation of the locking loop and the removal of the safety cord, the Gore Cardioform atrial septal defect device prolapsed in the right atrium.

Information

Type
Letter to the Editor
Copyright
© The Author(s), 2021. Published by Cambridge University Press
Figure 0

Figure 1. Intra-procedural trans-oesophageal echocardiography. (a) Baseline atrial septal defect diameter, 15 mm. (b) Stretched diameter at the static sizing (22 mm). (c) Device after locking loop closure. (d) Device prolapse after safety cord removal.