Circulation, Vol 81, 312-318, Copyright © 1990 by American Heart Association
EB Sideris, SE Sideris, JP Fowlkes, RL Ehly, JE Smith and RE Gulde
The feasibility and safety of transvenous closure of atrial septal defects
by a new device was tested in 20 piglets, in which atrial septal defects
were created by foramen ovale dilatation with angioplasty balloons. The
device was small enough to be introduced in a 7F or 8F sheath, and it
measured 20-25 mm. It has no hooks and consists of a foam occluder from the
left atrium and a counter-occluder from the right atrium, buttoned
independently. The animals were observed by angiography and color flow
mapping, and they were electively killed at various intervals up to 2
months after occlusion. The device was not thrombogenic and had
endothelialized by 2-3 weeks. All atrial defects were found to be
completely occluded. Complications occurred only with the first three
prototype devices, including counter-occluder detachment, right atrial
perforation, and need for double occlusion and pulmonary artery
embolization. No such complications occurred in the last 17 experiments
because of modifications of the device and operator experience. These
observations showed the feasibility of occlusion of moderate-size atrial
septal defects in piglets by a new device introduced through a small
sheath. The method appears promising for potential human application.
ARTICLES
Transvenous atrial septal defect occlusion in piglets with a "buttoned" double-disk device
Heart Institute for CARE, Amarillo, Texas.
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