2003
DOI: 10.1590/s0066-782x2003001300001
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Initial experience in Brazil with the Helex septal occluder for percutaneous occlusion of atrial septal defects

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Cited by 16 publications
(14 citation statements)
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“…Recently, percutaneous device closure has been the preferred choice in the treatment of the secundum ASDs with various devices in patients with sufficient rims [1,2,5,10,11]. Despite the significant refinement in device technology, there is no ideal device that closes all of the secundum ASDs without significant complications either in early and immediate term or in the long term.…”
Section: Discussionmentioning
confidence: 99%
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“…Recently, percutaneous device closure has been the preferred choice in the treatment of the secundum ASDs with various devices in patients with sufficient rims [1,2,5,10,11]. Despite the significant refinement in device technology, there is no ideal device that closes all of the secundum ASDs without significant complications either in early and immediate term or in the long term.…”
Section: Discussionmentioning
confidence: 99%
“…Despite the significant refinement in device technology, there is no ideal device that closes all of the secundum ASDs without significant complications either in early and immediate term or in the long term. These complications are mostly device related such as embolization or dislocation of the device, thrombus formation and cardiac erosion [2,7,12]. Thus, the studies have been going on for the refinement of the patient selection criteria and development of the new devices in optimal structure and design for avoiding from device-related complications during and after the percutaneous closure.…”
Section: Discussionmentioning
confidence: 99%
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“…(13) The GORE-Helex device consists of a single nitinol wire attached to a continuous tape of polytetrafluoroethylene that forms two hybrid discs in the shape of a spiral that, when released, attach themselves to each side of the fistula. (14) Because the GORE-Helex device is more malleable than is the Oclutech Figulla device, we believed the former would be more appropriate to close the tracheoesophageal fistula for two reasons: first, because the two organs involved presented motility; and second, because we were concerned that a rigid device might widen the fistula. (14) If our initial results are corroborated by future studies, this might be a promising technique for the endoscopic treatment of fistulas in the tracheobronchial tree.…”
Section: Casementioning
confidence: 99%