2015
DOI: 10.1093/ejcts/ezv310
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A new device as an open stent graft for extended aortic repair: a multicentre early experience in Japan

Abstract: The safety and effectiveness of this investigational device was verified over a period up to 36 months after operation. A long-term follow-up would be necessary to further verify the effectiveness of the device in the future.

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Cited by 52 publications
(51 citation statements)
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“…According to incomplete data, spinal cord injury occurred in 1.9% (43/2216), including paraparesis in 13 cases (0.6%) and paraplegia in 30 (1.3%). This incidence was much lower than the 6.7% reported in the premarket trial [61], which may be the result of avoidance of implanting below T8, and earlier distal perfusion after delivery of stent graft [Hideki Kataoka. Personal communication (email), January 2016].…”
Section: J Graft Open Stent Graftmentioning
confidence: 89%
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“…According to incomplete data, spinal cord injury occurred in 1.9% (43/2216), including paraparesis in 13 cases (0.6%) and paraplegia in 30 (1.3%). This incidence was much lower than the 6.7% reported in the premarket trial [61], which may be the result of avoidance of implanting below T8, and earlier distal perfusion after delivery of stent graft [Hideki Kataoka. Personal communication (email), January 2016].…”
Section: J Graft Open Stent Graftmentioning
confidence: 89%
“…For distal anastomosis, four 4-0 polypropylene stay sutures are placed first, followed by running stiches of 4-0 polypropylene reinforced by a felt strip [62]. The arch vessels are reconstructed with a separate branched graft in an end-to-end fashion [61,63].…”
Section: Cronusmentioning
confidence: 99%
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“…This stress is called the spring-back force. 4,5) The J Graft Open Stent Graft (JOSG, Japan Lifeline Co., Ltd., Tokyo, Japan), which is currently the only commercially available device in Japan used in conducting the frozen elephant trunk technique, 6,7) has a considerable spring-back force. We hereby report a typical case of DSINE caused by the spring-back force of this device after the treatment of true saccular arch aneurysm.…”
Section: Introductionmentioning
confidence: 99%