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B型主动脉夹层动脉瘤植入血管内支架后诱发的逆行性A型主动脉夹层动脉瘤
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Retrograde type A aortic dissection after endovascular stent graft placement for treatment of type B dissection
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Dong ZH, Fu WG, Wang YQ, Guo DQ, Xu X, Ji Y, Chen B, Jiang JH, Yang J, Shi ZY, Zhu T, Shi Y
2009/5/29 18:39:00
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Circulation,
2009,
Volume 119,
Issue 5
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Background - Retrograde type A aortic dissection has been deemed a rare complication after endovascular stent graft placement for type B dissection. However, this life-threatening event appears to be underrecognized and is worth being investigated further. Methods and Results - Eleven of 443 patients developed retrograde type A aortic dissection during or after stent grafting for type B dissection from August 2000 to June 2007. Of these 11 patients, 3 had Marfan syndrome. The Kaplan-Meier estimate of the rate of freedom from this event at 36 months is 97.4% (95% confidence interval, 0.95 to 0.99). The new entry was located at the tip of the proximal bare spring of the stent graft in 9 patients, was within the anchoring area of the proximal bare spring in 1, and remained unknown in 1 patient. Eight patients were converted to open surgery, and 2 received medical treatment. One patient suddenly died 2 hours after the primary stent grafting, and 2 died within 1 week after the surgical conversion, so mortality reached 27.3%. During the follow-up from 3 to 50 months, type I endoleak was identified in 1 patient 3 months after the surgical exploration and disappeared at 6 months. Conclusions - Retrograde type A aortic dissection after stent grafting for type B dissection appears not to be rare and results from mixed causes. Fragility of the aortic wall and disease progression may predispose to it, whereas stent grafting-related factors make important and provocative contributions. Avoiding aortic arch stent grafting in Marfan patients, preferably selecting the endograft without the proximal bare spring for patients with a kinked aortic arch or with Marfan syndrome (if endografting is used), improving the device design, and standardizing endovascular manipulation might lessen its occurrence. © 2009 American Heart Association, Inc.
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Correspondence Address:
Fu, W.G.; Department of Vascular Surgery, Zhongshan Hospital, Fudan University, 180 Fenglin Rd, Shanghai 200032, China; email: fu.weiguo@zs-hospital.sh.cn
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疾病资源中心
摘自:《脑电图精粹》(主译:元小冬 许亚茹),北京大学医学出版社出版
男孩,8岁,出现双侧上肢和躯干抽搐发作,没有明显的意识改变。患者具有病毒性脑膜脑炎后的严重抑制性脑病,并出现失明和四肢瘫。患者没有应用中枢神经系统兴奋剂。
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