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首例玛格瑞斯®可吸收支架在伴有先天性主动脉缩窄的低体重婴儿中的应用及局限性。

First use and limitations of Magmaris® bioresorbable stenting in a low birth weight infant with native aortic coarctation.

机构信息

Department of Pediatric Cardiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Department of Congenital Heart Disease/Pediatric Cardiology, Deutsches Herzzentrum Berlin (DHZB), Berlin, Germany.

出版信息

Catheter Cardiovasc Interv. 2019 Jun 1;93(7):1340-1343. doi: 10.1002/ccd.28300. Epub 2019 Apr 19.

DOI:10.1002/ccd.28300
PMID:31001884
Abstract

We, herein, report the first use of a Magmaris® magnesium-based vascular scaffold for native aortic coarctation in a 1,980 g infant with multiple malformations. Due to the low body weight, complex illness, and clinical instability, it was decided to delay surgical correction. After insufficient results had been obtained by balloon angioplasty, Magmaris® implantation was chosen to bridge the patient to surgery by stabilizing left ventricular function and to allow for sufficient growth. Due to significant early stent restenosis and complete loss of radial force, the patient required balloon reangioplasty only 21 days after Magmaris® implantation and early surgical correction. In addition, high systemic sirolimus levels were detected 48 hr after the intervention (5 ng/mL). Although the bioresorbable scaffold was successfully used as a short-term bridge-to-surgery in our case, due to significant early stent failure (loss of radial force), this approach does not seem promising for long-term bridging of infants with aortic coarctation. In addition, the consequences of sirolimus-induced systemic immunosuppression may further limit the applicability of Magmaris® scaffolds in infants with congenital heart disease.

摘要

我们在此报告首例使用 Magmaris®镁基血管支架治疗 1980 克伴有多种畸形的先天性主动脉缩窄的病例。由于体重低、病情复杂和临床不稳定,决定延迟手术矫正。球囊血管成形术效果不佳后,选择 Magmaris®植入术通过稳定左心室功能和促进充分生长来为手术搭桥。由于早期支架再狭窄和径向力完全丧失,患者在 Magmaris®植入后仅 21 天需要再次进行球囊血管成形术和早期手术矫正。此外,在介入后 48 小时检测到全身性西罗莫司水平升高(5ng/mL)。尽管在我们的病例中,生物可吸收支架成功地用作短期桥接手术,但由于早期支架失败(径向力丧失),这种方法对于长期桥接主动脉缩窄的婴儿似乎并不理想。此外,西罗莫司引起的全身免疫抑制的后果可能进一步限制 Magmaris®支架在先天性心脏病婴儿中的适用性。

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