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50 例先天性心血管疾病患者血管封堵术中应用 Amplatzer 血管塞和 Amplatzer 血管塞 II。

The Amplatzer vascular plug and Amplatzer vascular plug II for vascular occlusion procedures in 50 patients with congenital cardiovascular disease.

机构信息

The Children's Hospital of Philadelphia, Division of Cardiology, Philadelphia, PA, USA.

出版信息

Catheter Cardiovasc Interv. 2010 Sep 1;76(3):411-7. doi: 10.1002/ccd.22370.

Abstract

OBJECTIVE

To describe the use of the Amplatzer vascular plug (plug 1) and Amplatzer vascular plug II (plug 2) in patients with congenital cardiovascular disease (CCVD).

BACKGROUND

Plugs 1 and 2 have recently been made available. We report our experience describing plugs 1 and 2 in patients with CCVD highlighting the versatility of these devices.

METHODS

All patients with CCVD who underwent a vascular occlusion procedure at the Children's Hospital of Philadelphia between August 1, 2004 and July 30, 2009 with plug 1 or 2 were included. A retrospective review was performed.

RESULTS

Fifty patients underwent vascular occlusion procedure with plug 1 or 2 at a median age of 2.0 years (range 1 day to 47 years) and median weight of 12.3 kg (range 3.1-98 kg). Fifty-eight plugs (43% plug 1, 57% plug 2) were placed in 52 vessels. Of these vessels, 20 (38%) were patent ductus arteriosus (PDA), 14 (27%) venous collaterals, 5 (10%) aorto-pulmonary collaterals, 4 (8%) modified Blalock Taussig shunts, 3 (5%) porto-systemic connections, and 6 (12%) miscellaneous structures. Excluding a patient who was lost to follow-up, complete occlusion was observed in 100% of vessels either at the time of the catheterization or at follow-up. There were two complications (3.8%).

CONCLUSIONS

Plugs 1 and 2 are safe and effective devices that can be used in a variety of blood vessels in patients with CCVD. Plug 2 is particularly useful in closure of high-flow, tubular structures, especially type C PDA's.

摘要

目的

描述在先天性心血管疾病(CCVD)患者中使用 Amplatzer 血管塞(塞 1)和 Amplatzer 血管塞 II(塞 2)的情况。

背景

塞 1 和塞 2 最近已投入使用。我们报告了在 CCVD 患者中使用塞 1 和塞 2 的经验,强调了这些设备的多功能性。

方法

所有在 2004 年 8 月 1 日至 2009 年 7 月 30 日期间在费城儿童医院接受血管闭塞手术且使用塞 1 或塞 2 的 CCVD 患者均被纳入研究。对这些患者进行了回顾性研究。

结果

50 例患者在中位年龄为 2.0 岁(范围为 1 天至 47 岁)和中位体重为 12.3kg(范围为 3.1-98kg)时接受了血管闭塞手术,使用塞 1 或塞 2。在这些血管中,有 58 个塞子(43%为塞 1,57%为塞 2)被放置在 52 个血管中。这些血管中,有 20 个(38%)为动脉导管未闭(PDA),14 个(27%)为静脉侧支,5 个(10%)为体肺侧支,4 个(8%)为改良的 Blalock-Taussig 分流,3 个(5%)为门腔静脉连接,6 个(12%)为其他结构。除了 1 例失访患者外,在导管检查时或随访时,所有血管均观察到完全闭塞,比例为 100%。仅发生了 2 例并发症(3.8%)。

结论

塞 1 和塞 2 是安全有效的装置,可用于 CCVD 患者的各种血管。塞 2 特别适用于闭合高流量、管状结构,尤其是 C 型 PDA。

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