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升主动脉到胸腹主动脉的一期替换。

One-stage replacement of the aorta from arch to thoracoabdominal region.

机构信息

Division of Cardiovascular Surgery, Department of Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

Division of Cardiovascular Surgery, Department of Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

J Thorac Cardiovasc Surg. 2018 Feb;155(2):498-504. doi: 10.1016/j.jtcvs.2017.09.048. Epub 2017 Sep 19.

Abstract

OBJECTIVES

We present our experience with one-stage replacement of thoracic aneurysm from the ascending aorta to the thoracoabdominal aorta.

PATIENTS AND METHODS

Fourteen patients (10 male and 4 female; mean age 53.6 ± 12.4 years) with extended thoracic aortic aneurysms underwent graft replacement. The pathology of the diseased aorta was chronic aortic dissection in 13 patients and intraoperative retrograde aortic dissection in 1 patient. Five patients had Marfan syndrome. In a previous operation, 1 patient had undergone the Bentall procedure, 4 had hemiarch replacement for acute type A dissection, and 1 had a Y-graft for abdominal aortic aneurysm. The approach to the aneurysm was posterolateral thoracotomy with rib-cross incision extended to the retroperitoneal abdominal aorta. Arterial inflow for cardiopulmonary bypass consisted of the femoral artery in 13 patients and abdominal aortic aneurysm graft in 2. Venous drainage site was the femoral vein in 7, femoral vein and pulmonary artery in 3, and pulmonary artery in 1. All patients had antegrade cerebral perfusion and visceral perfusion.

RESULTS

Hospital mortality occurred in 1 patient due to acute myocardial infarction. Actuarial survival at 5 years after the operations was 96.5 ± 9.8%. Freedom from the subsequent aortic events was 91.0 ± 2.9% at 5 years.

CONCLUSIONS

Our treatment method for extensive thoracic aneurysm, from the ascending aorta to the thoracoabdominal aorta, achieved satisfactory results via the use of specific strategies and appropriate organ protection according to the aneurysm extension in the selected patients.

摘要

目的

我们介绍一期替换升主动脉至胸腹主动脉的胸主动脉瘤的经验。

患者和方法

14 名患者(10 名男性和 4 名女性;平均年龄 53.6±12.4 岁)患有扩展型胸主动脉瘤,接受了移植物置换。13 名患者的病变主动脉为慢性主动脉夹层,1 名患者为术中逆行主动脉夹层。5 例患者患有马凡综合征。在先前的手术中,1 例患者接受了 Bentall 手术,4 例患者接受了急性 A 型夹层的半弓置换,1 例患者接受了腹主动脉瘤的 Y 型移植。动脉瘤的入路为后外侧开胸,肋骨交叉切口延伸至腹膜后主动脉。体外循环的动脉入路包括 13 例患者的股动脉和 2 例患者的腹主动脉瘤移植物。7 例患者采用股静脉,3 例患者采用股静脉和肺动脉,1 例患者采用肺动脉。所有患者均采用顺行性脑灌注和内脏灌注。

结果

1 例患者因急性心肌梗死死亡。手术后 5 年的生存率为 96.5±9.8%。5 年后,无后续主动脉事件的生存率为 91.0±2.9%。

结论

我们对升主动脉至胸腹主动脉的广泛胸主动脉瘤的治疗方法,通过在选定患者中根据动脉瘤的扩展使用特定的策略和适当的器官保护,取得了满意的结果。

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