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J Thorac Cardiovasc Surg 2008;135:699-701
© 2008 The American Association for Thoracic Surgery


Brief Communication

Thoracic endovascular aortic repair of adult patent ductus arteriosus with pulmonary hypertension

Yong-Qiang Lai, MDa,*, Shang-Dong Xu, MDa, Zhi-Zhong Li, MDb, Bao-Zhong Yang, MDc, Su Wang, MDb, Jin-Hua Li, MDa, Jing-Wei Li, MDa, Yi Luo, MDa, Zhao-Guang Zhang, MDa

a Division of Cardiac Surgery, Beijing Anzhen Hospital, Beijing Institute of Heart, Lung, & Vascular Diseases, Capital Medical University, Beijing, China
b Division of Cardiology, Beijing Anzhen Hospital, Beijing Institute of Heart, Lung, & Vascular Diseases, Capital Medical University, Beijing, China
c Division of Vascular Surgery, Beijing Anzhen Hospital, Beijing Institute of Heart, Lung, & Vascular Diseases, Capital Medical University, Beijing, China

Received for publication September 3, 2007; accepted for publication November 26, 2007.

* Address for reprints: Yong-Qiang Lai, MD, Division of Cardiac Surgery, Beijing Anzhen Hospital, 36 Wuluju Chaoyang District, Beijing, China, 100029. (Email: yongqianglai@yahoo.com).

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Figure 1
Drs Xu, J-W Li, Z-Z Li, J-H Li, and Wang (top row, left to right); Drs Yang, Luo, Zhang, and Lai (bottom row, left to right).


Thoracic endovascular aortic repair (TEVAR) has emerged as an alternative treatment for adult patent ductus arteriosus (PDA) in recent years.1Go We report here our preliminary experience in treating adult PDA with stent–grafts.

Clinical Summary

From September 2005 to March 2007, a total of 4 patients with a large PDA and pulmonary hypertension underwent TEVAR. All patients had exertional dyspnea. Transthoracic echocardiography, computed tomographic angiography, and right heart catheterization were conducted before the operation. All patients had severe pulmonary hypertension. Indications for stent–graft implantation were as follows: (1) adult patient with large PDA, (2) no other congenital cardiac defects, (3) no right-to-left shunt, (4) adequate landing zone (arch diameter <35 mm), and (5) adequate access route. The study was approved by the institutional review board, and informed consent was obtained. Clinical data are summarized in Go Table 1.


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