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

2008 ◽  
Vol 135 (3) ◽  
pp. 699-701 ◽  
Author(s):  
Yong-Qiang Lai ◽  
Shang-Dong Xu ◽  
Zhi-Zhong Li ◽  
Bao-Zhong Yang ◽  
Su Wang ◽  
...  
2016 ◽  
Vol 9 (4) ◽  
pp. 326-329 ◽  
Author(s):  
Yuki Orimoto ◽  
Hiroyuki Ishibashi ◽  
Ikuo Sugimoto ◽  
Tetsuya Yamada ◽  
Yuki Maruyama ◽  
...  

2020 ◽  
Vol 54 (8) ◽  
pp. 741-746
Author(s):  
Hiroki Mitsuoka ◽  
Yuki Orimoto ◽  
Takahiro Arima ◽  
Tsuneo Ishiguchi ◽  
Hiroyuki Ishibashi

Background: Pseudoaneurysms that develop after surgical repair of a patent ductus arteriosus (PDA) are more likely to rupture, but open surgery including a repeat thoracotomy would be highly invasive. We report 2 cases of thoracic endovascular aortic repair (TEVAR) for such pseudoaneurysms. Methods/Results: A 59-year-old woman who underwent PDA surgical ligation at 13 years of age presented with sudden hemoptysis. She was diagnosed with a ruptured distorted pseudoaneurysm sized 26 mm; emergency TEVAR was performed. A 23-year-old woman with a history of Down syndrome, endocardial cushion defect, and PDA underwent 2 thoracotomy surgeries including PDA ligation. During a medical checkup, an abnormal shadow was detected on chest radiography. She was diagnosed with a 15-mm pseudoaneurysm after PDA surgical repair; TEVAR was performed. In both cases, the postoperative course was uneventful. Conclusions: To the best of our knowledge, this is the first report of emergency TEVAR for ruptured pseudoaneurysms after PDA ligation. Thoracic endovascular aortic repair is an important therapeutic option for such cases as it eliminates the need for repeat thoracotomy.


1956 ◽  
Vol 31 (3) ◽  
pp. 268-285
Author(s):  
F. Henry Ellis ◽  
John W. Kirklin ◽  
John A. Callahan ◽  
Earl H. Wood

1968 ◽  
Vol 32 (11) ◽  
pp. 1571-1577 ◽  
Author(s):  
HIROHISA KATO ◽  
TEIICHI ODA ◽  
MIZUO HIROSE ◽  
YOSHIAKI YOSHIZAWA ◽  
KAZUO URYU ◽  
...  

2021 ◽  
Vol 70 (Suppl-4) ◽  
pp. S701-05
Author(s):  
Khushal Khan Khattak ◽  
Maad Ullah ◽  
Abdul Malik Sheikh ◽  
Asma Kanwal ◽  
Sajid Ali Shah ◽  
...  

Objective: To determine different treatment options in patients of Patent Ductus Arteriosus with pulmonary hypertension beyond neonatal period. Study Design: Descriptive cross sectional study. Place and Duration of Study: This study was carried out in Pediatric Cardiology department of Rawalpindi Institute of Cardiology, from Jan 2017 to Jan 2019. Methodology: Patients having PDA with pulmonary hypertension were included in the study. Treatment options were divided into percutaneous catheter device closure, surgical ligation of patent ductus arteriosus and palliative treatment. Any adverse event during the procedure was documented. Stratification was done in regard to gender and age group. Post stratification chi square test was applied and p-value less than or equal to 0.05 was considered as significant. Results: Total number of patients included in the study were 37. Mean age (years) of patients (Mean ± SD) was 19.21 ± 8.76. Mean ± SD pulmonary artery pressure was 56.43 ± 11.55 mmHg. Percutaneous catheter device closure was successful in 24 (64.9%) patients, in 7 (18.9%) patients primary surgical PDA ligation was done, 3 (8.1%) patients were advised palliative treatment and in 3 (8.1%) patients adverse events occurred during percutaneous device closure and were thus referred for surgical ligation. Patent ductus Arteriosus Occlutech device was used in 18 (48.6%) patients, Occlutech VSD device was used in 7 (18.5%) patients and in 1 (2.7%) patient AGA duct occluder was used. Conclusion: In patients with patent ductus arteriosus and pulmonary artery hypertension, percutaneous catheter device closure is a safe and effective procedure.


PEDIATRICS ◽  
1967 ◽  
Vol 39 (3) ◽  
pp. 446-448
Author(s):  
COLETTE M. KOHLER ◽  
DAN G. MCNAMARA

The presence of patent ductus arteriosus without a typical continuous murmur has long been recognized, especially in the presence of pulmonary hypertension, or a small ductus, or with associated cardiac defects; however, there are only a few reports of documented, intermittently disappearing murmurs occurring in individuals over 6 months of age with a substantial shunt in the absence of pulmonary hypertension or associated defects. Danilowicz, et al. have recently reported delayed closure of the ductus anteriosus up to 6 months of age in some premature infants. We present this case report of a 2½-year-old boy with patent ductus arteriosus with cardiac catheterizations during the disappearance and subsequent reappearance of a continuous murmur with documentation of absence of shunting when the murmur was absent and substantial shunting if the murmur was present.


Heart ◽  
1964 ◽  
Vol 26 (5) ◽  
pp. 600-605 ◽  
Author(s):  
J. M. Reid ◽  
J. G. Stevenson ◽  
E. N. Coleman ◽  
R. S. Barclay ◽  
T. M. Welsh ◽  
...  

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