ArticleJournal of cardiothoracic surgery2019
The surgical treatment of anomalous origin of one pulmonary artery from the ascending aorta.
Article in Journal of cardiothoracic surgery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 14 citations in OpenAlex.
- [Anomalous origin of the right pulmonary artery: Non-invasive diagnosis and early surgery].Revista medica del Instituto Mexicano del Seguro Social · 2026Article
- Long-term outcomes after surgical repair of anomalous origin of one pulmonary artery from the aorta in infants younger than 6 months.BMC surgery · 2026Article
- Anomalous Origin of a Pulmonary Artery from the Aorta: Prognosis, Risk Factors and Long-Term Outcomes.Pediatric cardiology · 2026Article
- Anomalous origin of a right pulmonary artery identified with echocardiography combined with CT: a case in a juvenile patient.Journal of cardiothoracic surgery · 2025Article
- Anomalous origin of the fetal pulmonary artery.Frontiers in pediatrics · 2023Article
- Abnormal Origin of the Pulmonary Artery from the Ascending Aorta in the Neonate.Brazilian journal of cardiovascular surgery · 2022Article
- Right Pulmonary Artery Originating from Ascending Aorta (Hemitruncus Arteriosus) with VACTERL Association in a Neonate: A Case Report.Children (Basel, Switzerland) · 2022Article
- Surgical treatment of the anomalous origin of the right pulmonary artery from the ascending aorta: report of two cases.Archivos peruanos de cardiologia y cirugia cardiovascularArticle
- Staged repair of the anomalous origin of the right pulmonary artery from the ascending aorta with aortic coarctation.Annals of pediatric cardiologyArticle
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThis study sought to summarize the clinical experience of surgical treatment of anomalous origin of pulmonary arteries from the ascending aorta (AOPA) in Fuwai hospital.
methodsFifty-two patients (28 males, 17.2 ± 27.2 months old and 8.7 ± 10.2 Kg weight) who have AOPA undertook surgical treatment between 1998 and 2017 were reviewed in this study, 47 out of 52 are anomalous origin of the right pulmonary artery (AORPA), among the rest of the patients are anomalous origin of left pulmonary artery (AOLPA). 27 out of 52 associate with simple cardiac abnormalities, 20 out of 52 associate with complex cardiac malformations, the remaining 5 patients without cardiac abnormalities. Among all patients who underwent surgical treatment, the direct end-to-side anastomosis strategy was applied in 26 patients, autologous pericardial-homograft patch and aortic flap were employed in 20 patients, and synthetic graft was used in 6 patients.
resultsNo patient died during the perioperative period. 50 out of 52 patients were followed-up for 100.1 ± 70.9 months. The rate of pulmonary arterial free restenosis for 2 years, 5 years, and 10 years is 98.0, 96.0 and 92.0%, respectively.
conclusionsThe correct diagnosis and appropriate surgical treatment for AOPA could obtain excellent early and medium-term result.
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