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期刊名:Pediatric cardiac surgery annual

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ISSN:1092-9126

e-ISSN:1876-4665

IF/分区:0.0/

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共收录本刊相关文章索引477
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Carlos M Mery,Ziv Beckerman Carlos M Mery
Anomalous aortic origin of a coronary artery (AAOCA) is associated with an increased risk of sudden cardiac death. Multiple surgical techniques have been developed to treat this anomaly. The optimal surgical technique to treat AAOCA is uncl...
Silvana Molossi,Shagun Sachdeva Silvana Molossi
Congenital coronary artery anomalies remain a leading cause of sudden cardiac death in the young. Within these, anomalous aortic origin of a coronary artery represents the largest group, with anomalies of the left coronary artery carrying h...
Justin Robinson,David S Winlaw Justin Robinson
Surgical management of isolated aortic valve pathology in adolescents primarily involves aortic valve repair and the Ross procedure, each with distinct advantages and limitations influenced by anatomical considerations. The optimal surgical...
Ayman Almousa,Andrew Behrmann,Paighton Miller et al. Ayman Almousa et al.
We explore the innovative use of atrial appendage tissue for creating pulmonary valves in children, focusing on its application in Tetralogy of Fallot repair. We discuss the background, preclinical studies, surgical approach, and early clin...
Bari Murtuza,Juan Lehoux,Victor O Morell Bari Murtuza
Aortic root translocation and double root translocation have emerged as potentially valuable surgical options for complex transposition of the great arteries or double outlet right ventricle with VSD and LV outflow tract obstruction (LVOTO)...
Justus G Reitz,Sofia Hanabergh,Eiri Kisamori et al. Justus G Reitz et al.
Mitral valve repair is often preferred over replacement due to the preservation of native valve function, allowing for somatic growth and resulting in fewer complications and reoperations. Although there are no randomized trials comparing r...
Luciana da Fonseca da Silva,Victor Morell,Mario Castro Medina et al. Luciana da Fonseca da Silva et al.
Following the Starnes procedure, a progressive reduction in the RV cavity occurs, suggesting that the RV was unsuitable for a biventricular repair. For that reason, those patients traditionally followed the single ventricle pathway. In 2019...
Emile A Bacha,Stephanie N Nguyen,Andrew B Goldstone et al. Emile A Bacha et al.
Hypoplastic left heart syndrome (HLHS)-a universally fatal condition only 40 years ago-remains one of the most challenging congenital heart defects. The advancements and insights gained from historical experiences with the Norwood operation...
Supreet P Marathe,Christopher W Baird Supreet P Marathe
Congenital aortic and truncal valve diseases pose significant challenges due to their complex anatomy, diverse clinical presentations, and impact on long-term outcomes. Surgical management requires a tailored approach, balancing the need fo...
Christopher Z Lam,Shi-Joon Yoo,Osami Honjo et al. Christopher Z Lam et al.
The borderline left ventricle (LV) encompasses a heterogenous group of cardiac defects that result in underdevelopment of the left heart. Data supporting decision making is difficult to interpret because borderline LV hypoplasia is a relati...