Thoracic endovascular aortic repair for high-risk Stanford type B aortic dissection in a 15-year-old patient with genetic mutations: a case report with follow-up of four years [0.03%]
Xu-Xian Qiu,Yi-Peng Hu,Dong-Lin Li
Xu-Xian Qiu
This case report presents mid- to long-term outcomes of thoracic endovascular aortic repair for high-risk type B aortic dissection in a 15-year-old patient with myosin heavy chain protein 11 genetic mutations. A CT scan showed the primary e...
Six-hour renal resistive index as an early marker of acute kidney injury after infant cardiac surgery: a prospective cohort study [0.03%]
Ahmed R Elsaoudi,Yasser Kazzaz,Sameh Rabie Ismail et al.
Ahmed R Elsaoudi et al.
Background: Acute kidney injury after infant congenital cardiac surgery is common and worsens outcomes. Renal resistive index may aid early postoperative risk stratification. ...
Systematic evaluation of extracardiac findings on cardiac CT angiography in children with CHD: a large single-centre experience [0.03%]
Halise Zeynep Genc,Ali Nazim Guzelbag,Demet Kangel et al.
Halise Zeynep Genc et al.
Introduction: Cardiac CT angiography has seen a steady increase in use for the evaluation of CHD in children. While its primary role is to assess cardiovascular structures, CT angiography also captures extracardiac region...
Karim Salhadar,Stephen M Langley,Daniel McKenna et al.
Karim Salhadar et al.
Double aortic arch with bilateral interruptions is a rare abnormality. Indeed, to the best of our knowledge, it has not previously been reported before. Rare variants, such as a double arch with ligamentous atresia of the left component and...
Larger lung volumes in fetuses with transposition of the great arteries and an intact ventricular septum compared to heart healthy fetuses and fetuses with transposition of the great arteries and a ventricular septal defect [0.03%]
Emil Krogh,Signe Gade Hellmuth,Ditte Staub Jørgensen et al.
Emil Krogh et al.
Background: Complex CHDs may impair organ development. One proposed mechanism is an altered relationship between blood flow, oxygen delivery, and subsequent organ growth. In this study, we examined whether fetal lung, int...
Navigating downtime as a cardiac data abstractor: ensuring data quality and registry submission [0.03%]
心脏数据抽象员的空档期管理：确保数据质量和注册表提交
Sarah Schukei,Kelli Shores,Marian Morris et al.
Sarah Schukei et al.
Introduction: Electronic medical records (EMRs) have become foundational to healthcare, improving communication, data access, and patient outcomes. However, increasing reliance on EMR's has increased vulnerabitlity during...
Postnatal manifestation of left heart failure following foetal-onset right heart failure in biventricular noncompaction with an MYH7 variant: a case report [0.03%]
致心肌非 Compactification 的胎儿期右心衰和产后左心衰综合症的一个病例报告
Yuya Yamada,Keiichi Hirono,Kazushi Yasuda
Yuya Yamada
We report a case of foetal-onset biventricular noncompaction with an MYH7 variant. Prenatal fetal hydrops and right heart failure resolved after birth, but progressive left heart failure developed at 5 months. This transition reflects how p...
Spontaneously resolved pseudoaneurysm after valve-sparing aortic root replacement in Marfan syndrome: a case report - CORRIGENDUM [0.03%]
马凡综合征瓣膜保存主动脉根部置换术后自发消退的假性动脉瘤一例报告-勘误
Eun Chae Kim,Jooncheol Min,Jae Gun Kwak
Eun Chae Kim
Published Erratum
Cardiology in the young. 2026 May 5:1. DOI:10.1017/S1047951126112852 2026
Characteristics and outcomes of patients with occlusion of the left main trunk caused by Kawasaki disease [0.03%]
川崎病所致左主干闭塞患者的临床特征及转归分析
Etsuko Tsuda
Etsuko Tsuda
Background: The outcome of a coronary artery aneurysm at the bifurcation of the left coronary artery caused by Kawasaki disease affects myocardial involvement, which is related to the left ventricular function and outcome of patients. Metho...
Outpatient presentation of ventricular fibrillation in paediatric left ventricular assist device patients: a case series with mechanistic insights [0.03%]
儿科左心室辅助装置患者的门诊室颤表现：案例系列及其机制探讨
Eser Doğan,Zülal Ülger Tutar,Mehmet Baki Beyter et al.
Eser Doğan et al.
Background: Ventricular fibrillation in paediatric recipients of left ventricular assist devices is rare but potentially fatal; however, because systemic perfusion may be temporarily maintained by the mechanical support, ...