
Structural and Congenital Heart Disease (formerly known as Congenital Heart Disease) is a peer-reviewed journal dedicated to the study and management of heart disease across the lifespan. The journal covers both congenital and structural heart diseases, reflecting the evolving landscape of cardiovascular research and clinical practice.
As the official journal of the Children’s Hospital of Nanjing Medical University, it is committed to publishing high-quality clinical studies, invited editorials, state-of-the-art reviews, case reports, articles addressing the history and development of heart disease, and continuing medical education (CME) materials.
All manuscripts, including invited submissions, undergo a rigorous and thorough editorial and peer-review process to ensure the reliability, scientific integrity, and clinical relevance of published research.
Formerly Congenital Heart Disease[Science Citation Index Expanded (Clarivate Analytics): 2024 Impact Factor: 1.2; Scopus CiteScore (Impact per Publication 2024): 0.9; SNIP (Source Normalized Impact per Paper 2024): 0.380; Journal Citation Report/Science Edition (JCR); etc.]
From Volume 21, Issue 1 2026, the journal formerly titled Congenital Heart Disease will be published as Structural and Congenital Heart Disease.
The journal remains dedicated to high-quality research in congenital and structural heart diseases and continues under the same editorial leadership and peer-review framework.
Read the formal announcement from the Editors-in-Chief, here.
Open Access
EDITORIAL
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.080525 - 31 March 2026
Abstract This article has no abstract. More >
Open Access
ARTICLE
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.077974 - 31 March 2026
Abstract Congenital heart disease (CHD) is a common birth defect in children, and surgical intervention is the primary treatment. The traditional standard median sternotomy (MS) has drawbacks such as significant trauma and obvious scarring. The right axillary incision (RAI) has gradually become a conventional approach due to its advantages of preserving thoracic cage integrity, small incision size, rapid recovery, and hidden scarring. However, there is currently a lack of relevant guidelines and consensus for its application. This consensus adopts the international Delphi process, systematically searching domestic and foreign literature on CHD from 1982 to 2024. It… More >
Open Access
ARTICLE
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.076648 - 31 March 2026
Abstract Backgorund: Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly of coronary artery anatomy, usually diagnosed in infancy, but adults may also be affected by this deformity. Objectives: The aim of this study is to examine long-term outcomes in patients with ALCAPA and analyze the relevant factors influencing postoperative outcomes. Methods: The records of patients with ALCAPA admitted from January 2015 to December 2024 were retrospectively reviewed. Clinical data of the patients were retrieved from the records. The follow-up data included mortality rates and complications. Kaplan-Meier survival curves were… More >
Open Access
ARTICLE
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.077612 - 31 March 2026
Abstract Background: This study evaluated the impact of a comprehensive prevention program, which integrated eight evidence-based measures consistent with current clinical guidelines and practice standards, on ventilator-associated pneumonia (VAP) rates in a pediatric cardiac surgical intensive care unit (ICU). Methods: A quasi-experimental study was conducted from 2023 to 2024. We compared VAP rates across a 5-month pre-intervention period, a 12-month intervention period, and a 7-month post-intervention period in patients receiving mechanical ventilation for over 48 h. Additional outcomes, including postoperative length of stay were also assessed before and after the intervention. Results: Among 829 at-risk patients and 5677… More >
Open Access
CASE REPORT
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.074189 - 31 March 2026
Abstract Background: Transcatheter closure of perimembranous ventricular septal defects (pmVSDs) with Lifetech™ Konar-Multifunctional Occluder (MFO) has demonstrated high procedural success and safety. However, long-term complications due to valve–device interaction are rarely reported. We describe a pediatric patient who developed progressive right ventricular outflow tract (RVOT) obstruction and severe tricuspid regurgitation 20 months after MFO closure, highlighting mechanisms, management, and outcomes. Case Description: A 13-year-old girl underwent successful MFO closure of a 6-mm pmVSD. Early follow-up showed trivial tricuspid regurgitation and mild subpulmonic stenosis. Pre-procedural imaging revealed right ventricular hypertrophy caused by long-standing jet-related turbulence from the pmVSD, with… More >
Open Access
CASE REPORT
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.071470 - 31 March 2026
Abstract We report a full-term newborn with pulmonary atresia with an intact ventricular septum who developed acute hypoxemia after ductal stent embolization. Emergency surgery was performed to remove the stent and create a central systemic-to-pulmonary shunt using a 3.5 mm GORE-TEX® graft via a modified Gates, Laks, and Johnson technique. Postoperative recovery was favorable. At 24 months, the shunt remained patent with adequate pulmonary artery growth. This case underscores prompt surgical rescue and supports central shunting as an effective mid-term solution. More >
Open Access
REVIEW
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.075858 - 31 March 2026
Abstract Hyperglycemia in pregnancy (HIP) is an important independent risk factor for congenital heart disease (CHD) in offspring. With an increasing number of women of childbearing age experiencing gestational hyperglycemia, the impact of an intrauterine hyperglycemic environment on fetal development has drawn significant attention. However, the teratogenic mechanisms underlying its effects on cardiac development remain incompletely understood. This review systematically analyzes relevant literature to summarize its underlying mechanisms and key findings: A hyperglycemic environment disrupts cardiac neural crest cell migration, differentiation, and the proliferation/apoptosis balance of cardiomyocytes by inducing oxidative stress, endoplasmic reticulum stress, and inflammatory… More >
Open Access
ARTICLE
Structural and Congenital Heart Disease, Vol.21, No.1, 2026, DOI:10.32604/schd.2026.072858 - 31 March 2026
Abstract Background: Hypoplastic left heart syndrome (HLHS) is a congenital heart disease (CHD), and accumulating evidence has implicated ferroptosis in the pathogenesis of HLHS. Therefore, exploring ferroptosis-related genes (FRGs) in HLHS is of clinical significance. Materials and Methods: Gene Expression Omnibus (GEO) was accessed to obtain analytical data. WGCNA was employed to screen relevant module genes, and the limma package was used to identify differentially expressed genes (DEGs). The rfe function in the R package caret and the glmnet package were utilized to conduct SVM-RFE and LASSO regression analyses, and the intersection of these two analyses was taken… More >