Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1053/j.jvca.2022.07.026 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Corrigendum: Development and validation of a questionnaire to measure the congenital heart disease of children's family stressor.
Front Public Health
December 2024
Department of Nursing, The First Affiliated Hospital of Kunming Medical University, Kunming, China.
[This corrects the article DOI: 10.3389/fpubh.2024.
View Article and Find Full Text PDFNeuromonitoring modalities predicting neurological impairment in pediatric congenital heart disease: a systematic review.
Front Neurol
December 2024
Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Unlabelled: The increased risk of neurodevelopmental impairment in children with congenital heart disease (CHD) has been established, but the search for targeted neurological predictors of adverse outcome is ongoing. This systematic review reports on the utility of three functional neuromonitoring modalities, Near-infrared Spectroscopy (NIRS), electroencephalography (EEG) and biochemical biomarkers, in predicting either clinical neurodevelopmental outcome or structural brain abnormalities after pediatric CHD surgery. Medline, Embase, CENTRAL, Web of Science, clinicaltrials.
View Article and Find Full Text PDFFirst-in-Central-Europe implantation of the self-expandable Pulsta valve in pulmonary position: Short-term results.
Kardiol Pol
January 2025
Department of Cardiology, Polish-Mother's Memorial Hospital Research Institute, Łódź, Poland.
Efficacy of the cross-union protocol in the treatment of congenital tibial pseudarthrosis: a comparative study.
BMC Musculoskelet Disord
January 2025
Department of Orthopaedics Surgery, National Children's Medical Center & Children's Hospital of Fudan University, Wanyuan Road 399, Minhang District, Shanghai, 201102, China.
Background: Congenital Pseudarthrosis of the Tibia (CPT) is a rare pediatric condition presenting substantial challenges for orthopedic surgeons. Aiming to achieve bone union, with subsequent complications such as refractures being common. The aim of the present study is to evaluate the results of our intentional cross-union protocol and to compare these outcomes with those obtained from our previously used techniques.
View Article and Find Full Text PDFWhole Exome Sequencing in a Population of Fetuses With Structural Anomalies.
Prenat Diagn
January 2025
Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Objective: To investigate the exome sequencing (ES) detection rate among fetuses with congenital anomalies and describe the rates in the setting of multiple versus isolated anomalies, perinatal autopsy, and family history of a previously affected child.
Methods: A single-center retrospective chart review was conducted on 397 anomalous fetuses that underwent ES from May 2012 through December 2023. Medical record review included demographics, imaging, and genetic testing.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!