Background: Despite advancements in imaging technologies, including CT scans and MRI, these modalities may still fail to capture intricate details of congenital heart defects accurately. Virtual 3D models have revolutionized the field of pediatric interventional cardiology by providing clinicians with tangible representations of complex anatomical structures. We examined the feasibility and accuracy of utilizing an automated, Artificial Intelligence (AI) driven, cloud-based platform for virtual 3D visualization of complex congenital heart disease obtained from 3D rotational angiography DICOM images.
Methods: Five patients selected at random with 3DRA performed in the pediatric cardiac catheterization suite were selected. 3DRA's were performed following published institutional protocols and segmentations performed by primary operators. The 3DRA DICOM images were anonymized as per protocol and exported. Images when then processed by Axial3D Artificial Intelligence (AI) driven cloud-based platform for virtual segmentation. Two separate expert operators were selected to subjectively analyze the segmentations and compare them to the operator reconstructions for anatomic accuracy.
Results: Comparing results with local reconstructions by expert operators, five different patient anatomies were analyzed, showcasing Axial3D's ability to produce highly detailed reconstructions with improved visual appeal, including color-coded segments for implanted materials like stents. The reconstructions exhibited superior segmentation of different intrathoracic structures when compared to local models, offering valuable insights for medical professionals and patients.
Conclusions: The use of the AI driven, cloud-based platform for 3D visualization of complex congenital heart lesions presents a promising advancement in pediatric interventional cardiology, facilitating enhanced patient care, procedural planning, and educational opportunities for trainees and patients alike.
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http://dx.doi.org/10.1186/s41205-024-00247-6 | DOI Listing |
Echocardiography
January 2025
Department of Ultrasound, Wuhan Asia Heart Hospital Affiliated to Wuhan University of Science and Technology, Wuhan Clinical Medical Research Center of Cardiovascular Imaging, Wuhan, China.
This manuscript presents a rare case of a complex pulmonary venous malposition with an intact atrial septum and ventricular septum. The study demonstrates the diagnostic utility of echocardiography and computed tomography in the evaluation of complex congenital heart disease.
View Article and Find Full Text PDFFront Mol Neurosci
January 2025
Department of Pediatric Surgery, Medical Faculty of Mannheim, University of Heidelberg, Mannheim, Germany.
Hirschsprung's disease (HSCR) is characterized by congenital absence of ganglion cells in the gastrointestinal tract, which leads to impaired defecation, constipation and intestinal obstruction. The current diagnosis of HSCR is based on Rectal Suction Biopsies (RSBs), which could be complex in newborns. Occasionally, there is a delay in diagnosis that can increase the risk of clinical complications.
View Article and Find Full Text PDFCureus
December 2024
Emergency Department, Bayhealth Hospital, Dover, USA.
Subglottic stenosis (SGS) presents a rare, yet challenging condition characterized by airway obstruction below the glottis, with diverse etiologies ranging from congenital to acquired factors like intubation or autoimmune diseases. Diagnosis and management of SGS during pregnancy are particularly complex due to limited literature and diagnostic consensus. This article presents a case of a 26-year-old pregnant woman presenting with escalating dyspnea and stridor attributed to SGS, most likely secondary to idiopathic etiology.
View Article and Find Full Text PDFCardiol Young
January 2025
Department of Cardiology, Medica Super Specialty Hospital, Kolkata, India.
Background: Transcatheter closure of large and complex atrial septal defect can pose challenges and complications during device placement. To improve stability, several assistive techniques have been developed.
Methods: This retrospective study evaluated the efficacy of the device-assisted device closure technique for large secundum atrial septal defects.
In Vitro Cell Dev Biol Anim
January 2025
Department of Oral and Maxillofacial Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, 250012, Shandong, China.
Cleft lip and palate (CL/P) are prevalent congenital anomalies with complex genetic causes. The G874A mutation of T-box transcription factor 22 (TBX-22) gene is notably associated with CL/P, while the underlying mechanism remains to be clarified. Studies have shown that the restriction of epithelial-mesenchymal transformation (EMT) process in medial edge epithelial cells (MEEs) is crucial for CL/P development.
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