Publications by authors named "Stephen Sanders"

A 15q11.2 (BP1-BP2) deletion was detected in a 4-day-old boy who had hypoplastic left heart syndrome (HLHS) diagnosed prenatally by echocardiography. Postmortem examination revealed an anomalous origin of the right coronary artery from the pulmonary trunk (ARCAPT).

View Article and Find Full Text PDF
Article Synopsis
  • Postmortem heart specimens are crucial for studying congenital heart defects but are increasingly difficult to obtain, prompting the need for effective archiving methods.
  • The study scanned 88 wax-infiltrated heart specimens using advanced imaging and 3D printing technology to create detailed digital models, forming an interactive online atlas.
  • The results highlighted a variety of heart defects in the specimens, and the methods developed are valuable for preserving and sharing these important anatomical resources.
View Article and Find Full Text PDF

Photocatalysis with plasmonic nanostructures has lately emerged as a transformative paradigm to drive and alter chemical reactions using light. At the surface of metallic nanoparticles, photoexcitation results in strong near fields, short-lived high-energy "hot" carriers, and light-induced heating, thus creating a local environment where reactions can occur with enhanced efficiencies. In this context, it is critical to understand how to manipulate the nonequilibrium processes triggered by light, as their ultrafast (femto- to picoseconds) relaxation dynamics compete with the process of energy transfer toward the reactants.

View Article and Find Full Text PDF
Article Synopsis
  • Disordered lymphatic drainage is common in congenital heart diseases, and this study focuses on the drainage patterns of the thoracic duct (TD) in patients with heterotaxy, a condition involving abnormal arrangement of internal organs.
  • Researchers analyzed 115 patients with heterotaxy who had cardiovascular imaging, noting that the TD was visualized in nearly half, with varying sidedness: left (25), right (29), and bilateral (2).
  • The study found that while various anatomical factors were associated with TD sidedness, only the sidedness of the superior vena cava and aortic arch were significant predictors, highlighting the complexity of lymphatic anatomy in heterotaxy for future medical interventions.
View Article and Find Full Text PDF

Ebstein anomaly (EA) is a rare congenital heart defect characterized by abnormal development of the tricuspid valve (TV) and right ventricular myocardium. This study documents 2 dramatic cases of fetal EA characterized by hydrops and cardiomegaly, leading to intrauterine or early neonatal death. These clinical outcomes were associated with morphological abnormalities including severe tricuspid regurgitation, unguarded TV orifice, pulmonary atresia, and flattened right ventricular myocardium.

View Article and Find Full Text PDF

This paper illustrates a valve-sparing cardiac dissection technique that keeps the atrioventricular and semilunar valves and other important cardiac structures intact. The technique minimizes disruption in heart specimens, so they remain suitable for teaching, demonstration, and further research. When performed following the perfusion-distension method of fixation, as our group previously described, this technique could optimize the preservation of heart specimens for teaching and digital archiving postdissection.

View Article and Find Full Text PDF

Background: As more pediatric patients become candidates for heart transplantation (HT), understanding pathological predictors of outcome and the accuracy of the pretransplantation evaluation are important to optimize utilization of scarce donor organs and improve outcomes. The authors aimed to investigate explanted heart specimens to identify pathologic predictors that may affect cardiac allograft survival after HT.

Methods: Explanted pediatric hearts obtained over an 11-year period were analyzed to understand the patient demographics, indications for transplant, and the clinical-pathological factors.

View Article and Find Full Text PDF

Audience And Type Of Curriculum: This longitudinal leadership curriculum is designed for emergency medicine residents at all levels, with individual sessions designed for each residency year.

Length Of Curriculum: This curriculum runs once annually over three to four years of emergency medicine residency.

Introduction: Leadership is a vital skill for emergency physicians but is often passively taught during residency training.

View Article and Find Full Text PDF
Article Synopsis
  • - This document serves as an evidence-based guideline for naming and classifying congenital bicuspid aortic valve and its associated conditions, aimed at a wide range of medical professionals.
  • - It is designed for use by pediatricians, cardiologists, surgeons, and researchers, ensuring clarity across various healthcare fields.
  • - The consensus is subject to updates as new research and key findings emerge, highlighting its dynamic nature in adapting to evolving medical knowledge.
View Article and Find Full Text PDF

Background: Falls are common in people with multiple sclerosis (MS), causing injuries, fear of falling, and loss of independence. Although targeted interventions (physical therapy) can help, patients underreport and clinicians undertreat this issue. Patient-generated data, combined with clinical data, can support the prediction of falls and lead to timely intervention (including referral to specialized physical therapy).

View Article and Find Full Text PDF

Background: Neo-aortic root dilatation can lead to significant late morbidity after the arterial switch operation (ASO) for dextro-transposition of the great arteries (d-TGA).

Objectives: We sought to examine the growth of the neo-aortic root in d-TGA.

Methods: A single-center, retrospective cohort study of patients who underwent the ASO between July 1, 1981 and September 30, 2022 was performed.

View Article and Find Full Text PDF
Article Synopsis
  • The study analyzed the histomorphologic characteristics of common wall tissue from patients with anomalous aortic origin of a coronary artery to check for correlations with clinical and imaging results.
  • A total of 20 patients (averaging 7-18 years old) were examined, revealing notable histological changes like elastic fiber alterations and mural fibrosis, primarily in those over 10 years old.
  • The research concluded that the wall of the anomalous coronary artery closely resembles the aorta histologically, but the severity of vascular changes didn't have a clear link to the imaging findings.
View Article and Find Full Text PDF
Article Synopsis
  • There are significant differences in sudden cardiac death (SCD) rates and the types of ventricular arrhythmias (VAs) in patients with congenital heart defects (CHD), categorized into two groups: Group A (with distinct anatomical structures) and Group B (with diffuse or less-defined issues).
  • Group A includes patients with clear pathways for ventricular tachycardia (VT), while Group B involves complex conditions like Ebstein anomaly and transposition of great arteries, which tend to have more severe arrhythmias like polymorphic VT and ventricular fibrillation.
  • For Group B patients, the effectiveness of tests like programmed ventricular stimulation is uncertain, and catheter ablation is less commonly used;
View Article and Find Full Text PDF

Patients with congenital heart disease associated with a higher risk for ventricular arrhythmias (VA) and sudden cardiac death (SCD) can be divided conceptually into those with discrete mechanisms for reentrant monomorphic ventricular tachycardia (VT) (Group A) and those with more diffuse substrates (Group B). Part I of this review addresses Group A lesions, which predominantly consist of tetralogy of Fallot and related variants. Well-defined anatomic isthmuses for reentrant monomorphic VT are interposed between surgical scars and the pulmonary or tricuspid annulus.

View Article and Find Full Text PDF

Surface-enhanced Raman spectroscopy (SERS) is enabled by local surface plasmon resonances (LSPRs) in metallic nanogaps. When SERS is excited by direct illumination of the nanogap, the background heating of the lattice and electrons can prevent further manipulation of the molecules. To overcome this issue, we report SERS in electromigrated gold molecular junctions excited remotely: surface plasmon polaritons (SPPs) are excited at nearby gratings, propagate to the junction, and couple to the local nanogap plasmon modes.

View Article and Find Full Text PDF

Background: Ventricular pacing can cause myocardial dysfunction, but how lead anchoring to the myocardium affects function has not been studied.

Objective: The purpose of this study was to evaluate patterns of regional and global ventricular function in patients with a ventricular lead using cine cardiac computed tomography (CCT) and histology.

Methods: This was a single-center retrospective study with 2 groups of patients with a ventricular lead: (1) those who underwent cine CCT from September 2020 to June 2021 and (2) those whose cardiac specimen was analyzed histologically.

View Article and Find Full Text PDF

Formalin-fixed whole heart specimens are essential for studying the anatomy of congenital heart defects. Because of the improvement in diagnostic imaging and treatment, and cultural transition, heart specimens with congenital heart defects have become more and more rare and irreplaceable but are at risk of accidental deterioration through dehydration during long-term storage. In this article, we share our experience in reconditioning our inadvertently dehydrated heart specimens using a simple Formol-Glycerol solution that allowed for rehydration and recovery of such specimens.

View Article and Find Full Text PDF
Article Synopsis
  • Spontaneous coronary artery dissection in infants is a very uncommon occurrence.* -
  • The study discusses two neonates who experienced severe heart issues caused by this condition.* -
  • Both infants lacked other health problems or conditions that could clarify why they had coronary artery dissection.*
View Article and Find Full Text PDF

A 2-month-old male infant, born premature with a birth weight of 865 g, was found to have a tricuspid valve mass mimicking thrombus and vegetation by echocardiogram on the fourth day of life. The patient was treated with antibiotics and anticoagulation with no change in the size of the mass on serial follow-up echocardiography. The patient died of severe pulmonary vein stenosis and complex neurological disability.

View Article and Find Full Text PDF

Background: Outcomes following congenital aortic valve (AoV) repair are plagued by progressive dysfunction of currently available leaflet substitute materials.

Objectives: We compared the long-term outcomes of congenital AoV repair using porcine intestinal submucosa vs autologous pericardium (AP).

Methods: This was a single-center retrospective review of all patients who underwent congenital AoV repair with either porcine intestinal submucosa or AP from October 2009 to March 2013.

View Article and Find Full Text PDF

Double aortic arch associated with atresia of the left arch proximal to the left common carotid artery has been considered a theoretical possibility. To our knowledge, we report the first patient with this anatomy confirmed by surgical observation.

View Article and Find Full Text PDF

• ALCAPA must be considered in an infant with ischemia and/or heart failure. • A rare variant with intramural aortic course may appear normal on 2D echo. • Retrograde color flow in the LCA is highly suspicious for this lesion.

View Article and Find Full Text PDF

Background: Neurodevelopmental impairment is common in survivors of congenital diaphragmatic hernia (CDH). Altered cerebral perfusion in utero may contribute to abnormal brain development in CDH patients.

Methods: 5 fetal lambs with surgical left-CDH and 5 controls underwent transuterine cranial Doppler and contrast enhanced ultrasound (CEUS).

View Article and Find Full Text PDF