175 results match your criteria: "SSM Health Cardinal Glennon Children's Hospital.[Affiliation]"

Systemic Lupus Erythematosus, Evans Syndrome, and Neurofibromatosis: An Unusual Combination in Pediatric Patient.

J Pediatr Hematol Oncol

May 2020

Division of Pediatric Hematology-Oncology, Saint Louis University School of Medicine, SSM Health Cardinal Glennon Children's Hospital, St Louis, MO.

Systemic lupus erythematosus (SLE) is an autoimmune disease that affects multiple organ systems. Patients can have hematologic manifestations, including Evans syndrome (ES), which is characterized by immune-mediated thrombocytopenia and anemia. The association of neurofibromatosis 1 (NF1) with autoimmune disorders is rarely reported.

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Anti-E alloimmunization is the third most common cause of neonatal hemolytic disease, typically causing mild to moderate hemolytic anemia. We report an unusual case of severe hydrops fetalis and persistent pulmonary hypertension (PPHN) in a neonate with anti-E alloimmunization. Our case emphasizes the importance of close surveillance for development of severe fetal hemolytic anemia and possible need for antenatal intervention.

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Background: Pediatric patients with inflammatory bowel disease (IBD) are at increased risk of gadolinium deposition given the potential need for multiple contrast-enhanced magnetic resonance enterography (MRE) exams over their lifetime.

Objective: To determine whether gadolinium-based contrast agents are necessary in assessing active bowel inflammation on MRE in pediatric patients with known or suspected IBD.

Materials And Methods: We conducted a retrospective study of 77 patients (7-18 years; 68.

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Background: To compare outcomes for complicated appendicitis treated with early versus interval appendectomy and to identify which patients would likely benefit from early appendectomy.

Methods: A retrospective review of complicated appendicitis was performed from 2010 to 2015. Patients were divided into early (EA) versus interval appendectomy (IA) groups.

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Background: Hydroxyurea (HU) reduces complications and improves quality and duration of life in sickle cell disease. Evidence supports the use of HU starting after nine months of age.

Procedures: We performed a retrospective study of patients starting HU at less than five years of age between January 1, 2008, and December 31, 2016.

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Standardized text messages improve 30-day patient follow-up for ACS pediatric NSQIP cases.

Pediatr Surg Int

April 2019

Division of Pediatric Surgery, SSM Health Cardinal Glennon Children's Hospital, Saint Louis University, 1465 S Grand Blvd, St. Louis, MO, 63104-6454, USA.

Purpose: Thirty-day follow-up is a critical and challenging component of the American College of Surgeons (ACS) National Surgical Quality Improvement Program (NSQIP). We hypothesized the simplicity and immediacy of text messaging would increase response rates while reducing workload.

Methods: For 6 months, text messages were the primary form of contact for first and second follow-up attempts.

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The purpose of this study was to determine whether trisomy 18 patients are at an increased risk of tumor development and require formal tumor screening recommendations. A literature search of trisomy 18 patients with reports of tumors or malignancies, and compilation of all previously reported as well as new unreported cases was performed. 67 patients with trisomy 18 were found to have documented malignancies.

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Systematic Review: Online Crowdsourcing to Assess Perceptual Speech Outcomes.

J Surg Res

December 2018

Division of Plastic Surgery, Saint Louis University School of Medicine, St. Louis, Missouri; SSM Health Cardinal Glennon Children's Hospital at SLU, St. Louis, Missouri. Electronic address:

Background: Speech is integral for human interaction and development. Speech assessments are critical in the growing child, especially in the surgical evaluation of patients undergoing cleft palate and speech surgeries. Online crowdsourcing enables layperson raters, allowing rapid and large-scale data collection.

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We reviewed the resource utilization of patients with human rhinovirus/enterovirus (HRV/ENT), influenza A/B (FLU), or respiratory syncytial virus (RSV). A total of 2013 patients with nasopharyngeal swabs positive for HRV/ENT, RSV, or FLU were included. Records were reviewed for respiratory support, vascular access procedures, emergency department care only versus admission versus pediatric intensive care unit (PICU) care, antibiotics, length of stay, and billing data.

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Pancreatic heterotopia in a neonatal abdominopelvic cyst.

Pediatr Radiol

March 2019

Department of Radiology, SSM Health Cardinal Glennon Children's Hospital, St. Louis University School of Medicine, 3635 Vista Avenue at Grand Boulevard, St. Louis, MO, 63110, USA.

Pancreatic heterotopia is a rare congenital anomaly more commonly incidentally found in adults. While intra-abdominal cysts found on prenatal imaging are not uncommon, we examine a case of pancreatic heterotopia presenting in an abdominopelvic cyst on prenatal imaging. At birth, the neonate was found to have hypoglycemia unresponsive to treatment that resolved after cyst resection.

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Introduction: Bubble continuous positive airway pressure (bCPAP) generates a variable pressure due to bubble size and frequency, and these pressure oscillations may contribute to lung recruitment and gas exchange. Single-outlet bCPAP devices generate larger pressure fluctuation than bCPAP devices with diffusers, but clinical efficacy is unclear. Our hypothesis was that a single-outlet bCPAP device (B&B Bubbler©) would decrease extubation failure and improve oxygenation compared with a bCPAP device with a diffuser (BabiPlus©).

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Objectives: Previous studies have not evaluated the utility of obtaining chest radiographs (CXR) in patients with acute asthma exacerbation reporting chest pain. The aims of this study were to evaluate the symptom of chest pain as a predictor for clinicians obtaining a CXR in these patients and to evaluate chest pain as a predictor of a positive CXR finding.

Methods: This was a retrospective chart review of patients, ages 2 to 18 years, presenting for acute asthma exacerbation to the emergency department from August 1, 2014, to March 31, 2016.

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Poisoning, Overdoses, Toxic Exposures.

Mo Med

August 2019

Andrea Rivera-Sepulveda, MD, MSc, FAAP, is in the Division of Pediatric Emergency Medicine, SSM Health Cardinal Glennon Children's Hospital, Saint Louis University School of Medicine, in St. Louis, Mo.

The national poison center movement originated in the Midwest with actions of the American Academy of Pediatrics in Chicago, Illinois, in 1972. The Missouri Poison Center (MPC) was established in 1974. The MPC and other regional poison centers are essential to the public health locally and nationally.

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Background: Congenital lung malformations exist along a spectrum of pathogenesis and disease severity. Extrapulmonary sequestration (EPS), in which nonfunctional lung tissue develops without connection to the tracheobronchial tree, is one rare manifestation of this disease. Atypical vascular anatomy with a systemic feeding vessel characterizes these lesions.

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Nano-evidence for joint microbleeds in hemophilia patients.

J Thromb Haemost

October 2018

Department of Pediatrics, Division of Pediatric Hematology/Oncology, SSM Health Cardinal Glennon Children's Hospital, Saint Louis University, St. Louis, MO, USA.

The concept of joint microbleeding in hemophilia patients was first proposed over 10 years ago. This was based on unexpected abnormalities found in medical imaging studies of asymptomatic joints. Since then, there have been no published studies confirming the presence of joint microbleeds.

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Laparoscopy is increasingly utilized in neonatal surgery with safe and effective outcomes. Air embolism from insufflation for pneumoperitoneum is a rare but known risk of laparoscopy. Here we present a rare case of air embolism during insufflation for laparoscopic peritoneal dialysis catheter placement treated with extracorporeal cardiopulmonary resuscitation.

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Community Healthcare and Technology to Enhance Communication in Pediatric Obesity Care.

Child Obes

October 2018

14 Department of Pediatrics, C.S. Mott Children's Hospital and Von Voigtlander Women's Hospital, University of Michigan, Ann Arbor, MI.

Childhood obesity continues to be a critical healthcare issue and a paradigm of a pervasive chronic disease affecting even our youngest children. When considered within the context of the socioecological model, the factors that influence weight status, including the social determinants of health, limit the impact of multidisciplinary care that occurs solely within the medical setting. Coordinated care that incorporates communication between the healthcare and community sectors is necessary to more effectively prevent and treat obesity.

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Right ventricular-dependent coronary circulation (RVDCC) is associated with pulmonary atresia with intact ventricular septum and is defined by two or more epicardial coronary arteries with atresia or severe stenosis resulting in the dependency of coronary supply by retrograde flow. The hypothesis of this study is that coronary Doppler flow patterns on echocardiography can be used to distinguish patients with RVDCC. Between 2007 and 2016, we reviewed 16 patients with pulmonary atresia or critical pulmonary stenosis.

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Temporomandibular Joint Septic Arthritis.

Plast Reconstr Surg Glob Open

January 2018

Division of Pediatric Plastic Surgery, SSM Health Cardinal Glennon Children's Hospital at Saint Louis University School of Medicine, St. Louis, Mo.; Department of Radiology, Neuroradiology Section, Saint Louis University School of Medicine, St. Louis, Mo.; and SSM Health Cardinal Glennon Children's Hospital at Saint Louis University School of Medicine, St. Louis, Mo.

Infection of the temporomandibular joint (TMJ) is a rare pediatric condition resulting from the introduction of pathogens into the joint by hematogenous seeding, local extension, or trauma. Early recognition of the typical signs and symptoms including fever, trismus, preauricular swelling, and TMJ region tenderness are critical in order to initiate further evaluation and prevent feared complications of fibrosis, ankylosis, abnormal facial structure, or persistence of symptoms. Contrast-enhanced computed tomography with ancillary laboratory analysis including erythrocyte sedimentation rate, C-reactive protein, and white blood cell count are beneficial in confirming the suspected diagnosis and monitoring response to therapy.

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Risk factors for low bone mineral density in pediatric inflammatory bowel disease: the positive role of physical activity.

Eur J Gastroenterol Hepatol

April 2018

Division of Pediatric Gastroenterology and Hepatology, SSM Health Cardinal Glennon Children's Hospital, Saint Louis Unviersity, St. Louis, Missouri, USA.

Article Synopsis
  • The study investigates low bone mineral density (BMD) and fracture prevalence in pediatric patients with inflammatory bowel disease (IBD), finding low BMD in 12.5% of spine cases and 27% in total body assessments.
  • Among 216 patients, lower BMD was linked to factors like menstrual irregularities and tube feeding, while higher BMD was associated with increased physical activity and better height measurements.
  • The results indicate a significant relationship between low BMD and fracture risk, highlighting the importance of physical activity in managing BMD in young IBD patients.
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Article Synopsis
  • * A study of 72 participants provided detailed analysis of SAS, going beyond previous limited reports to identify key clinical and genetic characteristics.
  • * Major findings highlight severe speech delays, palate and dental abnormalities, and behavioral issues, which can aid healthcare providers in diagnosis and management, offering better support for affected families.
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Article Synopsis
  • This study focuses on a newly identified autoinflammatory disease caused by mutations in a tRNA processing enzyme, particularly examining its clinical features, immune responses, and molecular mechanisms.
  • In nine patients diagnosed with congenital sideroblastic anemia, significant genetic mutations were found, along with elevated inflammatory cytokines and notable cellular abnormalities.
  • Treatment with a TNF inhibitor successfully reduced inflammation and improved patient outcomes, highlighting the importance of early molecular diagnosis for effective intervention.
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A 7-month-old female infant had clinical and laboratory evidence of severe warm autoimmune hemolytic anemia. She also had clinical evidence of an upper respiratory tract infection with molecular detection of Mycoplasma pneumoniae. Although reticulocytopenic initially, she responded to red blood cell transfusion, steroids, and intravenous immunoglobulin and remains well today.

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Catfish injuries are increasingly common from the recreational activities of hobbyists, fishermen, and "noodling" enthusiasts as well as in the commercial catfish industry, most commonly in Brazil. Injuries can range from mild skin abrasions to life-threatening infections and tissue damage requiring urgent treatment. Most injuries and subsequent morbidity associated with catfish encounters involve the dorsal and pectoral fins.

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Background: Squamosal craniosynostosis is seldom reported in the craniofacial literature. Given that this is an uncommon diagnosis, phenotype and management remain unclear. The authors present a case series and review the literature to define the phenotype and management of these patients.

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