18 results match your criteria: "Primary Children's Medical Center and University of Utah[Affiliation]"
J Pediatr
October 2015
Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, TN; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN. Electronic address:
Objective: To assess the relationship between secondhand smoke (SHS) exposure and disease severity among children hospitalized with community-acquired pneumonia (CAP).
Study Design: Children hospitalized with clinical and radiographic CAP were enrolled between January 1, 2010, and June 30, 2012 at 3 hospitals in Tennessee and Utah as part of the Centers for Disease Control and Prevention's Etiology of Pneumonia in the Community study. Household SHS exposure was defined based on the number of smokers in the child's home.
J Am Soc Echocardiogr
May 2015
Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Background: Several quantification algorithms for measuring left ventricular (LV) size and function are used in clinical and research settings. The aims of this study were to investigate the effects of measurement algorithm and beat averaging on the reproducibility of measurements of the left ventricle and to assess the magnitude of agreement among the algorithms in children with dilated cardiomyopathy.
Methods: Echocardiograms were obtained in 169 children from eight clinical centers.
Circulation
May 2014
From the Boston Children's Hospital and Harvard Medical School, Boston, MA (J.W.N., C.D.-M.); New England Research Institutes, Watertown, MA (L.A.S., S.C.); Children's Hospital of Wisconsin and Medical College of Wisconsin, Milwaukee (P.C.F.); National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (G.D.P.); Emory University, Atlanta, GA (W.T.M.); Hospital for Sick Children, Toronto, ON, Canada (S.M., S.K.); Morgan Stanley Children's Hospital of New York-Presbyterian, New York (I.A.W.); University of Michigan Medical School, Ann Arbor (C.S.G., R.G.O.); The Congenital Heart Institute of Florida, St. Petersburg (J.P.J.); Cincinnati Children's Medical Center, Cincinnati, OH (C.D.K.); Children's Hospital Los Angeles, Los Angeles, CA (A.B.L.); North Carolina Consortium: Duke University, Durham; East Carolina University, Greenville; Wake Forest University, Winston-Salem (S.K.P.); Nemours Cardiac Center, Wilmington, DE (C.P.); Primary Children's Medical Center and University of Utah, Salt Lake City (P.J.G.); Medical University of South Carolina, Charleston (A.M.A.); and Children's Hospital of Philadelphia and University of Pennsylvania Medical School, Philadelphia (J.W.G.).
Background: In the Single Ventricle Reconstruction (SVR) trial, 1-year transplantation-free survival was better for the Norwood procedure with right ventricle-to-pulmonary artery shunt (RVPAS) compared with a modified Blalock-Taussig shunt (MBTS). At 3 years, we compared transplantation-free survival, echocardiographic right ventricular ejection fraction, and unplanned interventions in the treatment groups.
Methods And Results: Vital status and medical history were ascertained from annual medical records, death indexes, and phone interviews.
J Thorac Cardiovasc Surg
August 2014
Department of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pa. Electronic address:
Objective: The study objective was to determine whether the extracardiac conduit Fontan confers an arrhythmia advantage over the intracardiac lateral tunnel Fontan.
Methods: This multicenter study of 1271 patients compared bradyarrhythmia (defined as need for pacing) and tachyarrhythmia (defined as needing antiarrhythmic therapy) between 602 patients undergoing the intracardiac Fontan and 669 patients undergoing the extracardiac Fontan. The median age at the time of the Fontan procedure was 2.
Pediatrics
November 2009
Department of Cardiothoracic, Primary Children's Medical Center and University of Utah, Salt Lake City, Utah 84113, USA.
Objective: We sought to compare perceptions of functional health status between children who had undergone a Fontan procedure and their parents.
Methods: Fontan procedure survivors 10 to 18 years of age were included in the study if the child completed the Child Health Questionnaire (CHQ) and the parent completed the parent form to assess the child's functional health status. Comparisons were made between raw domain scores for the parent- and child-completed CHQs.
Am J Clin Pathol
December 2007
Department of Pathology, Primary Children's Medical Center and University of Utah, Salt Lake City, UT 84113, USA.
Timely communication of significant or unexpected findings in surgical pathology can significantly improve patient care. Although surgical pathology critical values have been published, no systematic assessment in pediatric surgical pathology has been published. We surveyed pediatric pathologists and pediatric subspecialists to develop pediatric surgical pathology critical values for verbal reporting before the final pathology report.
View Article and Find Full Text PDFAm J Surg Pathol
March 2007
Department of Pathology, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City, Utah, USA.
Gardner fibroma (GAF) is a benign soft tissue lesion with a predilection for childhood and adolescence and an association with familial adenomatous polyposis (FAP) and desmoid type fibromatosis (desmoid). We report 45 patients with GAF with clinicopathologic correlation and immunohistochemical analysis for beta-catenin and related proteins. Forty-five patients with 57 GAFs were identified from surgical pathology and consultation files.
View Article and Find Full Text PDFPediatrics
September 2006
Department of Pediatrics, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City, Utah 84113, USA.
Objective: Although the electrocardiogram is commonly obtained in the evaluation of patients with pulmonary hypertension, its value as a screening test for right ventricular hypertrophy or pulmonary hypertension is unclear. Therefore, we sought to determine the value of an electrocardiogram in the diagnosis of right ventricular hypertrophy using echocardiography as the gold standard.
Methods: We identified children without congenital heart disease who underwent evaluation for suspected pulmonary hypertension that included both an electrocardiogram and echocardiography within a specified time frame.
Arch Pathol Lab Med
July 2006
Division of Pediatric Pathology, Department of Pathology, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City 84113, USA.
Context: Laboratory data are essential to the medical care of fetuses, infants, children, and adolescents. However, the performance and interpretation of laboratory tests on specimens from these patients, which may constitute a significant component of the workload in general hospitals and integrated health care systems as well as specialized perinatal or pediatric centers, present unique challenges to the clinical pathologist and the laboratory. Therefore, pathology residents should receive training in pediatric laboratory medicine.
View Article and Find Full Text PDFJ Pediatr Surg
November 2004
Division of Pediatric Surgery, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City, UT 84113, USA.
Three infants with progressive upper esophageal stenosis had bilateral vocal fold paralysis. The patients were apparently normal at birth and without neurologic abnormality. Cricopharyngeal myotomy, followed by serial dilatations, relieved esophageal stenosis and restored the swallowing function.
View Article and Find Full Text PDFPediatr Dev Pathol
August 2004
Department of Pathology, Primary Children's Medical Center and University of Utah School of Medicine, 100 North Medical Drive, Salt Lake City, UT 84113, USA.
Evaluation for celiac disease (CD), an autoimmune enteropathy triggered by grain proteins in wheat, barley, rye, and possibly oats, is a common indication for pediatric endoscopy and biopsy. Duodenal or jejunal biopsy remains key for the initial diagnosis of CD. Small intestinal pathology may be diffuse or focal in CD, and histologic findings are nonspecific and must be interpreted in conjunction with clinical and serologic findings.
View Article and Find Full Text PDFMod Pathol
September 2002
Department of Pathology, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City, Utah 84132, USA.
Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma. This immunohistochemical study investigates whether the ALK family of neoplasms includes fibroblastic-myofibroblastic, myogenic, and spindle cell tumors. Formalin-fixed paraffin-embedded archival tissues from 10 IMTs and 125 other soft tissue tumors were stained for ALK1 and p80 with standard immunohistochemistry.
View Article and Find Full Text PDFAnn Thorac Surg
January 2001
Department of Pediatrics, Primary Children's Medical Center and University of Utah, Salt Lake City 84113, USA.
Background: The purpose of this study was to prospectively assess the effects of azathioprine on the humoral immune response to HLA alloantigens and allograft function in children receiving cryopreserved valved allografts.
Methods: We randomized 13 children to receive azathioprine or not to receive azathioprine (controls) after receiving a cryopreserved valved allograft. Azathioprine patients received intraoperatively 4 mg/kg of azathioprine and 2.
Pediatr Dev Pathol
March 2001
Department of Pathology, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City 84132, USA.
Needle core biopsies (NCB) are widely used in adults but are less often used for the evaluation of pediatric tumors. To determine the diagnostic utility of NCB for pediatric tumors, we performed a retrospective analysis. Fifty NCB of masses from 1992 to 1998, subsequent pathologic specimens, and medical records were reviewed.
View Article and Find Full Text PDFPediatr Cardiol
July 2000
Department of Pediatrics, Primary Children's Medical Center and University of Utah, Salt Lake City, UT 84113, USA.
Total anomalous pulmonary venous connection (TAPVC) is an uncommon cardiac anomaly that has also rarely been associated with esophageal atresia. We report an unusual case of esophageal atresia with TAPVC with several varices and multiple drainage sites into the superior vena cava and portal vein.
View Article and Find Full Text PDFAnn Thorac Surg
July 1999
Department of Pediatrics, Primary Children's Medical Center and University of Utah, Salt Lake City 84113, USA.
Background: Pulmonary vein (PV) stenosis with anatomically normal connection is considered rare, unresponsive to treatment, progressive, and usually fatal.
Methods: We reviewed the records of 13 children with this diagnosis at our center since 1990.
Results: The number of stenosed PVs ranged from all PVs (n = 5); three PVs (n = 1); two PVs (n = 5); and one PV (n = 2).
J Pediatr Gastroenterol Nutr
January 1999
Department of Pathology, Primary Children's Medical Center and University of Utah, Salt Lake City 84113-1100, USA.
J Pediatr Surg
April 1998
Division of Pediatric Surgery, Primary Children's Medical Center and University of Utah School of Medicine, Salt Lake City 84113, USA.
Background: Gastric emptying scintiscans are currently used to select reflux patients for added pyloroplasty at the time of fundoplication. The accuracy of this scan selection approach has been assumed. If preoperative scintiscans do not reliably predict postfundoplication gastric emptying, however, the decision to add pyloroplasty to the fundoplication operation may be inappropriate and even harmful.
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