Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Warren E. Regelmann"'
Autor:
Charles E. Johnston, David J. Nuckley, David W. Polly, Charles Gerald T. Ledonio, Warren E. Regelmann, Benjamin E. Rosenstein
Publikováno v:
Journal of Orthopaedic Research. 35:175-182
Scoliosis deformity has been linked with deleterious changes in the thoracic cavity that affect pulmonary function. The causal relationship between spinal deformity and pulmonary function has yet to be fully defined. It has been hypothesized that def
Autor:
David J. Pasta, Lawrence Rasouliyan, Michael W. Konstan, Warren E. Regelmann, Michael S. Schechter, Margaret Rosenfeld, Wayne J. Morgan, Gregory S. Sawicki, Donald R. VanDevanter
Publikováno v:
Pediatric Pulmonology. 50:431-440
Summary Background Antibiotic treatment of cystic fibrosis pulmonary exacerbations is inconsistent. Previous research has indicated that intravenous antibiotics are used more frequently at sites with better pulmonary function but it is not clear unde
Autor:
Jeremiah S Menk, Theresa A. Laguna, Warren E. Regelmann, Philippe Gaillard, Christina L. Mikesell, Andrew Wey, Robert R. Kempainen
Publikováno v:
Respiratory care. 62(7)
BACKGROUND: Objective measures of adherence to high-frequency chest wall compression (HFCWC), a form of airway clearance therapy for patients with cystic fibrosis, are lacking. We used a novel electronic monitoring device integrated into an HFCWC ves
Autor:
Antoinette Moran, Laura A. McCauley, William Thomas, Theresa A. Laguna, Lynda E. Polgreen, Warren E. Regelmann
Publikováno v:
Annals of the American Thoracic Society. 11:198-204
Rationale: Recent literature suggests vitamin D has an effect on lung function and on the lung’s ability to fight infection, both important in the cystic fibrosis (CF) population as predictors of morbidity and mortality. Objectives: Our study asses
Autor:
Melena D. Bellin, Antoinette Moran, Terri A. Laguna, Jordan M. Dunitz, Joanne Billings, Warren E. Regelmann, Janice Leschyshyn
Publikováno v:
Pediatric Diabetes. 14:417-421
Cystic fibrosis related diabetes (CFRD) is characterized by progressive insulin insufficiency. It is extraordinarily prevalent in the cystic fibrosis (CF) population, occurring in 15–20% of adolescents and, eventually, more than half of adults (1).
Autor:
Michael W. Konstan, Michael S. Schechter, Eric P. Elkin, Warren E. Regelmann, David J. Pasta, Wayne J. Morgan, Jeffrey S. Wagener
Publikováno v:
Pediatric Pulmonology. 48:649-657
Background A standard definition of pulmonary exacerbation based on signs and symptoms would be useful for categorizing cystic fibrosis (CF) patients and as an outcome measure of therapy. The frequently used definition of treatment with intravenous a
Autor:
Lawrence Rasouliyan, Donald R. VanDevanter, Jeffrey S. Wagener, David J. Pasta, Warren E. Regelmann, Michael W. Konstan, Wayne J. Morgan
Publikováno v:
Pediatric Pulmonology. 48:666-673
Patients with cystic fibrosis (CF) experience frequent pulmonary exacerbations (PExs). Clinicians manage these episodes of worsening signs and symptoms in a variety of ways.To characterize the antibiotic management and associated change in lung funct
Publikováno v:
Pediatric Pulmonology. 47:736-742
Objectives Rapid and reliable confirmatory sweat testing following a positive newborn screen (NBS) for cystic fibrosis (CF) is preferred to allow for early diagnosis and to decrease parental anxiety. The Cystic Fibrosis Foundation (CFF) recently reco
Autor:
Kevin W Southern, Gregory S. Sawicki, Allen Lapey, Yulia Green, Jane C. Davies, Sarah Robertson, Warren E. Regelmann, Margaret Rosenfeld, Steve Cunningham, J. Cooke, William T. Harris
Publikováno v:
The Lancet. Respiratory medicine. 4(2)
Ivacaftor has been shown to be a safe, effective treatment for cystic fibrosis in patients aged 6 years or older with a CFTR gating mutation. We aimed to assess the safety, pharmacokinetics, and pharmacodynamics of ivacaftor in children aged 2-5 year
Autor:
Sarah Jane Schwarzenberg, Joanne Billings, Philippe Gaillard, Warren E. Regelmann, Ann M. Brearley, Jordan M. Dunitz, Bonnie Holme, James A. Phillips, Chad Best
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 53:453-458
OBJECTIVES The aim of the study was to assess the efficacy of gastrostomy tube (GT) placement on improving nutritional status and pulmonary function in patients with cystic fibrosis (CF). PATIENTS AND METHODS Data were collected from the Minnesota Cy