Bruce C MarshallSummaryAffiliation: University of Utah Country: USA Publications
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Publications
Influenza vaccination coverage level at a cystic fibrosis centerBruce C Marshall
Intermountain Cystic Fibrosis Center, Salt Lake City, Utah, USA
Pediatrics 109:E80-0. 2002..Annual vaccination is the most effective means to prevent or attenuate this illness. The vaccine is recommended for patients with cystic fibrosis (CF) older than 6 months, but the degree of adherence with this recommendation is unknown...
A survey of the utilization of anti-pseudomonal beta-lactam therapy in cystic fibrosis patientsJeffery T Zobell
Department of Pharmacy, Intermountain Primary Children s Medical Center, Salt Lake City, UT 84113, USA
Pediatr Pulmonol 46:987-90. 2011..While this is of concern, it is not known if optimization of dosing strategies according to guidelines recommendations will result in clinical benefit...
Selection of patients with cystic fibrosis for lung transplantationTheodore G Liou
Intermountain Cystic Fibrosis Center, Department of Internal Medicine, Division of Respiratory Critical Care and Occupational Pulmonary Medicine, University of Utah, Salt Lake City 84132, USA
Curr Opin Pulm Med 8:535-41. 2002..However, judicious use of the survival model to select patients for transplantation is likely to improve survival outcomes...
Heterogeneity of treatment response to azithromycin in patients with cystic fibrosisLisa Saiman
Department of Pediatics, Columbia University, NY 10032, USA
Am J Respir Crit Care Med 172:1008-12. 2005..2% improvement in the 168-d relative change in FEV1 among azithromycin participants compared with placebo participants...
Priorities for lung transplantation among patients with cystic fibrosisTheodore G Liou
JAMA 287:1523-4; author reply 1524-5. 2002
Impact of burkholderia infection on lung transplantation in cystic fibrosisSusan Murray
Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan 48109, USA
Am J Respir Crit Care Med 178:363-71. 2008..Infection with Burkholderia species is typically considered a contraindication to transplantation in CF. However, the risks posed by different Burkholderia species on transplantation outcomes are poorly defined...
Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic reviewVirginia A Stallings
Division of Gastroenterology, Hepatology, and Nutrition, The Children s Hospital of Philadelphia, 3535 Market St, Philadelphia, PA 19104, USA
J Am Diet Assoc 108:832-9. 2008..These Registry data-based recommendations are presented...
Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosisChristian A Merlo
The Johns Hopkins University School of Medicine, 1830 E Monument St Fifth Floor, Baltimore, MD 21205, USA
Chest 132:562-8. 2007..The main objective of the study was to estimate the incidence and identify risk factors for the acquisition of MARPA among individuals with CF...
Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelinesVicky A LeGrys
Division of Clinical Laboratory Science, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7145, USA
J Pediatr 151:85-9. 2007
Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypesDao Nguyen
Children s Hospital and Regional Medical Center, Seattle, Washington, USA
Pediatr Pulmonol 42:533-41. 2007..The in vitro effect of AZM on PLC correlates with FEV(1) response to AZM. This suggests that AZM anti-virulence effects may be predictive of clinical response and play a role in the mechanism of action of AZM in CF patients...
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trialLisa Saiman
Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY 10032 3784, USA
JAMA 290:1749-56. 2003..Treatment strategies for cystic fibrosis (CF) lung disease include antibiotics, mucolytics, and anti-inflammatory therapies. Increasing evidence suggests that macrolide antibiotics might be beneficial in patients with CF...
Pulmonary exacerbations in cystic fibrosis: it's time to be explicit!Bruce C Marshall
Am J Respir Crit Care Med 169:781-2. 2004
Cystic fibrosis adult care: consensus conference reportJames R Yankaskas
University of North Carolina, Chapel Hill, NC 27599, USA
Chest 125:1S-39S. 2004
Cystic fibrosisBruce C Marshall
Curr Opin Pulm Med 9:484-5. 2003
