Gary L McPhail

Summary

Affiliation: Cincinnati Children's Hospital Medical Center
Country: USA

Publications

  1. doi request reprint Ivacaftor: the first therapy acting on the primary cause of cystic fibrosis
    G L McPhail
    University of Cincinnati, Cincinnati, OH, USA
    Drugs Today (Barc) 49:253-60. 2013
  2. ncbi request reprint Cavitary lung lesions in a 2-year-old child
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
    Respiration 76:117-8. 2008
  3. doi request reprint Improving follow-up in hospitalised children
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    Qual Saf Health Care 19:e35. 2010
  4. doi request reprint Improving evidence-based care in cystic fibrosis through quality improvement
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
    Arch Pediatr Adolesc Med 164:957-60. 2010
  5. doi request reprint Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis
    Rhonda D Vandyke
    Division of Biostatistics and Epidemiology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
    Ann Am Thorac Soc 10:205-12. 2013
  6. doi request reprint Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, OH, USA
    J Pediatr 153:752-7. 2008
  7. doi request reprint Is adolescents' religious coping with cystic fibrosis associated with the rate of decline in pulmonary function?-A preliminary study
    Daniel H Grossoehme
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    J Health Care Chaplain 19:33-42. 2013
  8. doi request reprint Bronchiectasis in chronic pulmonary aspiration: risk factors and clinical implications
    Joseph C Piccione
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
    Pediatr Pulmonol 47:447-52. 2012
  9. doi request reprint Prevention of tracheostomy-related pressure ulcers in children
    R Paul Boesch
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229 3039, USA
    Pediatrics 129:e792-7. 2012
  10. pmc A review of the effects of sleep during the first year of life on cognitive, psychomotor, and temperament development
    Mathew Ednick
    Division of Pulmonary and Sleep Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229, USA
    Sleep 32:1449-58. 2009

Detail Information

Publications12

  1. doi request reprint Ivacaftor: the first therapy acting on the primary cause of cystic fibrosis
    G L McPhail
    University of Cincinnati, Cincinnati, OH, USA
    Drugs Today (Barc) 49:253-60. 2013
    ..With restoration of adequate CFTR function through pharmacotherapy, it is possible that the clinical course of patients with CF could be markedly improved, including longevity, quality of life and treatment burden...
  2. ncbi request reprint Cavitary lung lesions in a 2-year-old child
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
    Respiration 76:117-8. 2008
  3. doi request reprint Improving follow-up in hospitalised children
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    Qual Saf Health Care 19:e35. 2010
    ..To improve the clinic follow-up rate of paediatric inpatients in a tertiary care hospital...
  4. doi request reprint Improving evidence-based care in cystic fibrosis through quality improvement
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
    Arch Pediatr Adolesc Med 164:957-60. 2010
    ..To increase clinician adherence to prescribing guidelines for pulmonary medications in children with cystic fibrosis (CF)...
  5. doi request reprint Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis
    Rhonda D Vandyke
    Division of Biostatistics and Epidemiology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
    Ann Am Thorac Soc 10:205-12. 2013
    ..However, little is known about its clinical effectiveness on lung function outside randomized controlled trial settings; conventional analysis of existing registry data has heretofore been confounded by treatment selection bias...
  6. doi request reprint Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use
    Gary L McPhail
    Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children s Hospital Medical Center, Cincinnati, OH, USA
    J Pediatr 153:752-7. 2008
    ..To compare lung function and nutritional outcomes in cystic fibrosis (CF) for 2 birth cohorts in our CF center...
  7. doi request reprint Is adolescents' religious coping with cystic fibrosis associated with the rate of decline in pulmonary function?-A preliminary study
    Daniel H Grossoehme
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    J Health Care Chaplain 19:33-42. 2013
    ..Changes in pulmonary function suggest opportunities for chaplains to explore options to cognitively reframe negative religious coping...
  8. doi request reprint Bronchiectasis in chronic pulmonary aspiration: risk factors and clinical implications
    Joseph C Piccione
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
    Pediatr Pulmonol 47:447-52. 2012
    ..This study describes the prevalence, time course for development, and risk factors for bronchiectasis in children with CPA...
  9. doi request reprint Prevention of tracheostomy-related pressure ulcers in children
    R Paul Boesch
    Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229 3039, USA
    Pediatrics 129:e792-7. 2012
    ....
  10. pmc A review of the effects of sleep during the first year of life on cognitive, psychomotor, and temperament development
    Mathew Ednick
    Division of Pulmonary and Sleep Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229, USA
    Sleep 32:1449-58. 2009
    ....
  11. doi request reprint A semiparametric approach to estimate rapid lung function decline in cystic fibrosis
    Rhonda D Szczesniak
    Division of Biostatistics and Epidemiology, Cincinnati Children s Hospital Medical Center, Cincinnati, OH Division of Pulmonary Medicine, Cincinnati Children s Hospital Medical Center, Cincinnati, OH Electronic address
    Ann Epidemiol 23:771-7. 2013
    ..The purpose of this article was to estimate patient-specific timing and degree of rapid decline while appropriately characterizing natural progression and variation in CF...
  12. doi request reprint Obstructive lung disease is common in children with syndromic and congenital scoliosis: a preliminary study
    Gary L McPhail
    Divisions of Pulmonary Medicine Orthopaedic Surgery, Cincinnati Children s Hospital Medical Center, University of Cincinnati, Cincinnati, OH WordCraft, Medical Writing Consultants, Los Angeles, CA Division of Pulmonary Medicine, Seattle Children s Hospital, University of Washington, Seattle, WA
    J Pediatr Orthop 33:781-5. 2013
    ..It is well known that restrictive lung disease (RLD) is associated with scoliosis. This study identifies that obstructive lung disease (OLD) is associated with syndromic scoliosis and congenital scoliosis...