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Stephanie Davis, M.D.

Associate Professor; Chief, Division of Pediatric Pulmonology

Curriculum Vitae

Department of Pediatrics
    Division of Pediatric Pulmonology

Services:
Pediatrics, Pediatric Pulmonary Medicine

Procedures/Research:
Infant and preschool pulmonary function testing; cystic fibrosis; primary ciliary dyskinesia; and other chronic lung disease.
 
Clinical Appointment Phone:  (919) 966-1401

Website: http://www.ncchildrenshospital.org/ourservices/specialties/pulmonology
Stephanie D. Davis, M.D.


Certifications
Pediatrics Pulmonary - Board Certified  (2000)
Pediatrics - Board Certified  (1996)


Education and Training
Fellowship: Indiana University Medical Center, Indiana, 1996 - 1999
Area: Pediatric Pulmonology
Residency: Indiana University Medical Center, Indiana, 1994 - 1996
Area: Pediatrics
Internship: Indiana University Medical Center, Indiana, 1993 - 1994
Area: Pediatrics
Medical School: MD, Wake Forest School of Medicine, Winston-Salem, NC, 1993


Professional Positions
  1. Assistant Professor of Pediatrics, University of North Carolina, Chapel Hill, 1999-2006

  2. Associate Professor of Pediatrics, University of North Carolina, Chapel Hill, 2006-present

  3. Fellowship Program Director, University of North Carolina, Chapel Hill, 2007-present


Honors
  1. Distinguished Residents and Fellows, Asthma Education Scholarship Program, London, England, 1997

  2. Alpha Omega Alpha, Indiana University School of Medicine, 1998

  3. Society of Pediatric Research, University of North Carolina at Chapel Hill, 2006

  4. Academic Leadership Program, University of North Carolina at Chapel Hill, 2009


Presentations
  1. Pulmonary Function Testing as Applied to the Wheezing Infant
    Authors: Pulmonary Function Testing as Applied to the Wheezing Infant
    CHEST 9th Pediatric Fellows Conference, 2008

  2. Infant Pulmonary Function Testing State of Art
    Duke Airway Biology Forum, 2008

  3. Implementing Infant Pulmonary Function Testing into Clinical Practice
    American Thoracic Society Annual Conference, Clinical Workshop, 2008

  4. Clinical and Research Outcome Measures of CF Lung Disease
    American Thoracic Society Annual Conference, 2008

  5. Infant PFTs as a Clinical Outcome Measures: Are we there yet?
    Invited Speaker, Cincinnati Children's Hospital, 2008

  6. The Value of Monitoring Lung Function Throughout the Pediatric Age
    Authors:
    American Thoracic Society Annual Conference, 2009

  7. Review of Current Status of Studies Restoring Airway Surface Liquid
    Cystic Fibrosis Therapeutic Development Network, 2009


Publications
  1. Paediatric Pulmonary Function Testing
    Authors: Davis, S, Gappa, M, Rosenfeld, M. Respiratory Mechanics
    Prog. Respir Res, Basel, Karger; 33: 20-33, 2005

  2. AARC Clinical Practice Guideline: Infant/Toddler Pulmonary Function Tests
    Authors: Davis SD. Johnson RC, Flucke RL, Kisling JA, Myers TR
    Respiratory Care, 53 (7): 929-945, July, 2008

  3. Reduced Lung Function in Cystic Fibrosis: A primary or secondary phenotype? (editorial)
    Authors: Davis SD, Ratjen F
    Am J Respir Crit Care Med; 178 (1): 2-3, 2008

  4. Early Lung Disease in Young Children with Primary Ciliary Dyskinesia
    Authors: Brown DE, Pittman JE, Leigh MW, Fordham L, Davis SD
    Pediatr Pulmonol.;43(5):514-6, May, 2008

  5. Extracellular Purines are Biomarkers of Neutrophilic Airway Inflammation
    Authors: Esther CR, Alexis NE, Clas ML, Lazarowski ER, Donaldson SH, Pedrosa Ribeiro CM, Moore CG, Davis SD, Boucher RC
    Eur Respir J.; 31(5):949-56, May, 2008

  6. Quality Control for Spirometry in Preschool Children (author correspondence)
    Authors: Davis S, Aurora P, Eigen H, Beydon N, Lombardi E on behalf of the ATS/ERS Working Group on Infant and Young Children Pulmonary Function Testing
    Am. J. Respir. Crit. Care Med.; 178: 107 - 108, July, 2008

  7. Safety and Tolerability of Inhaled Hypertonic Saline in Young Children with Cystic Fibrosis
    Authors: Dellon EP, Donaldson SH, Johnson R, Davis SD
    Pediatr Pulmonol.; 43(11):1100-6, 2008 November

  8. Lung Function Testing in Infants
    Authors: Davis S, Pittman J
    Cystic Fibrosis, 2009; in press., 2009

  9. Clinical and Genetic Aspects of Primary Ciliary Dyskinesia/Kartagener Syndrome
    Authors: Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA
    Genetics in Medicine 2009; in press., 2009


Abstracts
  1. Multi-center lung function testing in preschool subjects
    Authors: Kerby GS, Rosenfeld M, Ren C, Mayer O, Castile R, Hart M, Hiatt P, Kloster M, Brumback L, Johnson R, Davis SD
    Ped Pulm Supp. 31 (abstracts issue), October 2008, 2008

  2. Inhaled 7% Hypertonic Saline is Well Tolerated in Infants and Toddlers with CF
    Authors: Rosenfeld M, Davis SD, Brumback L, Daniel S, Johnson R, Rowbotham R, McNamara S, Martin S, Barlow C, Ratjen F
    Ped Pulm Supp. 31 (abstracts issue), October 2008., 2008

  3. Age of Pseudomonas aeruginosa Infection and Severity of Lung Disease in Cystic Fibrosis Adolescents and Adults
    Authors: Pittman J, Calloway E, Yeatts J, Drumm M, Leigh M, Davis S, Van Rie A, Emond M, Knowles M
    Ped Pulm Supp. 31 (abstracts issue), October 2008: A332, p. 319., 2008

  4. Primary Ciliary Dyskinesia: Characteristics of Children under Six
    Authors: Pittman JE, Davis SD, Chawla KK, Brown DE, Knowles MR, Leigh MW
    Proceedings of the American Thoracic Society; 2008, A798., 2008

  5. Primary Ciliary Dyskinesia in Children: Dichotomy in Structural Versus Functional Changes in Airways
    Authors: Leigh MW, Ferkol TW, Dell SD, Davis SD, Knowles MR
    Am. J. Respir. Crit. Care Med., Apr 2009; 179: A3674., 2009

  6. Spirometry in Biracial Children: Assessing Adequacy of Current Race-Based Reference Equations
    Authors: Pittman JE, Davis SD
    Am. J. Respir. Crit. Care Med., Apr 2009; 179: A4850., 2009


Physician Referral:
You can request a physician referral by calling UNC HealthLink at (919) 966-7890,
8:30 a.m. to 5 p.m., Monday through Friday.