Patient Knowledge and Clinic Attendance in Adolescent Patients with Cystic Fibrosis

Traci M. Kazmerski, Elizabeth Miller, Kaleab Z. Abebe, Janice Matisko, Diane Schachner, Jonathan Spahr

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

Background: With the rising age of patients with cystic fibrosis (CF), strategies to improve adolescents' adherence to care are needed. This study investigates the association between knowledge of disease and objective markers of clinic attendance in an adolescent CF population. Methods: Patients with CF aged 13-20 years completed a CF knowledge survey (n=38). Associations of knowledge scores with attendance measures and health status data were assessed. Results: Higher overall knowledge scores were associated with regular evaluations by dietitians (OR 1.08, p=0.045) and timely completion of pulmonary function testing (PFTs; OR 1.13, p=0.009) and routine cultures (OR 1.12, p=0.012). Higher nutrition health and treatment knowledge scores were also associated with timely completion of routine PFTs (OR 1.14, p=0.005 and OR 1.09, p=0.012) and cultures (OR 1.10, p=0.022 and OR 1.08, p=0.019). Conclusions: This is the first study demonstrating an association between adolescent disease knowledge and objectively measured adherence to recommended clinic attendance and evaluation. More adherent patients have better knowledge of their disease. Targeting adolescent CF patients' knowledge may be a modifiable factor to improve attendance and long-term management.

Original languageEnglish (US)
Pages (from-to)107-111
Number of pages5
JournalPediatric, Allergy, Immunology, and Pulmonology
Volume28
Issue number2
DOIs
StatePublished - Jun 1 2015
Externally publishedYes

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ASJC Scopus subject areas

  • Immunology and Allergy
  • Pediatrics, Perinatology, and Child Health
  • Pulmonary and Respiratory Medicine

Cite this

Kazmerski, T. M., Miller, E., Abebe, K. Z., Matisko, J., Schachner, D., & Spahr, J. (2015). Patient Knowledge and Clinic Attendance in Adolescent Patients with Cystic Fibrosis. Pediatric, Allergy, Immunology, and Pulmonology, 28(2), 107-111. https://doi.org/10.1089/ped.2014.0475