Primary snoring and growth failure in a patient with cystic fibrosis

Kelvin D. MacDonald, Brian M. McGinley, David J. Brown, Laura M. Sterni, Beryl J. Rosenstein, Peter J. Mogayzel

    Research output: Contribution to journalArticle

    3 Scopus citations

    Abstract

    An 8-year-old female with pancreatic-insufficiency cystic fibrosis presented with recurrent pharyngitis, and reduction in body mass index and height velocity during the previous 2 years. Her symptoms (eg, snoring and restless sleep) suggested obstructive sleep apnea, and physical examination revealed tonsillar hypertrophy. While her respiratory disturbance index on nocturnal polysomnography was normal, there was evidence of prolonged periods of snoring, associated with hypercapnia. Adenotonsillectomy decreased the snoring, improved her sleep, and in the 18-month follow-up period she had substantial weight-gain and growth improvement. This case demonstrates that adenotonsillar hypertrophy associated with recurrent pharyngitis and primary snoring might hinder growth in a patient with cystic fibrosis.

    Original languageEnglish (US)
    Pages (from-to)1727-1731
    Number of pages5
    JournalRespiratory care
    Volume54
    Issue number12
    StatePublished - Dec 1 2009

    Keywords

    • Adenotonsillectomy
    • Cystic fibrosis
    • Growth
    • Obstructive sleep apnea
    • Pancreatic insufficiency
    • Pharyngitis
    • Sleep disturbance
    • Snoring
    • Somnography
    • Tonsillar hypertrophy

    ASJC Scopus subject areas

    • Pulmonary and Respiratory Medicine
    • Critical Care and Intensive Care Medicine

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  • Cite this

    MacDonald, K. D., McGinley, B. M., Brown, D. J., Sterni, L. M., Rosenstein, B. J., & Mogayzel, P. J. (2009). Primary snoring and growth failure in a patient with cystic fibrosis. Respiratory care, 54(12), 1727-1731.