Asthma in children with sickle cells disease and the association with acute chest syndrome

J Knight-Madden, T S Forrester, N A Lewis, A Greenough

    Research output: Contribution to journalArticlepeer-review

    162 Citations (Scopus)

    Abstract

    Background: Pulmonary complications are a major cause of morbidity and mortality in sickle cell disease (SCD). The relationship of asthma with SCD and acute chest syndrome ( ACS) remains uncertain. A study was undertaken to test the hypotheses that asthma and bronchial hyperreactivity (BHR) are more common in children with SCD than in ethnic matched controls and that SCD children with atopic asthma are more likely to have recurrent episodes of ACS. Methods: A modified International Study of Asthma and Allergies in Childhood ( ISAAC) questionnaire was administered and skin prick tests undertaken in 80 children with SCD and 80 ethnic matched controls aged 5 - 10 years. BHR was assessed by measurement of forced expiratory volume in 1 second before and after a bronchodilator ( albuterol 200 mg) or an exercise challenge. Results: Asthma ( 48% v 22%, p = 0.002) and BHR ( p = 0.02) but not atopy were more common in children with SCD than in controls. Atopy ( 66.6% v 29%, p = 0.007) and asthma ( 80% v 40%, p = 0.005), particularly atopic asthma ( 53% v 12%, p, 0.001), were more common in children with SCD who had suffered recurrent episodes of ACS than in those who had suffered a single or no episode. Conclusions: Asthma and BHR are more common in children with SCD than in ethnic matched controls, and atopic asthma appears to be associated with recurrent ACS. Early and effective anti- asthma therapy might reduce the pulmonary morbidity associated with SCD
    Original languageEnglish
    Pages (from-to)206 - 210
    Number of pages5
    JournalThorax
    Volume60
    Issue number3
    DOIs
    Publication statusPublished - Mar 2005

    Fingerprint

    Dive into the research topics of 'Asthma in children with sickle cells disease and the association with acute chest syndrome'. Together they form a unique fingerprint.

    Cite this