Longitudinal analysis of pulmonary function in adults with sickle cell disease

  • Joshua J. Field
  • , Jeffrey Glassberg
  • , Annette Gilmore
  • , Joanna Howard
  • , Sameer Patankar
  • , Yan Yan
  • , Sally C. Davies
  • , Michael R. DeBaun
  • , Robert C. Strunk

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Among adults with sickle cell disease (SCD), pulmonary complications are a leading cause of death. Yet, the natural history of lung function in adults with SCD is not well established. We conducted a retrospective cohort study of adults with SCD who had repeated pulmonary function tests performed over 20 years of age. Ninety-two adults were included in this cohort. Rate of decline in FEV1 for men and women with SCD was 49 cc/year (compared with 20-26 cc/year in the general population). Further studies are needed to identify factors which impact the rate of lung function decline in adults with SCD.

Original languageEnglish
Pages (from-to)574-576
Number of pages3
JournalAmerican journal of hematology
Volume83
Issue number7
DOIs
StatePublished - Jul 2008

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