Provider barriers to hydroxyurea use in adults with sickle cell disease: A survey of the sickle cell disease adult provider network

Sophie Lanzkron, Carlton Haywood, Kathryn L. Hassell, Cynthia Rand

Research output: Contribution to journalArticlepeer-review

Abstract

The FDA approved hydroxyurea for use in adults with sickle cell disease (SCD) in 1998. In 2002, the NHLBI published recommendations for the use of hydroxyurea in this patient population. The purpose of this study was to evaluate providers' awareness of the NHLBI recommendations regarding hydroxyurea prescribing, whether these recommendations have changed providers' practices and how these providers prescribed hydroxyurea. We chose to survey a select group of providers of care to adults with SCD, members of the Sickle Cell Adult Provider Network. The response rate was 47%. Eighty-one percent of respondents reported they had read the NHLBI recommendations on hydroxyurea use, and 76% of respondents agreed with the NHLBI recommendations. Only 45% of respondents to this survey reported that they prescribe hydroxyurea to every eligible patient. Black respondents reported a higher percentage of their eligible patients being on hydroxyurea than white respondents. Seventy-seven percent of respondents thought that hydroxyurea was effective or very effective in patients with SCD. Ninety-four percent of black versus 73% of white versus 40% of other race respondents thought that hydroxyurea was effective or very effective in SCD patients (p=0.006). The results of this survey suggest that lack of awareness, agreement and belief in the benefits of hydroxyurea contributes to providers underprescribing hydroxyurea.

Original languageEnglish (US)
Pages (from-to)968-973
Number of pages6
JournalJournal of the National Medical Association
Volume100
Issue number8
DOIs
StatePublished - Aug 2008

Keywords

  • Barriers
  • Hydroxyurea
  • Sickle cell anemia

ASJC Scopus subject areas

  • Medicine(all)

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