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<record>
  <contributors>
    <authors>
      <author>De La Vergne, Maggie</author>
    </authors>
    <secondary-authors>
      <author>Norman, Sharon</author>
    </secondary-authors>
  </contributors>
  <titles>
    <title>Transition to adult care for pediatric patients with sickle cell disease: a quality improvement project</title>
    <translated-title/>
    <tertiary-title/>
  </titles>
  <periodical>
    <full-title/>
  </periodical>
  <alt-periodical>
    <full-title/>
    <abbr-1/>
  </alt-periodical>
  <pages/>
  <section/>
  <volume/>
  <number/>
  <keywords>
    <keyword>Transition to Adult Care</keyword>
    <keyword>Pediatrics</keyword>
    <keyword>Hospitalization</keyword>
    <keyword>Child</keyword>
    <keyword>Quality Improvement</keyword>
    <keyword>Anemia, Sickle Cell</keyword>
  </keywords>
  <dates>
    <year>2021</year>
  </dates>
  <abstract>The purpose of this quality improvement project was to develop a standardized transition program for pediatric patients with sickle cell disease from pediatric to adult healthcare settings. Patients with sickle cell disease require long-term management strategies to prevent complications and hospitalizations for their disease. Developing a transition program can help patients learn how to manage their disease.</abstract>
  <publisher>Oregon Health and Science University</publisher>
  <issn/>
  <isbn/>
  <custom3/>
  <custom7/>
  <notes/>
  <work-type>Final project</work-type>
  <electronic-resource-num>10.6083/n009w299f</electronic-resource-num>
  <language/>
</record>

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