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The Benefits and Challenges of Preconsent in a Multisite, Pediatric Sickle Cell Intervention Trial

  • for the sickle cell working group of the Pediatric Emergency Care Applied Research Network (PECARN)
  • Medical College of Wisconsin
  • Children's Hospital of Michigan
  • Northwestern University
  • Children's National Medical Center
  • The Children's Hospital of Philadelphia
  • University of Pittsburgh
  • Baylor College of Medicine
  • Children's Memorial Hospital
  • University of Utah
  • Medical College of Wisconsin and Children's Research Institute of Children's Wisconsin

Producción científicarevisión exhaustiva

4 Citas (Scopus)

Resumen

Enrollment of patients in sickle cell intervention trials has been challenging due to difficulty in obtaining consent from a legal guardian and lack of collaboration between emergency medicine and hematology. We utilized education and preconsent in a pediatric multisite sickle cell intervention trial to overcome these challenges. Overall, 48 patients were enrolled after being preconsented. Variable Institutional Review Board policies related to preconsent validity and its allowable duration decreased the advantages of preconsent at some sites. The utility of preconsent for future intervention trials largely depends on local Institutional Review Board policies. Preeducation may also benefit the consent process, regardless of site differences.

Idioma originalEnglish
Páginas (desde-hasta)1649-1652
Número de páginas4
PublicaciónPediatric Blood and Cancer
Volumen63
N.º9
DOI
EstadoPublished - 1 sept 2016
Publicado de forma externa

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