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Barriers to enrollment in a pediatric critical care biorepository.
Paquette, Erin; Shukla, Avani; Smith, Tracie; Pendergrast, Tricia; Duyar, Susan; Rychlik, Karen; Davis, Matthew M.
Afiliação
  • Paquette E; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA. epaquette@luriechildrens.org.
  • Shukla A; Northwestern University Feinberg School of Medicine, Chicago, IL, USA. epaquette@luriechildrens.org.
  • Smith T; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
  • Pendergrast T; Mary Ann & J. Milburn Smith Child Health Research, Outcomes and Evaluation Center, Stanley Manne Children's Research Institute, Chicago, IL, USA.
  • Duyar S; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Rychlik K; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Davis MM; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Pediatr Res ; 94(2): 803-810, 2023 08.
Article em En | MEDLINE | ID: mdl-36755188
ABSTRACT

BACKGROUND:

Individuals of minority race/ethnicity have lower rates of participation in genomic research. This study evaluated sociodemographic characteristics associated with decisions to enroll in a pediatric critical care biorepository.

METHODS:

Parents of children admitted to the PICU between November 2014 and May 2017 were offered to enroll their child in a biorepository using a single-page opt-in consent. Missed enrollment was assessed by failure to complete the form or declining consent on the form. We conducted a retrospective chart review for sociodemographic and clinical information. Bivariate and multivariable regression analyses were performed.

RESULTS:

In 4055 encounters, representing 2910 patients with complete data, 1480 (50%) completed the consent form and 1223 (83%) enrolled. We found higher odds of incomplete consent for non-English-speaking parents (OR = 2.1, p < 0.0001) and parents of children of all races except non-Hispanic white (OR = 1.27-1.99, p < 0.0001). We found higher odds of declined consent in patients with Medicaid (OR = 1.67, p = 0.003) and parents of children of all races except non-Hispanic white (OR = 1.32-2.9, p < 0.0001).

CONCLUSION:

Inability to enroll patients in a critical care biorepository may be associated with several sociodemographic factors at various points in recruitment/enrollment. IMPACT Individuals of minority race/ethnicity are less likely to enroll in genomic research and in critical care research. This study evaluated sociodemographic characteristics associated with decisions to enroll a child in a pediatric critical care biorepository. Sociodemographic factors including race/ethnicity, primary language, and insurance status and patient clinical characteristics are associated with differential enrollment into a pediatric critical care biorepository. More research is needed to understand how study team-participant interactions may play a role in differential enrollment. Barriers to enrollment occur both at the time of approaching and consenting for enrollment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Etnicidade / Termos de Consentimento Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Etnicidade / Termos de Consentimento Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans País como assunto: America do norte Idioma: En Ano de publicação: 2023 Tipo de documento: Article