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Disparities in prognosis communication among parents of children with cancer: The impact of race and ethnicity.
Ilowite, Maya F; Cronin, Angel M; Kang, Tammy I; Mack, Jennifer W.
Afiliação
  • Ilowite MF; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Cronin AM; Division of Population Sciences' Center for Outcomes and Policy Research, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Kang TI; Division of Pediatric Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts.
  • Mack JW; Division of Population Sciences' Center for Outcomes and Policy Research, Dana-Farber Cancer Institute, Boston, Massachusetts.
Cancer ; 123(20): 3995-4003, 2017 Oct 15.
Article em En | MEDLINE | ID: mdl-28873224
ABSTRACT

BACKGROUND:

Most parents of children with cancer say they want detailed information about their child's prognosis. However, prior work has been conducted in populations of limited diversity. The authors sought to evaluate the impact of parental race/ethnicity on prognosis communication experiences among parents of children with cancer.

METHODS:

In total, 357 parents of children with cancer and the children's physicians were surveyed at Dana-Farber Cancer Institute/Boston Children's Hospital and Children's Hospital of Philadelphia. Outcome measures were parental preferences for prognostic information, physician beliefs about parental preferences, prognosis communication processes, and communication outcomes. Associations were assessed by logistic regression with generalized estimating equations to correct for physician clustering.

RESULTS:

Two hundred eighty-one parents (79%) were white, 23 (6%) were black, 29 (8%) were Hispanic, and 24 (7%) were Asian/other. Eighty-seven percent of parents wanted as much detail as possible about their child's prognosis, with no significant differences by race/ethnicity (P = .75). However, physician beliefs about parental preferences for prognosis communication varied based on parent race/ethnicity, with physicians considering black and Hispanic parents less interested in details about prognosis than whites (P = .003). Accurate understanding of a less favorable prognosis was greater among white (49%) versus nonwhite parents (range, 20%-29%), although this difference was not statistically significant (P = .14).

CONCLUSIONS:

Most parents, regardless of racial and ethnic background, want detailed prognostic information about their child's cancer. However, physicians underestimate the information needs of black and Hispanic parents. To meet parents' information needs, physicians should ask about parents' information preferences before prognosis discussions. Cancer 2017;1233995-4003. © 2017 American Cancer Society.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pais / Relações Médico-Paciente / Médicos / Revelação da Verdade / Atitude do Pessoal de Saúde / Comunicação / Preferência do Paciente / Neoplasias Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: America do norte Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pais / Relações Médico-Paciente / Médicos / Revelação da Verdade / Atitude do Pessoal de Saúde / Comunicação / Preferência do Paciente / Neoplasias Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: America do norte Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article