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Research article summary (published 30 Dec 2006):

Telling children and adolescents about their cancer diagnosis: Cross-cultural comparisons between pediatric oncologists in the US and Japan.

Full Abstract

PURPOSE:
Over the last 50 years, direct communication about cancer with adults has shifted from an approach of not telling to one of telling. Less is known about communication practices with children. The purpose of this study is to (1) describe patterns of communication at diagnosis between pediatric oncologists and children with cancer and (2) compare cultural differences in these practices in the US and Japan.

METHODS:
This 2003 survey, developed in English and translated into Japanese was mailed to members of the American Society of Pediatric Hematology/Oncology and the two Japanese Societies of Pediatric Hematology and Oncology; there were 350 US and 362 Japanese respondents. Descriptive statistics and logistic regressions were performed.

RESULTS:
US physicians had a consistent pattern of telling children (65% always told the child; less than 1% rarely or never told). Japanese physicians had greater variability in their patterns of telling (with only 9.5% always telling, 34.5% rarely or never telling). Direct communication with the child was influenced by personal attitudes, patient factors, and work culture in both countries. Many more variables emerged as influencing Japanese physicians' communication practices than for US physicians. US physicians were influenced by their own sense of responsibility for telling, while Japanese physicians were more influenced by personal attitudes, patient factors, and work culture.

CONCLUSIONS:
US and Japanese physicians differed when communicating directly with the child about his or her cancer. The impact of these practices on children and their parents should be explored and the parent and child's perspectives elicited. This information will help facilitate culturally sensitive patient and family centered communication.Copyright 2006 John Wiley & Sons, Ltd.

 

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Author information

Author/s: Parsons, Susan K (SK); Saiki-Craighill, Shigeko (S); Mayer, Deborah K (DK); Sullivan, Amy M (AM); Jeruss, Stefanie (S); Terrin, Norma (N); Tighiouart, Hocine (H); Nakagawa, Kaoru (K); Iwata, Yoko (Y); Hara, Junichi (J); Grier, Holcombe E (HE); Block, Susan (S);

Affiliation: Center on Child and Family Outcomes, Institute for Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston, MA 02111, USA. sparsons(-atsign-)tufts-nemc.org

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal: Psycho-oncology (Psychooncology), published in England. (Language: eng)

Reference: 2007-Jan; vol 16 (issue 1) : pp 60-8

Dates: Created 2007/01/03; Completed 2007/03/22;

PMID: 16874746, status: MEDLINE (last retrieval date: 12/26/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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