Literature DB >> 16874746

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

Susan K Parsons1, Shigeko Saiki-Craighill, Deborah K Mayer, Amy M Sullivan, Stefanie Jeruss, Norma Terrin, Hocine Tighiouart, Kaoru Nakagawa, Yoko Iwata, Junichi Hara, Holcombe E Grier, Susan Block.   

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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Year:  2007        PMID: 16874746     DOI: 10.1002/pon.1048

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  13 in total

1.  Information-sharing challenges between adolescents with cancer, their parents and health care providers: a qualitative study.

Authors:  Masoud Bahrami; Mahboobeh Namnabati; Fariborz Mokarian; Parastoo Oujian; Paul Arbon
Journal:  Support Care Cancer       Date:  2017-01-11       Impact factor: 3.603

2.  Why did I get cancer? Perceptions of childhood cancer survivors in Korea.

Authors:  Jaehee Yi; Min Ah Kim; Bridget G Parsons; Yelena P Wu
Journal:  Soc Work Health Care       Date:  2018-02-13

Review 3.  Communication in pediatric oncology: State of the field and research agenda.

Authors:  Bryan A Sisk; Jennifer W Mack; Rachel Ashworth; James DuBois
Journal:  Pediatr Blood Cancer       Date:  2017-07-27       Impact factor: 3.167

4.  Cardiac screening prior to stimulant treatment of ADHD: a survey of US-based pediatricians.

Authors:  Laurel K Leslie; Angie Mae Rodday; Tully S Saunders; Joshua T Cohen; John B Wong; Susan K Parsons
Journal:  Pediatrics       Date:  2012-01-16       Impact factor: 7.124

5.  Multilevel barriers and facilitators of communication in pediatric oncology: A systematic review.

Authors:  Bryan A Sisk; Kieandra Harvey; Annie B Friedrich; Alison L Antes; Lauren H Yaeger; Jennifer W Mack; James M DuBois
Journal:  Pediatr Blood Cancer       Date:  2021-10-18       Impact factor: 3.167

6.  Impact of psychological and cancer-related factors on HRQoL for Korean childhood cancer survivors.

Authors:  Myung Ah Rhee; Kyong Mee Chung; Yuri Lee; Hana K Choi; Jung Woo Han; Hyo Sun Kim; Sun Hee Kim; Yoon Jung Shin; Chuhl Joo Lyu
Journal:  Qual Life Res       Date:  2014-05-11       Impact factor: 4.147

7.  'Palliative care': a contradiction in terms? A qualitative study of cancer patients with a Turkish or Moroccan background, their relatives and care providers.

Authors:  Fuusje M de Graaff; Anneke L Francke; Maria Etc van den Muijsenbergh; Sjaak van der Geest
Journal:  BMC Palliat Care       Date:  2010-09-10       Impact factor: 3.234

8.  Japanese physicians' attitudes toward end-of-life discussion with pediatric patients with cancer.

Authors:  Saran Yoshida; Chitose Ogawa; Ken Shimizu; Mariko Kobayashi; Hironobu Inoguchi; Yoshio Oshima; Chikako Dotani; Rika Nakahara; Masashi Kato
Journal:  Support Care Cancer       Date:  2018-05-17       Impact factor: 3.603

9.  Primary care physicians and oncologists are partners in cancer announcement.

Authors:  Marie-Eve Rougé Bugat; Christelle Omnes; Cyrille Delpierre; Emile Escourrou; Nathalie Boussier; Stéphane Oustric; Jean-Pierre Delord; Eric Bauvin; Pascale Grosclaude
Journal:  Support Care Cancer       Date:  2015-12-14       Impact factor: 3.603

10.  Survey of United States child and adolescent psychiatrists' cardiac screening practices prior to starting patients on stimulants.

Authors:  Laurel K Leslie; Angie Mae Rodday; Tully S Saunders; Joshua T Cohen; John B Wong; R Christopher Sheldrick; Susan K Parsons
Journal:  J Child Adolesc Psychopharmacol       Date:  2012-10       Impact factor: 2.576

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