Literature DB >> 18196291

Cultural aspects of communication in cancer care.

Antonella Surbone1.   

Abstract

Cultural competence in oncology requires the acquisition of specific knowledge, clinical skills, and attitudes that facilitate effective cross-cultural negotiation in the clinical setting, thus, leading to improved therapeutic outcomes and decreased disparities in cancer care. Cultural competence in oncology entails a basic knowledge of different cultural attitudes and practices of communication of the truth and of decision-making styles throughout the world. Cultural competence always presupposes oncology professionals' awareness of their own cultural beliefs and values. To be able to communicate with cancer patients in culturally sensitive ways, oncologists should have knowledge of the concept of culture in its complexity and of the risks of racism, classism, sexism, ageism, and stereotyping that must be avoided in clinical practice. Oncologists should develop a sense of appreciation for differences in health care values, based on the recognition that no culture can claim hegemony over others and that cultures are evolving under their reciprocal influence on each other. Medical schools and oncology training can teach communication skills and cultural competence, while fostering in all students and young doctors those attitudes of humility, empathy, curiosity, respect, sensitivity, and awareness that are needed to deliver effective and culturally sensitive cancer care.

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Year:  2008        PMID: 18196291     DOI: 10.1007/s00520-007-0366-0

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  62 in total

1.  Defining cultural competence: a practical framework for addressing racial/ethnic disparities in health and health care.

Authors:  Joseph R Betancourt; Alexander R Green; J Emilio Carrillo; Owusu Ananeh-Firempong
Journal:  Public Health Rep       Date:  2003 Jul-Aug       Impact factor: 2.792

Review 2.  The illness trajectory of elderly cancer patients across cultures: SIOG position paper.

Authors:  A Surbone; M Kagawa-Singer; C Terret; L Baider
Journal:  Ann Oncol       Date:  2006-10-06       Impact factor: 32.976

3.  Negotiating cross-cultural issues at the end of life: "You got to go where he lives".

Authors:  M Kagawa-Singer; L J Blackhall
Journal:  JAMA       Date:  2001-12-19       Impact factor: 56.272

4.  Offering truth. One ethical approach to the uninformed cancer patient.

Authors:  B Freedman
Journal:  Arch Intern Med       Date:  1993-03-08

5.  The dynamics of change: cancer patients' preferences for information, involvement and support.

Authors:  P N Butow; M Maclean; S M Dunn; M H Tattersall; M J Boyer
Journal:  Ann Oncol       Date:  1997-09       Impact factor: 32.976

6.  Information needs of patients with incurable cancer.

Authors:  Elsbeth Voogt; Anna F van Leeuwen; Adriaan P Visser; Agnes van der Heide; Paul J van der Maas
Journal:  Support Care Cancer       Date:  2005-04-27       Impact factor: 3.603

Review 7.  Telling the truth to patients with cancer: what is the truth?

Authors:  Antonella Surbone
Journal:  Lancet Oncol       Date:  2006-11       Impact factor: 41.316

8.  "Do not tell": what factors affect relatives' attitudes to honest disclosure of diagnosis to cancer patients?

Authors:  Mustafa Ozdogan; Mustafa Samur; Hakan Sat Bozcuk; Erkan Coban; Mehmet Artac; Burhan Savas; Arzu Kara; Zekiye Topcu; Yeliz Sualp
Journal:  Support Care Cancer       Date:  2004-04-16       Impact factor: 3.603

9.  Cancer by another name: a randomized trial of the effects of euphemism and uncertainty in communicating with cancer patients.

Authors:  S M Dunn; P U Patterson; P N Butow; H H Smartt; W H McCarthy; M H Tattersall
Journal:  J Clin Oncol       Date:  1993-05       Impact factor: 44.544

10.  Family experience caring for terminally ill patients with cancer in Hong Kong.

Authors:  Esther Mok; Faye Chan; Vivian Chan; Ellen Yeung
Journal:  Cancer Nurs       Date:  2003-08       Impact factor: 2.592

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  40 in total

1.  "A Word can become a Seed": A Lesson Learned about Cultural Humility.

Authors:  Edward Kangsuhp Kim
Journal:  J Cancer Educ       Date:  2016-12       Impact factor: 2.037

2.  Identifying the informational and psychosocial needs of Chinese immigrant cancer patients: a focus group study.

Authors:  Jennifer Leng; Trevor Lee; Umut Sarpel; Jessy Lau; Yanjun Li; Connie Cheng; Ming-der Chang; Francesca Gany
Journal:  Support Care Cancer       Date:  2012-04-25       Impact factor: 3.603

Review 3.  Cultural and religious considerations in pediatric palliative care.

Authors:  Lori Wiener; Denice Grady McConnell; Lauren Latella; Erica Ludi
Journal:  Palliat Support Care       Date:  2012-05-22

4.  Psychosocial care for patients and their families is integral to supportive care in cancer: MASCC position statement.

Authors:  Antonella Surbone; Lea Baider; Tammy S Weitzman; Mary Jacqueline Brames; Cynthia N Rittenberg; Judith Johnson
Journal:  Support Care Cancer       Date:  2009-07-17       Impact factor: 3.603

Review 5.  Informational Support in Pediatric Oncology: Review of the Challenges Among Arab Families.

Authors:  Naïma Otmani; Mohammed Khattab
Journal:  J Cancer Educ       Date:  2018-08       Impact factor: 2.037

6.  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

7.  "Doctor, what do i have?" Knowledge of cancer diagnosis among immigrant/migrant minorities.

Authors:  Francesca Gany; Lalanthica Yogendran; Dana Massie; Julia Ramirez; Trevor Lee; Gary Winkel; Lisa Diamond; Jennifer Leng
Journal:  J Cancer Educ       Date:  2013-03       Impact factor: 2.037

8.  Heterogeneity in cancer guidelines: should we eradicate or tolerate?

Authors:  G Pentheroudakis; R Stahel; H Hansen; N Pavlidis
Journal:  Ann Oncol       Date:  2008-07-28       Impact factor: 32.976

9.  '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

10.  Cancer knowledge in the plural: queering the biopolitics of narrative and affective mobilities.

Authors:  Mary K Bryson; Jackie Stacey
Journal:  J Med Humanit       Date:  2013-06
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