Supportive Care in Cancer

, Volume 19, Issue 2, pp 281–290 | Cite as

From inside the bubble: migrants’ perceptions of communication with the cancer team

  • Phyllis N. Butow
  • Ming Sze
  • Priya Dugal-Beri
  • Michelle Mikhail
  • Maurice Eisenbruch
  • Michael Jefford
  • Penelope Schofield
  • Afaf Girgis
  • Madeleine King
  • David Goldstein
  • on behalf of the Psycho-Oncology Co-operative Research Group (PoCoG)
Original Article

Abstract

Purpose

Migrants with cancer struggle to communicate with their health care team. This study aimed to identify health-care related unmet needs and communication issues for migrants who develop cancer and factors associated with these challenges. In this paper, the findings related to communication issues are presented.

Patients and methods

Seventy-three cancer patients diagnosed within the previous 3 years and 18 carers, who had migrated to Australia and spoke the designated languages, participated in focus groups or structured interviews. Participants were recruited from ethnic community support organisations, support groups and Oncology clinics within three metropolitan hospitals in two states of Australia. Focus groups and semi-structured interviews were conducted in participants’ own language or English as preferred, audio-taped, transcribed and translated into English and analysed using qualitative methods.

Results

Four themes emerged: (1) cultural isolation, alienation and identification; (2) language and communication difficulties; (3) interpreter issues; and (4) advice for health professionals. Participants, especially those less acculturated, described feeling alone and misunderstood, failing to comprehend medical instructions, being unable to communicate questions and concerns and a lack of consistency in interpreters and interpretation.

Conclusions

Migrants with cancer experience additional challenges to those of native-born patients. Participants provided cogent advice regarding optimal communication with people from their culture. There is clearly a need to develop strategies to increase the cultural competence of care to people from different countries.

Keywords

Unmet needs Communication Migrants Cancer Multi-culturalism Cultural competence 

References

  1. 1.
    Australian Bureau of Statistics (2006) Australian social trends (4102.0). AGPS, CanberraGoogle Scholar
  2. 2.
    Du XL, Meyer TE, Franzini L (2007) Meta-analysis of racial disparities in survival in association with socioeconomic status among men and women with colon cancer. Cancer 109(11):2161–2170PubMedCrossRefGoogle Scholar
  3. 3.
    Krupski TL, Sonn G, Kwan L, Maliski S, Fink A, Litwin MS (2005) Ethnic variation in health-related quality of life among low-income men with prostate cancer. Ethn Dis 15(3):461–468PubMedGoogle Scholar
  4. 4.
    Gotay CC, Holup JL, Pagano I (2002) Ethnic differences in quality of life among early breast and prostate cancer survivors. Psycho-oncol 11(2):103–113CrossRefGoogle Scholar
  5. 5.
    Mayerowitz BE, Richardson J, Hudson S, Leedham B (1998) Ethnicity and cancer outcomes: behavioural and psychosocial considerations. Psycho Bull 123:47–70CrossRefGoogle Scholar
  6. 6.
    Buckle JM, Horn SD, Oates VM, Abbey H (1992) Severity of illness and resource use differences among white and black hospitalized elderly. Arch Intern Med 152:1596–1603PubMedCrossRefGoogle Scholar
  7. 7.
    Goldstein D, Thewes B, Butow P (2002) Communicating in a multicultural society II: Greek community attitudes towards cancer in Australia. Internal Medicine Journal. Intern Med J 32:289–296PubMedCrossRefGoogle Scholar
  8. 8.
    NBCC Exploring Cultural attitudes to breast cancer; Towards the development of culturally appropriate information resources for women from Greek, Italian, Arabic and Polish speaking backgrounds. ISBN 0-9586732-8-4, 1997Google Scholar
  9. 9.
    Gonzalez G (1997) Health care in the United States; A perspective from the front line. In: Surbone Z (ed) Communication with the cancer patient; Information and truth. The NY Academy of Sciences, NY, pp 211–222Google Scholar
  10. 10.
    Janz NK, Mujahid MS, Hawley ST, Griggs JJ, Hamilton AS, Katz SJ (2008) Racial/ethnic differences in adequacy of information and support for women with breast cancer. Cancer 113(5):1058–1067PubMedCrossRefGoogle Scholar
  11. 11.
    Chambers T (2000) Cross-cultural issues in caring for patients with cancer. Cancer Treat Res 102:23–37PubMedGoogle Scholar
  12. 12.
    Lindert J, Ehrenstein OS, Priebe S, Mielck A, Brahler E (2009) Depression and anxiety in labor migrants and refugees—a systematic review and meta-analysis. Soc Sci Med 69(2):246–257PubMedCrossRefGoogle Scholar
  13. 13.
    Parker G, Chan B, Tully L, Eisenbruch M (2005) Depression in the Chinese: the impact of acculturation (2005). Psychol Med 35(10):1475–1483PubMedCrossRefGoogle Scholar
  14. 14.
    Rissel C (1997) The development and application of a scale of acculturation, Australian and New Zealand. Journal of Public Health 21:606–613Google Scholar
  15. 15.
    Stenner P (1993) Discoursing jealousy. In: Parker I (ed) E Burman. Routledge, Discourse Analytic Research. London, pp 114–134Google Scholar
  16. 16.
    Davies B, Harre R (1990) Positioning: the discursive production of selves. Journal of the Theory of Social Behaviour 20:43–65CrossRefGoogle Scholar
  17. 17.
    Schwaderer KA (2007) Itano JK Bridging the healthcare divide with patient navigation: development of a research program to address disparities. Clin J Oncol Nurs 11(5):633–639PubMedCrossRefGoogle Scholar
  18. 18.
    Waitzkin H (1985) Information giving in medical care. JHealth SocBehav 26(2):81–101PubMedCrossRefGoogle Scholar
  19. 19.
    Johnson RL, Roter D, Powe NR, Cooper LA (2004) Patient race/ethnicity and quality of patient-physician communication during medical visits. Am J Public Health 94(12):2084–2090PubMedCrossRefGoogle Scholar
  20. 20.
    Ashing KT, Padilla G, Tejero J, Kagawa-Singer M (2003) Understanding the breast cancer experience of Asian American women. Psycho-oncology 12:38–58CrossRefGoogle Scholar
  21. 21.
    National Breast Cancer Centre & National Cancer Control Initiative (2002) Clinical practice guidelines for the psychosocial care of adults with cancer—draft for consultation. National Breast Cancer Centre & National Cancer Control Initiative, SydneyGoogle Scholar
  22. 22.
    Reisfield GM, Wilson GR (2004) Use of metaphor in the discourse on cancer. J Clin Oncol 22(19):4024–4027PubMedCrossRefGoogle Scholar
  23. 23.
  24. 24.
    Kaufert JM, Koolage WW (1984) Role conflict among ‘culture brokers’: the experience of native Canadian medical interpreters. Soc Sci Med 18:283–286PubMedCrossRefGoogle Scholar
  25. 25.
    Flores G (2005) The impact of medical interpreter services on the quality of health care: a systematic review. Med Care Res Rev 62:255–299PubMedCrossRefGoogle Scholar
  26. 26.
    Barlow-Stewart K, Yeo SS, Meiser B, Goldstein D, Tucker K, Eisenbruch M (2006) Towards cultural competence in cancer genetic counseling and genetics education: lessons learned from Chinese-Australians. Genet Med 8(1):1–9CrossRefGoogle Scholar
  27. 27.
    Interpreter use and satisfaction with interpersonal aspects of care for Spanish-speaking patients. Med. Care 36(10):1461–1470, 1998Google Scholar
  28. 28.
    Chu KC, Miller BA, Springfield SA (2007) Measures of racial/ethnic health disparities in cancer mortality rates and the influence of socioeconomic status. J Natl Med Assoc 99(10):1092–1100PubMedGoogle Scholar
  29. 29.
    Eshiett Michael UA, Parry EHO (2003) Migrants and health: a cultural dilemma. Clin Med 3:229–231PubMedGoogle Scholar

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Phyllis N. Butow
    • 1
    • 2
  • Ming Sze
    • 1
    • 2
  • Priya Dugal-Beri
    • 1
    • 2
  • Michelle Mikhail
    • 1
    • 2
  • Maurice Eisenbruch
    • 3
  • Michael Jefford
    • 4
    • 5
  • Penelope Schofield
    • 4
    • 5
  • Afaf Girgis
    • 6
  • Madeleine King
    • 1
    • 2
  • David Goldstein
    • 7
  • on behalf of the Psycho-Oncology Co-operative Research Group (PoCoG)
  1. 1.Psycho-Oncology Co-operative Research Group (PoCoG)University of SydneySydneyAustralia
  2. 2.School of PsychologyBrennan/McCallum Building (A18) University of SydneySydneyAustralia
  3. 3.School of PsychologyPsychiatry, and Psychological Medicine, Monash UniversityClaytonAustralia
  4. 4.Nursing and Supportive Care ResearchPeter MacCallum Cancer CentreEast MelbourneAustralia
  5. 5.Faculty of Medicine, Dentistry and Health SciencesUniversity of MelbourneMelbourneAustralia
  6. 6.Centre for Health Research and Psycho-Oncology (CHeRP)Cancer Council NSW, University of Newcastle and the Hunter Medical Research InstituteCallaghanAustralia
  7. 7.Department of Medical OncologyPrince of Wales HospitalRandwickAustralia

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