Literature DB >> 24827124

Immigrants' perceptions of the quality of their cancer care: an Australian comparative study, identifying potentially modifiable factors.

D Goldstein1, M L Bell2, P Butow3, M Sze2, L Vaccaro2, S Dong2, W Liauw4, R Hui5, M Tattersall6, W Ng7, R Asghari8, C Steer9, J Vardy10, P Parente11, M Harris12, N V Karanth13, M King2, A Girgis14, M Eisenbruch15, M Jefford16.   

Abstract

BACKGROUND: Recent data show a falling cancer mortality in the general population without a similar shift in immigrant outcomes, leading to a greater cancer burden and mortality for immigrants. Our aims were to compare perceived patterns of care in immigrants and native-born cancer patients. PATIENTS AND METHODS: This was a hospital-based sample of first-generation immigrants and Australian-born Anglo patients in the first year following diagnosis. It was restricted to Chinese, Arabic, or Greek speakers. Eligible participants, recruited via 16 oncology clinics, were over 18, with cancer (any type or stage), and having commenced treatment at least 1 month previously. Five hundred and seventy-one CALD patients (comprising 145 Arabic, 248 Chinese, and 178 Greek) and a control group of 274 Anglo-Australian patients participated.
RESULTS: Immigrants had difficulty communicating with the doctor (73% versus 29%) and understanding the health system (38% versus 10%). Differences were found in 'difficulty knowing who to see' (P = 0.0002), 'length of time to confirm diagnosis' (P = 0.04), wanting more choice about a specialist and hospital (P < 0.0001); being offered the opportunity to see a counselor (P < 0.0001); and actually seeing one (P < 0.0001). There were no significant self-reported differences regarding how cancer was detected, time to see a health professional, or type first seen; however, immigrants reported difficulty knowing who to see. Previous studies showed differences in patterns of care according to socioeconomic status (SES) and educational level. Despite adjusting for age, sex, education, marital status, SES, time since diagnosis, and type of cancer, we did not find significant differences. Instead, we found that understanding of the health system and confidence understanding English were important factors.
CONCLUSIONS: This study confirmed that immigrants with cancer perceive an inferior quality of cancer care. We highlight potentially modifiable factors including assistance in navigating the health system, translated information, and cultural competency training for health professionals.
© The Author 2014. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  cancer outcomes; care co-ordination; health services; immigrant health

Mesh:

Year:  2014        PMID: 24827124     DOI: 10.1093/annonc/mdu182

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  15 in total

1.  "I might not have cancer if you didn't mention it": a qualitative study on information needed by culturally diverse cancer survivors.

Authors:  Clare O'Callaghan; Penelope Schofield; Phyllis Butow; Linda Nolte; Melanie Price; Spiri Tsintziras; Ming Sze; Thida Thein; Dorothy Yiu; Shab Mireskandari; David Goldstein; Michael Jefford
Journal:  Support Care Cancer       Date:  2015-06-21       Impact factor: 3.603

2.  Disparities in hospital smoking cessation treatment by immigrant status.

Authors:  Jenny Chen; Ellie Grossman; Alissa Link; Binhuan Wang; Scott Sherman
Journal:  J Ethn Subst Abuse       Date:  2018-05-04       Impact factor: 1.507

3.  A meta-review of qualitative research on adult cancer survivors: current strengths and evidence gaps.

Authors:  Rebekah Laidsaar-Powell; Stephanie Konings; Nicole Rankin; Bogda Koczwara; Emma Kemp; Carolyn Mazariego; Phyllis Butow
Journal:  J Cancer Surviv       Date:  2019-11-19       Impact factor: 4.442

4.  Chinese-Australian women with breast cancer call for culturally appropriate information and improved communication with health professionals.

Authors:  Janelle V Levesque; Martha Gerges; Verena S Wu; Afaf Girgis
Journal:  Cancer Rep (Hoboken)       Date:  2019-09-10

5.  It's all good on the surface: care coordination experiences of migrant cancer patients in Australia.

Authors:  Joanne M Shaw; Heather L Shepherd; Ivana Durcinoska; Phyllis N Butow; Winston Liauw; David Goldstein; Jane M Young
Journal:  Support Care Cancer       Date:  2015-12-03       Impact factor: 3.603

Review 6.  Integrative Review of the Supportive Care Needs of Arab People Affected by Cancer.

Authors:  Ibrahim Alananzeh; Janelle Levesque; Cannas Kwok; Bronwyn Everett
Journal:  Asia Pac J Oncol Nurs       Date:  2016 Apr-Jun

7.  Minority ethnicity patient satisfaction and experience: results of the National Cancer Patient Experience Survey in England.

Authors:  Richard J Pinder; Jamie Ferguson; Henrik Møller
Journal:  BMJ Open       Date:  2016-06-28       Impact factor: 2.692

8.  Listening to the consumer voice: developing multilingual cancer information resources for people affected by liver cancer.

Authors:  Monica C Robotin; Mamta Porwal; Max Hopwood; Debbie Nguyen; Minglo Sze; Carla Treloar; Jacob George
Journal:  Health Expect       Date:  2016-02-29       Impact factor: 3.377

9.  Communication challenges experienced by migrants with cancer: A comparison of migrant and English-speaking Australian-born cancer patients.

Authors:  Amelia Hyatt; Ruby Lipson-Smith; Penelope Schofield; Karla Gough; Ming Sze; Lynley Aldridge; David Goldstein; Michael Jefford; Melanie L Bell; Phyllis Butow
Journal:  Health Expect       Date:  2017-03-05       Impact factor: 3.377

10.  A qualitative study of cancer care professionals' experiences of working with migrant patients from diverse cultural backgrounds.

Authors:  Alex Broom; Rhiannon Bree Parker; Emma Kirby; Renata Kokanović; Lisa Woodland; Zarnie Lwin; Eng-Siew Koh
Journal:  BMJ Open       Date:  2019-03-23       Impact factor: 2.692

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