from Asian American Breast Cancer Patients
Download
Report
Transcript from Asian American Breast Cancer Patients
What Is Lacking in Patient-Physician Communication:
from Asian American Breast Cancer Patients’ and Oncologists’ Perspectives
Sunmin Lee,1 Grace X. Ma,2,3 Carolyn Y. Fang2,3,4 Lu Chen, 1 Youngsuk Oh,1 Lynn Scully1
1 Department
of Epidemiology and Biostatistics, University of Maryland School of Public Health, College Park, Maryland
2 Department of Public Health, College of Health Professions, Temple University, Philadelphia, Pennsylvania
3 Center for Asian Health, Temple University, Philadelphia, Pennsylvania
4 Cancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, Pennsylvania
INTRODUCTION
Breast cancer is the leading cancer in incidence and among top
five in mortality in Chinese & Korean women (CKW) in the U.S.
(Miller et al., 2008)
Rapid and steady increase of breast cancer incidence in CKW
since 1980’s. (Gormez et al., 2010)
Patient-physician communication and coordination is essential in
the quality of cancer survivorship care. (Arora et al., 2011)
Asian American patients have reported lower satisfaction with
health care compared to Whites and Blacks. (Saha, Arbelaez &
Cooper, 2003)
Key Interview Questions
Patients
Oncologists
• How did you feel about the interaction
between you and your doctor?
• Do you have any barriers in
communicating with your doctor?
• Were there cultural differences in your
communication? If so, what were they?
How would you want to improve this?
• When it came to the decision of your
care, what did you do?
• How did you feel about your role in the
decision making?
•How would you describe your Asian
patients’ interaction with you compared
with White patients in the following
areas:
•Making decisions
•Asking questions
•Talking about fear & distress
• Are there any difficulties other than
language?
• If you do face a language or
communication barrier, what do you
do?
• What is your advice for those who want
to be more actively involved in
treatment?
OBJECTIVE
To explore patient-physician communication process in Asian
American breast cancer patients from both patients and oncologists
perspectives.
METHODS
Study Design
Face-to-face in-depth interviews with nine Chinese or Korean
breast cancer patients/survivors and three Asian oncologists
who routinely provided care for Asian patients in the
Washington DC metropolitan area.
Patients’ Perspective
Oncologists’ Perspective
Language Barrier
RESULTS
Patient Characteristics
n=9 (4 Chinese & 5 Koreans)
Participants were between 40-69 years of age. Majority were married
(78%) and had college or above education (77%).
Most of them have completed active cancer treatment (89%). More than
half were diagnosed with breast cancer within a year (56%).
Acknowledgments: This research is a pilot project
supported by NIH-NCI’s Community Network Program
Center, ACCHDC U54 CNPC (1U54CA 153513-01, PI: Grace
Ma)
Cultural Differences
• Expected the doctor to be
authority and were
disappointed when questions
were not answered.
• Dissatisfied with doctor’s
advice on physical activity and
diet which from the patients’
perspective was not
appropriate for Asians.
• In US culture, having breast
cancer is a badge of honor and
surviving is something to be
proud of. For some Asian
women it’s more of a stigma
and they are ashamed and
hesitant to discuss it.
• Many Asian patients want to
know very specifically what
they can and cannot eat, and
are surprised when told that
they should just eat a healthy
balanced diet.
Decision-Making on Treatment
• Physicians played a leading role • Some Asian patients are not
in most cases.
very assertive and will not
• The influence from family
express their concerns. Asians
members was more evident in
in general are not very
participants who were limited
proactive or assertive.
in speaking English.
• They do not want too much
• Many expressed the desire to
information from a physician,
be actively involved in decision
they expect the physician to be
making.
the expert and make the
decisions for them. If they do
not receive this they may even
switch doctors.
Participant Recruitment
A convenience sample of Chinese and Korean breast cancer
survivors living in Washington D.C. metropolitan area.
Patients were recruited from community based organizations,
posters on websites well known among Korean/Chinese
immigrants, and personal contacts.
Oncologists were recruited from personal contacts. They
were not necessarily oncologists of women we interviewed.
Data Collection and Analysis
Comprehensive interview guides were developed separately
for patients and oncologists based on literature review and
input from experts on breast cancer survivorship and
oncologists.
Interviews were recorded, transcribed, and translated.
Transcripts were analyzed by two independent coders and
their analysis was compared and contrasted, and finally
agreed upon in the research team.
• Language was the biggest
• If the women cannot speak
barrier to understanding
English then this serves as a
information and making
large barrier for understanding
treatment decisions.
information and
• Medical terms were a challenge communicating.
even for those who were fluent • Translation by family members
in English.
may not be accurate.
• For some patients, they could
• Some patients may neglect to
only rely on guessing and body ask questions due to concerns
language in extreme situations. of burdening family members.
CONCLUSION, IMPLICATIONS & NEXT STEP
Oncologist Characteristics
Oncologist #1 Oncologist #2 Oncologist #3
Age (in years)
Country of birth
Gender
Language spoken (other
than English)
Ever communicate with
patients in language other
than English?
Years practicing medicine
47
50
37
Korea
India
US
F
F
M
Korean, Spanish,
Tamil, Spanish
Portuguese
Korean
Yes
Yes
Yes
22
22
14
Language barrier, cultural difference and patient involvement are
key issues in patient-physician communication for Asian American
breast cancer survivors.
Proper patient education with linguistically and culturally
appropriate information and tools may help improve communication
with physician and decision-making process.
As a next step, we plan to design and implement a theory-based,
culturally and linguistically appropriate intervention to Korean breast
cancer survivors. This will include skills to enhance patientphysician communication.