2005
DOI: 10.1111/j.1525-1497.2005.0195.x
|View full text |Cite
|
Sign up to set email alerts
|

Patients’ attitudes toward health care providers collecting information about their race and ethnicity

Abstract: Most patients think HCPs should collect information about race/ethnicity, but many feel uncomfortable giving this information, especially among minorities. Health care providers can increase patients' comfort levels by telling them this will be used to monitor quality of care.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
68
0

Year Published

2008
2008
2023
2023

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 54 publications
(69 citation statements)
references
References 8 publications
1
68
0
Order By: Relevance
“…Support for collection of race and ethnicity data among clinicians in this study complements similar support among patients for such activities 29 and suggests that health care systems should implement programs to collect these data as a part of routine clinical care. 30 Our survey findings are consistent to prior surveys of cardiovascular specialists in some respects but different in others.…”
Section: Discussionmentioning
confidence: 91%
“…Support for collection of race and ethnicity data among clinicians in this study complements similar support among patients for such activities 29 and suggests that health care systems should implement programs to collect these data as a part of routine clinical care. 30 Our survey findings are consistent to prior surveys of cardiovascular specialists in some respects but different in others.…”
Section: Discussionmentioning
confidence: 91%
“…3,5 This has been reported to be due to the different gender roles in the family: men could go home earlier because they were more likely to be looked after by their partner. 19 The situation in Hong Kong is different. Children usually live with or close to their parents for cultural and social reasons.…”
Section: Discussionmentioning
confidence: 99%
“…However, data from patient surveys indicate that, while minority patients are wary of providing information about their race, they are generally willing to do so if it is clear that the purpose of collecting the data is to improve the quality of care. 80 We recommend that clinical settings first determine how data on race-ethnicity are currently collected, then improve data collection by training staff to sensitively and accurately capture these data (and also data on preferred language). Another potential barrier to monitoring quality of care by race-ethnicity is the availability of data on quality.…”
Section: Recommendationsmentioning
confidence: 99%