If you are seeing this message, you may be experiencing temporary network problems. Please wait a few minutes and refresh the page. If the problem persists, you may wish to report it to your local Network Manager.
It is also possible that your web browser is not configured or not able to display style sheets. In this case, although the visual presentation will be degraded, the site should continue to be functional. We recommend using the latest version of Microsoft or Mozilla web browser to help minimise these problems.
Wiley InterScience | |||||||||||||||||||||
![]() Health Services ResearchVolume 41 Issue 4p1, Pages 1501 - 1518 Published Online: 5 May 2006 © 2010 Health Research and Educational Trust Published on behalf of Health Research and Educational Trust in cooperation with AcademyHealth.
Abstract | References | Full Text: HTML, PDF (Size: 112K) | Related Articles | Citation Tracking Obtaining Data on Patient Race, Ethnicity, and Primary Language in Health Care Organizations: Current Challenges and Proposed Solutions Address correspondence to Romana Hasnain-Wynia, Ph.D., Vice President, Research, Health Research and Educational Trust/AHA, One North Franklin, 30th Floor, Chicago, IL 60606. David W. Baker, M.D., M.P.H., FACP, is Chief of the Division of General Internal Medicine, Feinberg School of Medicine of Northwestern University, Chicago, IL. Copyright © 2006 Health Research and Educational Trust KEYWORDS disparities • quality of care • patient-centered care • self-reported race/ethnicity • uniform framework • health care organizations ABSTRACTObjectives. To provide an overview of why health care organizations (HCOs) should collect race, ethnicity, and language data, review current practices, discuss the rationale for collecting this information directly from patients, and describe barriers and solutions. Principal Findings. Hospitals and HCOs with data from their own institutions may be more likely to look at disparities in care, design targeted programs to improve quality of care, and provide patient-centered care. Yet data collection is fragmented and incomplete within and across organizations. A major factor affecting the quality of data is the lack of understanding about how best to collect this information from patients. Conclusions. If HCOs make a commitment to systematically collect race/ethnicity and language data from patients, it would be a major step in enhancing the ability of HCOs to monitor health care processes and outcomes for different population groups, target quality initiatives more efficiently and effectively, and provide patient-centered care. |
|
| |||||||||||||||||||
FREE Special Article on Flu Vaccinations | ![]() |
Journal of School Health has published a special, early view article entitled “Strategies for Implementing School-Located Influenza Vaccination of Children: A Systematic Literature Review.” Read this important paper FREE for a limited time! | |