Standardizing Patient Race, Ethnicity and Language Data Collection: Overview October 1, 2010...

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Standardizing Patient Race, Ethnicity and Language Data Collection: Overview October 1, 2010 Memphis, TN Aligning Forces for Quality National Program Office

Transcript of Standardizing Patient Race, Ethnicity and Language Data Collection: Overview October 1, 2010...

Standardizing Patient Race, Ethnicity

and Language Data Collection:Overview

October 1, 2010Memphis, TN

Aligning Forces for Quality National Program Office

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Why are we here?

• Understand key decision points in implementing standardized race, ethnicity and language (R/E/L) data collection within your organization

• To provide you with the knowledge and tools to train staff on the standardized collection of R/E/L data

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What are disparities in health care quality?

• “Racial and ethnic minorities tend to receive a lower quality of healthcare than non-minorities”

• Less likely to receive:– Cancer screening– Cardiovascular therapy– Kidney dialysis– Transplants – Curative surgery for lung cancer– Hip and knee replacement  – Pain medicines in the ER

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National CABG rates

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year 1993 - 2005

Whitemen

Blackmen

Jha, NEJM, 2005

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Growing U.S. minority population

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2010 2015 2020 2025 2030 2035 2040 2045 2050

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Non-Hispanic White

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Population Projections, 2010 to 2050

Source: U.S. Census Bureau, 2009 National Population Projections (Supplemental) 4. Projections of the Population by Sex, Race, and Hispanic Origin for the United States: 2010 to 2050

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Increasing legislative and regulatory attention to R/E/L

data• American Recovery and Reinvestment Act of 2009

– Hospitals and providers will need to collect R/E/L data to be eligible for “meaningful use” incentive payments

– Race/Ethnicity categories to follow Office of Management and Budget guidelines

• Patient Protection and Affordable Care Act of 2010 – Health programs receiving federal money are required to

collect R/E/L data

• Revised Joint Commission standards– Expand requirements related to the collection of patient

language data, including preferred spoken language and written communication needs

– New requirement to collect patient-level demographic data on race and ethnicity

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OMB guidelines: Race, ethnicity and language

categoriesRace• Black• White• Asian• American

Indian/Alaska Native

• Native Hawaiian/ Pacific Islander

• Multiracial*• Declined*• Unavailable*

Language• English• Spanish• Other• Declined • Unavailable

*This designation indicates a modification to the OMB R/E categories

Ethnicity• Hispanic• Not Hispanic• Declined*• Unavailable*

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Three steps in addressing disparities

• Standardized collection of self-reported R/E/L data– Categories are standardized

– Patient self-reports

• Stratification and analysis of performance measures

• Use of stratified data to identify and develop quality improvement interventions targeted to specific patient populations

Disparities in care represent a failure in quality

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What is the current status of R/E/L data collection?

• Most hospitals collect data but not in a standardized manner– Few hospitals use data collected to

drive quality improvement

• Few ambulatory providers collect or use data– More common in health centers and

integrated health systems than in smaller physician practices

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What change needs to happen?

• Develop the capacity and infrastructure to collect standardized race, ethnicity and language information from all patients

• This will affect: – Registration system and processes– Staff training and workflow– Patient communications– How data are used to monitor quality

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What will we cover today?

• Building blocks toward equitable care– National health care disparities – Linking R/E/L data to quality– Increasing attention R/E/L data

• Key Decision Points– Changes at the organizational level

• Nuts and Bolts– Tools to train your staff

• Available resources