Attitudes Toward Cultural Competency in CA Medical Groups

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Presentation transcript:

Attitudes Toward Cultural Competency in CA Medical Groups P4P Summit Neil A. Solomon, MD NAS Consulting Services February 28, 2008

Research Endeavor Questions: Team Are CA medical groups collecting and using information about language, race, ethnicity (LRE)? Is there a need for program support in cultural competency, especially for chronic care? Is there a role for cultural competency in P4P? Team Sunita Mutha, MD – Center for Health Professions Neil Solomon, MD – NAS, CQC Roza Do – CQC, CAPG Sponsored by The California Endowment

Surveyed Provider Organizations 11 medical groups/IPAs (20 total interviews) All risk-bearing groups in CA Mix of urban and rural, North and South Sampled high achievers and those serving very diverse populations Spoke to organizational/clinical leader Semi-structured interviews

Areas Covered Current activities to collect and use information about patient LRE Current strategies to incorporate language and cultural issues into population-based programs (DM, UM, CM, etc.) Major challenges faced in caring for specific groups of patients Desires/needs for support in LRE care issues Opinions about recognition and rewards for culturally effective care Ways to measure and report this information

LRE Data: “No Need Now” Haven’t heard it’s a problem No call from providers or patients No external complaints about disparities Language issue is being handled Patients find providers and vice versa Use bilingual office staff Other local interpreter resources

Data Collection: “Not Our Job” Health plans Have the infrastructure and resources Required to collect by law; they should forward to medical groups Individual provider offices Know their own patients Document in medical records or registries Medi-Cal Gather info during enrollment

Data Collection: Early Efforts Infer from population demographics Internal surveys of physicians Plan to incorporate into system-wide EHR

Challenging Patient Populations Defined by disease, not by culture Some recognition of cultural issues Self-care behaviors End-of-Life views Distrust of physicians who are different from them Groups with most complicated populations have least resources to dedicate for QI efforts

What is Needed/Wanted Embed teaching and tools into chronic care and patient experience programs (as opposed to stand-alone training) Interpreter training and support for office staff Work with health plans to get data Help address potential regulatory requirements

Cultural Competency in P4P Not an issue, doesn’t belong Adding another measure wouldn’t motivate focus on the topic Lack valid measures Not fair to assess across groups serving very disparate populations

Cultural Competency in P4P Go Slow for Now Add questions to PAS to learn more about the size and shape of the problem (not to be used for recognition or rewards) Recognition before Rewards

Future Directions Identify strategies to increase awareness of health disparities given population diversity Develop/describe valid and reliable LRE data collection methods for groups to use Shared across health plans Via EHRs at physician offices Develop training and education Esp. chronic care and self-management support Office staff interpreter services Focus on measuring cultural competency by assessing patient experience