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Association of Asian Pacific Community Health Organizations
Collecting social determinants of health data Using PRAPARE to reduce disparities, improve outcomes and transform care Protocol for Responding to and Assessing Patients’ Assets, Risks, and Experiences Presented by: Tuyen Tran Association of Asian Pacific Community Health Organizations April 24, 2017 This project was made possible with funding from: Collecting Social Determinants of Health Data Using P.R.A.P.A.R.E. to Reduce Disparities, Improve Outcomes, and Transform Care © National Association of Community Health Centers, Inc., Association of Asian Pacific Community Health Organizations, Oregon Primary Care Association. PRAPARE and its resources are proprietary information of NACHC and its partners, intended for use by NACHC, its partners, and authorized recipients. Do not publish, copy, or distribute this information in part of whole without written consent from NACHC.
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PRESENTATION OBJECTIVES
Present AAPCHO’s collaboration in PRAPARE Discuss the importance of documenting and addressing social determinants of health for improving patient and population health Describe the PRAPARE protocol and how it was developed and implemented in four different Electronic Health Records at health centers nationally Learn about free resources and information about how to get started in data collection on the social determinants of health
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Association of Asian Pacific Community Health Organizations (AAPCHO)
Non-profit, national association established in 1987 with a mission to improve health status and access of Asian Americans, Native Hawaiians and other Pacific Islanders. Represents 35 community health organizations, mostly health centers serving primarily underserved Asian Americans, Native Hawaiians and other Pacific Islanders (AA&NHPI). BPHC funded National Cooperative Agreement holder providing T/TA to health centers serving AA&NHPI. The Association of Asian Pacific Community Health Organizations (AAPCHO) is a national association of 35 community health centers and organizations serving primarily Asian Americans, Native Hawaiians, and other Pacific Islanders. We are dedicated to promoting advocacy, collaboration, and leadership that improves the health status and access of these medically underserved communities. Together, our CHC members serve over 500,000 patients nationally and are at the forefront in providing community responsive, financially affordable and culturally and linguistically appropriate primary health care services.
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Storytelling with our data SELECTED SDOH DATA
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Average AA&NHPI Patients at AAPCHO Health Centers, 2015
29 AAPCHO members, 1375 national FQHCs Data Source: UDS 2015
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AAPCHO* HEALTH CENTER PATIENTS BY RACE, 2015 (% KNOWN)
AAPCHO member HCs served over 530,000 patients AA&NHPI patients accounted for almost 70% of those served NATIVE HAWAIIANS 11.8% PACIFIC ISLANDERS 3.7% Guamanian/Chamorro 0.1% Micronesian 0.6% Other Pacific Islanders 0.8% Samoan 2.0% Tongan 0.2% ASIAN GROUPS 65.2% Cambodian 0.6% Chinese 50.7% Filipino 4.6% Japanese 0.7% Korean 1.2% Laotian 0.2% Mien Mixed AA&NHOPI Other Asian 3.7% Thai 0.1% Vietnamese 2.6% *AAPCHO has 29 AA&NHOPI-serving FQHCs
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AAPCHO HEALTH CENTER PATIENTS BY LIMITED ENGLISH PROFICIENCY (LEP), 2000-2015
More than half of AAPCHO member HC patients were best served in a language other than English For some AAPCHO members, LEP patients represented up to 100% of their patient populations English 39.3% Cantonese 22.5% Mandarin 22.3% Unknown 4.8% Chinese 3.7% Vietnamese 2.2% Other 2.3% Korean 0.9% Cambodian 0.4% Spanish 0.5% Tagalog 0.2% Samoan Burmese 0.1% Hakka Japanese Karen Mien Laotian Chuukese <.10% Indonesian Malay Thai Tongan *AAPCHO has 29 AA&NHOPI-serving HCs
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AAPCHO members had a higher proportion of geriatric (age 65+) patients from 2007-2015
VL, please update.
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AAPCHO and national HCs’ proportions of uninsured patients have been on a declining trend while Medicaid has simultaneously risen.
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SELECTED CLINICAL DATA
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SELECTED CLINICAL DIFFERENCES
AAPCHO( %) National ( %) % Hepatitis B 2.6% 0.2% % TB 0.09% 0.04% % Abnormal breast findings 0.83% 0.6% % Abnormal cervical findings 0.94% 0.8%
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SELECTED QUALITY OF CARE MEASURES
AAPCHO ( %) National (%) Cervical cancer screening 58.3% 56.0% Hypertensive patients with patients with controlled BP 67.6% 68.7% Diabetic patients with HbA1c > 9 26.1% 29.8% Notice AAPCHO has lower percentage with controlled BP
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SELECTED ENCOUNTER & CO$T DATA
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AAPCHO had a higher average number of enabling service (ES) encounters compared to the national average
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In 2015, average AAPCHO Enabling Services FTEs were higher than the national average overall and particularly for case management, patient education, and interpretation VL update this slide with 2015 data
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AAPCHO total costs for enabling services per HC were higher than national average
VL update this slide with 2015 data Statistically significant
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Average AAPCHO medical costs per medical encounter were similar to the national average
AAPCHO centers spend significantly more per pt and per encounter so we REALLY need the data on SDH and ES to justify why we are doing so! Look what the UDS data says. How do we defend without data? No significant difference, t-test for medical costs per medical encounter. Average costs per patient therefore much higher and statistically significant. The graph is the average cost/MEDICAL encounter, which doesn’t include ES etc. It’s really just the medical staff and Lab. For some reason AAPCHO CHCs still have a higher cost for medical encounters. Also, the results of t-tests don’t really matter here, because we are not comparing another sample to the national HCs, we are really just comparing AAPCHO members (which weren’t randomly selected) to the national HCs. Higher average for AAPCHO members is higher average no matter statistically significant or not. T-test is telling us what’s the chance to have randomly selected a sample like the AAPCHO members from the national FQHCs (significant result means not likely, so the sample couldn’t have been selected from the national FQHCs, so the sample must have some different characteristic). AAPCHO Members ($) National HCs ($) Costs per patient 1,030.45 826.84 Costs per encounter 215.45 207.21
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CONTRIBUTION OF NON-CLINICAL SERVICES
AAPCHO centers have better health outcomes compared to national averages for pap test, hypertension, and diabetes. This may be due to the higher number of enabling services and resulting quality outcomes provided by AAPCHO centers compared to national health centers. This is what the UDS is showing, we need data to show it. We can’t make this conclusion with just UDS data, need pt level data.
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ENABLING SERVICES (ES)
non-clinical services that are provided to health center patients that promote, support and assist in the delivery of health care and facilitate access to quality patient care NACHC/MGMA 2000
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AAPCHO’S ENABLING SERVICES ACCOUNTABILITY PROJECT (ESAP)
PARTICIPATING CENTERS: Charles B. Wang Community Health Center NY, NY International Community Health Services Seattle, WA Kalihi-Palama Health Center Honolulu, HI Waianae Coast Comprehensive Health Center Waianae, HI This project developed out of the recognition by AAPCHO health centers that enabling services play an important role in the health of their patients, many of whom are immigrant, and face cultural and linguistic barriers to care. We believe that if these services are valued and if we can show this with our data, then adequate and sufficient funding should be explicitly directed to pay for them, to assure they are provided where and when needed in sufficient volume and with appropriate staffing levels. Further, the lack of data on enabling services impedes the ability to quantify the need and demand for services, or to demonstrate their effectiveness. So in 2004, we embarked on a pilot project to develop a standardized data collection model for enabling services. AAPCHO, in collaboration with 4 CHCs pilot sites, NACHC and other experts, implemented findings of the MGMA/NACHC Health Center Enabling Services Report and developed a practical system for CHCs. To address differences in staffing and IT capacity among multiple CHCs, we applied a simpler enabling services tracking system.
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LACK OF COMPREHENSIVE ES DATA ON UDS
UDS TABLE 5- STAFFING AND UTILIZATION Personnel by Major Service Category FTEs (a) Clinic Visits (b) Patients (c) Case Managers Patient/Community Education Specialists Outreach Workers Transportation Staff Eligibility Assistance Workers Interpretation Staff Community Health Workers Other Enabling Services So you’re thinking, but aren’t we already required to submit ES data to UDS? HCs are required to submit some information on their ES to the BPHC as part of their annual Data System reports but the UDS poorly tracks the scope of ES actually provided and needed by the health center. The current UDS fails to demonstrate the critical impact of these services and the need to adequately finance them, requiring them to report partial information about ES staffing for case managers, patient/community education specialists, outreach workers, transportation staff, eligibility assistance workers, interpretation staff and other enabling services. UDS also provides a limited accounting of patient users and patient visits for ES but only for those seen by case managers and education specialists and also does not indicate which patients are actually receiving these services. Case managers and health educators do not currently document patient visits or the time spent with each patient.
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ESAP GOALS Develop standard data collection protocol and database for ES at health centers nationally Describe utilization of ES at health centers and the patients who use them Evaluate the impact of enabling services on health access, outcomes and utilization of primary care Disseminate findings to health centers and policy makers to guide effective resource allocation Facilitate research and expansion opportunities to other health centers and networks CMS example- CMS had proposed a daily encounter rate based on national average cost-per-visit for the Medicare program. This rate is calculated by aggregating all of the data from all FQHCs and dividing their costs by their total visits. In other words, CMS will develop a single payment rate based on the average of ALL health centers, adjusting for geography and an upward adjuster for patients who are new or doing their initial primary care screening. This will adversely affect those health centers that provide a high number of ES since the proposed rate do not take them into account. Having ES data will show all the wrap-around services that we provide.
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DOMAINS OF STANDARDIZED ES
CATEGORY CODE Minutes CASE MANAGEMENT ASSESSMENT CM001 CASE MANAGEMENT TREATMENT AND FACILITATION CM002 CASE MANAGEMENT REFERRAL CM003 FINANCIAL COUNSELING/ELIGIBILITY ASSISTANCE FC001 HEALTH EDUCATION/SUPPORTIVE COUNSELING HE001 INTERPRETATION IN001 OUTREACH OR001 TRANSPORTATION TR001 OTHER OT001 Enabling Services Accountability Project (ESAP) The ONLY standardized data system to track and document non-clinical enabling services that help patients access care.
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SAMPLE ENABLING SERVICES EMR TEMPLATE
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.
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DATA EXAMPLE CHC 5,150 27,712 33 69% 91% Medicaid, 52%; Self Pay, 19%
Health Center # of Patients # of ES Encounters Average Age Gender (%Women) Non-English Speaking Patients Most Common Insurance Most Common ES used Most Common ES Provider type CHC 5,150 27,712 33 69% 91% Medicaid, 52%; Self Pay, 19% CM-Assessment followed by CM-Treatment Social Worker, Social Work Assistant If 91% of your patients are LEP and the most commonly used ES was CM-assessment, what does this say about your staff? Shouldn’t you get to brag about the fact that you have staff who’s not only providing an ES but is providing it in another language?!
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ESAP OUTCOMES: DIABETES
One of the health outcomes research questions we looked at were: Do users of Enabling Services have better outcomes on diabetes and children’s immunizations when compared with non-users? We first looked at the impact of ES on HbA1C. This study included patients aged between 18 and 75 as of 2007 with a diagnosis of type 1 or type 2 diabetes. Similar to the last study, patients were categories into two groups: one enabling services user group with all patients that had at least one enabling service in 2007; and one enabling services non-user group with all patients who didn’t have any enabling services in As seen in the figure, ES users had lower average HbA1c level than non-users, and patients using enabling services were more likely to have controlled diabetes with HbA1c levels below 7% than non-users (53% vs. 42%). Data source: all ESAP sites ES and clinical data T Test: P<0.05
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ESAP OUTCOMES: APPROPRIATE CHILD IMMUNIZATION
In this health outcomes example, we assessed the impact of enabling services on appropriate child immunization. With 2007 data collected using the standardized pilot protocol and definitions, this study looked at all nine categories of enabling services and two performance measures including diabetes and children immunizations. Further, it exposed key demographic differences between enabling services users and non-users at FQHCs. The goals of this study is to provide a better understanding of the relationship between enabling services utilization and process/health outcomes by AA & NHOPIs, and to provide useful information to help policy makers effectively address health center needs as they strive to improve access and quality care to medically underserved AA & NHOPIs and other safety net patients. Data source: all ESAP sites ES and clinical data
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DEMONSTRATING HEALTH CENTER VALUE
RESPONSE Standardized data on interventions NEED Standardized data on patient risk We then pieced together some more research and were seeing that some patients did not experience worse outcomes when they had more SDH barriers, so knowing which patients had which interventions as well as the volume and time clinic staff spend on those interventions with patients (through our ES data collection) gives much needed context to understand patient outcome data. Together both sets of data help demonstrate the value of health centers in effectively meeting the needs of complex patients and benefiting the overall health system. Simply stating that health center patients are sicker and experience more social determinants of health barriers doesn’t prove the extra work (and the extra funds needed) that CHCs are doing to address. BOTH are necessary to demonstrate health center value
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Why Is it Important to collect standardized data on the social determinants of health?
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Why collect data on social determinants of Health (SDH)
Why collect data on social determinants of Health (SDH)? SDH drive outcomes before patients receive care How well do we know our patients? Are services addressing SDH incentivized and sustainable? Are community partnerships adequate and integrated?
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Standardized data to see the big picture
why is addressing social determinants of health (SDH) important to community health centers? Provide Better Care Reduced Costs Community Connection Standardized data to see the big picture Take answers from audience Understanding SDOH can help clinics provide better care By identifying and understanding the people you serve—including their challenges and risks—you can tailor your services more appropriately and provide better care Reduced costs By treating root causes and better integrating services, health centers can reduce the volume of unnecessary visits Connection to the community By recognizing issues facing the community and addressing these issues through partnership and advocacy, health centers cans further solidify their role in the community Clinics can leverage their existing relationships and standing in communities—patients are more likely to trust their motivation for collecting data The data itself is the crux of this work; without a large enough sample size, we can’t draw meaningful conclusions Standardized protocol in terms of what data is being collected is critically important; Some clinics are already collecting data on SDH, but without a standard data set, it’s impossible to aggregate responses on the population level and see the big picture
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Assessment Tool to Identify Needs in EHR Protocol to Respond to Needs
What is prApare? Protocol for Responding to & Assessing Patients’ Assets, Risks & Experiences: A national standardized patient risk assessment protocol designed to engage patients in assessing & addressing social determinants of health (SDH). PRAPARE = SDH screening tool + implementation/action process + Assessment Tool to Identify Needs in EHR Protocol to Respond to Needs
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PRAPARE was designed to accelerate systemic change
for insured and uninsured patients
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Dissemination Develop PRAPARE tool
Timeline of Phase 1 Year 1 2014 Develop PRAPARE tool Year 2 2015 Pilot PRAPARE implementation in EHR and explore data utility Year 3 2016 PRAPARE Implementation & Action Toolkit Dissemination
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Developing PRAPARE Criteria
Experience of Existing Protocols Stakeholder Feedback Identified 15 Core Social Determinants of Health Sensitivity Burden of Data Collection Action-ability Literature Review Aligned with National Initiatives: * Healthy People 2020 * ICD-10 * Meaningful Use Stage 3 * NQF on Risk Adjustment Criteria
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What makes PRAPARE Unique and feasible
17 core questions 9 of which already collected by health centers through federal reporting (UDS) All align with national initiatives Design Vetted and stakeholder engaged development process In the EHR to facilitate assessment & interventions (free templates) Conversation starter and patient-centered Common core yet flexible: Able to make more granular and/or add questions Focus on standardizing the need, not question Can be used in combination with other tools/data
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PRAPARE aligns with other national initiatives
PRAPARE Domain UDS ICD-10 IOM Meaningful Use (2 and 3) HP2020 RWJF County Health Race/Ethnicity X Farmworker Status Veteran Status Seeking comments English Proficiency Income Insurance Status Housing Education Employment Material Security Social Integration Stress Transportation Also includes neighborhood and optional questions (incarceration history, refugee status, safety, domestic violence)
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Money & Resources Tab: If information was previously collected on any of the measures, the answer responses will populate on the left hand side in the gray boxes with the date of last documentation You can select previous if the answer choices have not changes for the last time the information was collected Again, you will see Add XXX diagnoses jump buttons populate depending on the patient’s answer choices
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What we’ve learned from implementation
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prapare pilot testing implementation teams and Electronic Health Records
Other EHRs in Development or Interested: Greenway Allscripts Athena Cerner
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Sample Workflows: a Variety of Approaches!
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Pilot results Easy to administer
Possible to implement using various workflows and staffing models Builds patient-provider relationship Identifies new needs Leads to positive changes at the patient, health center, and community/population levels Facilitates collaboration with community partners
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PILOT Data Results High stress
SDH risks vary by community Most common risks*: High stress Having less than a high school education Uninsured Unemployed Preference for language other than English But, patients are very socially integrated, Half of patients see people they care about 5+ times a week * Excludes low income
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patients experience multiple SDH risk factors (typically 4-7, excluding low income)
Percent of Patients with Number* of SDH “Tallies” N = 2,694 patients for all teams This health center pilot population had highest burden of chronic illness. * Excludes low income 3 CHCs 1 CHC 2 CHCs 1 CHC 7 CHCs
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Positive Correlation Between SDH Factors and Hypertension: All Teams
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HOW PRAPARE DATA HAS BEEN USED TO IMPROVE CARE DELIVERY AND HEALTH OUTCOMES
Better Understand INDIVIDUAL Patient’s Socioeconomic Situation Build services in-house for same-day use as clinic visit (children’s book corner, food banks, clothing closets, wellness center, transportation shuttle, etc) Ensure prescriptions and treatment plan match patient’s socioeconomic situation Guide work of local foundations (ex: New York housing) Build partnerships with local community based organizations to offer bi-directional referrals and discounts on services (ex: Iowa transportation) Better Understand Needs of Patient POPULATION Streamline care management plans for better resource allocation (ex: Hawaii) First and foremost: about good clinical care Transform Care Experience for Individual Patients Inform Care Team Members: Knows patient risks/needs to inform counseling and referrals Understand context of patient health concerns Empower patients through: Staff sensitivity training Patient-centered phrasing of questions Brings awareness to SDH issues affecting health Improve patient population management Identify disparities Inform allocation of resources and services Mobilize community resources Encourage local partnerships and bi-directional referrals Opportunity to meaningfully share data Guide local policy reform Inform both Medicaid and Medicare ACO discussions (ex: Iowa, New York) Drive STATE and NATIONAL Care Transformation Inform payment reform and APM discussions with state agencies (e.g., Medicaid) on caring for complex patients (ex: Oregon, Hawaii) Create risk score to inform risk adjustment (ex: Hawaii)
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PRAPARE Implementation and Action Toolkit www.nachc.org/prapare
Chapter 1: Understand the PRAPARE Project Chapter 2: Engage Key Stakeholders Chapter 3: Strategize the Implementation Process Chapter 4: Technical Implementation with EHR Templates Chapter 5: Develop Workflow Models Chapter 6: Develop a Data Strategy Chapter 7: Understand and Evaluate Your Data Chapter 8: Build Capacity to Respond to SDH Data Chapter 9: Respond to SDH Data with Interventions Chapter 10: Track Enabling Services
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PRAPARe Readiness Assessment
Culture of Organization Leadership and Management Workflow Process Improvement Technology Paper form: Online form: ADD link. Best to do as organization but report back
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Phase 2: PRAPARE Learning and Action Network (PLAN)
Build health center capacity to deploy a common, standardized patient-centered SDH assessment protocol Create a PRAPARE community of users with shared learning Accelerate spread of PRAPARE Document impact With support from the Kresge Foundation: Audience Health Centers PCAs/HCCNs Breadth Online PRAPARE Engagement Platform (promote shared learning, track use, provide resources and access to experts) PRAPARE Readiness resources for supporting members Depth PRAPARE Engagement Grants PRAPARE Train the Trainer Academy
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PRAPARE IS A NATIONAL MOVEMENT
Health centers and/or PCAs in every state including AK have expressed interest in PRAPARE Health centers in over 30 states including AK downloaded PRAPARE EHR Templates 7000+ hits on PRAPARE website Health and hospital systems are interested in PRAPARE What pilot sites are doing in NC pilot will benefit others with resources specific to special populations and circumstances unique to CA, etc National movement! Think of what we could do in terms of research, in terms of advocacy, in terms of informing policy, payment, and care transformation and accelerating community change. Nearly 200 members are on our PRAPARE listserv Nearly 100 EHR template downloads from PRAPARE website
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RESOURCES AVAILABLE NOW
Visit PRAPARE Tool PRAPARE Implementation and Action Toolkit Electronic Health Record PRAPARE Templates Readiness Assessment Webinars PRAPARE Overview EHR and Workflow-specific Frequently Asked Questions Contact: Michelle Jester at Visit AAPCHO’s Enabling Services Accountability Project protocol for data collection of non- clinical enabling services Enabling Services Data Collection Implementation Guide White Papers, Best Practices, Studies Contact Tuyen Tran at
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HOW QUESTIONS ARE ASKED JUST AS CRITICAL
RESOURCES ON EMPATHIC INQUIRY Waianae Demo: OPCA Demo: Play video
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For more information on PRAPARE, visit www.nachc.org/prapare
This project was made possible with funding from:
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