Our pledge: reliability, integrity and trust

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Presentation transcript:

Our pledge: reliability, integrity and trust Formerly Jefferson Health Information Exchange

Who We Are Neutral Third-Party since 2012 Non-Profit Membership Organization Volunteer Board of Directors Support providers, their patients and those who pay for their care to: Realize opportunities to improve health Improve the patient/client experience Optimize health care efficiency and coordination Manage health care costs JHIE is a grass-roots organization started by physicians, public health, mental health, hospitals and CCOs looking to improve health care quality, efficiency and reduce costs through better, more accessible patient information. JHIE puts the patient at the center of the universe; and puts great emphasis on the privacy and security of a patient’s health information. JHIE ensures that those who care for a patient have a seamless experience where they can view a patient’s health information in a concise record, fed by other providers in the care team, to support treatment decisions. That means that patients get the best care possible and do not have to be subjected to repeat tests and treatment. Reliance eHealth Collaborative Behavioral Health Overview

that follows the patient… What we do… Accurate, actionable information that follows the patient… Right at your fingertips As the health care environment transitions to electronic records, there has been a growing need to integrate data through health information exchange (HIE). HIE is the secure, electronic exchange of health information among authorized providers that is patient centered. So patient’s don’t have to carry their records with them; instead they follow the patient wherever they access health care. – such as health care providers, hospitals and public health agencies. This exchange of health care information improves patient care and reduces costs by fostering care collaboration and lowering administrative burden. For example, referrals can be done electronically with all the relevant information attached to help the specialist better care for the patient. It reduces the need for unnecessary testing and exposure to radiation for the patient and for the clinic, there is a more streamlined workflow that reduces the staff time needed to support a referral. The system also allows for the referral loop to be closed so the primary doctor knows when the patient has been seen and the plan of treatment that has been prescribed. Reliance eHealth Collaborative Behavioral Health Overview

Architecture

Participation Coverage Area 16 Oregon Counties 11 Hospitals ~300 practices/ clinics 264 Interfaces/127 ambulatory CCDs 12+ EHR vendors 6 Coordinated Care Organizations 4 CCBHCs 7 Substance Use Treatment Providers connecting

Patients by Zip Code

Privacy and Security Considerations (HIPAA Covered Health Information) Patient Non-Participation (opt-out) User Roles and Access Controls Based on patient-provider relationship Based on User’s “need to know” User training to reinforce appropriate use Privacy & security policies (HIPAA, 42CFR Part 2) Monitoring usage Sanctions for misuse

Consent Management Model for Behavioral Health Information Exchange

Purpose Bridge the information divide between physical health care and behavioral health care services and providers Support coordination across the care team Improve care for those with serious mental illness who are 3times more likely to have comorbidities (diabetes, diseases of the heart, respiratory disorders, stroke and arthritis)

Principles: BH Information Exchange Lawfully Integrate Physical and Behavioral Health Information Exchange Develop universal interpretation of law for the exchange, disclosure, and re-disclosure of drug, alcohol and mental health data Develop common consent management model (CMM) Common Release of Information form Requirements for electronic data exchange Implement CMM within Reliance technology to enable robust exchange Connect with behavioral health EHRs

Findings: Managing Consent Qualified Service Organization Agreement Required between Reliance and data contributors Consent must be captured for disclosure of: Addictions information (42 CFR Part 2) Psychotherapy notes Re-disclosure is not allowed without explicit patient consent Bona fide emergencies allow for disclosure without consent Patient has right to identify specific users and health information to be disclosed Patient has right to request an accounting of disclosures

Consent Model Parameters Supported Release of Information (ROI) Release must be given at each SUT facility Full record from SUT facility authorized for release Release must allow for: Provider Organization (e.g., PCP Office, Inpatient facility, etc…) All person’s treatment providers in the HIE Bona fide emergency access and reporting Partial consent will not be managed through Reliance Current workflow will continue to be used

Consent Model Functionality Consented period Defaults to 1 year May be changed based on ROI Role-Based User Access Controls Reporting of Disclosures Configurable reports for providers Patients/Clients can request a report CCO Data Routing Based on member’s consent and active coverage Fully Compliant with 42 CFR Part 2 as amended March 2017

Challenges Consensus on Legal Requirements Technology Challenges EHR Vendor Capabilities & Competition Removing Stigma & Communicating Benefits Consistent Message for Informed Consent

Opportunities* Expanding purpose of consent model Granting consent for other members of the care team social service organizations, patient advocates, health navigators, court-ordered treatment, etc. Fully integrating social, behavioral, physical and dental to care for whole patient/family based on patient consent. Uncharted territory and possibilities *Requires much thought and consideration to the patient’s rights and impact (+/-) on their wellbeing

Questions? Comments! Concerns…

Guiding Principles Patient-centered Community-driven Provider-led collaboration Secure and trusted Provides value to patients, the providers who care for them and those who pay for their care JHIE is a grass-roots organization started by physicians, public health, mental health, hospitals and CCOs looking to improve health care quality, efficiency and reduce costs through better, more accessible patient information. JHIE puts the patient at the center of the universe; and puts great emphasis on the privacy and security of a patient’s health information. JHIE ensures that those who care for a patient have a seamless experience where they can view a patient’s health information in a concise record, fed by other providers in the care team, to support treatment decisions. That means that patients get the best care possible and do not have to be subjected to repeat tests and treatment.