# Vision: Patient-centric health interop Status: draft for feedback, June 2022 :::info **Note for skeptics:** Patient-centric health interop doesn't need to be a "winning model" (e.g., by $$ or adoption ) to provide productive design pressure on the ecosystem . We can improve all forms of interop by accounting for this vision. Considering patient-centric health interop guides us to design flexible architectural components that include: identity management, authn, authz, affirmative consent, clinical content standards, clinical knowledge standards, query- and subscription-based data access, survey based data capture, data provenance and integrity controls, confidential decision support, comprehensive public reference data and utilities. ::: "*In this world, I have my choice of tools and support to...*" ## Get care when I need it * Find providers based on my * health information including just-in-time "triage" questions * insurance coverage * preferences * Schedule appointments including workflow for * onboarding to practice * collection case history * sharing health information * Automate [flow of information into my own tools](#Collect-my-health-information-in-one-place) ## Manage my health * Find **informational resources** (including [learning opportunities](#Learn-from-experts-and-peers)) * Apply **decision tools** (effectiveness, side effects, cost, time commitment, other personal preferences) * Connect **management tools** (e.g., hypertension) with tracking, adjustment, shared decision making * Reminders and automated scheduling for **preventive services** * ^^All these tools keep my data **confidential and "local" by default** (stored in a platform of my choice, not duplicated) ## Learn from experts and peers * connect with communities * connect with clinical researchers * understand my own health through models, tools and evaluations (e.g., risk evaluation, prognosis) ## Collect my health information in one place * Connect and synchronize with * provider orgs * payor orgs * health and fitness devices * ^^ all with automated updates * ^^ all with provenance and data integrity * Longitudinal record * Structured, unstructured * Pragmatic standardization (most standardized at "core") * Sharing controls ## Choose what to share * Provision access for friends, family, caregivers * Proactive policies for emergency care, advance directives, POLST, etc * Choice to donate data (and attention, surveys) for research