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Continuity of Care Record

Continuity of Care Record. Claudia Tessier, CAE, RHIA Co-Chair, ASTM E31 Workgroup on CCR Executive Director, MoHCA. What Is the CCR?. A snapshot in time: A core data set of the most relevant facts about a patient’s healthcare. Organized and transportable.

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Continuity of Care Record

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  1. Continuity of Care Record Claudia Tessier, CAE, RHIA Co-Chair, ASTM E31 Workgroup on CCR Executive Director, MoHCA

  2. What Is the CCR? • A snapshot in time: A core data set of the most relevant facts about a patient’s healthcare. • Organized and transportable. • Prepared by a practitioner at the conclusion of a healthcare encounter. • To enable the next practitioner to readily access such information. • May be prepared, displayed, and transmitted on paper or electronically.

  3. The CCR… • Provides information that is • Appropriate, succinct, organized, and up-to-date • Interoperable through use of specified XML code • A necessary bridge to a different environment, often with new practitioners who know little about the patient. • Will address specific domains through extensions: long-term care, acute care, disease management, personal health record, etc.

  4. Development of the CCR • Unique standards development effort • Consortium of sponsoring organizations • ASTM International • Massachusetts Medical Society • HIMSS • American Academy of Family Physicians • American Academy of Pediatrics • American Medical Association • Patient Safety Institute • American Health Care Association • National Association for the Support of LTC • Additional sponsoring organizations pending

  5. Sponsors represent: • ANSI-recognized standards development organization • Over 400,000 practitioners • Over 13,000 IT professionals • Over 12,000 institutions in the long-term care community that provide care to over 1.5 million elderly and disabled • Patients, patient advocates, data sources, corporations, provider institutions….

  6. This Unique Initiative Is… • Patient-focused • Not about what the system says to do but about what patient information is most relevant • Provider-focused • Practitioners determine what information is most relevant • Content-focused • Emphasis is on what providers need to know to deliver good patient care

  7. This Unique Initiative Is Also… • Stimulating cooperation among • Organizations, such as ASTM and HL7 • Professional specialty organizations and their practitioners • Provider institutions • Vendors • These diverse groups are working together • To develop and implement the CCR • To assure its interoperability • To develop demonstration projects • Generating interest among • Patients and patient advocates • Federal agencies, payers, others

  8. The CCR Is Not… • An EHR • It is not a complete electronic health record of a patient’s lifelong health status and healthcare • It is not universally accessible • It does not have a universal patient identifier • A progress note, discharge summary, or consultation • It is not limited to information from a single encounter • It is not free-text based • A loose dataset of health information • It is a defined set of core data in specified XML code

  9. Why Is the CCR Needed? • CCR addresses the lack of appropriate, succinct, and up-to-date patient health information for practitioners at a new point of care. • CCR data is essential to good patient care and serves as a necessary bridge to a different environment, often with new practitioners who know little about the patient.

  10. What’s in the CCR or Core Data Set?

  11. CCR Identifying Information Section 1 • Referring (“from”) practitioner • Referral (“to”) practitioner • Date • Purpose/reason for CCR

  12. Patient Identifying Information Section 2 • Required information to uniquely identify the subject patient • Not a centralized system or a national patient identifier, but a federated or distributed identification system that • Links various practitioners • Contains the core data set of identifying information that could be used by any record system to assign the individual their own identifier.

  13. Patient Insurance/Financial Information Section 3 • Basic information from which eligibility for insurance benefits may be determined for the patient.

  14. Advance Directives Section 4 • Indicators that resuscitation efforts are to be either unrestricted or to be limited in some way. • Includes what is commonly known as the DNR (Do Not Resuscitate) status of the patient as addressed in such documents as living wills, healthcare proxies, and powers of attorney.

  15. Patient Health Status Section 5 • Conditions/Diagnoses/Problems • Family History • Adverse Reactions/ Allergies/Clinical Warnings and Alerts • Social History and Health Risk Factors • Medications • Immunizations • Vital Signs and Physiologic Measurements • Laboratory Results and Observations • Procedures/Imaging • This section may be amplified in extensions for clinical specialty-specific information regarding patient.

  16. Care Documentation Section 6 • Some detail on the patient-practitioner encounter history, such as dates and purposes of recent pertinent visits and names of practitioners seen. • May be significantly expanded in future extensions.

  17. Care Plan Recommendation Section 7 • Includes planned or scheduled tests, procedures, or regimens of care for the patient.

  18. Practitioners Section 8 • Information about those healthcare practitioners who are participants in the patient’s care • Links as appropriate to Conditions/Diagnoses/ Problems and Care Documentation encounters

  19. A Sample Data Group • Medications • Definition: Generic name of current and relevant past prescribed substances, including OTC, herbal, and homeopathic substances. Brand name is inadequate. • Comments/Examples: Medication: Trimethoprim/Sulphamethozaxole • Required or Optional: Required • XML: <MEDICATION>

  20. Extensions for Additional Content • Enterprise and institution-specific, e.g., acute care, LTC • Clinical specialty-specific, e.g, pediatrics, nursing • Disease management • Disease-specific information, performance measures, guidelines, etc. • Payers: financial information/attachments • Patient-entered Personal Health Record

  21. The CCR Can Stimulate EHR Adoption Because… • Through specified XML code it is interoperable, so it will enable EHR systems to • Import and export all CCR data • Interchange the CCR between otherwise incompatible systems • Minimize workflow disruption for practitioners

  22. More about XML and the CCR • Through XML, CCR can be prepared, transmitted, and viewed • In a browser • In an HL7 CDA-compliant document • In secure email • In any XML-enabled word processing document • In multiple formats • It can also be • Printed as a paper document • Stored on a portable storage device for use as a personal health record

  23. Why So Much Interest in the CCR? • Multiple uses • Referral, transfer, discharge, or other instance when patient is seen by another provider • Other uses include personal health record, research, and public health initiatives • Introduction to electronic documentation and ultimately to EHR • Can stimulate use of computers in healthcare • Flexibility • Whatever patient information is relevant can be accommodated

  24. Why So Much Interest in the CCR? • It is not a top-down approach • End-users, i.e., practitioners have participated in its design • The originator determines the relevant content • It has support and leadership from organizations representing end-users, who are • Involving, advising, and assisting their constituents in its adoption • It allows options for implementation • Paper or electronic • It has potential to reduce inefficiencies and costs • Practitioners won’t have to search for relevant information • Fewer repeat lab tests and other evaluations

  25. Why So Much Interest in the CCR? • It offers support for patient safety and reduced medical errors • Through easy access to critical data such as medications and allergies • It encourages patient involvement and improved provider/patient relations • It is patient focused • It offers patients easy access to their health information • Patients don’t have to repeat same information over and over • It can help populate a personal health record • It can stimulate the patient to become more involved in and informed about their healthcare • It can involve patient in transfer of information (USB)

  26. In Summary: • Practitioners, provider institutions, patients, vendors, and other stakeholders perceive the CCR as • Relevant • Doable • Transportable and interoperable • Valuable

  27. Thank you! • For more information on the CCR • Claudia Tessier, RHIA 202-659-2699 ctessi@attglobal.net

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