United States Core Data for Interoperability (USCDI)
The United States Core Data for Interoperability (USCDI) is a standardized set of health data classes and constituent data elements for nationwide, interoperable health information exchange. Review the USCDI Fact Sheet to learn more.
A USCDI “Data Class” is an aggregation of various Data Elements by a common theme or use case.
A USCDI “Data Element” is the most granular level at which a piece of data is exchanged.
For example, Date of Birth is a Data Element rather than its component Day, Month, or Year, because Date of Birth is the unit of exchange.
USCDI ONC New Data Element & Class (ONDEC) Submission System
The public feedback period for Draft USCDI v3 closed on April 30, 2022. ONC thanks the many stakeholders who submitted comments. ONC plans on releasing the final USCDI v3 in July 2022.
USCDI V1
Please reference the USCDI version 1 document to the left for applicable standards versions associated with USCDI v1.
Represents harmful or undesirable physiological response associated with exposure to a substance.
Represents a health professional’s conclusions and working assumptions that will guide treatment of the patient.
The specific person(s) who participate or are expected to participate in the care team.
Represents narrative patient data relevant to the respective note types.
An expressed desired health state to be achieved by a subject of care (or family/group).
Health related matter that is of interest, importance, or worry to someone who may be the patient, patient’s family or patient’s health care provider.
Record of an administration of a vaccination or a record of a vaccination as reported by a patient, a clinician, or another party.
Information about a condition, diagnosis, or other event, situation, issue, or clinical concept that is documented.
An activity that is performed with or on a patient as part of the provision of care.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
Representing a patient’s smoking behavior.
A unique numeric or alphanumeric code that consists of a device identifier (DI) and a production identifier (PI).
Physiologic measurements of a patient that indicate the status of the body’s life sustaining functions.
USCDI V2
The USCDI v2 contains data classes and elements from USCDI v1 and new data classes and elements submitted through the ONDEC system. Please reference the USCDI Version 2 document to the left for applicable vocabulary standards versions associated with USCDI v2 and to the ONC Standards Bulletin 21-3 for more information about the process to develop USCDI v2 and future versions.
Represents harmful or undesirable physiological response associated with exposure to a substance.
Represents a health professional’s conclusions and working assumptions that will guide treatment of the patient.
The specific person(s) who participate or are expected to participate in the care team.
Represents narrative patient data relevant to the respective note types.
Includes non-imaging and non-laboratory tests performed on a patient that results in structured or unstructured (narrative) findings specific to the patient, such as electrocardiogram (ECG), visual acuity exam, macular exam, or graded exercise testing (GXT), to facilitate the diagnosis and management of conditions.
Tests that result in visual images requiring interpretation by a credentialed professional.
Information related to interactions between healthcare providers and the subject of care in which healthcare-related activities take place.
An expressed desired health state to be achieved by a subject of care (or family/group).
Health related matter that is of interest, importance, or worry to someone who may be the patient, patient’s family or patient’s health care provider.
Record of an administration of a vaccination or a record of a vaccination as reported by a patient, a clinician, or another party.
Information about a condition, diagnosis, or other event, situation, issue, or clinical concept that is documented.
An activity that is performed with or on a patient as part of the provision of care.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
Representing a patient’s smoking behavior.
A unique numeric or alphanumeric code that consists of a device identifier (DI) and a production identifier (PI).
Physiologic measurements of a patient that indicate the status of the body’s life sustaining functions.
Draft USCDI V3
The Draft USCDI v3 contains data classes and elements from USCDI v2, new
data classes and data elements, and those reclassified
from other data classes. Please reference the Draft USCDI Version 3 document to the left for applicable vocabulary standards versions associated with Draft USCDI v3 and to the ONC Standards Bulletin 22-1 for more information about the development of Draft USCDI v3 and how you can provide feedback on it. The deadline for feedback on Draft USCDI v3 through comments on this website is April 30, 2022.
Represents harmful or undesirable physiological response associated with exposure to a substance.
Represents a health professional’s conclusions and working assumptions that will guide treatment of the patient.
The specific person(s) who participate or are expected to participate in the care team.
Represents narrative patient data relevant to the respective note types.
Includes non-imaging and non-laboratory tests performed on a patient that results in structured or unstructured (narrative) findings specific to the patient, such as electrocardiogram (ECG), visual acuity exam, macular exam, or graded exercise testing (GXT), to facilitate the diagnosis and management of conditions.
Tests that result in visual images requiring interpretation by a credentialed professional.
Information related to interactions between healthcare providers and the subject of care in which healthcare-related activities take place.
An expressed desired health state to be achieved by a subject of care (or family/group).
Data related to an individual’s insurance coverage for health care.
Health-related matter of interest, importance, or worry to a patient, patient’s family, or patient’s healthcare provider.
Record of an administration of a vaccination or a record of a vaccination as reported by a patient, a clinician, or another party.
Information about a condition, diagnosis, or other event, situation, issue, or clinical concept that is documented.
An activity that is performed with or on a patient as part of the provision of care.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
A unique numeric or alphanumeric code that consists of a device identifier (DI) and a production identifier (PI).
Physiologic measurements of a patient that indicate the status of the body’s life sustaining functions.
In addition to “Comment” and “Level 1” criteria, Level 2 data elements demonstrate extensive existing use in systems and exchange between systems, and use cases that show significant value to current and potential users. These data elements would clearly improve nationwide interoperability. Any burdens or challenges would be reasonable to overcome relative to the overall impact of the data elements. Data elements listed below with the 
indicate these data elements were added to recently released Draft USCDI v3. ONC is accepting public feedback on these new data elements until April 30, 2022.
indicate these data elements were added to recently released Draft USCDI v3. ONC is accepting public feedback on these new data elements until April 30, 2022.
Level 2
Represents harmful or undesirable physiological response associated with exposure to a substance.
Material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.
The specific person(s) who participate or are expected to participate in the care team.
Represents narrative patient data relevant to the respective note types.
Data related to an individual’s insurance coverage for health care.
Record of an administration of a vaccination or a record of a vaccination as reported by a patient, a clinician, or another party.
Information about a condition, diagnosis, or other event, situation, issue, or clinical concept that is documented.
An activity that is performed with or on a patient as part of the provision of care.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
A unique numeric or alphanumeric code that consists of a device identifier (DI) and a production identifier (PI).
Physiologic measurements of a patient that indicate the status of the body’s life sustaining functions.
In addition to “Comment” level criteria, Level 1 data elements demonstrate limited existing use in electronic systems, limited exchange between systems and more well-defined use cases and value to potential users. There may still be some burdens associated with development and implementation.
Level 1
Material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.
Represents narrative patient data relevant to the respective note types.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
Physiologic measurements of a patient that indicate the status of the body’s life sustaining functions.
A data element designated as "Comment" level is represented by health care standard terminology such as SNOMED CT® or implementation specifications such as HL7® FHIR® 4. It may not have a well-defined use case or value to potential users. There may be significant or unknown burdens associated with development or implementation.
Comment
Represents harmful or undesirable physiological response associated with exposure to a substance.
Represents a health professional’s conclusions and working assumptions that will guide treatment of the patient.
Material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.
The specific person(s) who participate or are expected to participate in the care team.
Represents narrative patient data relevant to the respective note types.
Includes non-imaging and non-laboratory tests performed on a patient that results in structured or unstructured (narrative) findings specific to the patient, such as electrocardiogram (ECG), visual acuity exam, macular exam, or graded exercise testing (GXT), to facilitate the diagnosis and management of conditions.
Tests that result in visual images requiring interpretation by a credentialed professional.
Information related to interactions between healthcare providers and the subject of care in which healthcare-related activities take place.
An expressed desired health state to be achieved by a subject of care (or family/group).
Record of an administration of a vaccination or a record of a vaccination as reported by a patient, a clinician, or another party.
Information about a condition, diagnosis, or other event, situation, issue, or clinical concept that is documented.
An activity that is performed with or on a patient as part of the provision of care.
The metadata, or extra information about data, that can help answer questions such as when and who created the data.
Representing a patient’s smoking behavior.
For data class description and applicable standards supporting data elements, click to view the USCDI Version 1 (July 2020 errata) in PDF format below.
The USCDI ONC New Data Element and Class (ONDEC) Submission System supports a predictable, transparent, and collaborative process, allowing health IT stakeholders to submit new data elements and classes for future versions of USCDI. Click here for more information and to submit new data elements.
The USCDI standard will follow the Standards Version Advancement Process described in the Cures rule to allow health IT developers to update their systems to newer version of USCDI and provide these updates to their customers.
Comment
Submitted by Silvia Yee @ D… on 2022-05-01
This field is for general…
This field is for general comments on the USCDI. To submit new USCDI data classes and/or data elements, please use the USCDI ONDEC system: https://healthit.gov/ONDECSubmitted by ritork on 2022-05-01
HL7 Patient Empowerment PCD feedback on USCDI v3 and provenance
USCDI consists of categories of data elements representing information captured from different systems as well as by individuals. However, attribution of information created or supplied by an individual, as a patient or other role, is not reflected within the Provenance data class in the latest USCDI draft version 3 consisting of the following two (2) data elements: Author Time Stamp and Author Organization. We suggest at minimum the Author data element classified as Level 2 be added to USCDI v3. In addition to USCDI v3 Provenance not specifying Author, the data class is not fully inclusive of information created outside an organization (or changes to information such as updates). To better understand the origin and changes to data that can occur with or without exchange, and improve Provenance with context that identifies the type of actor or system creating or updating data, we recommend two (2) additional data elements:- Author Role to clarify the type of actor, such as patient, especially where information is contributed by individuals. Author should also accommodate device-generated data such as wearables.
- Updates to understand whether data has changed either from the point of creation or in exchange
- Demographics (include identity, race and ethnicity, sexual orientation and gender identity, and other data)
- Health Insurance Information
- Goals (Patient and SDOH)
- Problems (includes SDOH Problems/Health Concerns and dates from diagnosis and resolution)
- Health Status (Includes Health Concerns, Functional Status, Disability Status, Mental Function, and Smoking Status)
- Clinical Tests (currently only reflects those performed in lab though perhaps could be expanded to include self-administered at-home tests)
- Observations
- Assessments and Plan of Treatment (includes SDOH assessment)
- Advance Directives (not in USCDI v3)
- Vital signs (e.g. where capture from remote sensing devices)
Submitted by claricelmiller… on 2022-05-01
American Occupational Therapy Association's Comment on USCDI v3
The American Occupational Therapy Association (AOTA) appreciates the opportunity to comment on draft version 3 of the US Core Data for Interoperability (USCDI). AOTA is the national professional association representing the interests of more than 220,000 occupational therapists, students of occupational therapy (OT), and occupational therapy assistants. Occupational therapy defines “occupations” as any meaningful or purposeful activity, which can describe activities of daily living (ADLs), instrumental activities of daily living (IADLs), work, school, hobbies, and social participation. The practice of occupational therapy is person-centered, evidence-based, and enables people of all ages to live life to its fullest by promoting health and purposeful activity. AOTA believes that understanding a person’s whole health, including function, environment, and context is crucial. AOTA is pleased to see the addition of Health Status as a data class. We support the inclusion of health concerns, functional status, disability status, mental function, pregnancy status, and smoking status as key components of health status. AOTA encourages these items to also be aligned with social determinants of health as these factors can have a significant impact on an individual’s status. We also support the utilization of the International Classification of Function (ICF) when establishing a framework for health data exchange in regards to function, cognition, and mobility. The Occupational Therapy Practice Framework: Domain and Process –4th edition (OTPF4) was developed based on concepts and terminology from the ICF in an effort to promote standardized interdisciplinary communication. Please see attached for full comments from AOTASubmitted by AMIA_Policy on 2022-04-30
Comments on USCDI v3
Please see attached comments from the American Medical Informatics Association.Submitted by LACdcny@810 on 2022-04-30
Legal Action Center's comments on USCDI v. 3
The Legal Action Center (“LAC”) is the only non-profit law and policy organization in the United States whose sole mission is to fight discrimination against people with histories of addiction, HIV/AIDS, or criminal records, and to advocate for sound public policies in these areas. LAC appreciates the opportunity to submit the attached comments on the ONC’s draft United States Core Data for Interoperability, Version 3.Submitted by JenniferSistoGall on 2022-04-30
Phreesia comments on USCDI v3
Thank you for the opportunity to provide comments on the USCDI Draft v3. Please see comments from Phreesia attached.Submitted by ddoneski on 2022-04-30
NASL Comments on USCDI v3
The National Association for the Support of Long Term Care (NASL) is pleased to offer our attached comments on the Draft USCDI v3. NASL is a national trade association representing providers of ancillary care and services operating in the long term and post-acute care (LTPAC) sector, to include the health IT developers/vendors who serve the majority of LTPAC providers. NASL and its members welcome the opportunity to work with ONC in further developing and expanding the standardized set of health data classes and data elements contained in the USCDI.Submitted by trujillos@ochin.org on 2022-04-30
OCHIN Comments on USCDI Draft Version 3 and Process
Thank you for the opportunity to provide comments on USCDI Draft Version 3. Please see OCHIN's full comment letter included. Thank you.Submitted by Brian Vamstad on 2022-04-30
Submitted by Silvia Yee @ D… on 2022-05-01
DREDF Comments on USCDI v3
Please see attached the comments of Disability Rights Education and Defense Fund (DREDF) on USCDI v3. Thank you, Silvia YeeDREDF Comments_USCDI v3_4-30-22_0.docx