Domain
Clinical
EHR, ICD-10, LOINC, SNOMED CT, patient care and clinical documentation
16,101 clinical terms
An assessment score or quality rating assigned to an advance directive record or advance care planning process, such as completeness or compliance scores. Used in quality management programs to evaluate whether documented end-of-life wishes meet regulatory or accreditation standards.
A proportional value comparing advance directive completion counts to total eligible patients, used in quality and population health reporting. Supports HEDIS-aligned measures and CMS quality initiatives tracking the percentage of patients with documented end-of-life care preferences in a given population.
The explanation or clinical rationale documented for creating, updating, or revoking an advance directive. Captured in clinical records to provide context for changes to a patient's end-of-life care preferences, such as a new diagnosis, change in condition, or patient-initiated revision of care wishes.
The date on which a completed advance directive document was received and acknowledged by a healthcare facility or care team. Used in medical records management to establish the official intake date for legal and clinical purposes, ensuring the document is recognized as part of the active medical record.
Unique identifier or external pointer linking a patient's advance directive record to related clinical documents, such as living wills or healthcare proxy designations, enabling cross-system retrieval of end-of-life care instructions within EHR and HIS platforms.
The date on which a patient's advance directive was resolved, fulfilled, revoked, or superseded. Used in clinical systems to close active directive records and establish accurate timelines for end-of-life care planning and legal documentation management.
Documents a patient's stated wishes regarding mechanical ventilation or other respiratory interventions as specified in their advance directive. Captures preferences such as DNI status or ventilator withdrawal instructions to guide clinical decision-making at end of life.
Records the outcome or finding associated with reviewing, executing, or adjudicating a patient's advance directive, such as whether stated end-of-life care wishes were honored, modified, or contested during a clinical encounter or legal review process.
Tracks the version or iteration number of a patient's advance directive document, distinguishing updated instructions from prior versions. Ensures clinicians reference the most current end-of-life care preferences and maintains an auditable history of directive changes.
Captures any documented risk factors or concerns associated with a patient's advance directive, such as potential conflicts between stated wishes and clinical recommendations, family disputes, or legal challenges that may affect end-of-life care execution.
Specifies the method or pathway through which a patient's advance directive was received, submitted, or documented, such as via patient self-report, legal representative, notarized document upload, or state registry, supporting chain-of-custody tracking in clinical systems.
A calculated or assigned rating reflecting the completeness, clarity, or compliance level of a patient's advance directive documentation. Used by clinical teams to assess whether end-of-life instructions meet legal and institutional standards for actionability.
Numeric ordering value assigned to individual instructions or components within a patient's advance directive, enabling structured storage and retrieval of multiple end-of-life care preferences in the correct priority or logical order within clinical data systems.
Indicates the degree of clinical intervention restriction specified in a patient's advance directive, ranging from full resuscitation consent to complete comfort-measures-only status, helping care teams quickly assess the scope of documented end-of-life treatment limitations.
Records the patient's biological sex as documented at the time of advance directive creation, used for demographic validation and to ensure the directive is correctly associated with the intended patient record in clinical and legal health information systems.
Identifies the originating system, facility, individual, or legal entity from which a patient's advance directive was obtained, such as a state registry, attorney, prior care facility, or patient submission, supporting provenance tracking in health information systems.
The effective date on which a patient's advance directive becomes legally and clinically active. Used to determine when documented end-of-life care preferences should be applied during treatment decisions and to validate directive currency in clinical records.
The precise time at which a patient's advance directive became effective or was first documented in the clinical system. Supports accurate timestamping for legal and clinical purposes, particularly in urgent care scenarios where directive timing is critical.
The U.S. state or jurisdiction in which a patient's advance directive was legally executed. Relevant because directive requirements and legal enforceability vary by state, affecting how clinical staff interpret and apply end-of-life care instructions across care settings.
Indicates the current lifecycle state of a patient's advance directive, such as active, revoked, expired, pending, or superseded. Used by clinical workflows to determine whether documented end-of-life care wishes are valid and actionable at the point of care.