The force of circulating blood on the walls of the arteries. 55284-4
Based On VitalSign
Value:
_Value
|
|||
BodySite
|
must be
from BloodPressureBodySiteVS |
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. |
FindingMethod
|
must be
from BloodPressureMethodVS |
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. |
ObservationQualifier
|
must be
from BloodPressureQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
ObservationCode
|
is 55284-4
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
HeadTiltAngle
|
optional | The angle at which the head is tilted relative to a level position while physiologic tests are taken. | |
ObservationComponent
|
includes optional
SystolicPressure
includes optional DiastolicPressure
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The distance from the sole to the crown of the head. 8302-2
Based On VitalSign
Value:
Quantity
|
Units is cm (cm)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8302-2
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ObservationQualifier
|
must be
from BodyHeightQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The distance from the sole of the foot to the crown of the head, lying down (typically 0-2 years). 8306-3
Based On BodyHeight
Value:
Quantity
|
Units is cm (cm)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8306-3
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ObservationQualifier
|
must be
from BodyHeightQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
A general indicator of the body fat an individual is carrying based upon the ratio of weight to height. 39156-5
Based On VitalSign
Value:
Quantity
|
Units is kg/m2 (kg/m2)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
from http://hl7.org/fhir/ValueSet/observation-vitalsignresult (if covered) |
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ObservationQualifier
|
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The measure of the level of heat in a human or animal. 8310-5
Based On VitalSign
Value:
Quantity
|
Units is C (Cel)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8310-5
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
BodySite
|
must be
from BodyTemperatureBodySiteVS |
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. |
ObservationQualifier
|
must be
from BodyTemperatureQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The mass or quantity of heaviness of an individual. Does not include estimates of fetal bodyweight. 29463-7
Based On VitalSign
Value:
Quantity
|
Units is kg (kg)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 29463-7
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ObservationQualifier
|
must be
from BodyWeightQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The blood pressure after the contraction of the heart while the chambers of the heart refill with blood, when the pressure is lowest. 8462-4
Based On ObservationComponent
Value:
Quantity
|
Units is mmHg (mm[Hg])
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8462-4
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. |
Circumference of the head (typically 0-2 years). 8287-5
Based On VitalSign
Value:
Quantity
|
Units is cm (cm)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8287-5
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ObservationQualifier
|
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The angle at which the head is tilted relative to a level position while physiologic tests are taken. 8360-0
Value:
Quantity
|
Units is deg (deg)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR |
The number of times the heart ventricles contract per unit of time, usually per minute. 8867-4
Based On VitalSign
Value:
Quantity
|
Units is /min (/min)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8867-4
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ObservationQualifier
|
must be
from HeartRateQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
FindingMethod
|
must be
from HeartRateMethodVS |
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
Oxygen saturation in Arterial blood by Pulse oximetry. 59408-5
Based On VitalSign
Value:
Quantity
|
Units is % (%)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 59408-5
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
BodySite
|
must be
from OxygenSaturationBodySiteVS |
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ObservationQualifier
|
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The rate of breathing (inhalation and exhalation) measured within in a unit time, expressed as breaths per minute. 9279-1
Based On VitalSign
Value:
Quantity
|
Units is /min (/min)
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 9279-1
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ObservationQualifier
|
must be
from RespiratoryRateQualifierVS |
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. |
FindingMethod
|
must be
from RespiratoryRateMethodVS |
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |
The blood pressure during the contraction of the left ventricle of the heart, when blood pressure is at its highest. 8480-6
Based On ObservationComponent
Value:
Quantity
|
Units is mmHg (mm[Hg])
|
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
is 8480-6
|
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. |
No Description Vital Sign (8716-3)
Based On Observation
Value:
Quantity
|
must be
from http://hl7.org/fhir/ValueSet/ucum-vitals-common |
A quantity with units, whose value may be bounded from above or below, as defined in FHIR | |
ObservationCode
|
from http://hl7.org/fhir/ValueSet/observation-vitalsignresult (if covered) |
required | A code that represents what the finding concerns, for example, the subject's height, blood pressure, disease status, wound dimensions, diabetes risk, etc. Although named ObservationCode, in different contexts the same attribute might be more naturally referred to as a property, observable, or test code. In assertions (observations without an explicit question), the observation code is defaulted to a value representing 'assertion'. |
Subject
|
required | The person or thing that this entry relates to, usually the Person of Record. However, not all entries have health information specifically about the patient, but in different contexts, could refer to a fetus, family member (living or dead), device, location, organization, finding, condition, or intervention. | |
Category
|
includes vital-signs
|
1 or more | A class or division of people or things having particular shared characteristics |
ValueAbsentReason
|
optional | Provides a reason why the value of the observation is missing, if it is expected (some observations are not expected to have a value). | |
ClinicallyRelevantTime
|
optional | The time or time period that the finding addresses. The clinically relevant time is not necessarily when the information is gathered or when a test is carried out, but for example, when a specimen was collected, or the time period referred to by the question. Use a TimePeriod for a measurement or specimen collection continued over a significant period of time (e.g. 24 hour Urine Sodium). | |
FindingStatus
|
required | Indicates whether the finding is preliminary, amended, final, etc.. | |
BodySite
|
optional | A location or structure in the body, including tissues, regions, cavities, and spaces, for example, right elbow, or left ventricle of the heart. | |
ChangeFlag
|
optional | Indicator of significant change (delta) from the last or previous measurement. | |
Details
|
optional | An text note containing additional details, explanation, description, comment, or summarization. Details can discuss, support, explain changes to, or dispute information. | |
Interpretation
|
optional | A clinical interpretation of a finding. | |
ObservationQualifier
|
0 or more | A description of the conditions or context of an observation, for example, under sedation, fasting or post-exercise. Body position and body site are also qualifiers, but handled separately. A qualifier cannot modify the measurement type; for example, a fasting blood sugar is still a blood sugar. | |
Specimen
|
optional | Sample for analysis | |
Device
|
optional | A specific durable physical device used in diagnosis or treatment. The value is the coding for a type of device, for example, a CPAP machine. The same device might be used on multiple patients. | |
ReferenceRange
|
0 or more | The usual or acceptable range for a test result. | |
ObservationComponent
|
0 or more | A simplified, non-separable observation consisting of a observation code, value (or value absent reason), reference range, and interpretation. The subject of the observation component is the same as in the parent observation. | |
Members
|
required | Members represent the elements of a group of a related but independent observations. Examples are the measurements that compose a complete blood count (CBC), or the elements of a pathology report. Each member is an independent observation, but the grouping reflects a composite lab order, shared specimen, or a single report author. Typically the Category and Reason are not given for individual findings that are part of the panel, but rather given at the level of the panel itself. | |
FocalSubject
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FocalSubjectReference
|
optional | For use when FHIR's subject does not allow the desired type of Subject in the Finding.Subject field. | |
FindingMethod
|
optional | The technique used to create the finding, for example, the specific imaging technical, lab test code, or assessment vehicle. | |
Evidence
|
0 or more | A symptom, observation, or other item, for example, a radiology report, that serves as evidence for the current assessment. | |
RelatedEncounter
|
optional | If content was generated during a patient encounter, related encounter is the encounter where the information was gained. | |
Author
|
optional | The person or organization who created the entry and is responsible for (and may certify) the content. | |
Informant
|
optional | The person or entity that provided the information in the entry, as distinct from who created the entry, e.g. the subject (patient), medical professional, family member, device or software program. |