Clinical Observation logical model

Unique identifier for the observation

Date when the observation was recorded

Date or period of the observation

Person, organisation or device that recorded the observation

The professional that performed the observation

The patient that this observation is about

The request that this observation is fulfilling

Part of referenced procedure

The specimen that was used when this observation was made

The device used to generate the observation data

A code that classifies the general type of observation being made

Describes what was observed. Sometimes this is called the observation 'name'

The value of the observation - typically a code, an amount or a date

Other observations that are part of this observation

The status of the result value.

A categorical assessment of an observation value

Guidance on how to interpret the value by comparison to a normal or recommended range

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Low Range, if relevant

High Range, if relevant

The site on the subject's body where the observation was made (i.e. the target site)

A subjective assessment of the quality of the observation

Comments about the observation or the results

Clinical Observation logical model

Unique identifier for the observation

Date when the observation was recorded

Date or period of the observation

Person, organisation or device that recorded the observation

The professional that performed the observation

The patient that this observation is about

The request that this observation is fulfilling

Part of referenced procedure

The specimen that was used when this observation was made

The device used to generate the observation data

A code that classifies the general type of observation being made

Describes what was observed. Sometimes this is called the observation 'name'

The value of the observation - typically a code, an amount or a date

Other observations that are part of this observation

The status of the result value.

A categorical assessment of an observation value

Guidance on how to interpret the value by comparison to a normal or recommended range

Low Range, if relevant

High Range, if relevant

The site on the subject's body where the observation was made (i.e. the target site)

A subjective assessment of the quality of the observation

Comments about the observation or the results

Clinical Observation logical model

Unique identifier for the observation

Date when the observation was recorded

Date or period of the observation

Person, organisation or device that recorded the observation

The professional that performed the observation

The patient that this observation is about

The request that this observation is fulfilling

Part of referenced procedure

The specimen that was used when this observation was made

The device used to generate the observation data

A code that classifies the general type of observation being made

Describes what was observed. Sometimes this is called the observation 'name'

The value of the observation - typically a code, an amount or a date

Other observations that are part of this observation

The status of the result value.

A categorical assessment of an observation value

Guidance on how to interpret the value by comparison to a normal or recommended range

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Low Range, if relevant

High Range, if relevant

The site on the subject's body where the observation was made (i.e. the target site)

A subjective assessment of the quality of the observation

Comments about the observation or the results