A logical model representing child report data elements.

Patient/subject information

Business identifier for the document

Author(s) by whom the resource was/were authored. Multiple authors could be provided.

Date and time of the last update to the document/information

The date of the child report is the date when the report was created, not the date of the examination or observation. In case of reports migrated from KMEHR, the date is the date of the conversion, not the KMEHR message creation, which is unknown.

Status of the resource

A base64 encoded PDF file with the remaining child report information (biometric data, charts, etc.).

Document title

The mother of the child is the related subject in this report.

Patient/subject information

A person related to the patient/subject, such as a family member or guardian.

The relationship of the related person to the patient/subject. This can include roles such as mother, father, guardian, etc.

Details about the pregnancy.

[BeObservation] The duration of pregnancy in weeks, as an observation.

subject

Length of gestation at birth

The duration of pregnancy in weeks

Indicates whether CMV infection occurred during pregnancy.

subject

CMV infection during pregnancy

The value indicates whether the mother had a CMV infection during pregnancy.

Indicates whether bacterial meningitis occurred during pregnancy.

Code

The mother of the child is the related subject in this report.

The value indicates whether the mother had a bacterial meningitis during pregnancy.

Details about the neonatal hearing screening.

Code

The date of neonatal hearing screening.

The child that the report is about.

Result of neonatal hearing screening for the left ear.

Result of neonatal hearing screening - left

Neonatal hearing screening result for the left ear.

Result of neonatal hearing screening for the right ear.

Result of neonatal hearing screening - right

Neonatal hearing screening result for the right ear.

Indicates whether the hearing test was refused.

Date of encoding of the information

Unique identifier

Is the patient's unique identifier. The unique identifier must be the patient's national patient registry number (NISS) or BIS number.

Is the unique identifier of either the healthcare professional responsible for the encrypted content, or the patient encoding his or her own wishes, or a representative of the patient encoding the patient's wishes. The unique identifier must be the National Register Number (NISS) or BIS number.

The representative is the person who acts on behalf of the applicant (patient) when he is no longer able to express his wishes. For example: the confidant is the person who guides the patient through his steps and assists him during medical appointments. He guarantees the follow-up of the wishes of the patient when he can no longer express his wishes clearly.

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.

Role of the representative (e.g. confidant, administrator, guardian...)

Type of relationship of the representative with the patient (e.g. father, mother, son, neighbour...)

Enables you to attach a document

Type of patient wishes.

The patient's wishes (euthanasia, no vaccination, no intubation...)

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.

Indicates the status of the patient's will (draft, proposes, active, ...)

Validity of the will

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.

Date the will comes into effect

Date the will expires

Comments

Indicates whether severe head trauma was identified.

The child that the report is about.

Date of reporting the trauma.

Code

The value indicates whether severe head trauma was identified in the child.

Details about the eye screening.

The patient or subject to whom the observation applies.

A code that identifies the type of observation being made, such as a clinical measurement or assessment.

The value of the observation, which can be a quantity, a coded value, or a string.

The time or period during which the observation was made.

The status of the observation, indicating whether it is preliminary, final, etc.

The reason for the current status of the observation.

The individual or organization that performed the observation.

Components of the observation, which can include additional measurements or assessments related to the main observation.

A code that identifies the component of the observation.

The value of the component observation, which can be a quantity, a coded value, or a string.

An interpretation of the observation, such as normal, abnormal, etc.

Additional notes or comments related to the observation.

The child that the report is about.

The date of eye screening.

Code

Result of eye screening.

Age of eye screening.

Details about the eyes.

Details about the inspection of the pupil.

Details about the inspection of the pupil.

The patient or subject to whom the observation applies.

A code that identifies the type of observation being made, such as a clinical measurement or assessment.

The value of the observation, which can be a quantity, a coded value, or a string.

The time or period during which the observation was made.

The status of the observation, indicating whether it is preliminary, final, etc.

The reason for the current status of the observation.

The individual or organization that performed the observation.

Components of the observation, which can include additional measurements or assessments related to the main observation.

A code that identifies the component of the observation.

The value of the component observation, which can be a quantity, a coded value, or a string.

An interpretation of the observation, such as normal, abnormal, etc.

Additional notes or comments related to the observation.

The child that the report is about.

The date of eye screening.

Inspection pupil abnormal

Inspection pupil abnormal

[BeObservation] Findings about the eye movement and position

The patient or subject to whom the observation applies.

A code that identifies the type of observation being made, such as a clinical measurement or assessment.

The value of the observation, which can be a quantity, a coded value, or a string.

The time or period during which the observation was made.

The status of the observation, indicating whether it is preliminary, final, etc.

The reason for the current status of the observation.

The individual or organization that performed the observation.

Components of the observation, which can include additional measurements or assessments related to the main observation.

A code that identifies the component of the observation.

The value of the component observation, which can be a quantity, a coded value, or a string.

An interpretation of the observation, such as normal, abnormal, etc.

Additional notes or comments related to the observation.

The child that the report is about.

The date of eye screening.

Code

Result of testing eye movement and position.

Free text remarks about the eyes.

The patient or subject to whom the observation applies.

A code that identifies the type of observation being made, such as a clinical measurement or assessment.

The value of the observation, which can be a quantity, a coded value, or a string.

The time or period during which the observation was made.

The status of the observation, indicating whether it is preliminary, final, etc.

The reason for the current status of the observation.

The individual or organization that performed the observation.

Components of the observation, which can include additional measurements or assessments related to the main observation.

A code that identifies the component of the observation.

The value of the component observation, which can be a quantity, a coded value, or a string.

An interpretation of the observation, such as normal, abnormal, etc.

Additional notes or comments related to the observation.

The child that the report is about.

The date of eye screening.

Eye movement and position

Result of testing eye movement and position

Details about treatment with an ophthalmologist.

The patient or subject to whom the observation applies.

A code that identifies the type of observation being made, such as a clinical measurement or assessment.

The value of the observation, which can be a quantity, a coded value, or a string.

The time or period during which the observation was made.

The status of the observation, indicating whether it is preliminary, final, etc.

The reason for the current status of the observation.

The individual or organization that performed the observation.

Components of the observation, which can include additional measurements or assessments related to the main observation.

A code that identifies the component of the observation.

The value of the component observation, which can be a quantity, a coded value, or a string.

An interpretation of the observation, such as normal, abnormal, etc.

Additional notes or comments related to the observation.

Date of remarks about treatment with ophthalmologist.

Code

Treatment with ophthalmologist.

A logical model representing child report data elements.

The date of the child report is the date when the report was created, not the date of the examination or observation. In case of reports migrated from KMEHR, the date is the date of the conversion, not the KMEHR message creation, which is unknown.

A base64 encoded PDF file with the remaining child report information (biometric data, charts, etc.).

The mother of the child is the related subject in this report.

Details about the pregnancy.

[BeObservation] The duration of pregnancy in weeks, as an observation.

subject

Length of gestation at birth

The duration of pregnancy in weeks

Indicates whether CMV infection occurred during pregnancy.

subject

CMV infection during pregnancy

The value indicates whether the mother had a CMV infection during pregnancy.

Indicates whether bacterial meningitis occurred during pregnancy.

Code

The mother of the child is the related subject in this report.

The value indicates whether the mother had a bacterial meningitis during pregnancy.

Details about the neonatal hearing screening.

Code

The date of neonatal hearing screening.

The child that the report is about.

Result of neonatal hearing screening for the left ear.

Result of neonatal hearing screening - left

Neonatal hearing screening result for the left ear.

Result of neonatal hearing screening for the right ear.

Result of neonatal hearing screening - right

Neonatal hearing screening result for the right ear.

Indicates whether the hearing test was refused.

Indicates whether severe head trauma was identified.

The child that the report is about.

Date of reporting the trauma.

Code

The value indicates whether severe head trauma was identified in the child.

Details about the eye screening.

The child that the report is about.

The date of eye screening.

Code

Result of eye screening.

Age of eye screening.

Details about the eyes.

Details about the inspection of the pupil.

Details about the inspection of the pupil.

The child that the report is about.

The date of eye screening.

Inspection pupil abnormal

Inspection pupil abnormal

[BeObservation] Findings about the eye movement and position

The child that the report is about.

The date of eye screening.

Code

Result of testing eye movement and position.

Free text remarks about the eyes.

The child that the report is about.

The date of eye screening.

Eye movement and position

Result of testing eye movement and position

Details about treatment with an ophthalmologist.

Date of remarks about treatment with ophthalmologist.

Code

Treatment with ophthalmologist.

A logical model representing child report data elements.

Patient/subject information

Business identifier for the document

Author(s) by whom the resource was/were authored. Multiple authors could be provided.

Date and time of the last update to the document/information

The date of the child report is the date when the report was created, not the date of the examination or observation. In case of reports migrated from KMEHR, the date is the date of the conversion, not the KMEHR message creation, which is unknown.

Status of the resource

A base64 encoded PDF file with the remaining child report information (biometric data, charts, etc.).

Document title

The mother of the child is the related subject in this report.

Patient/subject information

A person related to the patient/subject, such as a family member or guardian.

The relationship of the related person to the patient/subject. This can include roles such as mother, father, guardian, etc.

Details about the pregnancy.

[BeObservation] The duration of pregnancy in weeks, as an observation.

subject

Length of gestation at birth

The duration of pregnancy in weeks

Indicates whether CMV infection occurred during pregnancy.

subject

CMV infection during pregnancy

The value indicates whether the mother had a CMV infection during pregnancy.

Indicates whether bacterial meningitis occurred during pregnancy.

Code

The mother of the child is the related subject in this report.

The value indicates whether the mother had a bacterial meningitis during pregnancy.

Details about the neonatal hearing screening.

Code

The date of neonatal hearing screening.

The child that the report is about.

Result of neonatal hearing screening for the left ear.

Result of neonatal hearing screening - left

Neonatal hearing screening result for the left ear.

Result of neonatal hearing screening for the right ear.

Result of neonatal hearing screening - right

Neonatal hearing screening result for the right ear.

Indicates whether the hearing test was refused.

Date of encoding of the information

Unique identifier

Is the patient's unique identifier. The unique identifier must be the patient's national patient registry number (NISS) or BIS number.

Is the unique identifier of either the healthcare professional responsible for the encrypted content, or the patient encoding his or her own wishes, or a representative of the patient encoding the patient's wishes. The unique identifier must be the National Register Number (NISS) or BIS number.

The representative is the person who acts on behalf of the applicant (patient) when he is no longer able to express his wishes. For example: the confidant is the person who guides the patient through his steps and assists him during medical appointments. He guarantees the follow-up of the wishes of the patient when he can no longer express his wishes clearly.

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