TEMPLATE Nephro_klinische Eckdaten (Nephro_klinische Eckdaten)

TEMPLATE IDNephro_klinische Eckdaten
ConceptNephro_klinische Eckdaten
DescriptionZur Darstellung von klinischen Eckdaten des Patienten innerhalb des Nephro-Digital Projektes.
UseZur Repräsentation der klinischen Eckdaten eines Patienten (Vitalparameter, Infektionen etc.)
PurposeZur Darstellung von klinischen Eckdaten des Patienten innerhalb des Nephro-Digital Projektes.
References
AuthorsName: Nina Schewe; Organisation: Medizinische Hochschule Hannover; Email: schewe.nina@mh-hannover.de
Other Details LanguageName: Nina Schewe; Organisation: Medizinische Hochschule Hannover; Email: schewe.nina@mh-hannover.de
Other Details (Language Independent)
  • MetaDataSet:Sample Set : Template metadata sample set
KeywordsKlinische Daten; Blutdruck; Puls; Trinkmenge; Immunitätsstatus; Infektion; Transplantation; Hepatitis; HIV; Dialyse
Language useden
Citeable Identifier1246.169.1046
Root archetype idopenEHR-EHR-COMPOSITION.report.v1
Klinische EckdatenKlinische Eckdaten: Document to communicate information to others, commonly in response to a request from another party.
Other Context
Case identificationCase identification: To record case identification details for public health purposes.
Case identifierCase identifier: The identifier of this case.
DialyseDialyse: A clinical activity carried out for screening, investigative, diagnostic, curative, therapeutic, evaluative or palliative purposes.
Name der DialyseName der Dialyse: Identification of the procedure by name.
Coding of the specific procedure with a terminology is preferred, where possible.
Terminology: SNOMED-CT
  • Renal dialysis (procedure) 
Methode der DialyseMethode der Dialyse: Identification of specific method or technique for the procedure.
Use this data element to record simple terms or a narrative description. If the requirements for recording the method require more complex modelling then this can be represented by additional archetypes within the 'Procedure detail' SLOT in this archetype. If the method is included in the 'Procedure name' via precoordinated codes, this data element becomes redundant.
Terminology: SNOMED-CT
  • Hemodialysis (procedure) 
  • Peritoneal dialysis (procedure) 
StartdatumStartdatum: The date and/or time on which the procedure is intended to be performed.
Only for use in association with the 'Procedure scheduled' pathway step.
TransplantationTransplantation: A clinical activity carried out for screening, investigative, diagnostic, curative, therapeutic, evaluative or palliative purposes.
Procedure nameProcedure name: Identification of the procedure by name.
Coding of the specific procedure with a terminology is preferred, where possible.
Terminology: SNOMED-CT
  • Transplant of kidney (procedure) 
Art der TransplantationArt der Transplantation: Identification of specific method or technique for the procedure.
Use this data element to record simple terms or a narrative description. If the requirements for recording the method require more complex modelling then this can be represented by additional archetypes within the 'Procedure detail' SLOT in this archetype. If the method is included in the 'Procedure name' via precoordinated codes, this data element becomes redundant.
  • Lebendspende
  • Todspende
TransplantationsdatumTransplantationsdatum: The date and/or time on which the procedure is intended to be performed.
Only for use in association with the 'Procedure scheduled' pathway step.
CommentComment: Additional narrative about the activity or care pathway step not captured in other fields.
Hepatitis ImmunitätsstatusHepatitis Immunitätsstatus: The result, including findings and the laboratory's interpretation, of an investigation performed on specimens collected from an individual or related to that individual.
LaborabnahmeLaborabnahme: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Test nameTest name: Name of the laboratory investigation performed on the specimen(s).
A test result may be for a single analyte, or a group of items, including panel tests. It is strongly recommended that 'Test name' be coded with a terminology, for example LOINC or SNOMED CT. For example: 'Glucose', 'Urea and Electrolytes', 'Swab', 'Cortisol (am)', 'Potassium in perspiration' or 'Melanoma histopathology'. The name may sometimes include specimen type and patient state, for example 'Fasting blood glucose' or include other information, as 'Potassium (PNA blood gas)'.
Terminology: SNOMED-CT
  • Hepatitis A virus antibody measurement (procedure) 
  • Hepatitis C antibody measurement (procedure) 
  • Hepatitis D antibody measurement (procedure) 
  • Hepatitis E antibody measurement (procedure) 
  • Hepatitis Be antibody measurement (procedure) 
Laboratory analyte resultLaboratory analyte result: The result of a laboratory test for a single analyte value.
VirusVirus: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
Terminology: LOINC
  • Hepatitis A virus IgG Ab [Presence] in Serum 
  • Hepatitis A virus IgG Ab [Presence] in Serum by Immunoassay 
  • Hepatitis D virus IgG Ab [Presence] in Serum 
  • Hepatitis D virus IgG Ab [Presence] in Serum by Immunoassay 
  • Hepatitis B virus core IgG Ab [Presence] in Serum 
  • Hepatitis B virus core IgG Ab [Presence] in Serum by Immunoassay 
  • Hepatitis C virus IgG Ab [Presence] in Serum 
  • Hepatitis C virus IgG Ab [Presence] in Serum by Immunoblot 
  • Hepatitis C virus IgG Ab [Presence] in Serum or Plasma by Immunoassay 
  • Hepatitis C virus IgG Ab [Presence] in Serum, Plasma or Blood by Rapid immunoassay 
  • Hepatitis E virus IgG Ab [Presence in Serum 
  • Hepatitis E virus IgG Ab [Presence] in Serum by Immunoassay 
NachweisNachweis: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • IgG positiv
  • IgG negativ
CommentComment: Additional narrative about the test result not captured in other fields.
Confounding factorsConfounding factors: Issues or circumstances that impact on the accurate interpretation of the measurement or test result.
'Confounding factors' should be reserved for uncontrolled/unplanned issues of patient state/physiology that might affect interpretation, for example 'recent exercise' or 'recent tobacco smoking'. Known or required preconditions, such as 'fasting' should be carried in the 'Sampling conditions' element within the CLUSTER.specimen archetype . In some cases preconditions are captured as part of the test name, for example 'Fasting blood glucose'. Known issues with specimen collection or handling, such as 'prolonged use of tourniquet' or 'sample haemolysed', should be carried in the 'Specimen quality' elements within CLUSTER.specimen archetype. Coding with a terminology is desirable, where possible.
HIV ImmunitätsstatusHIV Immunitätsstatus: The result, including findings and the laboratory's interpretation, of an investigation performed on specimens collected from an individual or related to that individual.
LaborabnahmeLaborabnahme: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Test nameTest name: Name of the laboratory investigation performed on the specimen(s).
A test result may be for a single analyte, or a group of items, including panel tests. It is strongly recommended that 'Test name' be coded with a terminology, for example LOINC or SNOMED CT. For example: 'Glucose', 'Urea and Electrolytes', 'Swab', 'Cortisol (am)', 'Potassium in perspiration' or 'Melanoma histopathology'. The name may sometimes include specimen type and patient state, for example 'Fasting blood glucose' or include other information, as 'Potassium (PNA blood gas)'.
Terminology: SNOMED-CT
  • Measurement of Human immunodeficiency virus 1 antibody (procedure) 
  • Measurement of Human immunodeficiency virus 2 antibody (procedure) 
Laboratory analyte resultLaboratory analyte result: The result of a laboratory test for a single analyte value.
Analyte nameAnalyte name: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
Terminology: LOINC
  • HIV 2 IgG Ab [Presence] in Serum 
  • HIV 2 IgG Ab [Presence] in Serum by Immunoblot 
  • HIV 1 IgG Ab [Presence] in Serum 
  • HIV 1 IgG Ab [Presence] in Serum by Immunoblot 
NachweisNachweis: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • IgG positiv
  • IgG negativ
CommentComment: Additional narrative about the test result not captured in other fields.
Confounding factorsConfounding factors: Issues or circumstances that impact on the accurate interpretation of the measurement or test result.
'Confounding factors' should be reserved for uncontrolled/unplanned issues of patient state/physiology that might affect interpretation, for example 'recent exercise' or 'recent tobacco smoking'. Known or required preconditions, such as 'fasting' should be carried in the 'Sampling conditions' element within the CLUSTER.specimen archetype . In some cases preconditions are captured as part of the test name, for example 'Fasting blood glucose'. Known issues with specimen collection or handling, such as 'prolonged use of tourniquet' or 'sample haemolysed', should be carried in the 'Specimen quality' elements within CLUSTER.specimen archetype. Coding with a terminology is desirable, where possible.
CMV ImmunitätsstatusCMV Immunitätsstatus: The result, including findings and the laboratory's interpretation, of an investigation performed on specimens collected from an individual or related to that individual.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Test nameTest name: Name of the laboratory investigation performed on the specimen(s).
A test result may be for a single analyte, or a group of items, including panel tests. It is strongly recommended that 'Test name' be coded with a terminology, for example LOINC or SNOMED CT. For example: 'Glucose', 'Urea and Electrolytes', 'Swab', 'Cortisol (am)', 'Potassium in perspiration' or 'Melanoma histopathology'. The name may sometimes include specimen type and patient state, for example 'Fasting blood glucose' or include other information, as 'Potassium (PNA blood gas)'.
Terminology: SNOMED-CT
  • Serologic test for cytomegalovirus (procedure) 
Laboratory analyte resultLaboratory analyte result: The result of a laboratory test for a single analyte value.
Analyte nameAnalyte name: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
Terminology: LOINC
  • Cytomegalovirus IgG Ab [Titer] in Serum or Plasma 
  • Cytomegalovirus IgG Ab [Titer] in Serum or Plasma by Immunofluorescence 
NachweisNachweis: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • IgG positiv
  • IgG negativ
CommentComment: Additional narrative about the test result not captured in other fields.
Confounding factorsConfounding factors: Issues or circumstances that impact on the accurate interpretation of the measurement or test result.
'Confounding factors' should be reserved for uncontrolled/unplanned issues of patient state/physiology that might affect interpretation, for example 'recent exercise' or 'recent tobacco smoking'. Known or required preconditions, such as 'fasting' should be carried in the 'Sampling conditions' element within the CLUSTER.specimen archetype . In some cases preconditions are captured as part of the test name, for example 'Fasting blood glucose'. Known issues with specimen collection or handling, such as 'prolonged use of tourniquet' or 'sample haemolysed', should be carried in the 'Specimen quality' elements within CLUSTER.specimen archetype. Coding with a terminology is desirable, where possible.
EBV ImmunitätsstatusEBV Immunitätsstatus: The result, including findings and the laboratory's interpretation, of an investigation performed on specimens collected from an individual or related to that individual.
LaborabnahmeLaborabnahme: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Test nameTest name: Name of the laboratory investigation performed on the specimen(s).
A test result may be for a single analyte, or a group of items, including panel tests. It is strongly recommended that 'Test name' be coded with a terminology, for example LOINC or SNOMED CT. For example: 'Glucose', 'Urea and Electrolytes', 'Swab', 'Cortisol (am)', 'Potassium in perspiration' or 'Melanoma histopathology'. The name may sometimes include specimen type and patient state, for example 'Fasting blood glucose' or include other information, as 'Potassium (PNA blood gas)'.
Terminology: SNOMED-CT
  • Epstein-Barr virus serologic test (procedure) 
Laboratory analyte resultLaboratory analyte result: The result of a laboratory test for a single analyte value.
Analyte nameAnalyte name: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
Terminology: LOINC
  • Epstein Barr virus nuclear IgG Ab [Titer] in Serum 
  • Epstein Barr virus nuclear IgG Ab [Titer] in Serum by Immunofluorescence 
  • Epstein Barr virus capsid IgG Ab [Titer] in Serum 
  • Epstein Barr virus capsid IgG Ab [Titer] in Serum by Immunofluorescence 
  • Epstein Barr virus early IgG Ab [Titer] in Serum 
  • Epstein Barr virus early IgG Ab [Titer] in Serum by Immunofluorescence 
NachweisNachweis: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • IgG positiv
  • IgG negativ
CommentComment: Additional narrative about the test result not captured in other fields.
Confounding factorsConfounding factors: Issues or circumstances that impact on the accurate interpretation of the measurement or test result.
'Confounding factors' should be reserved for uncontrolled/unplanned issues of patient state/physiology that might affect interpretation, for example 'recent exercise' or 'recent tobacco smoking'. Known or required preconditions, such as 'fasting' should be carried in the 'Sampling conditions' element within the CLUSTER.specimen archetype . In some cases preconditions are captured as part of the test name, for example 'Fasting blood glucose'. Known issues with specimen collection or handling, such as 'prolonged use of tourniquet' or 'sample haemolysed', should be carried in the 'Specimen quality' elements within CLUSTER.specimen archetype. Coding with a terminology is desirable, where possible.
Body weightBody weight: Measurement of the body weight of an individual.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
WeightWeight: The weight of the individual.
0..1000; 0..1000000
Units:
  • kg
  • g
Height/LengthHeight/Length: Height, or body length, is measured from crown of head to sole of foot.
Height is measured with the individual in a standing position and body length in a recumbent position.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Height/LengthHeight/Length: The length of the body from crown of head to sole of foot.
0..1000 cm
Pulse/Heart beatPulse/Heart beat: The rate and associated attributes for a pulse or heart beat.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
RateRate: The rate of the pulse or heart beat, measured in beats per minute.
0..1000 /min
Blood pressureBlood pressure: The local measurement of arterial blood pressure which is a surrogate for arterial pressure in the systemic circulation.
Most commonly, use of the term 'blood pressure' refers to measurement of brachial artery pressure in the upper arm.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
SystolicSystolic: Peak systemic arterial blood pressure - measured in systolic or contraction phase of the heart cycle.
0..1000 mmHg
DiastolicDiastolic: Minimum systemic arterial blood pressure - measured in the diastolic or relaxation phase of the heart cycle.
0..1000 mmHg
Mean arterial pressureMean arterial pressure: The average arterial pressure that occurs over the entire course of the heart contraction and relaxation cycle.
0..1000 mmHg
Pulse pressurePulse pressure: The difference between the systolic and diastolic pressure.
0..1000 mmHg
klinische Untersuchungklinische Untersuchung: Findings observed during the physical examination of a subject of care.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
DescriptionDescription: Narrative description of the overall findings observed during a physical examination of a patient.
May be used to record a narrative summary of the complete clinical examination or key aspects of clinical examination findings, which will be supported by structured data. Details of specific structured findings can be included using CLUSTER archetypes in the 'Examination Detail' slot. This data element may be used to capture legacy data that is not available in a structured format.
Verlauf des GesundheitszustandesVerlauf des Gesundheitszustandes: Narrative summary or overview about a patient, specifically from the perspective of a healthcare provider, and with or without associated interpretations.
VerlaufstextVerlaufstext: The summary, assessment, conclusions or evaluation of the clinical findings.