ID

29611

Descripción

http://openehr.org/ckm/ To record laboratory test results as a single value or in a panel/battery format common to clinical pathology testing such as biochemistry, haematology and immunology. Normally used in conjunction with a parent Laboratory test result (Observation) archetype. The name attribute of the Laboratory test panel/Result value element is normally replaced in a template or at run-time to carry the name of the specific analyte e.g. 'Haemoglobin', often coded with a reference terminology such as LOINC, SNOMED CT or NPU. Where other more complex result patterns are required it may be helpful to specialise this archetype or substitute another.

Link

http://openehr.org/ckm/

Palabras clave

  1. 10/4/18 10/4/18 - Halim Ugurlu
Titular de derechos de autor

openEHR Foundation

Subido en

10 de abril de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0

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openEHR-EHR-CLUSTER.laboratory_test_panel.v0

openEHR-EHR-CLUSTER.laboratory_test_panel.v0

  1. StudyEvent: openEHR-EHR-CLUSTER.laboratory_test_panel.v0
    1. openEHR-EHR-CLUSTER.laboratory_test_panel.v0
openEHR-EHR-CLUSTER.laboratory_test_panel.v0.xml
Descripción

openEHR-EHR-CLUSTER.laboratory_test_panel.v0.xml

Alias
UMLS CUI-1
C0200378
Laboratory test panel
Descripción

Laboratory test result as a single value or in a panel/battery format common to clinical pathology testing.

Tipo de datos

text

Alias
UMLS CUI [1]
C0200378
Result value
Descripción

Actual value of the result. The name of this element is normally replaced in a template or at run-time to relfect the actual analyte e.g. Serum sodium and will often be coded.

Tipo de datos

text

Alias
UMLS CUI [1]
C2348527
Laboratory result
Descripción

Specific detailed result, including both the value of the result item, and additional information that may be useful for clinical interpretation.

Tipo de datos

text

Alias
UMLS CUI [1]
C0587081
Comment
Descripción

Comment about the Result.

Tipo de datos

text

Alias
UMLS CUI [1]
C0947611
Reference range guidance
Descripción

Additional advice on the applicability of the reference range.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0150600
Result status
Descripción

The status of the result value.

Tipo de datos

text

Alias
UMLS CUI [1]
C2346633
Result status timestamp
Descripción

The date and/or time that the entire result was issued for the recorded ‘Result status’.

Tipo de datos

datetime

Alias
UMLS CUI [1]
C1705482
Other detail
Descripción

Further details including the specimen for the panel or a further nested panel.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1522508
UMLS CUI [1,2]
C0205394
Result detail
Descripción

Further detail regarding an individual result.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1522508
UMLS CUI [1,2]
C1274040

Similar models

openEHR-EHR-CLUSTER.laboratory_test_panel.v0

  1. StudyEvent: openEHR-EHR-CLUSTER.laboratory_test_panel.v0
    1. openEHR-EHR-CLUSTER.laboratory_test_panel.v0
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
openEHR-EHR-CLUSTER.laboratory_test_panel.v0.xml
C0200378 (UMLS CUI-1)
Laboratory test panel
Item
Laboratory test panel
text
C0200378 (UMLS CUI [1])
Result value
Item
Result value
text
C2348527 (UMLS CUI [1])
Laboratory result
Item
Laboratory result
text
C0587081 (UMLS CUI [1])
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Reference range guidance
Item
Reference range guidance
text
C0883335 (UMLS CUI [1,1])
C0150600 (UMLS CUI [1,2])
Item
Result status
text
C2346633 (UMLS CUI [1])
Code List
Result status
CL Item
Registered (1)
CL Item
Interim (2)
CL Item
Final (3)
CL Item
Amended (4)
CL Item
Cancelled/Aborted (5)
CL Item
Not requested (6)
Result status timestamp
Item
Result status timestamp
datetime
C1705482 (UMLS CUI [1])
Other detail
Item
Other detail
text
C1522508 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Result detail
Item
Result detail
text
C1522508 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])

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