ID

11833

Beskrivning

http://openehr.org/ckm/

Länk

http://openehr.org/ckm/

Nyckelord

  1. 2015-08-06 2015-08-06 - Martin Dugas
Rättsinnehavare

OpenEHR / FHIR

Uppladdad den

6 augusti 2015

DOI

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Creative Commons BY-NC 3.0

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Adverse Reaction Risk (OpenEHR)

Adverse Reaction Risk (OpenEHR)

Adverse reaction
Beskrivning

Adverse reaction

Alias
UMLS CUI-1
C0559546
Substance
Beskrivning

Identification of a substance, or a class of substances, that is considered to be responsible for the adverse reaction.

Datatyp

text

Alias
UMLS CUI [1]
C0439861
Status
Beskrivning

Assertion about the propensity, or potential risk, of a reaction to the identified 'Substance'.

Datatyp

integer

Alias
UMLS CUI [1]
C1547775
Criticality
Beskrivning

An indication of the potential for critical system organ damage or life threatening consequence

Datatyp

integer

Alias
UMLS CUI [1]
C3858539
Reaction type
Beskrivning

Identification of the underlying physiological mechanism for the adverse reaction

Datatyp

integer

Alias
UMLS CUI [1]
C0745111
Reaction type
Beskrivning

Reaction type

Datatyp

text

Substance category
Beskrivning

Category of the identified 'Substance'.

Datatyp

integer

Alias
UMLS CUI [1]
C0439861
Substance category
Beskrivning

Substance category

Datatyp

text

Alias
UMLS CUI [1]
C0439861
Date of last reaction
Beskrivning

Represents the date and/or time of the last known occurrence of a reactlon event

Datatyp

datetime

Alias
UMLS CUI [1]
C3260033
Comment
Beskrivning

Additional narrative about the propensity for the adverse reaction, not captured in other fields.

Datatyp

text

Alias
UMLS CUI [1]
C0947611
Details about each adverse reaction event linked to exposure to the identified 'Substance'
Beskrivning

Details about each adverse reaction event linked to exposure to the identified 'Substance'

Alias
UMLS CUI-1
C0877248
Specific substance
Beskrivning

Identification of the specific substance considered to be responsible for the adverse reaction event. For example: 'Amoxycillin '.

Datatyp

text

Alias
UMLS CUI [1]
C0439861
Certainty
Beskrivning

Certainty

Datatyp

integer

Alias
UMLS CUI [1]
C0332146
Manifestation
Beskrivning

Clinical symptoms and/or signs that are observed or associated with the adverse reaction

Datatyp

text

Alias
UMLS CUI [1]
C0205319
Reaction description
Beskrivning

Narrative description about the adverse reaction as a whole, including details of the manifestation if required

Datatyp

text

Alias
UMLS CUI [1]
C0443286
Onset of the reaction
Beskrivning

Record of the date and/or time of the onset of the reaction

Datatyp

datetime

Alias
UMLS CUI [1]
C0574845
Duration of reaction
Beskrivning

The total amount of time that the manifestation of the adverse reaction persisted

Datatyp

durationDatetime

Alias
UMLS CUI [1]
C0237585
Severity of reaction
Beskrivning

Clinical assessment of the severity of the reaction event as a whole, potentially considering multiple different manifestations

Datatyp

integer

Alias
UMLS CUI [1]
C0442720
Reaction details
Beskrivning

Additional details about the adverse reaction, including anatomical location and Common Toxicity Criteria

Datatyp

text

Alias
UMLS CUI [1]
C3840507
Initial exposure
Beskrivning

Record of the date and/or time of the first exposure to the Substance for this Reaction Event

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0205265
UMLS CUI [1,2]
C2220266
Duration of exposure
Beskrivning

The total amount of time the individual was exposed to the identified 'Specific substance'

Datatyp

durationDatetime

Alias
UMLS CUI [1]
C2826870
Route of exposure
Beskrivning

Identification of the route by which the subject was exposed to the identified 'Specific substance'.

Datatyp

text

Alias
UMLS CUI [1]
C0683172
Exposure description
Beskrivning

Narrative description about exposure to the identified 'Specific substance'

Datatyp

text

Alias
UMLS CUI [1]
C0332157
Exposure details
Beskrivning

Additional details about exposure to the 'Specific substance', especially in Situations where there may have been multiple or cumulative exposures can be provided

Datatyp

text

Alias
UMLS CUI [1]
C0332157
Clinical management description
Beskrivning

Narrative description about the clinical management provided

Datatyp

text

Alias
UMLS CUI [1]
C1516615
Clinical management details
Beskrivning

Additional structured details about clinical management for this reaction event can be provided

Datatyp

text

Alias
UMLS CUI [1]
C1516615
Reporting details
Beskrivning

Additional structured details required for reporting to regulatory bodies can be provided

Datatyp

text

Alias
UMLS CUI [1]
C0700287
Information source
Beskrivning

Details about the provenance of the information can be provided

Datatyp

text

Alias
UMLS CUI [1]
C0683836
Reaction comment
Beskrivning

Additional narrative about the adverse reaction event not captured in other fields

Datatyp

text

Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C0877248

Similar models

Adverse Reaction Risk (OpenEHR)

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Adverse reaction
C0559546 (UMLS CUI-1)
Substance
Item
Substance
text
C0439861 (UMLS CUI [1])
Item
Status
integer
C1547775 (UMLS CUI [1])
Code List
Status
CL Item
Unconfirmed (1)
C1547326 (UMLS CUI-1)
CL Item
Confirmed (2)
C0750484 (UMLS CUI-1)
CL Item
Resolved (3)
C3714811 (UMLS CUI-1)
CL Item
Refuted (4)
C3245471 (UMLS CUI-1)
Item
Criticality
integer
C3858539 (UMLS CUI [1])
Code List
Criticality
CL Item
low (1)
C0205251 (UMLS CUI-1)
CL Item
high (2)
C0205250 (UMLS CUI-1)
CL Item
indeterminate (3)
C0205258 (UMLS CUI-1)
Item
Reaction type
integer
C0745111 (UMLS CUI [1])
Code List
Reaction type
CL Item
Immune mediated (1)
C0020964 (UMLS CUI-1)
CL Item
Non-immune mediated (2)
C1518422 (UMLS CUI-1)
C0020964 (UMLS CUI-2)
Reaction type
Item
Reaction type
text
Item
Substance category
integer
C0439861 (UMLS CUI [1])
Code List
Substance category
CL Item
Food (1)
C0016452 (UMLS CUI-1)
CL Item
Medication (2)
C0013227 (UMLS CUI-1)
CL Item
Environment (3)
C0014406 (UMLS CUI-1)
Substance category
Item
Substance category
text
C0439861 (UMLS CUI [1])
Date last reaction
Item
Date of last reaction
datetime
C3260033 (UMLS CUI [1])
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Item Group
Details about each adverse reaction event linked to exposure to the identified 'Substance'
C0877248 (UMLS CUI-1)
Specific substance
Item
Specific substance
text
C0439861 (UMLS CUI [1])
Item
Certainty
integer
C0332146 (UMLS CUI [1])
Code List
Certainty
CL Item
Unlikely (1)
C0750558 (UMLS CUI-1)
CL Item
Likely (2)
C0750492 (UMLS CUI-1)
CL Item
Confirmed (3)
C0750484 (UMLS CUI-1)
Manifestation
Item
Manifestation
text
C0205319 (UMLS CUI [1])
Reaction description
Item
Reaction description
text
C0443286 (UMLS CUI [1])
Onset of the reaction
Item
Onset of the reaction
datetime
C0574845 (UMLS CUI [1])
Duration of reaction
Item
Duration of reaction
durationDatetime
C0237585 (UMLS CUI [1])
Item
Severity of reaction
integer
C0442720 (UMLS CUI [1])
Code List
Severity of reaction
CL Item
Mild (1)
C2945599 (UMLS CUI-1)
CL Item
Moderate (2)
C1547226 (UMLS CUI-1)
CL Item
Severe (3)
C0205082 (UMLS CUI-1)
Reaction details
Item
Reaction details
text
C3840507 (UMLS CUI [1])
Initial exposure
Item
Initial exposure
datetime
C0205265 (UMLS CUI [1,1])
C2220266 (UMLS CUI [1,2])
Duration of exposure
Item
Duration of exposure
durationDatetime
C2826870 (UMLS CUI [1])
Route of exposure
Item
Route of exposure
text
C0683172 (UMLS CUI [1])
Exposure description
Item
Exposure description
text
C0332157 (UMLS CUI [1])
Exposure details
Item
Exposure details
text
C0332157 (UMLS CUI [1])
Clinical management description
Item
Clinical management description
text
C1516615 (UMLS CUI [1])
Clinical management details
Item
Clinical management details
text
C1516615 (UMLS CUI [1])
Reporting details
Item
Reporting details
text
C0700287 (UMLS CUI [1])
Information source
Item
Information source
text
C0683836 (UMLS CUI [1])
Reaction comment
Item
Reaction comment
text
C0947611 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])

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