ID
42513
Beschrijving
Preliminary case definition Children and adolescents 0–19 years of age with measured or self-reported fever ≥ 3 days AND two or more of the following: a) Rash or bilateral non-purulent conjunctivitis or muco-cutaneous inflammation signs (oral, hands or feet) b) Hypotension or shock c) Features of myocardial dysfunction, or pericarditis, or valvulitis, or coronary abnormalities (clinical features, ECHO findings, or laboratory markers such as elevated Troponin/NT-proBNP) d) Evidence of coagulopathy (such as abnormal PT, PTT, elevated d-Dimers) e) Acute gastrointestinal problems (such as diarrhoea, vomiting or abdominal pain) AND Elevated markers of inflammation such as ESR, C-reactive protein or procalcitonin AND No other obvious microbial cause of inflammation, including bacterial sepsis, staphylococcal or streptococcal shock syndromes AND Evidence of current or previous COVID-19 (RT-PCR, antigen test or serology positive) or likely contact with patients with COVID NB Consider this syndrome in children with features of typical or atypical Kawasaki disease or toxic shock syndrome. Based on CRF on https://isaric.org/research/covid-19-clinical-research-resources/multisystem-inflammatory-syndrome-mis-c/ This Case Report Form (CRF) has been developed by ISARIC in cooperation with WHO's working group (https://www.who.int/news-room/commentaries/detail/multisystem-inflammatory-syndrome-in-children-and-adolescents-with-covid-19) to use as a standalone CRF for children and adolescents presenting with syndrome of suspected Multisystem Inflammatory Syndrome (MIS-C). This Module is to be completed at time of discharge or death.
Link
Trefwoorden
Versies (1)
- 11-08-21 11-08-21 -
Houder van rechten
ISARIC on behalf of Oxford University
Geüploaded op
11 augustus 2021
DOI
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Licentie
Creative Commons BY-SA 4.0
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Multisystem inflammatory syndrome (MIS) in children and adolescents temporally related to COVID-19
MODULE 2: OUTCOME CASE REPORT FORM
- StudyEvent: ODMjoin
Beschrijving
Summary of clinical features of current illness (include all signs identified any time between admission and discharge/death)
Alias
- UMLS CUI-1
- C0242482
- UMLS CUI-2
- C2348519
- UMLS CUI-3
- C0205210
- UMLS CUI-4
- C0521116
- UMLS CUI-5
- C0221423
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0015967
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0439237
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
float
Maateenheden
- F
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0456628
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
text
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0806909
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ If not applicable write "NA".
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0015230
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
text
Alias
- UMLS CUI [1,1]
- C0015230
- UMLS CUI [1,2]
- C0332307
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0238767
- UMLS CUI [1,2]
- C0009763
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Examples include redness, swelling, or dryness of the lips; redness of the throat; strawberry tongue.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0026639
- UMLS CUI [1,2]
- C0021368
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Examples include pain, swelling, or redness of the fingers, toes, hands, or feet.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205100
- UMLS CUI [1,2]
- C0221912
- UMLS CUI [1,3]
- C0021368
- UMLS CUI [1,4]
- C0037088
- UMLS CUI [1,5]
- C0018563
- UMLS CUI [2,1]
- C0205100
- UMLS CUI [2,2]
- C0221912
- UMLS CUI [2,3]
- C0021368
- UMLS CUI [2,4]
- C0037088
- UMLS CUI [2,5]
- C0016504
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Please follow the normal standard ranges for blood pressure appropriate to the age, size, and sex of the child.
Datatype
integer
Alias
- UMLS CUI [1]
- C0020649
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Please follow the normal standard ranges for heart rate appropriate to the age, size, and sex of the child.
Datatype
integer
Alias
- UMLS CUI [1]
- C0039231
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ A normal capillary refill time should be 2 seconds or less.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0439590
- UMLS CUI [1,2]
- C0425716
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0151907
- UMLS CUI [2,1]
- C0302133
- UMLS CUI [2,2]
- C1123023
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0857073
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1287298
- UMLS CUI [1,2]
- C1532580
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0008031
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Please follow the normal standard ranges for respiratory rate appropriate to the age, size, and sex of the child.
Datatype
integer
Alias
- UMLS CUI [1]
- C0231835
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0476273
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0000737
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0011991
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1]
- C0042963
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
Beschrijving
Please include all signs and symptoms clinically assessed between admission and discharge/death. Clinically assessed according to local standard ranges, or for information see the WHO standardised age-ranges for children see the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Beschrijving
Laboratory results (record the most abnormal result during the hospital admission up to the time of discharge/death) (*record units if different from those listed)
Alias
- UMLS CUI-1
- C1254595
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0518015
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0023508
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0948762
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0948762
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0200635
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0200635
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- %
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0018935
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0018935
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0032181
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0032181
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0030605
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C1272061
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0030605
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C1272061
- UMLS CUI [2,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- sec
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0033707
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0033707
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0525032
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0525032
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0016006
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0016006
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- ng/mL
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mg/L
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mm/hr
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mg/L
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- pg/mL
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- pg/mL
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- umol/L
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337443
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0337443
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202194
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0202194
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0005845
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C0523961
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0005845
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C0523961
- UMLS CUI [2,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337438
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0337438
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- pg/mL
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- ng/mL
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- U/L
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- U/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202236
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0202236
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- U/L
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- umol/L
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- U/L
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- g/dL
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0201838
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0201838
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- mmol/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
float
Maateenheden
- ng/mL
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0373607
Beschrijving
Please record the most abnormal result between admission up to the time of discharge/death. If the unit of measurement is different from those listed, please record the units. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. For individual parameters see guidance in section 1h.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0373607
- UMLS CUI [1,2]
- C1272696
Beschrijving
Imaging and pathogen testing (include the most abnormal results from admission up to the time of discharge/death)
Alias
- UMLS CUI-1
- C0011923
- UMLS CUI-2
- C0450254
- UMLS CUI-3
- C0039593
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if X-ray and/or CT were performed, even if no infiltrates were present.
Datatype
integer
Alias
- UMLS CUI [1]
- C0039985
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if X-ray and/or CT were performed, even if no infiltrates were present.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0243095
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if X-ray and/or CT were performed, even if no infiltrates were present.
Datatype
integer
Alias
- UMLS CUI [1]
- C0202823
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if X-ray and/or CT were performed, even if no infiltrates were present.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0243095
- UMLS CUI [1,3]
- C0332448
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if X-ray and/or CT were performed, even if no infiltrates were present.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0243095
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1]
- C0013516
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0340515
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0031046
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0018826
- UMLS CUI [1,3]
- C0021368
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1704258
- UMLS CUI [1,3]
- C1522318
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if an ECG was performed, even if the result was normal. Indicate any significant findings.
Datatype
integer
Alias
- UMLS CUI [1]
- C0013798
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if an ECG was performed, even if the result was normal. Indicate any significant findings.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record if an ECG was performed, even if the result was normal. Indicate any significant findings.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C0243095
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
Datatype
date
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0011008
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
Datatype
text
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0332307
- UMLS CUI [1,4]
- C1521902
- UMLS CUI [2,1]
- C2936236
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C1274040
- UMLS CUI [2,4]
- C1521902
- UMLS CUI [2,5]
- C1522166
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
Datatype
text
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1522166
- UMLS CUI [1,4]
- C1274040
- UMLS CUI [1,5]
- C1521902
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please record if the patient was tested for bacterial pathogens and the result.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C0039593
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please record if the patient was tested for bacterial pathogens and the result.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C1446409
- UMLS CUI [1,4]
- C1521902
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [1,4]
- C1515974
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0729856
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0729856
- UMLS CUI [1,4]
- C0200345
- UMLS CUI [1,5]
- C1515974
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0368676
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
- UMLS CUI [1,3]
- C0475208
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
- UMLS CUI [1,3]
- C0475208
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1521902
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1274040
Beschrijving
Please specify any other pathogen tests that were done and provide the results in the space provided. Results that were rejected by the clinical team (e.g. contaminated microbiology results) should not be reported.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
Beschrijving
Please specify any other pathogen tests that were done and provide the results in the space provided. Results that were rejected by the clinical team (e.g. contaminated microbiology results) should not be reported.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Beschrijving
Please include the most abnormal results post- admission or post-first day MIS clinically assessed up to the time of discharge/death. Please complete all of this section even if the tests were not done or the result was negative. Please provide the site of specimen collection or the titre where indicated.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C5203670
- UMLS CUI [1,2]
- C0332140
Beschrijving
Treatment: at any time during the hospital admission, did the patient receive any of the following:
Alias
- UMLS CUI-1
- C0087111
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please record if the patient received fluids via a feeding tube, oral or intravenously.
Datatype
integer
Alias
- UMLS CUI [1]
- C2013463
- UMLS CUI [2,1]
- C0349717
- UMLS CUI [2,2]
- C0429791
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please record if the patient received fluids via a feeding tube, oral or intravenously.
Datatype
integer
Alias
- UMLS CUI [1]
- C1289919
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
integer
Alias
- UMLS CUI [1]
- C0003451
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0035525
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0674432
- UMLS CUI [2]
- C0292818
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C3541969
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1609165
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0245109
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0022322
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0002199
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0015980
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed.
Datatype
boolean
Alias
- UMLS CUI [1]
- C4726677
Beschrijving
Other Antiviral agent
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0003451
- UMLS CUI [1,3]
- C1521902
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
integer
Alias
- UMLS CUI [1]
- C0239126
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0027365
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0013153
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0806909
- UMLS CUI [1,3]
- C2348070
- UMLS CUI [2,1]
- C0239126
- UMLS CUI [2,2]
- C0806909
- UMLS CUI [2,3]
- C1519795
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0239126
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0239126
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. ‘Corticosteroids’ (commonly referred to as ‘steroids’). Examples include: prednisolone, prednisone, methyl-prednisolone, dexamethasone, hydrocortisone, fluticasone, betamethasone (note that other examples exist). Please include the route and the maximum daily dose.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0239126
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
integer
Alias
- UMLS CUI [1]
- C0085297
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C2348070
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0808070
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0449238
Beschrijving
At any time during the hospital admission post- admission or post-first day MIS clinically assessed up to the time of discharge/death), did the patient receive any of the treatments listed. Please provide the daily dose and the number of days of treatment.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0806909
- UMLS CUI [1,3]
- C2348070
- UMLS CUI [2,1]
- C0085297
- UMLS CUI [2,2]
- C0806909
- UMLS CUI [2,3]
- C1519795
Beschrijving
‘Antibiotic’ refers to any agent(s) are substances naturally produced by microorganisms or their derivatives that selectively target microorganisms. These substances are used in the treatment of bacterial and other microbial infections. Topical preparations are not included.
Datatype
integer
Alias
- UMLS CUI [1]
- C0338237
Beschrijving
‘Antibiotic’ refers to any agent(s) are substances naturally produced by microorganisms or their derivatives that selectively target microorganisms. These substances are used in the treatment of bacterial and other microbial infections. Topical preparations are not included.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0450442
Beschrijving
Antibiotic therapy - duration
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
Beschrijving
Antibiotic therapy duration unknown
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0439673
Beschrijving
‘Antifungal agent’ refers to any agent(s) prescribed specifically to treat systemic or topical infections caused by fungi. Examples include fluconazole, amphotericin, caspofungin, anidulafungin, posaconazole, itraconazole (note that other examples exist). Topical preparations should not be recorded.
Datatype
integer
Alias
- UMLS CUI [1]
- C0003308
Beschrijving
Supportive care
Alias
- UMLS CUI-1
- C0344211
Beschrijving
At any time during the hospital admission, did the patient receive any of the following:
Datatype
integer
Alias
- UMLS CUI [1]
- C0583239
- UMLS CUI [2]
- C1301858
Beschrijving
At any time during the hospital admission, did the patient receive any of the following:
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0021708
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Complete this field for all patients. If any supplemental oxygen (at any concentration) was given by any means of delivery at any point until the time of submission of Module 1, place a cross in the box marked ‘yes’. This includes any supplementary oxygen (O2) delivered via non-invasive facemasks/nasal cannula/mask or via invasive mechanical ventilation. Please also indicate the maximum O2 flow volume. If it is not possible to access record of the absolute highest O2 volume delivered during the admission indicate the highest known.
Datatype
integer
Alias
- UMLS CUI [1]
- C0919655
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Complete this field for all patients. If any supplemental oxygen (at any concentration) was given by any means of delivery at any point until the time of submission of Module 1, place a cross in the box marked ‘yes’. This includes any supplementary oxygen (O2) delivered via non-invasive facemasks/nasal cannula/mask or via invasive mechanical ventilation. Please also indicate the maximum O2 flow volume. If it is not possible to access record of the absolute highest O2 volume delivered during the admission indicate the highest known.
Datatype
text
Alias
- UMLS CUI [1,1]
- C1960999
- UMLS CUI [1,2]
- C0806909
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Complete this field for all patients. If any supplemental oxygen (at any concentration) was given by any means of delivery at any point until the time of submission of Module 1, place a cross in the box marked ‘yes’. This includes any supplementary oxygen (O2) delivered via non-invasive facemasks/nasal cannula/mask or via invasive mechanical ventilation. Please also indicate the maximum O2 flow volume. If it is not possible to access record of the absolute highest O2 volume delivered during the admission indicate the highest known.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0699733
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Complete this field for all patients. If any supplemental oxygen (at any concentration) was given by any means of delivery at any point until the time of submission of Module 1, place a cross in the box marked ‘yes’. This includes any supplementary oxygen (O2) delivered via non-invasive facemasks/nasal cannula/mask or via invasive mechanical ventilation. Please also indicate the maximum O2 flow volume. If it is not possible to access record of the absolute highest O2 volume delivered during the admission indicate the highest known.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Beschrijving
At any time during the hospital admission, did the patient receive any of the following. If the patient received prone positioning at any time during their hospital stay, please tick ‘yes’.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0033422
Beschrijving
At any time during the hospital admission, did the patient receive any of the following. If the patient received prone positioning at any time during their hospital stay, please tick ‘yes’.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0033422
- UMLS CUI [1,2]
- C0449238
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: If the patient received non-invasive ventilation (NIV), defined as the provision of ventilatory support through the patient's upper airway using a mask or similar device, at any time until discharge or death, please tick ‘yes’ and enter the total duration in days if known.
Datatype
integer
Alias
- UMLS CUI [1]
- C1997883
- UMLS CUI [2]
- C1956423
- UMLS CUI [3]
- C0199451
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: If the patient received non-invasive ventilation (NIV), defined as the provision of ventilatory support through the patient's upper airway using a mask or similar device, at any time until discharge or death, please tick ‘yes’ and enter the total duration in days if known.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0033422
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: If the patient received non-invasive ventilation (NIV), defined as the provision of ventilatory support through the patient's upper airway using a mask or similar device, at any time until discharge or death, please tick ‘yes’ and enter the total duration in days if known.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0449238
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
integer
Alias
- UMLS CUI [1]
- C1868981
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
integer
Maateenheden
- cm H2O
Alias
- UMLS CUI [1,1]
- C0032740
- UMLS CUI [1,2]
- C0806909
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
integer
Maateenheden
- %
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0428167
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
integer
Maateenheden
- cm H2O
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0445176
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C1822070
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0391840
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Invasive ventilation means that patient has undergone tracheal intubation, the mode of intubation may be orotracheal, nasotracheal, or via a cricothyrotomy or tracheotomy. If the patient received invasive ventilation at any time until until discharge or death, please tick ‘yes’, enter the maximum ventilation parameters, and enter the duration in days.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C1868981
- UMLS CUI [1,2]
- C0449238
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Vasopressor agents include norepinephrine, epinephrine, vasopressin, terlipressin and phenylephrine. Commonly used ‘positive’ inotropes include dobutamine, dopamine, milrinone and adrenaline (epinephrine). If the patient received a vasopressor or inotrope for at least one hour during their hospital stay, please tick ‘yes’ and provide the generic name in the space provided.
Datatype
integer
Alias
- UMLS CUI [1]
- C0304509
- UMLS CUI [2]
- C0042397
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Vasopressor agents include norepinephrine, epinephrine, vasopressin, terlipressin and phenylephrine. Commonly used ‘positive’ inotropes include dobutamine, dopamine, milrinone and adrenaline (epinephrine). If the patient received a vasopressor or inotrope for at least one hour during their hospital stay, please tick ‘yes’ and provide the generic name in the space provided.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304509
- UMLS CUI [1,2]
- C1521902
- UMLS CUI [2,1]
- C0042397
- UMLS CUI [2,2]
- C1521902
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Datatype
integer
Alias
- UMLS CUI [1]
- C3869463
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C3869463
- UMLS CUI [1,2]
- C0449238
Beschrijving
At any time during the hospital admission, did the patient receive any of the following:
Datatype
integer
Alias
- UMLS CUI [1]
- C0032113
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: High frequency oscillatory ventilation (HFOV) is a type of mechanical ventilation which utilises a high respiratory rate and low tidal volume.
Datatype
integer
Alias
- UMLS CUI [1]
- C0419017
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Blood transfusion is the administration of any blood product.
Datatype
integer
Alias
- UMLS CUI [1]
- C0005841
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Please include any form of continuous renal replacement therapy or intermittent haemodialysis.
Datatype
integer
Alias
- UMLS CUI [1]
- C0206074
- UMLS CUI [2]
- C0011946
Beschrijving
At any time during the hospital admission, did the patient receive any of the following: Please include any form of continuous renal replacement therapy or intermittent haemodialysis.
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0206074
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [2,1]
- C0011946
- UMLS CUI [2,2]
- C0449238
Beschrijving
Outcome
Alias
- UMLS CUI-1
- C1547647
Beschrijving
Discharged alive can mean discharge to their usual place of residence before their illness, to the home of a relative or friend, or to a social care facility, because their illness is no longer severe enough to warrant treatment in a medical facility. Hospitalized means they are still in hospital but have recovered from COVID-19 infection and the form has been completed as the patient is in a part of the hospital for care of other conditions and where the form will not be completed at a later date. Transfer to other facility means they have been transferred to another facility that provides medical care. This could be a specialist centre for more intensive treatment or a step-down for rehabilitation. It does not include facilities that solely provide social care (these patients should be listed as discharged alive). Death means the patient died in the hospital. Palliative discharge means the patient has been discharged with the expectation that they will not recover from this or other co-existing illness. This could be to a specialist hospice facility, or to their usual home address with anticipatory end of life medications.
Datatype
integer
Alias
- UMLS CUI [1]
- C1547647
Beschrijving
Please state the date for the outcome listed above.
Datatype
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
Beschrijving
Please state the date for the outcome listed above.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0439673
Beschrijving
Care needs at discharge versus before illness: if the patient requires care at discharge (in terms of activities of daily living) at the same level as before they developed illness then tick ‘same as before illness’. If their care needs have decreased or increased, then tick the appropriate box (‘worse’ or ‘better’).
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3871203
- UMLS CUI [1,2]
- C1521721
- UMLS CUI [1,3]
- C1514873
- UMLS CUI [1,4]
- C0443172
Beschrijving
Clinician assessment of diagnosis on death or discharge.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C5389369
Beschrijving
Clinician assessment of diagnosis on death or discharge.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
Beschrijving
Clinician assessment of diagnosis on death or discharge.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
- UMLS CUI [1,3]
- C0205182
Beschrijving
Clinician assessment of diagnosis on death or discharge. Please specify if a final diagnosis not listed above was given.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0600327
Beschrijving
Clinician assessment of diagnosis on death or discharge.
Datatype
text
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0205394
Beschrijving
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0243088
- UMLS CUI [1,2]
- C3871203
Beschrijving
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0243088
- UMLS CUI [1,2]
- C3871203
- UMLS CUI [1,3]
- C1521902
Similar models
MODULE 2: OUTCOME CASE REPORT FORM
- StudyEvent: ODMjoin
C2348519 (UMLS CUI-2)
C0205210 (UMLS CUI-3)
C0521116 (UMLS CUI-4)
C0221423 (UMLS CUI-5)
C0439237 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
C0456628 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
C0806909 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
C0332307 (UMLS CUI [1,2])
C0009763 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,2])
C0221912 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,3])
C0037088 (UMLS CUI [1,4])
C0018563 (UMLS CUI [1,5])
C0205100 (UMLS CUI [2,1])
C0221912 (UMLS CUI [2,2])
C0021368 (UMLS CUI [2,3])
C0037088 (UMLS CUI [2,4])
C0016504 (UMLS CUI [2,5])
C0425716 (UMLS CUI [1,2])
C0302133 (UMLS CUI [2,1])
C1123023 (UMLS CUI [2,2])
C1532580 (UMLS CUI [1,2])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0518015 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0948762 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0200635 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0018935 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0032181 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0030605 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C1272061 (UMLS CUI [2,2])
C1272696 (UMLS CUI [1,2])
C1272061 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
C0033707 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0525032 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0016006 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0337443 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0202194 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0005845 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C0523961 (UMLS CUI [2,2])
C1272696 (UMLS CUI [1,2])
C0523961 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
C0337438 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0202236 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0201838 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0373607 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0450254 (UMLS CUI-2)
C0039593 (UMLS CUI-3)
C0243095 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,2])
C0332448 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0340515 (UMLS CUI [1,2])
C0031046 (UMLS CUI [1,2])
C0018826 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,3])
C1704258 (UMLS CUI [1,2])
C1522318 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0243095 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C2936236 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1274040 (UMLS CUI [2,3])
C1521902 (UMLS CUI [2,4])
C1522166 (UMLS CUI [2,5])
C0205394 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
C0450254 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C0450254 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0599161 (UMLS CUI [1,2])
C0599161 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C1515974 (UMLS CUI [1,4])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,4])
C1515974 (UMLS CUI [1,5])
C0456962 (UMLS CUI [1,2])
C0368676 (UMLS CUI [1,3])
C0014441 (UMLS CUI [1,2])
C0014441 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
C4054524 (UMLS CUI [1,2])
C4054524 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0332140 (UMLS CUI [1,2])
C0349717 (UMLS CUI [2,1])
C0429791 (UMLS CUI [2,2])
C0292818 (UMLS CUI [2])
C0003451 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0027365 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C0239126 (UMLS CUI [2,1])
C0806909 (UMLS CUI [2,2])
C1519795 (UMLS CUI [2,3])
C0239126 (UMLS CUI [1,2])
C0239126 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,2])
C0239126 (UMLS CUI [1,3])
C2348070 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C0085297 (UMLS CUI [2,1])
C0806909 (UMLS CUI [2,2])
C1519795 (UMLS CUI [2,3])
C0450442 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C1301858 (UMLS CUI [2])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0033422 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C1956423 (UMLS CUI [2])
C0199451 (UMLS CUI [3])
C0033422 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C0428167 (UMLS CUI [1,2])
C0445176 (UMLS CUI [1,2])
C1822070 (UMLS CUI [1,2])
C0391840 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0042397 (UMLS CUI [2])
C1521902 (UMLS CUI [1,2])
C0042397 (UMLS CUI [2,1])
C1521902 (UMLS CUI [2,2])
C0449238 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2])
C0449238 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C1521721 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0443172 (UMLS CUI [1,4])
C5389369 (UMLS CUI [1,2])
C0026691 (UMLS CUI [1,2])
C0026691 (UMLS CUI [1,2])
C0205182 (UMLS CUI [1,3])
C0600327 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C3871203 (UMLS CUI [1,2])
C3871203 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])