ID
42513
Description
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
Keywords
Versions (1)
- 8/11/21 8/11/21 -
Copyright Holder
ISARIC on behalf of Oxford University
Uploaded on
August 11, 2021
DOI
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License
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
Description
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
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0015967
Description
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/
Data type
float
Measurement units
- °C
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0439237
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Description
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/
Data type
float
Measurement units
- F
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0456628
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Description
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/
Data type
text
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0806909
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Description
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".
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
Description
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/
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0015230
Description
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/
Data type
text
Alias
- UMLS CUI [1,1]
- C0015230
- UMLS CUI [1,2]
- C0332307
Description
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/
Data type
integer
Alias
- UMLS CUI [1,1]
- C0238767
- UMLS CUI [1,2]
- C0009763
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0026639
- UMLS CUI [1,2]
- C0021368
Description
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.
Data type
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
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0020649
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0039231
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0439590
- UMLS CUI [1,2]
- C0425716
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0151907
- UMLS CUI [2,1]
- C0302133
- UMLS CUI [2,2]
- C1123023
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0857073
Description
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/
Data type
integer
Alias
- UMLS CUI [1,1]
- C1287298
- UMLS CUI [1,2]
- C1532580
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0008031
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0231835
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0476273
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0000737
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0011991
Description
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/
Data type
integer
Alias
- UMLS CUI [1]
- C0042963
Description
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/
Data type
integer
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
Description
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/
Data type
text
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Description
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
Description
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.
Data type
float
Measurement units
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0518015
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0023508
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0948762
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0948762
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0200635
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0200635
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- %
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0018935
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018935
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0032181
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0032181
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0030605
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C1272061
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0030605
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C1272061
- UMLS CUI [2,2]
- C1272696
Description
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.
Data type
float
Measurement units
- sec
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0033707
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0033707
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0525032
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0525032
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0016006
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0016006
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- ng/mL
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mg/L
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mm/hr
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mg/L
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- pg/mL
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- pg/mL
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- umol/L
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337443
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0337443
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202194
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0202194
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0005845
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C0523961
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0005845
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C0523961
- UMLS CUI [2,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337438
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0337438
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- pg/mL
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- ng/mL
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- U/L
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- U/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202236
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0202236
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- U/L
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- umol/L
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- U/L
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- g/dL
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0201838
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0201838
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- mmol/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Description
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.
Data type
float
Measurement units
- ng/mL
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0373607
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0373607
- UMLS CUI [1,2]
- C1272696
Description
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
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0039985
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0243095
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0202823
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0243095
- UMLS CUI [1,3]
- C0332448
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0243095
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0013516
Description
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.
Data type
date
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0340515
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0031046
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0018826
- UMLS CUI [1,3]
- C0021368
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1704258
- UMLS CUI [1,3]
- C1522318
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0013798
Description
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.
Data type
date
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C0243095
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
Description
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.
Data type
date
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0011008
Description
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.
Data type
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
Description
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.
Data type
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
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C0039593
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C1446409
- UMLS CUI [1,4]
- C1521902
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [1,4]
- C1515974
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0729856
Description
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.
Data type
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
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0368676
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
- UMLS CUI [1,3]
- C0475208
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
- UMLS CUI [1,3]
- C0475208
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1521902
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1274040
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C5203670
- UMLS CUI [1,2]
- C0332140
Description
Treatment: at any time during the hospital admission, did the patient receive any of the following:
Alias
- UMLS CUI-1
- C0087111
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C2013463
- UMLS CUI [2,1]
- C0349717
- UMLS CUI [2,2]
- C0429791
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C1289919
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0003451
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0035525
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0674432
- UMLS CUI [2]
- C0292818
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C3541969
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C1609165
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0245109
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0022322
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0002199
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C0015980
Description
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.
Data type
boolean
Alias
- UMLS CUI [1]
- C4726677
Description
Other Antiviral agent
Data type
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0003451
- UMLS CUI [1,3]
- C1521902
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0239126
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0027365
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0013153
Description
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.
Data type
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
Description
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.
Data type
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0239126
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0239126
Description
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.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0239126
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0085297
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C2348070
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Description
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.
Data type
date
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0808070
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0449238
Description
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.
Data type
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
Description
‘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.
Data type
integer
Alias
- UMLS CUI [1]
- C0338237
Description
‘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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0450442
Description
Antibiotic therapy - duration
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
Description
Antibiotic therapy duration unknown
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0439673
Description
‘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.
Data type
integer
Alias
- UMLS CUI [1]
- C0003308
Description
Supportive care
Alias
- UMLS CUI-1
- C0344211
Description
At any time during the hospital admission, did the patient receive any of the following:
Data type
integer
Alias
- UMLS CUI [1]
- C0583239
- UMLS CUI [2]
- C1301858
Description
At any time during the hospital admission, did the patient receive any of the following:
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0021708
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0919655
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C1960999
- UMLS CUI [1,2]
- C0806909
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0699733
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Description
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’.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0033422
Description
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’.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0033422
- UMLS CUI [1,2]
- C0449238
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C1997883
- UMLS CUI [2]
- C1956423
- UMLS CUI [3]
- C0199451
Description
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.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0033422
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0449238
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C1868981
Description
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.
Data type
integer
Measurement units
- cm H2O
Alias
- UMLS CUI [1,1]
- C0032740
- UMLS CUI [1,2]
- C0806909
Description
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.
Data type
integer
Measurement units
- %
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0428167
Description
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.
Data type
integer
Measurement units
- cm H2O
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0445176
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C1822070
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0391840
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C1868981
- UMLS CUI [1,2]
- C0449238
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0304509
- UMLS CUI [2]
- C0042397
Description
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.
Data type
text
Alias
- UMLS CUI [1,1]
- C0304509
- UMLS CUI [1,2]
- C1521902
- UMLS CUI [2,1]
- C0042397
- UMLS CUI [2,2]
- C1521902
Description
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Data type
integer
Alias
- UMLS CUI [1]
- C3869463
Description
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C3869463
- UMLS CUI [1,2]
- C0449238
Description
At any time during the hospital admission, did the patient receive any of the following:
Data type
integer
Alias
- UMLS CUI [1]
- C0032113
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0419017
Description
At any time during the hospital admission, did the patient receive any of the following: Blood transfusion is the administration of any blood product.
Data type
integer
Alias
- UMLS CUI [1]
- C0005841
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C0206074
- UMLS CUI [2]
- C0011946
Description
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.
Data type
integer
Measurement units
- days
Alias
- UMLS CUI [1,1]
- C0206074
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [2,1]
- C0011946
- UMLS CUI [2,2]
- C0449238
Description
Outcome
Alias
- UMLS CUI-1
- C1547647
Description
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.
Data type
integer
Alias
- UMLS CUI [1]
- C1547647
Description
Please state the date for the outcome listed above.
Data type
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
Description
Please state the date for the outcome listed above.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0439673
Description
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’).
Data type
integer
Alias
- UMLS CUI [1,1]
- C3871203
- UMLS CUI [1,2]
- C1521721
- UMLS CUI [1,3]
- C1514873
- UMLS CUI [1,4]
- C0443172
Description
Clinician assessment of diagnosis on death or discharge.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C5389369
Description
Clinician assessment of diagnosis on death or discharge.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
Description
Clinician assessment of diagnosis on death or discharge.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
- UMLS CUI [1,3]
- C0205182
Description
Clinician assessment of diagnosis on death or discharge. Please specify if a final diagnosis not listed above was given.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0600327
Description
Clinician assessment of diagnosis on death or discharge.
Data type
text
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0205394
Description
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0243088
- UMLS CUI [1,2]
- C3871203
Description
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Data type
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])