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

https://isaric.org/research/covid-19-clinical-research-resources/multisystem-inflammatory-syndrome-mis-c/

Trefwoorden

  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

Participant Identification
Beschrijving

Participant Identification

Alias
UMLS CUI-1
C3165543
Participant Identification Numbers
Beschrijving

Participant Identification Numbers

Datatype

text

Alias
UMLS CUI [1]
C3165543
Date of patient assessment
Beschrijving

This is the date when the patient was first clinically assessed for MIS. This may be the same data as the date of admission to hospital, or for patients already admitted to hospital, who later develop or are later assessed for symptoms consistent with MIS, enter the date MIS is first clinically assessed.

Datatype

date

Alias
UMLS CUI [1]
C2985720
Summary of clinical features of current illness (include all signs identified any time between admission and discharge/death)
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
Fever
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
Maximum temperature during the admission:
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
°C
Maximum temperature during the admission:
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
F
If not applicable write "NA".
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
Duration of fever during the admission
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
days
If not applicable write "NA".
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
days
Rash
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
If yes, type of rash:
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
Bilateral conjunctivitis
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
Oral mucosal inflammation signs
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
Peripheral cutaneous inflammation signs (hands or feet)
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
Hypotension (age appropriate)
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
Tachycardia (age appropriate)
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
Prolonged capillary refill time
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
Pale/motted skin
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
Cold hands/feet
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
Urinary output <2mL/kg/hr
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
Chest pain
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
Tachypnoea (age appropriate)
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
Respiratory distress
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
Abdominal pain
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
Diarrhoea
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
Vomiting
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
Other clinical features
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
Other clinical features, specify
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
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)
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
Haemoglobin (g/L)
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
g/L
Haemoglobin (g/L) measurement not done?
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
Total WBC count (x10^9/L)
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
x10^9/L
Total WBC count (x10^9/L) not done?
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
Neutrophils (x10^9/L)
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
x10^9/L
Neutrophils (x10^9/L) measurement not done?
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
Lymphocytes (x10^9/L)
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
x10^9/L
Lymphocytes (x10^9/L) measurement not done?
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
Haematocrit (%)
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
%
Haematocrit (%) measurement not done?
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
Platelets (x10^9/L)
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
x10^9/L
Platelets (x10^9/L) measurement not done?
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
APTT/APTR
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
APTT/APTR measurement not done?
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
PT (seconds)
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
sec
PT (seconds) measurement not done?
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
INR
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
INR measurement not done?
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
Fibrinogen (g/L)
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
g/L
Fibrinogen (g/L) measurement not done?
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
Procalcitonin (ng/mL)
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
ng/mL
Procalcitonin (ng/mL) measurement not done?
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
CRP (mg/L)
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
mg/L
CRP (mg/L) measurement not done?
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
ESR (mm/hr)
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
mm/hr
ESR (mm/hr) measurement not done?
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
D-Dimer (mg/L)
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
mg/L
D-Dimer (mg/L) measurement not done?
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
IL-6 (pg/mL)
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
pg/mL
IL-6 (pg/mL) measurement not done?
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
IL-10 (pg/mL)
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
pg/mL
IL-10 (pg/mL) measurement not done?
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
Creatinine (umol/L)
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
umol/L
Creatinine (umol/L) measurement not done?
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
Sodium (mmol/L)
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
mmol/L
Sodium (mmol/L) measurement not done?
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
Potassium (mmol/L)
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
mmol/L
Potassium (mmol/L) measurement not done?
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
Urea (BUN) (mmol/L)
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
mmol/L
Urea (BUN) (mmol/L) measurement not done?
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
Glucose (mmol/L)
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
mmol/L
Glucose (mmol/L) measurement not done?
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
Pro-BNP (pg/mL)
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
pg/mL
Pro-BNP (pg/mL) measurement not done?
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
Troponin (ng/mL)
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
ng/mL
Troponin (ng/mL) measurement not done?
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
Creatine kinase (U/L)
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
U/L
Creatine kinase (U/L) measurement not done?
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
LDH (U/L)
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
U/L
LDH (U/L) measurement not done?
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
Triglyceride
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
Triglyceride measurement not done?
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
ALT/SGPT (U/L)
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
U/L
ALT/SGPT (U/L) measurement not done?
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
Total bilirubin (umol/L)
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
umol/L
Total bilirubin (umol/L) measurement not done?
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
AST/GOT (U/L)
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
U/L
AST/GOT (U/L) measurement not done?
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
Albumin (g/dL)
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
g/dL
Albumin (g/dL) measurement not done?
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
Lactate (mmol/L)
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
mmol/L
Lactate (mmol/L) measurement not done?
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
Ferritin (ng/mL)
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
ng/mL
Ferritin (ng/mL) measurement not done?
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
Imaging and pathogen testing (include the most abnormal results from admission up to the time of discharge/death)
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
Chest X-ray performed
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
If yes, findings:
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
Chest CT performed
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
If yes, were infiltrates present?:
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
If yes, other findings:
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
Echocardiography performed?
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
If yes, what was the date of the most abnormal echocardiogram?
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
On that echocardiogram were there: features of myocardial dysfunction?
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
On that echocardiogram were there: features of pericarditis?
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
On that echocardiogram were there: features of valvulitis?
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
On that echocardiogram were there: features of coronary abnormalities?
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
ECG performed?
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
If yes, what was the date of the most abnormal ECG?
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
On that ECG what were the findings?
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
Other cardiac imaging performed?
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
If yes, date
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
If yes, specify name of imaging and most abnormal results
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
If yes, specify most abnormal results
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
Bacterial pathogen
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
If positive, specify
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
SARS-CoV-2 testing, RT-PCR
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
SARS-CoV-2 testing, RT-PCR site of specimen collection
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
SARS-CoV-2 testing, rapid antigen test
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
SARS-CoV-2 testing, rapid antigen test site of specimen collection
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
SARS-CoV-2 testing, rapid antibody test
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
SARS-CoV-2 testing, ELISA
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
SARS-CoV-2 testing, ELISA if done, titres
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
SARS-CoV-2 testing, Neutralization test
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
SARS-CoV-2 testing, Neutralization test if done, titres
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
Other test?
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
If other test, specification
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
If other test, results
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
Other viral pathogen
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
If positive, specify:
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
If no pathogen testing: clinically diagnosed COVID-19?
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
Treatment: at any time during the hospital admission, did the patient receive any of the following:
Beschrijving

Treatment: at any time during the hospital admission, did the patient receive any of the following:

Alias
UMLS CUI-1
C0087111
Oral / orogastric fluids?
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
Intravenuous fluids?
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
Antiviral?
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
If yes, Ribavirin?
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
If yes, Lopinavir/Ritonavir?
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
If yes, Neuraminidase inhibitor?
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
If yes, Tocilizumab?
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
If yes, Anakinra?
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
If yes, Ivermectin?
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
If yes, Interferon alpha?
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
If yes, Interferon beta?
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
If yes, Remdesivir?
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
If other, specify:
Beschrijving

Other Antiviral agent

Datatype

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0003451
UMLS CUI [1,3]
C1521902
Corticosteroid (not topical)?
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
If yes, specify name
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
If yes, specify route
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
If yes, please provide maximum daily dose and unit
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
If yes, date commenced:
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
Duration:
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
days
Duration: unknown
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
IV immune globulin?
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
If yes, daily dose
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
Number of days of treatment:
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
days
If yes, date commenced:
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
Duration:
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
days
Max daily dose and unit:
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
Antibiotic?
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
Agent:
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
Duration:
Beschrijving

Antibiotic therapy - duration

Datatype

integer

Maateenheden
  • days
Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0449238
days
Duration: unknown
Beschrijving

Antibiotic therapy duration unknown

Datatype

boolean

Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0439673
Antifungal agent?
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
Supportive care
Beschrijving

Supportive care

Alias
UMLS CUI-1
C0344211
ICU or high dependency unit admission?
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
If yes, number of days in ICU
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
days
Oxygen supplementation therapy?
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
If yes, max O2 flow
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
If yes, interface
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
If yes, number of days of oxygen therapy?
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
Prone positioning
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
If yes, duration
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
days
Non-invasive ventilation (any e.g. BiPAP/CPAP)
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
If yes, prone position?
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
If yes, duration in days?
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
days
Invasive ventilation (any)?
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
If yes, maximum PEEP
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
cm H2O
If yes, maximum FiO2
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
%
If yes, maximum plateau pressure
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
cm H2O
If yes, maximum PaCO2
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
If yes, maximum PaO2
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
If yes, duration in days?
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
days
Inotropes/Vasopressors?
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
If yes, specify name
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
Extracorporal (ECMO) support
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
If yes, total duration:
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
days
Plasma exchange?
Beschrijving

At any time during the hospital admission, did the patient receive any of the following:

Datatype

integer

Alias
UMLS CUI [1]
C0032113
HFOV
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
Blood transfusion
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
Renal replacement therapy (RRT) or dialysis?
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
If yes, total duration:
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
days
Outcome
Beschrijving

Outcome

Alias
UMLS CUI-1
C1547647
Please select only one outcome
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
Outcome date
Beschrijving

Please state the date for the outcome listed above.

Datatype

date

Alias
UMLS CUI [1,1]
C1547647
UMLS CUI [1,2]
C0011008
Outcome date: unknown
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
If discharged alive: care needs at discharge versus before illness
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
What was the physician's impression of the final diagnosis? Multisystem inflammatory syndrome
Beschrijving

Clinician assessment of diagnosis on death or discharge.

Datatype

integer

Alias
UMLS CUI [1,1]
C1546485
UMLS CUI [1,2]
C5389369
Kawasaki disease
Beschrijving

Clinician assessment of diagnosis on death or discharge.

Datatype

integer

Alias
UMLS CUI [1,1]
C1546485
UMLS CUI [1,2]
C0026691
Atypical kawasaki disease
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
Toxic shock syndrome
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
Other, specify:
Beschrijving

Clinician assessment of diagnosis on death or discharge.

Datatype

text

Alias
UMLS CUI [1,1]
C1546485
UMLS CUI [1,2]
C0205394
Were there any sequelae present at the time of discharge:
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
If yes, specify
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

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Participant Identification
C3165543 (UMLS CUI-1)
Participant Identification Numbers
Item
Participant Identification Numbers
text
C3165543 (UMLS CUI [1])
Date of patient assessment
Item
Date of patient assessment
date
C2985720 (UMLS CUI [1])
Item Group
Summary of clinical features of current illness (include all signs identified any time between admission and discharge/death)
C0242482 (UMLS CUI-1)
C2348519 (UMLS CUI-2)
C0205210 (UMLS CUI-3)
C0521116 (UMLS CUI-4)
C0221423 (UMLS CUI-5)
Item
Fever
integer
C0015967 (UMLS CUI [1])
Code List
Fever
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Fever, maximum temperature in degrees celsius during the admission:
Item
Maximum temperature during the admission:
float
C0005903 (UMLS CUI [1,1])
C0439237 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
Fever, maximum temperature in degrees fahrenheit during the admission:
Item
Maximum temperature during the admission:
float
C0005903 (UMLS CUI [1,1])
C0456628 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
Fever, maximum temperature during the admission, not applicable
Item
If not applicable write "NA".
text
C0005903 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
Fever, duration during the admission:
Item
Duration of fever during the admission
integer
C0015967 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
Fever, duration during the admission, not applicable
Item
If not applicable write "NA".
integer
C0015967 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
Item
Rash
integer
C0015230 (UMLS CUI [1])
Code List
Rash
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Rash, Type
Item
If yes, type of rash:
text
C0015230 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Item
Bilateral conjunctivitis
integer
C0238767 (UMLS CUI [1,1])
C0009763 (UMLS CUI [1,2])
Code List
Bilateral conjunctivitis
CL Item
Yes, purulent (1)
CL Item
Yes, non-purulent (2)
CL Item
No  (3)
CL Item
Unknown (4)
Item
Oral mucosal inflammation signs
integer
C0026639 (UMLS CUI [1,1])
C0021368 (UMLS CUI [1,2])
Code List
Oral mucosal inflammation signs
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Peripheral cutaneous inflammation signs (hands or feet)
integer
C0205100 (UMLS CUI [1,1])
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])
Code List
Peripheral cutaneous inflammation signs (hands or feet)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Hypotension (age appropriate)
integer
C0020649 (UMLS CUI [1])
Code List
Hypotension (age appropriate)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Tachycardia (age appropriate)
integer
C0039231 (UMLS CUI [1])
Code List
Tachycardia (age appropriate)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Prolonged capillary refill time
integer
C0439590 (UMLS CUI [1,1])
C0425716 (UMLS CUI [1,2])
Code List
Prolonged capillary refill time
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Pale/motted skin
integer
C0151907 (UMLS CUI [1])
C0302133 (UMLS CUI [2,1])
C1123023 (UMLS CUI [2,2])
Code List
Pale/motted skin
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Cold hands/feet
integer
C0857073 (UMLS CUI [1])
Code List
Cold hands/feet
CL Item
Yes (1)
CL Item
no (2)
CL Item
Unknown (3)
Item
Urinary output <2mL/kg/hr
integer
C1287298 (UMLS CUI [1,1])
C1532580 (UMLS CUI [1,2])
Code List
Urinary output <2mL/kg/hr
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Chest pain
integer
C0008031 (UMLS CUI [1])
Code List
Chest pain
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Tachypnoea (age appropriate)
integer
C0231835 (UMLS CUI [1])
Code List
Tachypnoea (age appropriate)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Respiratory distress
integer
C0476273 (UMLS CUI [1])
Code List
Respiratory distress
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Abdominal pain
integer
C0000737 (UMLS CUI [1])
Code List
Abdominal pain
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Diarrhoea
integer
C0011991 (UMLS CUI [1])
Code List
Diarrhoea
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Vomiting
integer
C0042963 (UMLS CUI [1])
Code List
Vomiting
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other clinical features
integer
C0205210 (UMLS CUI [1,1])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Code List
Other clinical features
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Other clinical features, to specify
Item
Other clinical features, specify
text
C0205210 (UMLS CUI [1,1])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Item Group
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)
C1254595 (UMLS CUI-1)
Worst Haemoglobin
Item
Haemoglobin (g/L)
float
C1522166 (UMLS CUI [1,1])
C0518015 (UMLS CUI [1,2])
Haemoglobin not done
Item
Haemoglobin (g/L) measurement not done?
boolean
C0518015 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst total WBC count
Item
Total WBC count (x10^9/L)
float
C1522166 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
Total WBC count not done
Item
Total WBC count (x10^9/L) not done?
boolean
C0023508 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst neutrophils
Item
Neutrophils (x10^9/L)
float
C1522166 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
Neutrophils not done
Item
Neutrophils (x10^9/L) measurement not done?
boolean
C0948762 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst lymphocytes
Item
Lymphocytes (x10^9/L)
float
C1522166 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
Lymphocytes not done
Item
Lymphocytes (x10^9/L) measurement not done?
boolean
C0200635 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst haematocrit
Item
Haematocrit (%)
float
C1522166 (UMLS CUI [1,1])
C0018935 (UMLS CUI [1,2])
Haematocrit not done
Item
Haematocrit (%) measurement not done?
boolean
C0018935 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst platelets
Item
Platelets (x10^9/L)
float
C1522166 (UMLS CUI [1,1])
C0032181 (UMLS CUI [1,2])
Platelets not done
Item
Platelets (x10^9/L) measurement not done?
boolean
C0032181 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest APTT/APTR
Item
APTT/APTR
float
C1522410 (UMLS CUI [1,1])
C0030605 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C1272061 (UMLS CUI [2,2])
APTT/APTR not done
Item
APTT/APTR measurement not done?
boolean
C0030605 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
C1272061 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
Highest prothrombin time
Item
PT (seconds)
float
C1522410 (UMLS CUI [1,1])
C0033707 (UMLS CUI [1,2])
Prothrombin time not done
Item
PT (seconds) measurement not done?
boolean
C0033707 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest INR
Item
INR
float
C1522410 (UMLS CUI [1,1])
C0525032 (UMLS CUI [1,2])
INR not done
Item
INR measurement not done?
boolean
C0525032 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst fibrinogen
Item
Fibrinogen (g/L)
float
C1522166 (UMLS CUI [1,1])
C0016006 (UMLS CUI [1,2])
Fibrinogen not done
Item
Fibrinogen (g/L) measurement not done?
boolean
C0016006 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest procalcitonin
Item
Procalcitonin (ng/mL)
float
C1535922 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Procalcitonin not done
Item
Procalcitonin (ng/mL) measurement not done?
boolean
C1535922 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest CRP
Item
CRP (mg/L)
float
C0201657 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
CRP not done
Item
CRP (mg/L) measurement not done?
boolean
C0201657 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest ESR
Item
ESR (mm/hr)
float
C1176468 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
ESR not done
Item
ESR (mm/hr) measurement not done?
boolean
C1176468 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest D-Dimer
Item
D-Dimer (mg/L)
float
C2826333 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
D-Dimer not done
Item
D-Dimer (mg/L) measurement not done?
boolean
C2826333 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest IL-6
Item
IL-6 (pg/mL)
float
C0919829 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
IL-6 not done
Item
IL-6 (pg/mL) measurement not done?
boolean
C0919829 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest IL-10
Item
IL-10 (pg/mL)
float
C0085295 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
IL-10 not done
Item
IL-10 (pg/mL) measurement not done?
boolean
C0085295 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest creatinine
Item
Creatinine (umol/L)
float
C0201975 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Creatinine not done
Item
Creatinine (umol/L) measurement not done?
boolean
C0201975 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst sodium
Item
Sodium (mmol/L)
float
C1522166 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
Sodium not done
Item
Sodium (mmol/L) measurement not done?
boolean
C0337443 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst potassium
Item
Potassium (mmol/L)
float
C1522166 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
Potassium not done
Item
Potassium (mmol/L) measurement not done?
boolean
C0202194 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest urea (BUN)
Item
Urea (BUN) (mmol/L)
float
C1522410 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C0523961 (UMLS CUI [2,2])
Urea (BUN) not done
Item
Urea (BUN) (mmol/L) measurement not done?
boolean
C0005845 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
C0523961 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
Worst glucose
Item
Glucose (mmol/L)
float
C1522166 (UMLS CUI [1,1])
C0337438 (UMLS CUI [1,2])
Glucose not done
Item
Glucose (mmol/L) measurement not done?
boolean
C0337438 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest pro-BNP
Item
Pro-BNP (pg/mL)
float
C3272900 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Pro-BNP not done
Item
Pro-BNP (pg/mL) measurement not done?
boolean
C3272900 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest Troponin
Item
Troponin (ng/mL)
float
C0523952 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Troponin not done
Item
Troponin (ng/mL) measurement not done?
boolean
C0523952 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest creatine kinase
Item
Creatine kinase (U/L)
float
C0201973 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Creatine kinase not done
Item
Creatine kinase (U/L) measurement not done?
boolean
C0201973 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest LDH
Item
LDH (U/L)
float
C0202113 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
LDH not done
Item
LDH (U/L) measurement not done?
boolean
C0202113 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst triglyceride
Item
Triglyceride
float
C1522166 (UMLS CUI [1,1])
C0202236 (UMLS CUI [1,2])
Triglyceride not done
Item
Triglyceride measurement not done?
boolean
C0202236 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest ALT/SGPT
Item
ALT/SGPT (U/L)
float
C0201836 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
ALT/SGPT not done
Item
ALT/SGPT (U/L) measurement not done?
boolean
C0201836 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest total bilirubin
Item
Total bilirubin (umol/L)
float
C0201913 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Total bilirubin not done
Item
Total bilirubin (umol/L) measurement not done?
boolean
C0201913 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest AST/GOT
Item
AST/GOT (U/L)
float
C0201899 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
AST/GOT not done
Item
AST/GOT (U/L) measurement not done?
boolean
C0201899 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Worst albumin
Item
Albumin (g/dL)
float
C1522166 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
Albumin not done
Item
Albumin (g/dL) measurement not done?
boolean
C0201838 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest lactate
Item
Lactate (mmol/L)
float
C0202113 (UMLS CUI [1,1])
C1522410 (UMLS CUI [1,2])
Lactate not done
Item
Lactate (mmol/L) measurement not done?
boolean
C0202113 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Highest ferritin
Item
Ferritin (ng/mL)
float
C1522410 (UMLS CUI [1,1])
C0373607 (UMLS CUI [1,2])
Ferritin not done
Item
Ferritin (ng/mL) measurement not done?
boolean
C0373607 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Item Group
Imaging and pathogen testing (include the most abnormal results from admission up to the time of discharge/death)
C0011923 (UMLS CUI-1)
C0450254 (UMLS CUI-2)
C0039593 (UMLS CUI-3)
Item
Chest X-ray performed
integer
C0039985 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Chest X-ray findings
Item
If yes, findings:
text
C0039985 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
Item
Chest CT performed
integer
C0202823 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
If yes, were infiltrates present?:
integer
C0202823 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
C0332448 (UMLS CUI [1,3])
Code List
If yes, were infiltrates present?:
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Chest CT other findings
Item
If yes, other findings:
text
C0202823 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,3])
Item
Echocardiography performed?
integer
C0013516 (UMLS CUI [1])
Code List
Echocardiography performed?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Date of worst echocardiogram
Item
If yes, what was the date of the most abnormal echocardiogram?
date
C0013516 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
On that echocardiogram were there: features of myocardial dysfunction?
integer
C0013516 (UMLS CUI [1,1])
C0340515 (UMLS CUI [1,2])
Code List
On that echocardiogram were there: features of myocardial dysfunction?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
On that echocardiogram were there: features of pericarditis?
integer
C0013516 (UMLS CUI [1,1])
C0031046 (UMLS CUI [1,2])
Code List
On that echocardiogram were there: features of pericarditis?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
On that echocardiogram were there: features of valvulitis?
integer
C0013516 (UMLS CUI [1,1])
C0018826 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,3])
Code List
On that echocardiogram were there: features of valvulitis?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
On that echocardiogram were there: features of coronary abnormalities?
integer
C0013516 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1522318 (UMLS CUI [1,3])
Code List
On that echocardiogram were there: features of coronary abnormalities?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
ECG performed?
integer
C0013798 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Date of worst ECG
Item
If yes, what was the date of the most abnormal ECG?
date
C0013798 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
ECG finding
Item
On that ECG what were the findings?
text
C0013798 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
Item
Other cardiac imaging performed?
integer
C2936236 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Code List
Other cardiac imaging performed?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Other cardiac imaging date
Item
If yes, date
date
C2936236 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Other cardiac imaging type and most abnormal result specification
Item
If yes, specify name of imaging and most abnormal results
text
C2936236 (UMLS CUI [1,1])
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])
Other cardiac imaging most abnormal results specification
Item
If yes, specify most abnormal results
text
C2936236 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
Item
Bacterial pathogen
text
C0004623 (UMLS CUI [1,1])
C0450254 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
Code List
Bacterial pathogen
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
Bacterial pathogen positive specification
Item
If positive, specify
text
C0004623 (UMLS CUI [1,1])
C0450254 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Item
SARS-CoV-2 testing, RT-PCR
text
C5203676 (UMLS CUI [1,1])
C0599161 (UMLS CUI [1,2])
Code List
SARS-CoV-2 testing, RT-PCR
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
SARS-CoV-2 testing, RT-PCR site of specimen collection
Item
SARS-CoV-2 testing, RT-PCR site of specimen collection
text
C5203676 (UMLS CUI [1,1])
C0599161 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C1515974 (UMLS CUI [1,4])
Item
SARS-CoV-2 testing, rapid antigen test
text
C5203676 (UMLS CUI [1,1])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
Code List
SARS-CoV-2 testing, rapid antigen test
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
SARS-CoV-2 testing, rapid antigen test site of specimen collection
Item
SARS-CoV-2 testing, rapid antigen test site of specimen collection
text
C5203676 (UMLS CUI [1,1])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,4])
C1515974 (UMLS CUI [1,5])
Item
SARS-CoV-2 testing, rapid antibody test
text
C5203676 (UMLS CUI [1,1])
C0456962 (UMLS CUI [1,2])
C0368676 (UMLS CUI [1,3])
Code List
SARS-CoV-2 testing, rapid antibody test
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
Item
SARS-CoV-2 testing, ELISA
text
C5203676 (UMLS CUI [1,1])
C0014441 (UMLS CUI [1,2])
Code List
SARS-CoV-2 testing, ELISA
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
SARS-CoV-2 testing, ELISA titres
Item
SARS-CoV-2 testing, ELISA if done, titres
text
C5203676 (UMLS CUI [1,1])
C0014441 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
Item
SARS-CoV-2 testing, Neutralization test
text
C5203676 (UMLS CUI [1,1])
C4054524 (UMLS CUI [1,2])
Code List
SARS-CoV-2 testing, Neutralization test
CL Item
Positive (1)
CL Item
Negative (2)
CL Item
Not done (3)
SARS-CoV-2 testing, Neutralization test specimen titres
Item
SARS-CoV-2 testing, Neutralization test if done, titres
text
C5203676 (UMLS CUI [1,1])
C4054524 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
Other SARS-CoV-2 testing?
Item
Other test?
boolean
C0205394 (UMLS CUI [1,1])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
Other SARS-CoV-2 testing, specify
Item
If other test, specification
text
C0205394 (UMLS CUI [1,1])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Other SARS-CoV-2 testing, results
Item
If other test, results
text
C0205394 (UMLS CUI [1,1])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Other viral pathogen
text
C0450254 (UMLS CUI [1,1])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Code List
Other viral pathogen
CL Item
positive (1)
CL Item
negative  (2)
CL Item
not done (3)
Other viral pathogen, specification
Item
If positive, specify:
text
C0450254 (UMLS CUI [1,1])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Item
If no pathogen testing: clinically diagnosed COVID-19?
integer
C5203670 (UMLS CUI [1,1])
C0332140 (UMLS CUI [1,2])
Code List
If no pathogen testing: clinically diagnosed COVID-19?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Treatment: at any time during the hospital admission, did the patient receive any of the following:
C0087111 (UMLS CUI-1)
Item
Oral / orogastric fluids?
integer
C2013463 (UMLS CUI [1])
C0349717 (UMLS CUI [2,1])
C0429791 (UMLS CUI [2,2])
Code List
Oral / orogastric fluids?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Intravenuous fluids?
integer
C1289919 (UMLS CUI [1])
Code List
Intravenuous fluids?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Antiviral?
integer
C0003451 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Ribavirin
Item
If yes, Ribavirin?
boolean
C0035525 (UMLS CUI [1])
Lopinavir/Ritonavir
Item
If yes, Lopinavir/Ritonavir?
boolean
C0674432 (UMLS CUI [1])
C0292818 (UMLS CUI [2])
Neuraminidase inhibitor
Item
If yes, Neuraminidase inhibitor?
boolean
C3541969 (UMLS CUI [1])
Tocilizumab
Item
If yes, Tocilizumab?
boolean
C1609165 (UMLS CUI [1])
Anakinra
Item
If yes, Anakinra?
boolean
C0245109 (UMLS CUI [1])
Ivermectin
Item
If yes, Ivermectin?
boolean
C0022322 (UMLS CUI [1])
Interferon alpha
Item
If yes, Interferon alpha?
boolean
C0002199 (UMLS CUI [1])
Interferon beta
Item
If yes, Interferon beta?
boolean
C0015980 (UMLS CUI [1])
Remdesivir
Item
If yes, Remdesivir?
boolean
C4726677 (UMLS CUI [1])
Other Antiviral agent
Item
If other, specify:
text
C0205394 (UMLS CUI [1,1])
C0003451 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item
Corticosteroid (not topical)?
integer
C0239126 (UMLS CUI [1])
Code List
Corticosteroid (not topical)?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Corticosteroid name
Item
If yes, specify name
text
C0239126 (UMLS CUI [1,1])
C0027365 (UMLS CUI [1,2])
Item
If yes, specify route
text
C0239126 (UMLS CUI [1,1])
C0013153 (UMLS CUI [1,2])
Code List
If yes, specify route
CL Item
oral/rectal (1)
CL Item
parenteral (IM/IV)  (2)
CL Item
inhaled  (3)
CL Item
unknown (4)
Corticosteroid: maximum daily dosage and unit
Item
If yes, please provide maximum daily dose and unit
text
C0239126 (UMLS CUI [1,1])
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])
Corticosteroid - Start date
Item
If yes, date commenced:
date
C0808070 (UMLS CUI [1,1])
C0239126 (UMLS CUI [1,2])
Corticosteroid duration
Item
Duration:
integer
C0449238 (UMLS CUI [1,1])
C0239126 (UMLS CUI [1,2])
Corticosteroid duration unknown
Item
Duration: unknown
boolean
C0449238 (UMLS CUI [1,1])
C0439673 (UMLS CUI [1,2])
C0239126 (UMLS CUI [1,3])
Item
IV immune globulin?
integer
C0085297 (UMLS CUI [1])
Code List
IV immune globulin?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
IV immune globulin, daily dose
Item
If yes, daily dose
text
C0085297 (UMLS CUI [1,1])
C2348070 (UMLS CUI [1,2])
IV immune globulin, number of days
Item
Number of days of treatment:
integer
C0085297 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
IV immune globulin, start date
Item
If yes, date commenced:
date
C0085297 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
IV immune globulin, duration
Item
Duration:
integer
C0085297 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
IV immune globulin, max. daily dose and unit
Item
Max daily dose and unit:
text
C0085297 (UMLS CUI [1,1])
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])
Item
Antibiotic?
integer
C0338237 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Antibiotic agent
Item
Agent:
text
C0338237 (UMLS CUI [1,1])
C0450442 (UMLS CUI [1,2])
Antibiotic therapy - duration
Item
Duration:
integer
C0338237 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Antibiotic therapy duration unknown
Item
Duration: unknown
boolean
C0338237 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
Item
Antifungal agent?
integer
C0003308 (UMLS CUI [1])
Code List
Antifungal agent?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Supportive care
C0344211 (UMLS CUI-1)
Item
ICU or high dependency unit admission?
integer
C0583239 (UMLS CUI [1])
C1301858 (UMLS CUI [2])
Code List
ICU or high dependency unit admission?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Number of days in ICU
Item
If yes, number of days in ICU
integer
C0021708 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Item
Oxygen supplementation therapy?
integer
C0919655 (UMLS CUI [1])
Code List
Oxygen supplementation therapy?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
If yes, max O2 flow
text
C1960999 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
Code List
If yes, max O2 flow
CL Item
1-5 L/min (1)
CL Item
6-10 L/min (2)
CL Item
11-15 L/min (3)
CL Item
>15 L/min (4)
CL Item
Unknown (5)
Item
If yes, interface
text
C0919655 (UMLS CUI [1,1])
C0699733 (UMLS CUI [1,2])
Code List
If yes, interface
CL Item
Nasal prongs (1)
CL Item
HF nasal cannula (2)
CL Item
Mask (3)
CL Item
Mask with reservoir (4)
CL Item
CPAP/NIV mask (5)
CL Item
Unknown (6)
Oxygen supplementation therapy, number of days
Item
If yes, number of days of oxygen therapy?
integer
C0919655 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Item
Prone positioning
integer
C0919655 (UMLS CUI [1,1])
C0033422 (UMLS CUI [1,2])
Code List
Prone positioning
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Prone positioning duration
Item
If yes, duration
integer
C0033422 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item
Non-invasive ventilation (any e.g. BiPAP/CPAP)
integer
C1997883 (UMLS CUI [1])
C1956423 (UMLS CUI [2])
C0199451 (UMLS CUI [3])
Code List
Non-invasive ventilation (any e.g. BiPAP/CPAP)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
If yes, prone position?
integer
C1997883 (UMLS CUI [1,1])
C0033422 (UMLS CUI [1,2])
Code List
If yes, prone position?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Non-invasive ventilation, duration
Item
If yes, duration in days?
integer
C1997883 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item
Invasive ventilation (any)?
integer
C1868981 (UMLS CUI [1])
Code List
Invasive ventilation (any)?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Maximum PEEP
Item
If yes, maximum PEEP
integer
C0032740 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
Maximum FiO2
Item
If yes, maximum FiO2
integer
C0806909 (UMLS CUI [1,1])
C0428167 (UMLS CUI [1,2])
Maximum plateau pressure
Item
If yes, maximum plateau pressure
integer
C0806909 (UMLS CUI [1,1])
C0445176 (UMLS CUI [1,2])
Maximum PaCO2
Item
If yes, maximum PaCO2
text
C0806909 (UMLS CUI [1,1])
C1822070 (UMLS CUI [1,2])
Maximum PaO2
Item
If yes, maximum PaO2
text
C0806909 (UMLS CUI [1,1])
C0391840 (UMLS CUI [1,2])
Invasive ventilation, duration
Item
If yes, duration in days?
integer
C1868981 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item
Inotropes/Vasopressors?
integer
C0304509 (UMLS CUI [1])
C0042397 (UMLS CUI [2])
Code List
Inotropes/Vasopressors?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Inotropes/Vasopressors specification
Item
If yes, specify name
text
C0304509 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
C0042397 (UMLS CUI [2,1])
C1521902 (UMLS CUI [2,2])
Item
Extracorporal (ECMO) support
integer
C3869463 (UMLS CUI [1])
Code List
Extracorporal (ECMO) support
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Extracorporal support, duration
Item
If yes, total duration:
integer
C3869463 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item
Plasma exchange?
integer
C0032113 (UMLS CUI [1])
Code List
Plasma exchange?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
HFOV
integer
C0419017 (UMLS CUI [1])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Blood transfusion
integer
C0005841 (UMLS CUI [1])
Code List
Blood transfusion
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Renal replacement therapy (RRT) or dialysis?
integer
C0206074 (UMLS CUI [1])
C0011946 (UMLS CUI [2])
Code List
Renal replacement therapy (RRT) or dialysis?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Renal replacement therapy, dialysis duration
Item
If yes, total duration:
integer
C0206074 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Item Group
Outcome
C1547647 (UMLS CUI-1)
Item
Please select only one outcome
integer
C1547647 (UMLS CUI [1])
Code List
Please select only one outcome
CL Item
Discharged alive (1)
CL Item
Hospitalized (2)
CL Item
Transfer to other facility (3)
CL Item
Death (4)
CL Item
Left against medical advice (5)
CL Item
Unknown (6)
Outcome date
Item
Outcome date
date
C1547647 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Outcome date unknown
Item
Outcome date: unknown
boolean
C1547647 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
Item
If discharged alive: care needs at discharge versus before illness
integer
C3871203 (UMLS CUI [1,1])
C1521721 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0443172 (UMLS CUI [1,4])
Code List
If discharged alive: care needs at discharge versus before illness
CL Item
Same as before illness (1)
CL Item
Worse (2)
CL Item
Better (3)
CL Item
Unknown (4)
Item
What was the physician's impression of the final diagnosis? Multisystem inflammatory syndrome
integer
C1546485 (UMLS CUI [1,1])
C5389369 (UMLS CUI [1,2])
Code List
What was the physician's impression of the final diagnosis? Multisystem inflammatory syndrome
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Kawasaki disease
integer
C1546485 (UMLS CUI [1,1])
C0026691 (UMLS CUI [1,2])
Code List
Kawasaki disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Atypical kawasaki disease
integer
C1546485 (UMLS CUI [1,1])
C0026691 (UMLS CUI [1,2])
C0205182 (UMLS CUI [1,3])
Code List
Atypical kawasaki disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Toxic shock syndrome
integer
C1546485 (UMLS CUI [1,1])
C0600327 (UMLS CUI [1,2])
Code List
Toxic shock syndrome
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Final diagnosis: Other
Item
Other, specify:
text
C1546485 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Sequelae present at the time of discharge
Item
Were there any sequelae present at the time of discharge:
boolean
C0243088 (UMLS CUI [1,1])
C3871203 (UMLS CUI [1,2])
Sequelae at the time of discharge, specification
Item
If yes, specify
text
C0243088 (UMLS CUI [1,1])
C3871203 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])

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