ID
42513
Descripción
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
Palabras clave
Versiones (1)
- 11/8/21 11/8/21 -
Titular de derechos de autor
ISARIC on behalf of Oxford University
Subido en
11 de agosto de 2021
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-SA 4.0
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Multisystem inflammatory syndrome (MIS) in children and adolescents temporally related to COVID-19
MODULE 2: OUTCOME CASE REPORT FORM
- StudyEvent: ODMjoin
Descripción
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
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015967
Descripción
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/
Tipo de datos
float
Unidades de medida
- °C
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0439237
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Descripción
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/
Tipo de datos
float
Unidades de medida
- F
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0456628
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0184666
Descripción
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/
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0806909
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Descripción
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".
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
Descripción
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/
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0184666
- UMLS CUI [1,4]
- C1272460
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015230
Descripción
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/
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0015230
- UMLS CUI [1,2]
- C0332307
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0238767
- UMLS CUI [1,2]
- C0009763
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0026639
- UMLS CUI [1,2]
- C0021368
Descripción
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.
Tipo de datos
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
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0020649
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0039231
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0439590
- UMLS CUI [1,2]
- C0425716
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0151907
- UMLS CUI [2,1]
- C0302133
- UMLS CUI [2,2]
- C1123023
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0857073
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1287298
- UMLS CUI [1,2]
- C1532580
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0008031
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0231835
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0476273
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0000737
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0011991
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0042963
Descripción
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/
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
Descripción
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/
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C2348519
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Descripción
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
Descripción
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.
Tipo de datos
float
Unidades de medida
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0518015
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0023508
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0948762
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0948762
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0200635
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0200635
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- %
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0018935
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0018935
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- x10^9/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0032181
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0032181
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0030605
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C1272061
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0030605
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C1272061
- UMLS CUI [2,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- sec
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0033707
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0033707
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0525032
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0525032
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- g/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0016006
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0016006
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- ng/mL
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1535922
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mg/L
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201657
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mm/hr
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1176468
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mg/L
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2826333
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- pg/mL
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0919829
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- pg/mL
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0085295
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- umol/L
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337443
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0337443
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202194
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202194
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0005845
- UMLS CUI [2,1]
- C1522410
- UMLS CUI [2,2]
- C0523961
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0005845
- UMLS CUI [1,2]
- C1272696
- UMLS CUI [2,1]
- C0523961
- UMLS CUI [2,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mmol/L
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0337438
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0337438
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- pg/mL
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C3272900
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- ng/mL
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0523952
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- U/L
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201973
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- U/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0202236
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202236
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- U/L
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- umol/L
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- U/L
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- g/dL
Alias
- UMLS CUI [1,1]
- C1522166
- UMLS CUI [1,2]
- C0201838
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201838
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- mmol/L
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1522410
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202113
- UMLS CUI [1,2]
- C1272696
Descripción
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.
Tipo de datos
float
Unidades de medida
- ng/mL
Alias
- UMLS CUI [1,1]
- C1522410
- UMLS CUI [1,2]
- C0373607
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0373607
- UMLS CUI [1,2]
- C1272696
Descripción
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
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0039985
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0243095
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0202823
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0243095
- UMLS CUI [1,3]
- C0332448
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0202823
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0243095
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0013516
Descripción
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.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0340515
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0031046
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C0018826
- UMLS CUI [1,3]
- C0021368
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0013516
- UMLS CUI [1,2]
- C1704258
- UMLS CUI [1,3]
- C1522318
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0013798
Descripción
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.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C1522166
- UMLS CUI [1,3]
- C0011008
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C0243095
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
Descripción
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.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2936236
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0011008
Descripción
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.
Tipo de datos
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
Descripción
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.
Tipo de datos
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
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C0039593
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C0450254
- UMLS CUI [1,3]
- C1446409
- UMLS CUI [1,4]
- C1521902
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0599161
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [1,4]
- C1515974
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0729856
Descripción
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.
Tipo de datos
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
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0368676
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C0014441
- UMLS CUI [1,3]
- C0475208
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C5203676
- UMLS CUI [1,2]
- C4054524
- UMLS CUI [1,3]
- C0475208
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1521902
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C5203676
- UMLS CUI [1,3]
- C0039593
- UMLS CUI [1,4]
- C1274040
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0450254
- UMLS CUI [1,2]
- C0521026
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1521902
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C5203670
- UMLS CUI [1,2]
- C0332140
Descripción
Treatment: at any time during the hospital admission, did the patient receive any of the following:
Alias
- UMLS CUI-1
- C0087111
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C2013463
- UMLS CUI [2,1]
- C0349717
- UMLS CUI [2,2]
- C0429791
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1289919
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0003451
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0035525
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0674432
- UMLS CUI [2]
- C0292818
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3541969
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1609165
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0245109
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0022322
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0002199
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0015980
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C4726677
Descripción
Other Antiviral agent
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0003451
- UMLS CUI [1,3]
- C1521902
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0239126
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0027365
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0239126
- UMLS CUI [1,2]
- C0013153
Descripción
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.
Tipo de datos
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
Descripción
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.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0239126
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0239126
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0239126
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0085297
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C2348070
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Descripción
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.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0808070
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0085297
- UMLS CUI [1,2]
- C0449238
Descripción
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.
Tipo de datos
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
Descripción
‘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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0338237
Descripción
‘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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0450442
Descripción
Antibiotic therapy - duration
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
Descripción
Antibiotic therapy duration unknown
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0338237
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [1,3]
- C0439673
Descripción
‘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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0003308
Descripción
Supportive care
Alias
- UMLS CUI-1
- C0344211
Descripción
At any time during the hospital admission, did the patient receive any of the following:
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0583239
- UMLS CUI [2]
- C1301858
Descripción
At any time during the hospital admission, did the patient receive any of the following:
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0021708
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0919655
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1960999
- UMLS CUI [1,2]
- C0806909
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0699733
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C1265611
Descripción
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’.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0919655
- UMLS CUI [1,2]
- C0033422
Descripción
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’.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0033422
- UMLS CUI [1,2]
- C0449238
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1997883
- UMLS CUI [2]
- C1956423
- UMLS CUI [3]
- C0199451
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0033422
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C1997883
- UMLS CUI [1,2]
- C0449238
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1868981
Descripción
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.
Tipo de datos
integer
Unidades de medida
- cm H2O
Alias
- UMLS CUI [1,1]
- C0032740
- UMLS CUI [1,2]
- C0806909
Descripción
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.
Tipo de datos
integer
Unidades de medida
- %
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0428167
Descripción
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.
Tipo de datos
integer
Unidades de medida
- cm H2O
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0445176
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C1822070
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0806909
- UMLS CUI [1,2]
- C0391840
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C1868981
- UMLS CUI [1,2]
- C0449238
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0304509
- UMLS CUI [2]
- C0042397
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0304509
- UMLS CUI [1,2]
- C1521902
- UMLS CUI [2,1]
- C0042397
- UMLS CUI [2,2]
- C1521902
Descripción
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3869463
Descripción
At any time during the hospital admission, did the patient receive any of the following: ECMO refers to Extra Corporeal Membrane Oxygenation.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C3869463
- UMLS CUI [1,2]
- C0449238
Descripción
At any time during the hospital admission, did the patient receive any of the following:
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0032113
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0419017
Descripción
At any time during the hospital admission, did the patient receive any of the following: Blood transfusion is the administration of any blood product.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0005841
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0206074
- UMLS CUI [2]
- C0011946
Descripción
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.
Tipo de datos
integer
Unidades de medida
- days
Alias
- UMLS CUI [1,1]
- C0206074
- UMLS CUI [1,2]
- C0449238
- UMLS CUI [2,1]
- C0011946
- UMLS CUI [2,2]
- C0449238
Descripción
Outcome
Alias
- UMLS CUI-1
- C1547647
Descripción
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.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1547647
Descripción
Please state the date for the outcome listed above.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
Descripción
Please state the date for the outcome listed above.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0439673
Descripción
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’).
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C3871203
- UMLS CUI [1,2]
- C1521721
- UMLS CUI [1,3]
- C1514873
- UMLS CUI [1,4]
- C0443172
Descripción
Clinician assessment of diagnosis on death or discharge.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C5389369
Descripción
Clinician assessment of diagnosis on death or discharge.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
Descripción
Clinician assessment of diagnosis on death or discharge.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0026691
- UMLS CUI [1,3]
- C0205182
Descripción
Clinician assessment of diagnosis on death or discharge. Please specify if a final diagnosis not listed above was given.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0600327
Descripción
Clinician assessment of diagnosis on death or discharge.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1546485
- UMLS CUI [1,2]
- C0205394
Descripción
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0243088
- UMLS CUI [1,2]
- C3871203
Descripción
Specify if the patient had any remaining sequelae from this illness episode at the time of discharge, as assessed by a physician/clinician.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0243088
- UMLS CUI [1,2]
- C3871203
- UMLS CUI [1,3]
- C1521902
Similar models
MODULE 2: OUTCOME CASE REPORT FORM
- StudyEvent: ODMjoin
C2348519 (UMLS CUI-2)
C0205210 (UMLS CUI-3)
C0521116 (UMLS CUI-4)
C0221423 (UMLS CUI-5)
C0439237 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
C0456628 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0184666 (UMLS CUI [1,4])
C0806909 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,3])
C1272460 (UMLS CUI [1,4])
C0332307 (UMLS CUI [1,2])
C0009763 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,2])
C0221912 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,3])
C0037088 (UMLS CUI [1,4])
C0018563 (UMLS CUI [1,5])
C0205100 (UMLS CUI [2,1])
C0221912 (UMLS CUI [2,2])
C0021368 (UMLS CUI [2,3])
C0037088 (UMLS CUI [2,4])
C0016504 (UMLS CUI [2,5])
C0425716 (UMLS CUI [1,2])
C0302133 (UMLS CUI [2,1])
C1123023 (UMLS CUI [2,2])
C1532580 (UMLS CUI [1,2])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348519 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0518015 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0948762 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0200635 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0018935 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0032181 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0030605 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C1272061 (UMLS CUI [2,2])
C1272696 (UMLS CUI [1,2])
C1272061 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
C0033707 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0525032 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0016006 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0337443 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0202194 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0005845 (UMLS CUI [1,2])
C1522410 (UMLS CUI [2,1])
C0523961 (UMLS CUI [2,2])
C1272696 (UMLS CUI [1,2])
C0523961 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
C0337438 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0202236 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0201838 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C1522410 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0373607 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0450254 (UMLS CUI-2)
C0039593 (UMLS CUI-3)
C0243095 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,2])
C0332448 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0340515 (UMLS CUI [1,2])
C0031046 (UMLS CUI [1,2])
C0018826 (UMLS CUI [1,2])
C0021368 (UMLS CUI [1,3])
C1704258 (UMLS CUI [1,2])
C1522318 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0243095 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C2936236 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1274040 (UMLS CUI [2,3])
C1521902 (UMLS CUI [2,4])
C1522166 (UMLS CUI [2,5])
C0205394 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
C0450254 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C0450254 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0599161 (UMLS CUI [1,2])
C0599161 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C1515974 (UMLS CUI [1,4])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
C0456962 (UMLS CUI [1,2])
C0729856 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,4])
C1515974 (UMLS CUI [1,5])
C0456962 (UMLS CUI [1,2])
C0368676 (UMLS CUI [1,3])
C0014441 (UMLS CUI [1,2])
C0014441 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
C4054524 (UMLS CUI [1,2])
C4054524 (UMLS CUI [1,2])
C0475208 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C5203676 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0521026 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0332140 (UMLS CUI [1,2])
C0349717 (UMLS CUI [2,1])
C0429791 (UMLS CUI [2,2])
C0292818 (UMLS CUI [2])
C0003451 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0027365 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C0239126 (UMLS CUI [2,1])
C0806909 (UMLS CUI [2,2])
C1519795 (UMLS CUI [2,3])
C0239126 (UMLS CUI [1,2])
C0239126 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,2])
C0239126 (UMLS CUI [1,3])
C2348070 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C0085297 (UMLS CUI [2,1])
C0806909 (UMLS CUI [2,2])
C1519795 (UMLS CUI [2,3])
C0450442 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C1301858 (UMLS CUI [2])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0439228 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0033422 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C1956423 (UMLS CUI [2])
C0199451 (UMLS CUI [3])
C0033422 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C0428167 (UMLS CUI [1,2])
C0445176 (UMLS CUI [1,2])
C1822070 (UMLS CUI [1,2])
C0391840 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0042397 (UMLS CUI [2])
C1521902 (UMLS CUI [1,2])
C0042397 (UMLS CUI [2,1])
C1521902 (UMLS CUI [2,2])
C0449238 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2])
C0449238 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C1521721 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0443172 (UMLS CUI [1,4])
C5389369 (UMLS CUI [1,2])
C0026691 (UMLS CUI [1,2])
C0026691 (UMLS CUI [1,2])
C0205182 (UMLS CUI [1,3])
C0600327 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C3871203 (UMLS CUI [1,2])
C3871203 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])