Eligibility criteria

  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Descrizione

Inclusion Criteria

adults > 18 years
Descrizione

adults > 18 years

Tipo di dati

boolean

Alias
UMLS CUI-1
C0001779
able to give informed consent
Descrizione

able to give informed consent

Tipo di dati

boolean

Alias
UMLS CUI-1
C0021430
a history of chest pain
Descrizione

a history of chest pain

Tipo di dati

boolean

Alias
UMLS CUI-1
C0008031
other symptoms suggestive of an ACS leading to admission at the emergency unit
Descrizione

other symptoms suggestive of an ACS leading to admission at the emergency unit

Tipo di dati

boolean

Alias
UMLS CUI-1
C0948089
Exclusion Criteria
Descrizione

Exclusion Criteria

< 18 years of age
Descrizione

< 18 years of age

Tipo di dati

boolean

Alias
UMLS CUI-1
C0001779
Unwillingness or incapacity to provide informed consent
Descrizione

Unwillingness or incapacity to provide informed consent

Tipo di dati

boolean

Alias
UMLS CUI-1
C0021430
Prior admission resulting in inclusion in the present study
Descrizione

Prior admission resulting in inclusion in the present study

Tipo di dati

boolean

Alias
UMLS CUI-1
C0422740

Similar models

Eligibility criteria

  1. StudyEvent: ODM
    1. Eligibility criteria
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion Criteria
Age
Item
adults > 18 years
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
able to give informed consent
boolean
C0021430 (UMLS CUI-1)
Chest pain
Item
a history of chest pain
boolean
C0008031 (UMLS CUI-1)
Acute coronary syndrome
Item
other symptoms suggestive of an ACS leading to admission at the emergency unit
boolean
C0948089 (UMLS CUI-1)
Item Group
Exclusion Criteria
Age
Item
< 18 years of age
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
Unwillingness or incapacity to provide informed consent
boolean
C0021430 (UMLS CUI-1)
Study patient
Item
Prior admission resulting in inclusion in the present study
boolean
C0422740 (UMLS CUI-1)