Engelsk

Eligibility Criteria

6 Formulär  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    3. Subject ID, sample ID, study ID, and sample use variable obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    4. Subject ID, primary phenotype status, day when subject died in hospital, age, sex, race, primary risk factors associated with participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    5. Sample ID, body site where sample was collected, analyte type, tumor status of sample, and histological type of samples obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    6. Sample ID, body site where sample was collected, analyte type, tumor status of sample, and histological type of sample obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
Inclusion and exclusion criteria
Beskrivning

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Inclusions:
Beskrivning

Inclusions:

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
Caucasian
Beskrivning

Caucasian

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0043157
Controls: patients at-risk for development of ARDS based on the presence of an ARDS risk factor (e.g., sepsis, pneumonia, trauma, aspiration, pancreatitis, massive transfusion) but who did not develop ARDS during their hospital course.
Beskrivning

Controls: patients at-risk for development of ARDS based on the presence of an ARDS risk factor (e.g., sepsis, pneumonia, trauma, aspiration, pancreatitis, massive transfusion) but who did not develop ARDS during their hospital course.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009932
UMLS CUI [1,2]
C1444641
UMLS CUI [1,3]
C2887484
UMLS CUI [1,4]
C0035648
UMLS CUI [1,5]
C0243026
UMLS CUI [1,6]
C0030305
UMLS CUI [1,7]
C0349707
UMLS CUI [1,8]
C0032285
UMLS CUI [1,9]
C3714660
UMLS CUI [1,10]
C0456675
UMLS CUI [2,1]
C0009932
UMLS CUI [2,2]
C2887484
UMLS CUI [2,3]
C4534490
Cases: patients with ARDS as defined by: 1) acute onset with P/F <300, 2) bilateral chest infiltrates on chest radiograph, 3) absence of clinical evidence for left atrial hypertension, and 4) use of invasive positive pressure mechanical ventilation.
Beskrivning

Cases: patients with ARDS as defined by: 1) acute onset with P/F <300, 2) bilateral chest infiltrates on chest radiograph, 3) absence of clinical evidence for left atrial hypertension, and 4) use of invasive positive pressure mechanical ventilation.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1706256
UMLS CUI [1,2]
C2887484
UMLS CUI [1,3]
C1276802
UMLS CUI [1,4]
C1698575
UMLS CUI [1,5]
C3842377
UMLS CUI [1,6]
C2939072
UMLS CUI [1,7]
C0332125
UMLS CUI [1,8]
C0238705
UMLS CUI [1,9]
C2349751
Exclusions:
Beskrivning

Exclusions:

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
Metastatic cancer
Beskrivning

Metastatic cancer

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0027627
Hemodialysis dependence
Beskrivning

Hemodialysis dependence

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2939452
Hepatic failure
Beskrivning

Hepatic failure

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0085605
Immunosuppression
Beskrivning

Immunosuppression

Datatyp

boolean

Alias
UMLS CUI [1,1]
C4048329
Burns
Beskrivning

Burns

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0006434
Pregnancy
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0032961
Clinical evidence of elevated left atrial pressures
Beskrivning

Clinical evidence of elevated left atrial pressures

Datatyp

boolean

Alias
UMLS CUI [1,1]
C5554846
UMLS CUI [1,2]
C4531219
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Similar models

Eligibility Criteria

6 Formulär
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    3. Subject ID, sample ID, study ID, and sample use variable obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    4. Subject ID, primary phenotype status, day when subject died in hospital, age, sex, race, primary risk factors associated with participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    5. Sample ID, body site where sample was collected, analyte type, tumor status of sample, and histological type of samples obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
    6. Sample ID, body site where sample was collected, analyte type, tumor status of sample, and histological type of sample obtained from participants with or without acute respiratory distress syndrome and involved in the "ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)" project.
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Inclusions:
Item
Inclusions:
boolean
C1512693 (UMLS CUI [1,1])
Caucasian
Item
Caucasian
boolean
C0043157 (UMLS CUI [1,1])
Controls: patients at-risk for development of ARDS based on the presence of an ARDS risk factor (e.g., sepsis, pneumonia, trauma, aspiration, pancreatitis, massive transfusion) but who did not develop ARDS during their hospital course.
Item
Controls: patients at-risk for development of ARDS based on the presence of an ARDS risk factor (e.g., sepsis, pneumonia, trauma, aspiration, pancreatitis, massive transfusion) but who did not develop ARDS during their hospital course.
boolean
C0009932 (UMLS CUI [1,1])
C1444641 (UMLS CUI [1,2])
C2887484 (UMLS CUI [1,3])
C0035648 (UMLS CUI [1,4])
C0243026 (UMLS CUI [1,5])
C0030305 (UMLS CUI [1,6])
C0349707 (UMLS CUI [1,7])
C0032285 (UMLS CUI [1,8])
C3714660 (UMLS CUI [1,9])
C0456675 (UMLS CUI [1,10])
C0009932 (UMLS CUI [2,1])
C2887484 (UMLS CUI [2,2])
C4534490 (UMLS CUI [2,3])
Cases: patients with ARDS as defined by: 1) acute onset with P/F <300, 2) bilateral chest infiltrates on chest radiograph, 3) absence of clinical evidence for left atrial hypertension, and 4) use of invasive positive pressure mechanical ventilation.
Item
Cases: patients with ARDS as defined by: 1) acute onset with P/F <300, 2) bilateral chest infiltrates on chest radiograph, 3) absence of clinical evidence for left atrial hypertension, and 4) use of invasive positive pressure mechanical ventilation.
boolean
C1706256 (UMLS CUI [1,1])
C2887484 (UMLS CUI [1,2])
C1276802 (UMLS CUI [1,3])
C1698575 (UMLS CUI [1,4])
C3842377 (UMLS CUI [1,5])
C2939072 (UMLS CUI [1,6])
C0332125 (UMLS CUI [1,7])
C0238705 (UMLS CUI [1,8])
C2349751 (UMLS CUI [1,9])
Exclusions:
Item
Exclusions:
boolean
C0680251 (UMLS CUI [1,1])
Metastatic cancer
Item
Metastatic cancer
boolean
C0027627 (UMLS CUI [1,1])
Hemodialysis dependence
Item
Hemodialysis dependence
boolean
C2939452 (UMLS CUI [1,1])
Hepatic failure
Item
Hepatic failure
boolean
C0085605 (UMLS CUI [1,1])
Immunosuppression
Item
Immunosuppression
boolean
C4048329 (UMLS CUI [1,1])
Burns
Item
Burns
boolean
C0006434 (UMLS CUI [1,1])
Pregnancy
Item
Pregnancy
boolean
C0032961 (UMLS CUI [1,1])
Clinical evidence of elevated left atrial pressures
Item
Clinical evidence of elevated left atrial pressures
boolean
C5554846 (UMLS CUI [1,1])
C4531219 (UMLS CUI [1,2])
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