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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.

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.
pht003601
Beskrivning

pht003601

Alias
UMLS CUI [1,1]
C3846158
De-identified subject ID
Beskrivning

subject_id

Datatyp

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348585
ALI or no ALI
Beskrivning

primary_phenotype_status

Datatyp

text

Alias
UMLS CUI [1,1]
C0242488
Severity of ALI based on VFD count
Beskrivning

secondary_phenotype_status

Datatyp

text

Måttenheter
  • categorical
Alias
UMLS CUI [1,1]
C0242488
UMLS CUI [1,2]
C0439793
UMLS CUI [1,3]
C0750480
Vent-Free Days during 28-day hospital stay [from 1-129 days]
Beskrivning

VFD

Datatyp

text

Måttenheter
  • Days
Alias
UMLS CUI [1,1]
C0556971
UMLS CUI [1,2]
C0332296
UMLS CUI [1,3]
C0199470
Day subject died in hospital [1-29 day of death]
Beskrivning

death_day

Datatyp

text

Måttenheter
  • Days
Alias
UMLS CUI [1,1]
C0421616
UMLS CUI [1,2]
C0872291
UMLS CUI [1,3]
C0439228
Age [18-90 years old]
Beskrivning

yoa

Datatyp

text

Måttenheter
  • Years
Alias
UMLS CUI [1,1]
C0001779
Sex
Beskrivning

gender

Datatyp

text

Alias
UMLS CUI [1,1]
C0079399
Race
Beskrivning

race

Datatyp

text

Alias
UMLS CUI [1,1]
C0034510
Primary risk factor trauma
Beskrivning

trauma

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C3714660
Primary risk factor sepsis
Beskrivning

sepsis

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0243026
Primary risk factor-transfusion
Beskrivning

transf

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C1879316
Primary risk factor aspiration
Beskrivning

aspir

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C2712334
Primary risk factor pneumonia
Beskrivning

pneumo

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0032285
Primary risk factor other
Beskrivning

other

Datatyp

text

Alias
UMLS CUI [1,1]
C0035648
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0205394
Original source of samples
Beskrivning

source_site

Datatyp

text

Alias
UMLS CUI [1,1]
C0205313
UMLS CUI [1,2]
C0449416
UMLS CUI [1,3]
C0370003
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Similar models

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.

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
pht003601
C3846158 (UMLS CUI [1,1])
subject_id
Item
De-identified subject ID
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Item
ALI or no ALI
text
C0242488 (UMLS CUI [1,1])
primary_phenotype_status
Code List
ALI or no ALI
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Severity of ALI based on VFD count
text
C0242488 (UMLS CUI [1,1])
C0439793 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
secondary_phenotype_status
Code List
Severity of ALI based on VFD count
CL Item
Not applicable (0)
C1272460 (UMLS CUI [1,1])
CL Item
Low VFD (severe) (1)
CL Item
High VFD (mild) (2)
Item
Vent-Free Days during 28-day hospital stay [from 1-129 days]
text
C0556971 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
C0199470 (UMLS CUI [1,3])
VFD
Code List
Vent-Free Days during 28-day hospital stay [from 1-129 days]
CL Item
Missing (-99)
Item
Day subject died in hospital [1-29 day of death]
text
C0421616 (UMLS CUI [1,1])
C0872291 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
death_day
Code List
Day subject died in hospital [1-29 day of death]
CL Item
Missing (-99)
CL Item
Survived (0)
Item
Age [18-90 years old]
text
C0001779 (UMLS CUI [1,1])
yoa
Code List
Age [18-90 years old]
CL Item
Missing (-99)
Item
Sex
text
C0079399 (UMLS CUI [1,1])
gender
Code List
Sex
CL Item
Missing (-99)
CL Item
Male (1)
C0086582 (UMLS CUI [1,1])
CL Item
Female (2)
C0086287 (UMLS CUI [1,1])
Item
Race
text
C0034510 (UMLS CUI [1,1])
race
Code List
Race
CL Item
Missing (-99)
CL Item
Caucasian (1)
CL Item
African American (2)
CL Item
Hispanic (3)
CL Item
Asian+Islander (4)
CL Item
Native (5)
CL Item
No race (6)
C0034510 (UMLS CUI [1,1])
Item
Primary risk factor trauma
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C3714660 (UMLS CUI [1,3])
trauma
Code List
Primary risk factor trauma
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Primary risk factor sepsis
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0243026 (UMLS CUI [1,3])
sepsis
Code List
Primary risk factor sepsis
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Primary risk factor-transfusion
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C1879316 (UMLS CUI [1,3])
transf
Code List
Primary risk factor-transfusion
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Primary risk factor aspiration
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C2712334 (UMLS CUI [1,3])
aspir
Code List
Primary risk factor aspiration
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Primary risk factor pneumonia
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0032285 (UMLS CUI [1,3])
pneumo
Code List
Primary risk factor pneumonia
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Primary risk factor other
text
C0035648 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
other
Code List
Primary risk factor other
CL Item
Missing (-99)
CL Item
NO (0)
CL Item
YES (1)
Item
Original source of samples
text
C0205313 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,3])
source_site
Code List
Original source of samples
CL Item
HSPH_HarvardSchoolPublicHealth (1)
CL Item
ARDSnet (2)
CL Item
Vanderbilt (3)
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