age at least 18 Years
Item
age at least 18 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Severe sepsis or septic shock according to ACCP/SCCM criteria
Item
Severe sepsis or septic shock according to ACCP/SCCM criteria
boolean
C1719672 (UMLS CUI 2011AA)
R65.2 (ICD-10-CM Version 2010)
995.92 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0036983 (UMLS CUI 2011AA)
76571007 (SNOMED CT 2011_0131)
10040070 (MedDRA 14.1)
785.52 (ICD-9-CM Version 2011)
C0332290 (UMLS CUI 2011AA)
385433004 (SNOMED CT 2011_0131)
C0596070 (UMLS CUI 2011AA)
C0557806 (UMLS CUI 2011AA)
224864007 (SNOMED CT 2011_0131)
C0586857 (UMLS CUI 2011AA)
309345004 (SNOMED CT 2011_0131)
C0037459 (UMLS CUI 2011AA)
C1319411 (UMLS CUI 2011AA)
408478003 (SNOMED CT 2011_0131)
CL414621 (UMLS CUI 2011AA)
Onset of severe sepsis or septic shock <24 h
Item
Onset of severe sepsis or septic shock <24 h
boolean
C0332162 (UMLS CUI 2011AA)
77374008 (SNOMED CT 2011_0131)
C1719672 (UMLS CUI 2011AA)
R65.2 (ICD-10-CM Version 2010)
995.92 (ICD-9-CM Version 2011)
C0036983 (UMLS CUI 2011AA)
76571007 (SNOMED CT 2011_0131)
10040070 (MedDRA 14.1)
785.52 (ICD-9-CM Version 2011)
C0439092 (UMLS CUI 2011AA)
276139006 (SNOMED CT 2011_0131)
LT (HL7 V3 2006_05)
C0205447 (UMLS CUI 2011AA)
38112003 (SNOMED CT 2011_0131)
C0439228 (UMLS CUI 2011AA)
258703001 (SNOMED CT 2011_0131)
D (HL7 V3 2006_05)
Informed consent
Item
Informed Consent
boolean
C0021430 (UMLS CUI 2011AA)
Pregnant or breast-feeding women
Item
Pregnant or breast-feeding women
boolean
C0549206 (UMLS CUI 1)
10036586 (MedDRA 1)
C0006147 (UMLS CUI 2)
10006247 (MedDRA 2)
Fertile female women without effective contraception
Item
Fertile female women without effective contraception
boolean
CL426012 (UMLS CUI 2011AA)
C0043210 (UMLS CUI 2011AA)
224526002 (SNOMED CT 2011_0131)
C0332197 (UMLS CUI 2011AA)
2667000 (SNOMED CT 2011_0131)
C0700589 (UMLS CUI 2011AA)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
Participation in interventional clinical trial within the last 30 days
Item
Participation in interventional clinical trial within the last 30 days
boolean
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
CL432484 (UMLS CUI 2011AA)
Current participation in any study
Item
Current participation in any study
boolean
C0521116 (UMLS CUI 2011AA)
15240007 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
CL407060 (UMLS CUI 2011AA)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Former participation in this trial
Item
Former participation in this trial
boolean
C2348568 (UMLS CUI 2011AA)
Selenium intoxication
Item
Selenium intoxication
boolean
C0036581 (UMLS CUI 2011AA)
22038003 (SNOMED CT 2011_0131)
MTHU007657 (LOINC Version 232)
C0728899 (UMLS CUI 2011AA)
75478009 (SNOMED CT 2011_0131)
10022727 (MedDRA 14.1)
No commitment to full patient support (i.e. DNR order)
Item
No commitment to full patient support (i.e. DNR order)
boolean
C1705492 (UMLS CUI 2011AA)
C0680240 (UMLS CUI 2011AA)
C0030705 (UMLS CUI 2011AA)
116154003 (SNOMED CT 2011_0131)
C1521721 (UMLS CUI 2011AA)
C0079252 (UMLS CUI 2011AA)
Patient's death is considered imminent due to coexisting disease
Item
Patient's death is considered imminent due to coexisting disease
boolean
C2363727 (UMLS CUI 2011AA)
10068311 (MedDRA 14.1)
CL420107 (UMLS CUI 2011AA)
C0243087 (UMLS CUI 2011AA)
Relationship of the patient to study team member (i.e. colleague, relative)
Item
Relationship of the patient to study team member (i.e. colleague, relative)
boolean
C0699792 (UMLS CUI 2011AA)
263498003 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C1552089 (UMLS CUI 2011AA)
STF (HL7 V3 2006_05)
C0681088 (UMLS CUI 2011AA)
C0080103 (UMLS CUI 2011AA)
125677006 (SNOMED CT 2011_0131)
Infection where guidelines recommend a longer duration of antimicrobial therapy (i.e. endocarditis, tuberculosis, malaria etc)
Item
Infection where guidelines recommend a longer duration of antimicrobial therapy (i.e. endocarditis, tuberculosis, malaria etc)
boolean
C0021311 (UMLS CUI 2011AA)
257551009 (SNOMED CT 2011_0131)
10021789 (MedDRA 14.1)
C0034866 (UMLS CUI 2011AA)
MTHU036724 (LOINC Version 232)
RMD (HL7 V3 2006_05)
C1136254 (UMLS CUI 2011AA)
250428009 (SNOMED CT 2011_0131)
MTHU014499 (LOINC Version 232)
C0039798 (UMLS CUI 2011AA)
C0014118 (UMLS CUI 2011AA)
56819008 (SNOMED CT 2011_0131)
10014665 (MedDRA 14.1)
424.90 (ICD-9-CM Version 2011)
C0041296 (UMLS CUI 2011AA)
56717001 (SNOMED CT 2011_0131)
10044755 (MedDRA 14.1)
MTHU020835 (LOINC Version 232)
A15-A19 (ICD-10-CM Version 2010)
010-018.99 (ICD-9-CM Version 2011)
C0024530 (UMLS CUI 2011AA)
61462000 (SNOMED CT 2011_0131)
10025487 (MedDRA 14.1)
B54 (ICD-10-CM Version 2010)
084.6 (ICD-9-CM Version 2011)
Immunocompromised patients
Item
Patient immunocompromised
boolean
C0085393 (UMLS CUI 2011AA)
370388006 (SNOMED CT 2011_0131)