Age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Vascular Surgical Procedure atherosclerotic elective Scheduled
Item
scheduled for atherosclerotic vascular elective surgery with presumed fast-track,
boolean
C0042381 (UMLS CUI [1,1])
C0333482 (UMLS CUI [1,2])
C0439608 (UMLS CUI [1,3])
C0205539 (UMLS CUI [1,4])
At risk Myocardial Ischemia
Item
cardiac ischaemic risk supported by:
boolean
C1444641 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
Myocardial Infarction Disease length
Item
history of myocardial infarction older than 1 month and/or
boolean
C0027051 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Stable angina Asymptomatic | Treatment | Treatment Absent
Item
documented stable angina (asymptomatic ± medical treatment) and/or
boolean
C0340288 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Coronary revascularisation
Item
history of coronary revascularisation, and/or
boolean
C0877341 (UMLS CUI [1])
Revised cardiac risk index
Item
surgical risk index ("lee" index) ≥ 3.
boolean
C3164217 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Unstable Angina Recent
Item
unstable angina within the last 30 days,
boolean
C0002965 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Uncontrolled hypertension
Item
non controlled arterial hypertension .
boolean
C1868885 (UMLS CUI [1])
Heart failure Severe New York Heart Association Classification
Item
severe cardiac heart failure (nyha iv)
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
Severe chronic obstructive pulmonary disease
Item
severe chronic obstructive pulmonary disease
boolean
C0730607 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial, Randomized
Item
patient already randomized in another ongoing clinical trial
boolean
C2348568 (UMLS CUI [1])
C0206034 (UMLS CUI [2])
Myocardial Infarction Recent
Item
patient with recent myocardial infarction (m.i) (less than one month )
boolean
C0027051 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patient already included in a clinical trial
boolean
C2348568 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Hypersensitivity Xenon | Propofol allergy | Allergy to sevoflurane | Desflurane allergy | Isoflurane allergy
Item
history of hypersensitivity to study drugs( i.e xenon, propofol, sevoflurane, desflurane, isoflurane)
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0043339 (UMLS CUI [2,2])
C0570632 (UMLS CUI [3])
C2711572 (UMLS CUI [4])
C0570641 (UMLS CUI [5])
C0570639 (UMLS CUI [6])
Malignant fever
Item
malignant hyperthermia
boolean
C2930828 (UMLS CUI [1])
Intracranial Hypertension
Item
documented elevated intracranial pressure
boolean
C0151740 (UMLS CUI [1])
Pre-Eclampsia | Eclampsia
Item
preeclampsia or eclampsia
boolean
C0032914 (UMLS CUI [1])
C0013537 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnancy and lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Uncooperative behavior Suspected | Legal capacity Lacking
Item
presumed uncooperativeness or legal incapacity
boolean
C0424350 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0683673 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])