Eligibility Cardiovascular Disease NCT00860925

1 moduli

StudyEvent: Eligibility
1. Eligibility Cardiovascular Disease NCT00860925

Name

genere

Description | Question | Decode (Coded Value)

Tipo di dati

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

Operative Surgical Procedures | Exception Cardiac Surgery

Item

patients undergoing noncardiac surgery who fulfill the following criteria:

boolean

C0543467 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0018821 (UMLS CUI [2,2])

Age

Item

age ≥ 45 years

boolean

C0001779 (UMLS CUI [1])

Hospital admission Overnight Postoperative Expected | Operative Surgical Procedures | Exception Cardiac Surgery

Item

expected to require at least an overnight hospital admission after noncardiac surgery, and fulfill any 1 of the following criteria:

boolean

C0184666 (UMLS CUI [1,1])
C0439583 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
C1517001 (UMLS CUI [1,4])
C0543467 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0018821 (UMLS CUI [3,2])

Coronary Artery Disease

Item

history of coronary artery disease

boolean

C1956346 (UMLS CUI [1])

Peripheral Vascular Diseases

Item

peripheral vascular disease

boolean

C0085096 (UMLS CUI [1])

Cerebrovascular accident

Item

stroke

boolean

C0038454 (UMLS CUI [1])

Vascular Surgical Procedures Major | Vascular Surgical Procedures | Exception Arteriovenous shunt | Exception Stripping of vein | Exception Carotid Endarterectomy

Item

undergoing major vascular surgery (i.e., vascular surgery except arteriovenous shunt, vein stripping procedures, and carotid endarterectomies)

boolean

C0042381 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0042381 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0684204 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0149807 (UMLS CUI [4,2])
C1705847 (UMLS CUI [5,1])
C0014099 (UMLS CUI [5,2])

Risk Criteria Quantity

Item

or any 3 of 9 risk criteria:

boolean

C0035647 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])

Major surgery | Operative Surgical Procedures Intraperitoneal | Thoracic Surgical Procedures | Orthopedic Surgical Procedures

Item

1. undergoing major surgery [i.e., intraperitoneal, intrathoracic, or orthopedic surgery]

boolean

C0679637 (UMLS CUI [1])
C0543467 (UMLS CUI [2,1])
C0442120 (UMLS CUI [2,2])
C0524832 (UMLS CUI [3])
C1136201 (UMLS CUI [4])

Congestive heart failure

Item

2. history of congestive heart failure

boolean

C0018802 (UMLS CUI [1])

Transient Ischemic Attack

Item

3. transient ischemic attack

boolean

C0007787 (UMLS CUI [1])

Diabetes Mellitus | Oral hypoglycemic | Insulin

Item

4. diabetes and currently taking an oral hypoglycemic agent or insulin

boolean

C0011849 (UMLS CUI [1])
C0359086 (UMLS CUI [2])
C0021641 (UMLS CUI [3])

Age

Item

5. age = or > than 70 years

boolean

C0001779 (UMLS CUI [1])

Hypertensive disease

Item

6. hypertension

boolean

C0020538 (UMLS CUI [1])

Creatinine measurement, serum

Item

7. serum creatinine > 175 µmol/l

boolean

C0201976 (UMLS CUI [1])

Tobacco use

Item

8. history of smoking within 2 years of surgery, or

boolean

C0543414 (UMLS CUI [1])

Emergency surgery

Item

9. undergoing emergent/urgent surgery

boolean

C4264510 (UMLS CUI [1])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

Aspirin

Item

patients has taken asa < or = to 72 hours before scheduled surgery

boolean

C0004057 (UMLS CUI [1])

Aspirin allergy | Clonidine allergy

Item

history of asa or clonidine hypersensitivity or allergy

boolean

C0004058 (UMLS CUI [1])
C0570975 (UMLS CUI [2])

Systolic Pressure

Item

systolic blood pressure < 105 mm hg

boolean

C0871470 (UMLS CUI [1])

Heart rate

Item

heart rate < 55 beats per minute

boolean

C0018810 (UMLS CUI [1])

Second degree atrioventricular block | Complete atrioventricular block | Artificial cardiac pacemaker Absent

Item

second or third degree heart block without a pacemaker

boolean

C0264906 (UMLS CUI [1])
C0151517 (UMLS CUI [2])
C0030163 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])

Peptic Ulcer

Item

patient has active peptic ulcer disease

boolean

C0030920 (UMLS CUI [1])

Bare metal stent

Item

patient has had a bare metal stent in the six weeks prior to randomization

boolean

C2825200 (UMLS CUI [1])

Drug-Eluting Stents

Item

patient has had a drug eluting stent in the year prior to randomization

boolean

C1322815 (UMLS CUI [1])

Alpha 2 agonist | alpha-methyldopa | Reserpine | clopidogrel | Ticlopidine

Item

patient is currently taking an alpha-2 agonist, alpha methyldopa, reserpine, clopidogrel, or ticlopidine

boolean

C1268904 (UMLS CUI [1])
C0025741 (UMLS CUI [2])
C0035179 (UMLS CUI [3])
C0070166 (UMLS CUI [4])
C0040207 (UMLS CUI [5])

Intracranial surgery | Carotid Endarterectomy | Operation on retina

Item

patient undergoing intracranial surgery, carotid endarterectomy, or retinal surgery

boolean

C0745377 (UMLS CUI [1])
C0014099 (UMLS CUI [2])
C0197770 (UMLS CUI [3])

Study Subject Participation Status Surgeon Unwilling | Clonidine Trial perioperative | Aspirin Trial perioperative

Item

surgeon unwilling to have patient participate in a participate in a perioperative clonidine/asa trial

boolean

C2348568 (UMLS CUI [1,1])
C0582175 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0009014 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C1518988 (UMLS CUI [2,3])
C0004057 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C1518988 (UMLS CUI [3,3])

Enrollment Clinical Trial Specified

Item

prior enrolment in the poise-2 pilot trial

boolean

C1516879 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])

Informed Consent Unable | Informed Consent Refused

Item

unable to obtain or refusal to consent prior to surgery

boolean

C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])

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Eligibility Cardiovascular Disease NCT00860925