Diabetes Mellitus Absent | Diabetes Mellitus, Non-Insulin-Dependent | Acute myocardial infarction Suspected
Item
both nondiabetic patients and patients with non-insulin-requiring type 2 diabetes mellitus admitted with a suspected ami are eligible if they meet the following criteria:
boolean
C0011849 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0011860 (UMLS CUI [2])
C0155626 (UMLS CUI [3,1])
C0750491 (UMLS CUI [3,2])
Sign or Symptom Acute myocardial infarction | Electrocardiographic changes | ST segment elevated persistent Lead measurement Quantity | Left Bundle-Branch Block New
Item
signs or symptoms of ami with definite ecg changes, defined as persistent st-segment elevation (> or = than 1 mm)in two or more contiguous leads, or new left bundle branch block
boolean
C3540840 (UMLS CUI [1,1])
C0155626 (UMLS CUI [1,2])
C0855329 (UMLS CUI [2])
C2216134 (UMLS CUI [3,1])
C0524167 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0023211 (UMLS CUI [4,1])
C0205314 (UMLS CUI [4,2])
Onset of Symptoms Before Hospital visit
Item
onset of symptoms within 24 hours before hospital presentation
boolean
C0332162 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0545092 (UMLS CUI [1,4])
Capillary blood glucose measurement
Item
capillary blood glucose level on presentation > or = 8.0 mmol/l (144 mg/dl)
boolean
C0457578 (UMLS CUI [1])
Patient need for Insulin
Item
patient with conditions that require the administration of insulin, including:
boolean
C0686904 (UMLS CUI [1,1])
C0021641 (UMLS CUI [1,2])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes mellitus, defined by a documented history of diabetes mellitus before the age of 30
boolean
C0011854 (UMLS CUI [1])
Insulin regime Non-Insulin-Dependent Diabetes Mellitus
Item
type 2 diabetes mellitus that was treated with insulin prior to ami presentation
boolean
C0557978 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
Non-Insulin-Dependent Diabetes Mellitus Poorly controlled Very | Capillary blood glucose measurement | Blood glucose increased
Item
type 2 diabetes mellitus that is known to be very poorly controlled (e.g. admission capillary blood glucose > 16.0 mmol/l (288 mg/dl)or marked elevation in glucose for which the site investigator plans to treat with insulin therapy)
boolean
C0011860 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0442824 (UMLS CUI [1,3])
C0457578 (UMLS CUI [2])
C0595877 (UMLS CUI [3])
Hypoglycaemic episodes Severe
Item
a history of severe hypoglycemic episodes (defined as hypoglycemia with symptoms which the patient is unable to reverse without the assistance of another person) within the past two years
boolean
C0745153 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
End Stage Liver Disease | End Stage Liver Disease Suspected | Risk Hypoglycemia | Liver Dysfunction | Regulation Impaired Glucose homeostasis
Item
known or suspected end-stage liver disease (due to the risk of hypoglycemia in the setting of liver dysfunction and consequent impaired regulation of glucose homeostasis)
boolean
C0745744 (UMLS CUI [1])
C0745744 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0035647 (UMLS CUI [3,1])
C0020615 (UMLS CUI [3,2])
C0086565 (UMLS CUI [4])
C1327622 (UMLS CUI [5,1])
C0221099 (UMLS CUI [5,2])
C1326961 (UMLS CUI [5,3])
Shock, Cardiogenic
Item
cardiogenic shock on admission (due to the inaccuracy of glucose meter readings)
boolean
C0036980 (UMLS CUI [1])
Pregnancy
Item
documented pregnancy
boolean
C0032961 (UMLS CUI [1])
Comorbidity Limiting Life Expectancy | Malignant Neoplasms
Item
any concomitant disease (e.g. cancer) that might limit life expectancy to less than 90 days
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2])
Protocol Compliance Poor | Factor compromises Follow-up | Address Lacking | Residence Remote
Item
anticipated poor adherence with study treatments or an other factor that might jeopardize 90-day follow-up (e.g. no fixed address, long distance to hospital, etc.)
boolean
C0525058 (UMLS CUI [1,1])
C0542537 (UMLS CUI [1,2])
C1521761 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C3274571 (UMLS CUI [2,3])
C1442065 (UMLS CUI [3,1])
C0332268 (UMLS CUI [3,2])
C0237096 (UMLS CUI [4,1])
C0205157 (UMLS CUI [4,2])
Study Subject Participation Status | ST segment elevation myocardial infarction
Item
prior enrollment in this trial or current enrollment in another trial of st-segment elevation myocardial infarction
boolean
C2348568 (UMLS CUI [1])
C1536220 (UMLS CUI [2])