The Association Between Peri-Operative Hyperglycemia and Major Morbidity and Mortality
Hyperglycemia
About this trial
This is an interventional treatment trial for Hyperglycemia focused on measuring glycemic control, diabetes, obesity, comorbidities
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for non emergent surgery under either general or regional anesthesia deemed to have moderate to high physiologic stress
- Male and female subjects over the age of 18 with or without a diagnosis of diabetes mellitus
- Patients must be able to provide informed consent
Exclusion Criteria:
- Cognitively impaired
- Non-English or Spanish speaking with no relative present who is fluent in reading and comprehending English or Spanish.
- Female patients of child bearing age who have a positive pregnancy test on admission.
Sites / Locations
- University Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
intensive glycemic control
conventional glycemic control
In the intensive treatment group, continuous insulin infusion (50 IU of Novolin R [Novo Nordisk]) in 50ml of 0.9% saline via infusion pump will be started when the blood glucose level exceeds 110 mg / dL on two consecutive samples and will be adjusted to maintain the blood glucose level between 80 and 110 mg / dL. If the glucose level falls below 80 mg / dL, the insulin infusion will be tapered and discontinued.
In this group if the subject's blood glucose level should exceed 200 mg/dL the subject will be treated with a continuous insulin infusion to maintain blood glucose levels between 180-200mg/dL