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| Name | Class |
|---|---|
| Fundação de Amparo à Pesquisa do Estado de São Paulo | OTHER_GOV |
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To evaluate the efficacy and safety of three insulin algorithms in medical ICU patients (MICU).
Strict glycemic control has been recommended for critically ill patients. However, its implementation may face difficulties with increased nursing workload, inadequate glucose control and higher risk of hypoglycemia.
We designed a computer guided protocol to adjust endovenous insulin infusion aiming glucose levels between 100mg/dl and 130 mg/dl. This trial evaluates the efficacy and safety of this protocol (algorithm A), compared to a standard endovenous insulin infusion protocol (algorithm B) and a conventional subcutaneous insulin protocol (algorithm C).
Methods : MICU patients with at least one blood glucose ≥ 150 mg/dL and who are on mechanical ventilation, or had SIRS, or are admitted because of trauma or burn will be randomized to one of the following treatments: algorithm A - continuous insulin infusion with adjustments guided by hand held device or desktop software targeting glucose levels between 100mg/dL-130mg/dL; algorithm B - continuous insulin aiming glucose levels between 80mg/dl-110mg/dl using Van den Berghe's insulin protocol; algorithm C - conventional treatment - intermittent subcutaneous administration of insulin if blood glucose levels exceeds 150mg/dL; insulin will be administered as IV boluses in hypotensive patients.
The randomization list was generated in blocks of six by computer software. Patients will be randomly assigned in a 1:1:1 ratio to have their glucose controlled by one of the three insulin algorithms with the use of a central, computerized system accessed by Internet, permitting concealment of allocation list. Randomization will be stratified according to study site.
The study is planned to enroll 165 patients in order to have 80% power to detect a 20mg/dl difference in blood glucose means between groups, assuming standard deviation equal to 33 mg/dl and two-tailed alpha equal to 0.05. Efficacy will be measured by the mean of patients' median blood glucose and safety measured by the incidence of hypoglycemia (≤40 mg/dL). Analysis will follow the intention-to-treat principle.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| A | Experimental |
| |
| B | Experimental |
| |
| C | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Computer-assisted IV insulin infusion protocol (algorithm A) | Procedure | Computer assisted insulin protocol (CAIP), with continuous intravenous insulin adjustments aiming blood glucose levels between 100 mg/dl and 130 mg/dl. |
| Measure | Description | Time Frame |
|---|---|---|
| Efficacy: mean of patients' median blood glucose during ICU stay | ICU Stay | |
| Safety: incidence of hypoglycemia (≤40 mg/dL)during ICU stay | ICU stay |
| Measure | Description | Time Frame |
|---|---|---|
| Death from any cause | ICU and in-hospital | |
| ICU and hospital length of stay | ICU and in-hospital | |
| Five-day variation in SOFA score |
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Inclusion Criteria:
Criteria 1, 2 and 3 must be present:
Clinical patients admitted to an Intensive Care Unit
At least one blood glucose measurement >= 150 mg/dL (capilar, venous or arterial blood)
At least one of the following:
Patient on mechanical ventilation for an acute process, with expected duration of mechanical ventilation of at least 24 hours
Polytrauma patients
Severe burn patients
Systemic Inflammatory Response Syndrome (modified criteria), with at least three of the following: core temperature >=38°C or <=36°C; heart rate >=90 beats/min, except in patients with a medical condition or receiving a medication known to prevent tachycardia; respiratory heart rate >= 20 breaths/min or a PaCO2 <=32mmHg, or the use of mechanical ventilation for an acute process; white-cell count of >=12.000/mm3 or <=4.000/mm3 or a differential count showing >10% percent immature neutrophils
Exclusion Criteria:
Age < 21 years
Surgical patients (surgery less than 24hs before admission to ICU)
Diabetic ketoacidosis
Non-ketotic hyperosmolar state
Patients with defined diagnosis of brain death
Moribund state in which death is perceived to be imminent
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| Name | Affiliation | Role |
|---|---|---|
| Alexandre B Cavalcanti, MD | Hospital Israelita Albert Einstein | Study Chair |
| Eliezer Silva, PhD | Hospital Israelita Albert Einstein | Study Director |
| Jose Eluf-Neto, PhD | Departamento de Medicina Preventiva, Faculdade de Medicina da Universidade de Sao Paulo | Study Director |
| Milton Caldeira, MD | Hospital Regional Sao Jose | Principal Investigator |
| Glauco Westphal, MD | Centro Hospitalar UNIMED | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Complexo Hospitalar UNIMED | Joinville | Santa Catarina | Brazil | |||
| Hospital Dona Helena |
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| Leuven Strict glycemic control protocol (Algorithm B) | Procedure | Leuven protocol: continuous intravenous insulin infusion aimiming blood glucose levels between 80mg/dl and 110mg/dl. |
|
| Conventional Intermittent Insulin Protocol (Algorithm C) | Procedure | Conventional treatment: intermitent subcutaneous insulin according to a sliding scale, starting with blood glucose levels higher than 150mg/dl. |
|
| Five days |
| 90-day health status | 90 days |
| Days on mechanical ventilation |
| Initiation of dialysis |
| Days on antibiotics |
| Days on inotropic of vasopressor support |
| Necessity of red blood cell transfusions |
| Bilirubin peak |
| Platelets through |
| Joinville |
| Santa Catarina |
| Brazil |
| Hospital Regional Sao Jose | Joinville | Santa Catarina | Brazil |
| Hospital Estadual Mario Covas | Santo André | São Paulo | Brazil |
| Hospital Israelita Albert Einstein | São Paulo | São Paulo | 05651-901 | Brazil |
| ID | Term |
|---|---|
| D007333 | Insulin Resistance |
| D006943 | Hyperglycemia |
| D007003 | Hypoglycemia |
| ID | Term |
|---|---|
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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