None listed
Conditions
Brief summary
The purpose of this study is to determine the optimum blood glucose target for critically ill patients with high blood glucose levels. This will be done by changing the insulin protocol in ICU for a period of 6 months to compare to the current standard protocol.
Interventions
The intervention is a change in insulin protocol in the Intensive Care Unit (ICU) patients with chronic hyperglycaemia or poorly controlled pre-existing type 2 diabetes. Patients will be identified by a Hba1c test (glycated haemoglobin) on admission to ICU. Patients with a HbA1c >6.9% (or 51 mmol/mol) will be treated with a new Insulin protocol. This study will be performed sequentially; initially (6 months) the study will observe the current Insulin regimen, followed by a 2nd 6 month period in which the intervention (an altered Insulin regimen) will be implemented. The 2 study periods will be separated by 1 month to prevent patients from the control period being included in the intervention period. The new protocol targets blood glucose levels of 10-14 mmol/L in chronic hyperglycaemic patients and poorly controlled type 2 diabetic patients. The current insulin protocol targets blood glucose levels of 6-10 mmol/L. This will involve a change in practice for the bedside nurse who will administer insulin as required to reach the target blood glucose level. The new protocol will result in the administration of less insulin than the current protocol. All patients (including diabetic patients) with a HbA1c of 6.9% or below will continue with the control Insulin regimen if required.
Sponsors
Study design
Eligibility
Inclusion criteria
New admission to ICU HbA1c greater than 6.9% or 51 mmol/mol Anticipated to remain in ICU for 48 hours or greater
Exclusion criteria
HbA1c less than 6.9% Type-1 diabetes. Expected to die within 48 hours Not expected to stay for at least 48 hours Readmission to ICU