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Clinical Process Improvement With A Bedside Computerized Insulin Therapy Protocol For Blood Glucose Control (eProtocol-insulin) in Adult And Pediatric ICU Patients:Further Refinement and Validation of eProtocol-insulin
The Purpose of this study is to: 1. Refine and validate a computerized bedside decision support tool blood glucose management in critically ill adult and pediatric ICU patients. 2. Monitor how often low blood sugar levels occur during use of the bedside tool. 3. Determine how the computerized tool effects the workload of the ICU nurses.
This first phase will be a prospective cohort study. We will validate the bedside tool in at least 4 adult and at least 4 pediatric ICUs and if necessary we will modify the bedside tool. The computerized bedside tool will be considered refined if \>90% of the generated instructions are accepted and if the percent of glucose values in the 70-110 mg/dl range are equivalent to our pilot experience rate of 55%, and if the rate of glucose values less than or equal to 40 mg/dl is less than 0.5% of glucose measurements.
Age
0 - No limit years
Sex
ALL
Healthy Volunteers
No
Yale University
New Haven, Connecticut, United States
Johns Hopkins University
Baltimore, Maryland, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
Baystate Medical Center
Springfield, Massachusetts, United States
Wake Forest Medical Center
Winston-Salem, North Carolina, United States
Pennsylvania State Children's Hospital
Hersey, Pennsylvania, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Vanderbilt University
Nashville, Tennessee, United States
LDS Hospital
Salt Lake City, Utah, United States
Primary Children's Hospital
Salt Lake City, Utah, United States
Start Date
February 1, 2006
Primary Completion Date
December 1, 2017
Completion Date
December 1, 2018
Last Updated
February 26, 2015
200
ESTIMATED participants
glucose control with computer generated recommendations
PROCEDURE
Lead Sponsor
Intermountain Health Care, Inc.
NCT07448805
NCT07222007
Data Source & Attribution
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