About this trial
The goal of this study is to measure the prevalence and risks of hyperglycemia in surgical patients with prediabetes. The main questions it aims to answer are:
* What is the prevalence of hyperglycemia in surgical patients with prediabetes? * What is the relative risk of postoperative complications associated with hyperglycemia?
To answer these questions, surgical patients with prediabetes will undergo universal glucose measurement in the perioperative period. Glucose data will be analyzed in conjunction with electronic health record (EHR) data describing patient outcomes.
Eligibility criteria
Qualifiers
Hemoglobin A1c measurement between 6 and 6.4%
Scheduled for non-cardiac surgery
Disqualifiers
Age>18
Pregnancy
Any formal diabetes diagnosis
Current use of medications that influence blood glucose regardless of the indication
Trial design
Treatments tested in this trial
- Not listed