Guidelines for Prescribing FreeStyle Libre 3 for Diabetes Management
FreeStyle Libre 3 should be prescribed for patients with diabetes who require intensive insulin therapy, experience frequent hypoglycemia, or have difficulty achieving glycemic targets with conventional monitoring methods. 1
Patient Selection Criteria
Primary Indications
- Patients with Type 1 diabetes on multiple daily injections or insulin pump therapy 2
- Patients with Type 2 diabetes on intensive insulin regimens 2
- Individuals with unexplainable severe hypoglycemia, recurrent hypoglycemia, or nocturnal hypoglycemia 1
- Patients with high glycemic variability despite optimized insulin therapy 1
Special Populations
- Chronic Kidney Disease: Use with caution in patients on hemodialysis as accuracy may be reduced (MARD 19.5% vs standard 7.8% in stable patients) 2
- Peritoneal Dialysis: Not recommended for patients on peritoneal dialysis due to potential interference with glucose measurements 2
Device Specifications and Performance
- FreeStyle Libre 3 is a factory-calibrated continuous glucose monitoring system with 14-day wear duration 3
- Latest generation shows improved accuracy with overall MARD of 7.8% compared to venous blood glucose reference 3
- Performance remains stable throughout the 14-day wear period, though slightly less accurate on days 1 and 14 4
- System provides real-time glucose readings without requiring fingerstick calibration 2
Prescription Process
Documentation Requirements:
- Diagnosis of diabetes (Type 1 or Type 2)
- Current insulin regimen (multiple daily injections or pump)
- History of hypoglycemia or glycemic variability
- Previous self-monitoring blood glucose (SMBG) records showing need for more intensive monitoring
Initial Prescription:
- Prescribe one sensor every 14 days (2-3 sensors per month)
- Include reader device if patient doesn't have compatible smartphone
- Specify "FreeStyle Libre 3 Continuous Glucose Monitoring System"
Follow-up Plan:
- Schedule follow-up within 2-4 weeks of initiation to review data
- Assess time in range, hypoglycemic episodes, and glycemic variability
- Adjust insulin regimen based on CGM data patterns
Patient Education Requirements
- Proper sensor application on the upper arm (primary site) 5
- Alternative sites (chest, back) may be used but with potentially reduced accuracy 5
- Scanning technique and frequency (minimum once every 8 hours)
- Data interpretation using ambulatory glucose profile
- Technical troubleshooting for common issues
- Understanding limitations in specific situations (rapid glucose changes, exercise)
Clinical Benefits to Emphasize
- Reduction in hypoglycemia time and severity 2, 1
- Improved glycemic control without increasing hypoglycemia risk 1
- Better understanding of glucose patterns and trends 1
- Immediate feedback allowing for informed decisions about food intake and insulin dosing 1
Important Considerations and Limitations
Accuracy Considerations:
Device Comparison:
Cost and Coverage:
- Verify insurance coverage before prescribing
- Consider patient's ability to afford ongoing sensor costs
Documentation for Insurance Approval
- Document medical necessity based on:
- Hypoglycemia risk or history
- Glycemic variability
- Intensive insulin regimen
- Failed attempts to achieve targets with conventional monitoring
- Need for improved glucose data to optimize therapy
By following these guidelines, clinicians can appropriately prescribe FreeStyle Libre 3 to patients who will benefit most from continuous glucose monitoring technology, leading to improved glycemic control, reduced hypoglycemia risk, and better quality of life.