What is the proper format for writing a prescription for a FreeStyle Libre (flash glucose monitoring system) device?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 10, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

How to Write a Prescription for FreeStyle Libre Blood Glucose Monitoring Device

Write the prescription for FreeStyle Libre as a routine, ongoing supply with continuous sensor replacement every 14 days, not as a PRN or one-time order, because CGM devices must be used "as close to daily as possible for maximal benefit" and require uninterrupted access to supplies to minimize gaps in continuous glucose monitoring. 1

Essential Prescription Components

Device Specification

  • Specify "FreeStyle Libre 3 System" or the specific model (FreeStyle Libre, FreeStyle Libre 2, or FreeStyle Libre 3) on the prescription 1
  • Include both the sensor and reader device in the initial prescription, as the system requires pairing with a device-specific app or reader 2

Quantity and Duration

  • Prescribe sensors for continuous replacement cycles: typically 2-3 sensors per month (each sensor lasts 14 days) 1, 3
  • Specify the total duration of therapy (e.g., 3 months, 6 months, or ongoing) to ensure uninterrupted access 1
  • Include refills to maintain continuous monitoring without gaps 1

Usage Instructions

  • Direct the patient to scan the sensor at minimum once every 8 hours to capture complete 24-hour glucose data 1
  • Instruct to insert the new sensor before removing the old one when changing sensors to avoid gaps in data collection 1
  • Note that the device measures interstitial glucose continuously and displays data when scanned with the reading device 1

Clinical Documentation Requirements

Key Metrics to Document

  • Average glucose level, percentage of time in hypoglycemia ranges, percentage of time in target range, and percentage of time in hyperglycemia range should be documented in patient records 4
  • Confirm that the CGM continuously measured glucose and displayed data in real-time >95% of the time for the duration specified in the product label 4

Alert Configuration

  • Document settings for real-time alerts and alarms for hypoglycemia, hyperglycemia, and rapid rates of change 4
  • Ensure visual and audible alerts are properly configured for appropriate clinical response 4

Special Population Considerations

Patients with Advanced Chronic Kidney Disease

  • Use FreeStyle Libre with caution in hemodialysis patients, as accuracy is reduced during dialysis sessions (MARD 18.2-22.8% during hemodialysis vs. 11.3-19.3% overall) 2
  • Do NOT prescribe FreeStyle Libre for patients on peritoneal dialysis until more evidence becomes available, as there are no studies assessing whether icodextrin interferes with the sensor 2
  • In hemodialysis patients, use the device to assess glucose patterns rather than focusing on specific glucose values given lower accuracy compared to other CGM systems 2
  • Consider that 97.9% of readings were within clinically acceptable zones A+B on hemodialysis days in recent studies 2

Pediatric Patients

  • FreeStyle Libre is approved for children aged ≥4 years 5
  • Be aware of higher interindividual variability in accuracy in children, with MARD inversely related to age (younger children have higher MARD) 5
  • Sensor detachment is more common in pediatric patients (43.3% reported sensor problems, mainly early detachment), requiring special attention to sensor placement and adhesive reinforcement 5

Accuracy Considerations

Sensor Age Effects

  • Accuracy is lowest during the first day (MARD 14.5%) and last day (MARD 14.7%) of the 14-day sensor life, with optimal accuracy occurring on days 5-7 (MARD 7.8%) 3
  • Only 1.9% of readings fall in potentially dangerous zones C, D, or E during the first day, decreasing to 0.2-0.4% during mid-life and end-of-life 3

Medication Interferences

  • Document any use of high doses of acetaminophen, salicylic acid, or ascorbic acid, as these may affect sensor accuracy 4
  • Note that the FreeStyle Libre uses wired-enzyme technology that is NOT susceptible to acetaminophen interference at therapeutic doses, unlike some other CGM systems 2

Common Pitfalls to Avoid

  • Never prescribe as PRN or "as needed" – inconsistent use reduces clinical value and limits ability to improve quality of life and health outcomes 1
  • Do not prescribe as a one-time order – these devices are designed for regular, ongoing use to monitor glucose trends over time 1
  • Avoid prescribing without adequate patient education on scanning frequency (minimum every 8 hours) and sensor replacement procedures 1
  • Do not rely solely on estimated HbA1c from CGM data without documenting correlation with laboratory HbA1c measurements 4
  • Never fail to document instances where the CGM indicated questionable accuracy or withheld data 4

Sample Prescription Format

FreeStyle Libre 3 System

  • Sensors: 2-3 sensors per month (each lasts 14 days)
  • Reader device: 1 (if not using smartphone app)
  • Duration: 3 months supply with refills
  • Instructions: Apply new sensor every 14 days. Scan at least once every 8 hours. Insert new sensor before removing old sensor to avoid data gaps.
  • Indication: Continuous glucose monitoring for diabetes mellitus management
  • Refills: As needed for ongoing therapy

References

Guideline

Continuous Glucose Monitoring with FreeStyle Libre 3

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Continuous Glucose Monitoring System Documentation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.