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Tools for CGM users

Calculators for CGM Users

Eight tools built around continuous glucose monitor data. Estimate A1C from your average, predict per-meal glucose response, count net carbs for insulin dosing, and track the underlying insulin sensitivity that CGM patterns reflect.

The eight tools

How CGM data fits with the lab A1C

Continuous glucose monitors (Dexcom G7, Libre 3, Medtronic Guardian) compute "GMI" — Glucose Management Indicator — using essentially the same Nathan 2008 ADAG formula as lab A1C estimation, but applied to 14+ days of CGM data rather than the ~120 days of red blood cell glycation history a lab A1C reflects. The 2018 Bergenstal consensus paper in Diabetes Care renamed the metric from "estimated A1C" to GMI specifically because individual A1C-GMI gaps were clinically meaningful and shouldn\'t be ignored.

The practical implication: use both. CGM data gives you fast-feedback metabolic information — within days you know if a diet change is moving your average glucose. Lab A1C gives you the longer-term standardised measurement that endocrinologists, insurance, and clinical trials use. The two should track in the same direction; a persistent gap is worth discussing with your care team.

The five CGM metrics that matter

  1. Time in Range (TIR): percentage of readings 70–180 mg/dL. ≥70% is the 2019 Battelino consensus target.
  2. Average glucose: drives the estimated A1C / GMI calculation.
  3. Glucose Management Indicator (GMI): A1C equivalent of your CGM data.
  4. Coefficient of Variation (CV): measures glucose variability. Target <36% — lower values indicate more stable glucose patterns.
  5. Time Above Range / Time Below Range: percentage above 180 (hyperglycemia) and below 70 (hypoglycemia). Both should be minimised.

The 2019 Battelino consensus established these as the standard CGM metrics for clinical and research use. Most CGM apps display all five automatically. The Glycemic Load and Net Carbs calculators above help you predict and prevent the spikes that hurt TIR and drive Time Above Range higher.

Practical workflow for non-diabetic CGM users

A growing number of non-diabetic adults wear CGMs for metabolic health insight (Levels, Nutrisense, Veri, Stelo, January AI). For this population:

Related

FAQ

Why does my CGM GMI differ from my lab A1C?
GMI (Glucose Management Indicator) uses essentially the same Nathan 2008 ADAG formula as lab A1C estimation but applied to 14+ days of CGM data rather than the ~120 days of red blood cell history a lab A1C reflects. The 2018 Bergenstal et al. consensus paper renamed the metric from "estimated A1C" to GMI specifically because individual GMI-A1C gaps were clinically meaningful — about 50% of T1D and T2D adults have gaps over 0.3% and about 10% have gaps over 0.7%. Both numbers can be correct; they're measuring different averaging windows and individual glycation kinetics differ.
How long does my CGM data need to cover for an accurate A1C estimate?
Minimum 14 days of CGM wear time with at least 70% data capture, per the 2019 International Consensus on Time in Range (Battelino et al., Diabetes Care). The 14-day window correlates ~0.84 with subsequent 90-day A1C in stable subjects. 30 days is better; 90 days approaches the full A1C measurement period. After major treatment changes (new medication, significant diet shift), the CGM-based estimate will be ahead of the lagging lab A1C until ~6 weeks after the change stabilises.
What's "Time in Range" and how does it compare to A1C?
Time in Range (TIR) measures the percentage of CGM readings between 70–180 mg/dL (3.9–10.0 mmol/L) — the consensus target window for most adults with diabetes. The 2019 Battelino consensus established TIR ≥70% as the standard target, with each 10% improvement in TIR corresponding to approximately 0.5% reduction in A1C. TIR captures glucose variability that A1C cannot — two people with identical 7.0% A1Cs can have radically different TIR depending on spike patterns. For CGM users, TIR is the more actionable daily metric; A1C remains the standard for cross-population comparisons and clinical trials.
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