What are the target blood glucose levels for normal Continuous Blood Glucose (CBG) monitoring trends in individuals with diabetes?

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Normal CGM Monitoring Trends: Target Blood Glucose Levels

For most nonpregnant adults with diabetes, the target is to maintain Time in Range (TIR) >70% (glucose 70-180 mg/dL or 3.9-10.0 mmol/L), with Time Below Range <4% and Time <54 mg/dL <1%. 1

Core CGM Metrics and Targets

Time in Range (TIR) Goals

  • Standard target for most adults: >70% of readings between 70-180 mg/dL (3.9-10.0 mmol/L), which translates to >16 hours and 48 minutes per day 1
  • Older adults or high-risk individuals: >50% TIR (>12 hours per day) with more relaxed targets to minimize hypoglycemia risk 1
  • Each 5% increase in TIR provides clinically significant benefits for reducing microvascular complications 1

Time Below Range (TBR) - Hypoglycemia Prevention

  • Level 1 hypoglycemia (54-69 mg/dL): <4% of time (<1 hour per day) for most adults 1
  • Level 2 hypoglycemia (<54 mg/dL): <1% of time (<15 minutes per day) for all adults 1
  • High-risk/older adults: Combined TBR <1% (<15 minutes per day) to prioritize safety 1

Time Above Range (TAR) - Hyperglycemia Limits

  • Level 1 hyperglycemia (181-250 mg/dL): <25% of time (<6 hours per day) for most adults 1
  • Level 2 hyperglycemia (>250 mg/dL): <5% of time (<1 hour 12 minutes per day) for most adults 1
  • Older adults: Combined TAR <50% (<12 hours per day), with Level 2 <10% 1

Glycemic Variability

  • Coefficient of variation (%CV): Target ≤36% to minimize dangerous glucose fluctuations 1
  • Some evidence suggests targeting <33% provides additional protection against hypoglycemia for those on insulin or sulfonylureas 1

Data Collection Requirements

Minimum Monitoring Duration

  • 14 days of CGM wear is required for pattern management and accurate assessment 1
  • 70% active CGM time over those 14 days strongly correlates with 3-month mean glucose and time in range metrics 1
  • For CGM use between 45-95% over 90 days, 14 days minimum sampling is sufficient for mean glucose, TIR, and TAR metrics 2
  • Assessment of hypoglycemia requires longer sampling: 28-35 days for time <54 mg/dL regardless of CGM use frequency 2

Special Population Targets

Advanced Chronic Kidney Disease/ESKD

  • TIR target: >50% (more conservative due to heightened hypoglycemia risk from impaired kidney gluconeogenesis and decreased insulin clearance) 1
  • TBR target: <1% (stricter hypoglycemia prevention given increased risk) 1
  • Use Glucose Management Indicator (GMI) instead of HbA1c when discordance exists, as HbA1c has low accuracy in advanced CKD 1

Hospitalized Patients

  • Target range: 70-180 mg/dL with priority on hypoglycemia prevention 3
  • Keep time <70 mg/dL at <1%, with heightened awareness when glucose is 72-106 mg/dL, especially with downward CGM trend arrows 3
  • While 70% TIR is ideal, hypoglycemia prevention takes priority during acute illness 3

Pregnancy and Gestational Diabetes

  • Tighter target range: 63-140 mg/dL (3.5-7.8 mmol/L) instead of the standard 70-180 mg/dL 1
  • More stringent monitoring required with specific postprandial targets 4

Practical Implementation Algorithm

Step 1: Verify Adequate Data Collection

  • Confirm ≥14 days of CGM data with ≥70% active time before making treatment decisions 1
  • If assessing hypoglycemia patterns, extend to 28-35 days of data collection 2

Step 2: Assess Primary Metrics in Order

  1. First priority - Safety: Check TBR <54 mg/dL is <1% and TBR 54-69 mg/dL is <4% 1
  2. Second priority - Efficacy: Verify TIR 70-180 mg/dL is >70% (or >50% for high-risk patients) 1
  3. Third priority - Variability: Confirm %CV is ≤36% 1
  4. Fourth priority - Hyperglycemia: Check TAR >250 mg/dL is <5% and TAR 181-250 mg/dL is <25% 1

Step 3: Use Ambulatory Glucose Profile (AGP) for Pattern Recognition

  • Standardized single-page AGP reports with visual cues showing median (50th percentile) and interquartile ranges (25th-75th percentiles) should guide treatment adjustments 1
  • AGP displays glucose patterns as if occurring in a single day, making it easier to identify timing of hyperglycemia or hypoglycemia 1

Critical Pitfalls to Avoid

Don't Ignore Hypoglycemia Despite Good TIR

  • Even individuals with low TBR percentages can experience substantial numbers of severe hypoglycemic events 1
  • Monitor frequency of hypoglycemic events separately, not just percentage of time below range 1

Don't Accept Suboptimal CGM Use Without Adjustment

  • For CGM use <70%, recognize that 14 days may not adequately capture hypoglycemia patterns, requiring 28-35 days of data 2
  • Coefficient of variation requires 28 days of sampling regardless of CGM use percentage 2

Don't Apply Standard Targets to All Populations

  • Patients with advanced CKD require more conservative TIR targets (>50% vs >70%) due to altered glucose metabolism and increased hypoglycemia risk 1
  • Older adults with frailty should target >50% TIR with <1% combined TBR to prioritize safety over tight control 1

Don't Rely on Mean Glucose or GMI Alone

  • While mean glucose and GMI provide useful averages, they miss critical information about time spent in hypoglycemia and hyperglycemia ranges 1
  • A patient can have acceptable mean glucose but dangerous glycemic variability with significant time in both hypo- and hyperglycemia 1

Don't Forget to Adjust for Real-World Achievability

  • Research shows that even patients achieving HbA1c <7.5% only maintain approximately 60% of readings in target range (72-180 mg/dL), with up to 30% of readings >180 mg/dL being common 5
  • This suggests the 70% TIR target, while evidence-based, represents optimal rather than typical control 5

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.

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