Continuous Glucose Monitoring and Long-Term Glycemic and Kidney Outcomes - Scorecard - MDSpire
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Continuous Glucose Monitoring in Relation to Long-Term Glycemic Control and Kidney Outcomes

  • By

  • Andrew J. Karter

  • Melissa M. Parker

  • Holly Finertie

  • Joshua R. Nugent

  • Lisa K. Gilliam

  • Ajit Mahapatra

  • October 7, 2026

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Clinical Scorecard: Continuous Glucose Monitoring in Relation to Long-Term Glycemic Control and Kidney Outcomes

At a Glance

CategoryDetail
ConditionType 2 diabetes; study of the association of real-time continuous glucose monitoring (rtCGM) with glycemic and kidney outcomes.
Key MechanismsCGM uses subcutaneous sensors to measure interstitial-fluid glucose. The source describes rtCGM as delivering immediate feedback and intermittently scanned CGM as requiring manual scanning.
Target PopulationAdults aged 19 years or older with type 2 diabetes, no prior CGM exposure, and either HbA1c greater than 8% within the preceding 12 months or a hypoglycemia-related emergency department visit or inpatient admission within the preceding 36 months.
Care SettingObservational comparative-effectiveness study using electronic health records and durable medical equipment claims at Kaiser Permanente Northern California.

Key Highlights

  • The study emulated a target trial comparing initiation and continued use of rtCGM with no CGM use.
  • Outcomes included HbA1c, urinary albumin-creatinine ratio (UACR), and estimated glomerular filtration rate (eGFR).
  • Monthly risk sets with temporally matched controls were assembled from January 2015 through June 2023.
  • Follow-up was planned for up to 36 months; the supplied excerpt does not provide the full censoring details.
  • The supplied article text describes the study design and outcomes but does not report study results.

Guideline-Based Recommendations

Diagnosis

  • Target-trial eligibility required type 2 diabetes and either HbA1c greater than 8% within the preceding 12 months or a hypoglycemia-related emergency department visit or inpatient admission within the preceding 36 months.

Management

  • The study compared initiating and maintaining rtCGM with not initiating CGM; the supplied text does not state clinical treatment recommendations.

Monitoring & Follow-up

  • Study outcomes were HbA1c, UACR, and eGFR; the supplied excerpt does not specify the measurement setting or follow-up interval schedule.

Risks

  • The authors noted limited prior evidence on long-term CGM effects and whether CGM preserves kidney function or reduces kidney damage.
  • The study used observational data and target trial emulation to address limitations including time-varying confounding.

Patient & Prescribing Data

Adults aged 19 years or older with type 2 diabetes, no previous CGM exposure, and either poor glycemic control or a history of hypoglycemia as defined by the study.

rtCGM initiation was identified through durable medical equipment claims for specified devices or supplies. The emulated per-protocol comparison was continued rtCGM use versus no CGM use.

Clinical Best Practices

  • Interpret the study as an observational target trial emulation, not a randomized clinical trial.
  • The analysis restricted CGM exposure to rtCGM to reduce heterogeneity.
  • Controls were sampled from monthly risk sets and assigned baseline dates within the selection month to match initiators temporally.
  • The study followed STROBE and TARGET reporting guidance.

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