Evidence map›Paper›PMID 41858085›Full record

ArticleDiabetic medicine : a journal of the British Diabetic Association2026

Sampling duration matters: Intraindividual variation of glycaemic metrics in type 1 diabetes using automated insulin delivery.

Bo Martin Bibby, Ermina Bach, Mia Christensen, Sanne Fisker, Klavs Würgler Hansen

Abstract read
In one paragraph

Article in Diabetic medicine : a journal of the British Diabetic Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Bo Martin BibbySection for Biostatistics, Department of Public Health, Aarhus University, Aarhus C, Denmark.
Ermina BachMedical Diagnostic Center, Viborg Regional Hospital, Viborg, Denmark.
Mia ChristensenMedical Diagnostic Center, Silkeborg Regional Hospital, Silkeborg, Denmark.
Sanne FiskerSteno Diabetes Center, Aarhus, Aarhus University Hospital, Aarhus N, Denmark.
Klavs Würgler HansenSteno Diabetes Center, Aarhus, Aarhus University Hospital, Aarhus N, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionUnderstanding intraindividual variability in glycaemic metrics among users of automated insulin delivery (AID) is essential for interpreting data from continuous glucose monitoring (CGM).

methodsCGM data over 56 days were collected from 142 individuals with type 1 diabetes using AID systems. Glycaemic metrics were derived from four 14-day periods and two 28-day periods.

resultsThe 95% limit of agreement for the difference between two measurements of time in range (TIR) from the same individual over 14-day periods was ±13.4%. The risk that two 14-day TIR values from the same individual differed by more than 5% points was 46.5%. If TIR was based on two 28-day periods, the 95% limit of agreement decreased to ±9.0%. The risk that two 28-day TIR values from the same individual differed by more than 5% points was 27.6%.

conclusionA 28-day CGM sampling period is recommended to minimise random variation and obtain more reliable glycaemic metrics.

Indexed as

Blood GlucoseDiabetes Mellitus, Type 1Hypoglycemic AgentsInsulinInsulin Infusion SystemsAdultBlood Glucose Self-MonitoringContinuous Glucose MonitoringFemaleHumansIntelligent SystemsMaleMiddle AgedTime FactorsYoung AdultBlood GlucoseHypoglycemic AgentsInsulinautomated insulin deliverycontinuous glucose monitoringtime in rangetype 1 diabetesvariability

Identifiers

PMID41858085
PMCPMC13257906

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.