Evidence map›Paper›PMID 22047051›Full record

ArticleDiabetes technology & therapeutics2012

A comparison of average daily risk range scores for young children with type 1 diabetes mellitus using continuous glucose monitoring and self-monitoring data.

Susana R Patton, L Kurt Midyett, Lawrence M Dolan, Scott W Powers

Abstract read
In one paragraph

Article in Diabetes technology & therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

15 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Identification and prediction of group-based glycemic control trajectories during the transition to adolescence.Health psychology : official journal of the Division of Health Psychology, American Psychological Association · 2014
    Article
  11. Average Daily Risk Range (ADRR) in Young Children With Type 1 Diabetes.Journal of diabetes science and technology · 2014
    Article
  12. Review
  13. Review
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Susana R PattonDepartment of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas 66160, USA. Spatton2@kumc.edu
L Kurt Midyett
Lawrence M Dolan
Scott W Powers

Funding

Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
Behavioral Treatment for Dietary Adherence in ChildrenK24DK059973 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI POWERS, SCOTT W · 2001 to 2010
$1.3M
Improving Mealtime Functioning in Families of Young Children with Type 1 DiabetesK23DK076921 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PATTON, SUSANA R · 2007 to 2011
$566k
NCATS NIH HHS UL1 TR000077NIDDK NIH HHS K23-DK076921NIDDK NIH HHS K24-DK59973
6 · The paper itself

Abstract

backgroundYoung children with type 1 diabetes are vulnerable to glycemic excursion. Continuous glucose monitoring (CGM), combined with variability statistics, can offer a richer and more complete picture of glycemic variability in young children. In particular, we present data for the Average Daily Risk Range (ADRR) and compare ADRR scores calculated using CGM versus self-monitoring of blood glucose (SMBG) data for young children.

methodsCGM and SMBG data from 48 young children with type 1 diabetes (mean age, 5.1 years) were used to calculate two separate ADRR scores, using SMBG data (ADRRs) and CGM data (ADRRc), for each child. Additionally, we calculated mean amplitude of glycemic excursion (MAGE) scores for children to examine the concurrent validity of the ADRRs and ADRRc.

resultsYoung children's mean ADRRc score was significantly greater than their ADRRs score (55±12 and 46±11, respectively; P<0.001). In addition, 74% of the time the children's ADRRc score reflected greater variability risk than their ADRRs score. Examining the concurrent validity, children's ADRRc scores correlated positively with MAGE scores calculated using their CGM and SMBG data, whereas their ADRRs scores only correlated with MAGE scores calculated using SMBG.

conclusionsADRR scores generated for young children with type 1 diabetes demonstrate a high risk for glucose variability, but ADRR scores generated from CGM data may provide a more sensitive measure of variability than ADRR scores generated from SMBG. In young children with type 1 diabetes, ADRR scores calculated from CGM data may be superior to scores calculated from SMBG for measuring risk of excursion.

Indexed as

Blood GlucoseBlood Glucose Self-MonitoringChildChild, PreschoolDiabetes Mellitus, Type 1FemaleHumansHyperglycemiaHypoglycemiaMaleReproducibility of ResultsRisk AssessmentSurveys and QuestionnairesUnited StatesBlood Glucose

Identifiers

PMID22047051
PMCPMC3284697

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.