Cited by 16Clinical Laboratory Practices and Quality ControlDiabetes Management and ResearchIndigenous Health and Education

Results from 15 years of quality surveillance for a National Indigenous Point-of-Care Testing Program for diabetes

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Shephard, Mark, Shephard, Anne, McAteer, Bridgit, Regnier, Tamika, Barancek, Kristina·2017·Clinical Biochemistry

Abstract

INTRODUCTION Diabetes is a major health problem for Australia's Aboriginal and Torres Strait Islander peoples. Point-of-care testing for haemoglobin A1c (HbA1c) has been the cornerstone of a long-standing program (QAAMS) to manage glycaemic control in Indigenous people with diabetes and recently, to diagnose diabetes. METHODS The QAAMS quality management framework includes monthly testing of quality control (QC) and external quality assurance (EQA) samples. Key performance indicators of quality include imprecision (coefficient of variation [CV%]) and percentage acceptable results. This paper reports on the past 15years of quality testing in QAAMS and examines the performance of HbA1c POC testing at the 6.5% cut-off recommended for diagnosis. RESULTS The total number of HbA1c EQA results submitted from 2002 to 2016 was 29,093. The median imprecision for EQA testing by QAAMS device operators averaged 2.81% (SD 0.50; range 2.2 to 3.9%) from 2002 to 2016 and 2.44% (SD 0.22; range 2.2 to 2.9%) from 2009 to 2016. No significant difference was observed between the median imprecision achieved in QAAMS and by Australasian laboratories from 2002 to 2016 (p=0.05; two-tailed paired t-test) and from 2009 to 2016 (p=0.17; two-tailed paired t-test). For QC testing from 2009 to 2016, imprecision averaged 2.5% and 3.0% for the two levels of QC tested. Percentage acceptable results averaged 90% for QA testing from 2002 to 2016 and 96% for QC testing from 2009 to 2016. The DCA Vantage was able…

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Crossref · 10.1016/j.clinbiochem.2017.07.007

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  • Deviations near key clinical thresholds, such as 6.5% for diagnosis or 7.0-8.0% for treatment decisions, may result in misclassification and inappropriate therapeutic interventions.

    “Notably, deviations near key clinical thresholds, such as 6.5% for diagnosis or 7.0-8.0% for treatment decisions, may result in misclassification and inappropriate therapeutic interventions (9,10).”

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Authors
Shephard, M., Shephard, A., McAteer, B., Regnier, T., & Barancek, K.
Affiliations
  • Flinders University (AU)
  • Royal College of Pathologists of Australasia (AU)
Corresponding author
Shephard, Anne
Venue
Clinical Biochemistry
Publisher
Elsevier BV
Published
2017-12
Volume
50
Issue
18
Pages
1159-1163
ISSN
0009-9120 (ISSN-L)
OpenAlex
W2736818726
Cited by
16
References
1
Citations by year
2026: 2 · 2025: 2 · 2024: 1 · 2023: 2 · 2022: 3 · 2021: 1 · 2020: 2 · 2019: 3
FWCI
1.01
Type
journal article
Language
en
Open access
Locations
  • Clinical Biochemistry (publishedVersion)
  • PubMed (publishedVersion)
  • Flinders Academic Commons (Flinders University) (acceptedVersion, cc-by-nc-nd)
Funders
Australian Government
Topics
  • Health Sciences › Medicine › Physiology › Clinical Laboratory Practices and Quality Control
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Health Professions › General Health Professions › Indigenous Health and Education
Keywords
point-of-care testing, HbA1c, diabetes diagnosis, Aboriginal and Torres Strait Islander peoples, quality assurance, external quality assessment, glycemic control, imprecision, coefficient of variation, Indigenous health
MeSH terms
Australian Aboriginal and Torres Strait Islander Peoples, Diabetes Mellitus, Female, Glycated Hemoglobin, Humans, Male, Quality of Health Care, Point-of-Care Systems

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