Acknowledgements
The authors acknowledge the support of the Australasian Association for Clinical Biochemistry and Laboratory Medicine (AACB) and the Royal College of Pathologists of Australasia (RCPA). This abstract reflects the views of the authors who are members of the AACB-RCPA Harmonisation Glucose Preanalytical Working Group.
Aim
To conduct a narrative review of contemporary approaches to minimise preanalytical glycolysis in oral glucose tolerance test (OGTT) samples with a focus on GDM diagnosis using criteria derived from the Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) study. The challenges of implementing each approach across a diverse Australian healthcare setting were explored.
Results
Many Australian sites currently collect and transport OGTT samples at ambient temperature in sodium fluoride (NaF) tubes which likely leads to missed diagnosis of GDM in a significant proportion of cases. Alternative preanalytical solutions should be pragmatic and tailored to individual settings and as close as possible to the preanalytical conditions of the HAPO study for correct interpretation of OGTT results.
Rapid centrifugation of barrier tubes to separate plasma could be suitable in urban settings provided time to centrifugation is strictly controlled (estimated 1.8-fold increase in GDM). Tubes containing NaF and citrate could be useful for remote or resource poor settings with long delays to analysis but the impact on the interpretation of OGTT results should be carefully considered (estimated 1.4- to 4.2-fold increase in GDM). Testing venous blood glucose at the point-of-care bypasses the need for glycolytic inhibition but requires careful selection of devices with robust analytical performance (estimated impact on GDM not reported).
Conclusions
Studies to evaluate the potential error of each solution compared to the HAPO protocol are required to assess the magnitude of misdiagnosis and inform clinicians regarding the potential impact on patient safety and healthcare costs.