Diagnostic significance of different plasma glucose analytical techniques in the clinical daily routine concerning the diagnostics of gestation diabetes
Introduction: Since 2012 plasma glucose analyses in the diagnostics of gestation diabetes (GDM) has exclusively allowed the use of venous blood instead of capillary blood. Objective: The question now is whether the change in this diagnostic standard influences relevant results. Methods: To find a fe...
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Published in | Experimental and Clinical Endocrinology & Diabetes |
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Main Authors | , , , , |
Format | Conference Proceeding |
Language | English |
Published |
07.03.2013
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Online Access | Get full text |
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Summary: | Introduction:
Since 2012 plasma glucose analyses in the diagnostics of gestation diabetes (GDM) has exclusively allowed the use of venous blood instead of capillary blood.
Objective:
The question now is whether the change in this diagnostic standard influences relevant results.
Methods:
To find a feasible solution, we simultaneously used 5 different oGTT analysis techniques in 90 pregnant women. Everytime plasma was used. The analysis techniques used included: venous blood in an NaF-monovette (ivL), venous blood in Hemocue (ivH) and SuperGL easy+(ivS), capillary blood in Hemocue (kH) and SuperGL easy+(cS). GDM was diagnosed if the SuperGL easy+ showed at least one pathological value.
Results:
There are significant differences in all analytical techniques. However, the prevalence for GDM using Hemocue and Super GL easy+ with venous or capillary blood showed no significant difference. But using the NaF system GDM was diagnosed significantly less frequently.
ivL: 4.7 ± 0.7/9.0 ± 2.0/6.7 ± 1.8; GDM 24%
ivH: 5.0 ± 0.8/8.4 ± 2.1/7 ± 0.7; GDM 52%
kH: 5.2 ± 0.7/8.9 ± 2.0/7.4 ± 1.7; GDM 57%
kS: 4.9 ± 0.7/9.0 ± 2.0/7.1 ± 1.8; GDM 43%
ivS: 4.8 ± 0.6/8.7 ± 2.0/7 ± 1.8; GDM 45.7%
p < 0.05 all vs. NaF, p < 0.05 capillary vs. i.v.
76% of the participants who were not diagnosed with GDM using the NaF technique developed a condition liable to obligatory therapy.
Using sodium fluoride a chemical stabilisation of glucose is achieved too late. Therefore the results are too low which leads to diagnostic errors.
Sarstedt AG has now introduced a new system using liquid citrate buffer which is currently used for comparison measurements. Those results could not be included in this analysis.
Conclusion:
Considering the low reproducibility of the oGTT clinical markers including maternal risk factors and fetal parameters have to be taken into account.
A less invasive analysis technique using capillary blood is if clinical parameters are also considered a valid method for diagnosing GDM. |
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ISSN: | 0947-7349 1439-3646 |
DOI: | 10.1055/s-0033-1336781 |