Diabetes Clinical Trial
Official title:
Prospective and Multi-centric Study on Diabetes During Pregnancy in Belgium
The General hypothesis is that the IADPSG screening strategy for gestational diabetes (GDM)
will lead to an important increase in the work load and the prevalence of GDM in Belgium but
that this might not be cost effective concerning the prevention of adverse pregnancy
outcomes. The risk to develop type 2 diabetes postpartum will probably be lower than for
women diagnosed with the two-step screening strategy.
In this prospective multicentric cohort study, women will be universally screened for
pregestational diabetes and GDM at the first prenatal visit during the first trimester by
measuring the fasting plasma glucose. In the second trimester, women without diagnosis of
diabetes or GDM in the first trimester, will be universally screened for GDM using the 50g
glucose challenge test (GCT) and the 75g oral glucose tolerance test (OGTT) with the IADPSG
criteria for GDM. Diagnosis of GDM will be based on the 75g OGTT.
Accurate data on the prevalence of gestational diabetes (GDM) are lacking in Belgium and the
current practice for screening for GDM varies across different centers. The discrepancy in
recommendations is due to the lack of data based on research in our population concerning the
best screening strategy for pregestational diabetes in early pregnancy and the lack of data
on the best screening strategy for GDM. A substantial number of centers in Belgium already
use the IADPSG screening strategy although not always a an universal screening strategy or
not always as an one-step screening strategy.
The General hypothesis is that the IADPSG screening strategy will lead to an important
increase in the work load and the prevalence of GDM in Belgium but that this might not be
cost effective concerning the prevention of adverse pregnancy outcomes. The risk to develop
type 2 diabetes postpartum will probably be lower than for women diagnosed with the two-step
screening strategy.
In this prospective cohort study, women will be universally screened for pregestational
diabetes and GDM at the first prenatal visit during the first trimester by measuring the
fasting plasma glucose. GDM will be defined as a fasting plasma glucose ≥100-125mg/dl. This
will allow to identify the most important risk factors for the development of GDM.
In the second trimester, women will be universally screened for GDM using the 50g glucose
challenge test (GCT) and the 75g oral glucose tolerance test (OGTT)with the IADPSG criteria
for GDM. Compared to the IADPSG screening strategy used in normal routine, the 50g GCT will
be an extra test specific for the study. Diagnosis of GDM will be based on the 75g OGTT.
Participants and researchers will therefore be blinded for the result of the GCT. The results
of the GCT test will be used at the end of the study for research purposes only. The use of a
GCT as an universal screening tool in a two-step approach with the use of the 75g 2-hour OGTT
with the IADPSG criteria only if the GCT is abnormal, is not yet validated and will be
evaluated in the study, since this could be a practical solution. Differences in GDM
prevalence and pregnancy outcomes will be analyzed using different diagnostic criteria based
on the 75g OGTT: the Carpenter & Coustan criteria, the IADPSG criteria, and threshold values
if diagnostic criteria would be based on an odds ratio of 2.0. The evaluation of different
screening strategies and different diagnostic criteria will allow to explore the most cost
effective methods for identifying women at risk for adverse pregnancy outcomes and at high
risk for the development of type 2 diabetes after pregnancy. By using a multivariable risk
estimation model based on the most relevant clinical risk factors and biochemical measures
for GDM in our own population, the aim is to develop a simple and cost effective screening
algorithm.
This study will also allow to evaluate the best short-term follow up strategy postpartum for
women with a previous history of GDM. Different screening tests will be used three months
postpartum: a fasting plasma glucose, Hba1c and 75g OGTT.
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