Detecting Late-Onset Gestational Diabetes After Initial Screening
Women who develop clinical signs or symptoms suggestive of gestational diabetes after a negative initial screening at 24-28 weeks should undergo a repeat OGTT, as this can identify an additional 23.5% of GDM cases that would otherwise be missed. 1
Risk Factors for Late-Onset GDM
Women at higher risk for developing late-onset GDM (after initial negative screening) include those with:
- History of previous GDM (2.6 times higher risk) 1
- Higher glucose values on initial screening (even if below diagnostic threshold) 1
- Early abnormal glucose metabolism (fasting glucose 110-125 mg/dL or A1C 5.9-6.4%) 2
- Marked obesity 3
- Strong family history of diabetes 3
- Previous macrosomic infant 3
Clinical Indicators for Repeat Testing
Repeat OGTT should be performed when any of these clinical signs develop after initial negative screening:
- Fetal growth abnormalities (most common indicator, yields 22.7% positive results) 1
- Polyhydramnios
- Glycosuria
- Symptoms of hyperglycemia (polydipsia, polyuria)
- Recurrent infections (especially urinary tract or vaginal)
Approach to Repeat Testing
Timing: Perform repeat testing as soon as clinical signs or symptoms develop in the third trimester 1
Method: Use the same diagnostic test as recommended for initial screening:
- Two-step approach: 50g glucose challenge test (GCT) followed by 100g OGTT if abnormal
- One-step approach: 75g OGTT directly 3
Diagnostic criteria: Same as initial screening
Predictive Values from Initial Screening
Initial OGTT values can help identify women at higher risk for late-onset GDM:
- Fasting glucose ≥4.8 mmol/L on initial OGTT: PPV 32%, NPV 83% 1
- 2-hour glucose ≥6.5 mmol/L on initial OGTT: PPV 47%, NPV 90% 1
Clinical Implications
Early detection and treatment of late-onset GDM is crucial as it reduces risks of:
- Preeclampsia
- Macrosomia
- Shoulder dystocia
- Other adverse pregnancy outcomes 3
Pitfalls to Avoid
- Assuming a negative initial screening eliminates all risk of GDM
- Ignoring clinical signs of GDM that develop after initial screening
- Failing to consider repeat testing in women with borderline results on initial screening
- Missing opportunities for intervention in women who develop late-onset GDM
The evidence clearly demonstrates that a single screening at 24-28 weeks may miss cases of GDM that develop later in pregnancy. Vigilance for clinical signs and symptoms, particularly in high-risk women, with prompt repeat testing can identify these cases and allow for timely intervention to improve maternal and fetal outcomes.