Management of Gestational Diabetes Mellitus
Begin immediately with medical nutrition therapy and self-monitoring of blood glucose after diagnosis, targeting fasting glucose <95 mg/dL, 1-hour postprandial <140 mg/dL, or 2-hour postprandial <120 mg/dL; if these targets are not met within 1-2 weeks of lifestyle modification alone, initiate insulin as the first-line pharmacologic agent. 1
Initial Management Framework
The cornerstone of GDM management is lifestyle modification, which successfully controls glycemia in 70-85% of women without requiring medication. 2 This high success rate makes it essential to give lifestyle measures an adequate trial before escalating to pharmacotherapy.
Step 1: Medical Nutrition Therapy (Within First Week)
Refer urgently to a registered dietitian nutritionist familiar with GDM management within the first week of diagnosis. 1, 3 The nutrition plan must include:
- Minimum 175 g carbohydrate daily (approximately 35% of a 2,000-calorie diet) 2, 3
- Minimum 71 g protein daily 2, 3
- Minimum 28 g fiber daily 2, 3
- Emphasize monounsaturated and polyunsaturated fats while limiting saturated fats and avoiding trans fats entirely 2, 3
Critical pitfall to avoid: Never reduce carbohydrates below 175 g/day, as this risks fetal growth compromise and maternal ketosis. 1, 3 Women who substitute excessive fat for carbohydrate may unintentionally enhance lipolysis, promote elevated free fatty acids, and worsen maternal insulin resistance. 2
Distribute carbohydrates across 3 small-to-moderate meals and 2-4 snacks throughout the day, with an evening snack usually necessary to prevent accelerated ketosis overnight. 1, 3
Step 2: Physical Activity
Prescribe at least 150 minutes of moderate-intensity aerobic activity weekly, spread throughout the week. 1 Regular exercise lowers both fasting and postprandial glucose levels and should be used as an adjunct to nutrition therapy. 3
Step 3: Self-Monitoring of Blood Glucose
Instruct the patient to check:
- Fasting glucose daily upon waking 1
- Postprandial glucose after each main meal (breakfast, lunch, dinner) 1
- Choose either 1-hour OR 2-hour postprandial measurements consistently 1
Postprandial monitoring is superior to preprandial monitoring alone and is associated with better glycemic control and lower risk of preeclampsia. 1
Glycemic Targets
The specific targets that guide all management decisions are: 2, 1
- Fasting glucose <95 mg/dL (5.3 mmol/L)
- 1-hour postprandial <140 mg/dL (7.8 mmol/L) OR
- 2-hour postprandial <120 mg/dL (6.7 mmol/L)
Pharmacologic Management Algorithm
When to Initiate Medication
Start insulin immediately if glycemic targets are not achieved within 1-2 weeks of lifestyle modification alone. 1 Do not delay pharmacotherapy beyond this window if targets remain unmet.
First-Line: Insulin
Insulin is the preferred and recommended first-line pharmacologic agent because it does not cross the placenta to a measurable extent. 1 This is Level A evidence based on extensive safety data and unlimited dose-titration capacity. 1
Initial insulin dosing: 1
- Total daily dose: 0.7-1.0 units/kg of maternal weight
- Allocate approximately 40% as basal insulin
- Allocate approximately 60% as prandial insulin
Insulin requirements increase linearly by 5% per week through week 36, often resulting in a doubling of the pre-pregnancy dose. 2 Frequent titration is necessary to match changing requirements throughout pregnancy. 1
Oral Agents: When and Why to Avoid
Metformin and glyburide are NOT recommended as first-line therapy. 1 The evidence against their use as initial agents is compelling:
Metformin concerns: 1
- Crosses the placenta, producing umbilical-cord concentrations equal to or higher than maternal levels
- The MiG-TOFU follow-up study showed children aged 9 years exposed in utero had higher BMI, waist-to-height ratio, and waist circumference compared with insulin-exposed children
- 25-28% of women fail to achieve glycemic targets on metformin alone
- Should be avoided in women with hypertension, preeclampsia, or any condition predisposing to intrauterine growth restriction
- Crosses the placenta with fetal cord concentrations reaching 50-70% of maternal levels
- Associated with higher rates of neonatal hypoglycemia, macrosomia, and increased fetal abdominal circumference compared with insulin
- Failed to meet non-inferiority criteria versus insulin for composite neonatal outcomes
- 23% failure rate in achieving glycemic targets
- No long-term safety data for offspring
When oral agents may be considered: 1 Only when insulin administration is impractical or unsafe due to cost, language barriers, limited health literacy, or cultural factors, or when a well-informed patient declines insulin after comprehensive counseling. If an oral agent must be used, metformin is preferred over glyburide due to lower incidences of neonatal hypoglycemia and macrosomia. 1 Patients must be counseled that all oral agents cross the placenta and lack long-term offspring safety data. 1
If oral therapy is initiated and targets are not met within 1-2 weeks, transition promptly to insulin or add insulin to the regimen. 1
Fetal Surveillance
Ultrasound monitoring of fetal abdominal circumference should begin in the second and early third trimesters and be repeated every 2-4 weeks. 1
Management based on fetal growth: 1
- Fetal abdominal circumference <75th percentile (normal growth): Less intensified management may be adopted, but continue SMBG
- Fetal abdominal circumference ≥75th percentile (excessive growth): Lower glycemic targets or intensify pharmacologic therapy
Instruct mothers to monitor fetal movements during the last 8-10 weeks of pregnancy and report immediately any reduction. 1 Women whose fasting glucose exceeds 105 mg/dL or who progress beyond term require heightened surveillance for fetal demise. 1
Maternal Surveillance
Measure blood pressure and urinary protein at every prenatal visit to detect preeclampsia, as women with GDM have a 1.6-fold higher risk compared with non-diabetic pregnancies. 1
Fasting urine ketone testing may be useful to identify women with inadequate caloric or carbohydrate intake, particularly those on calorie-restricted diets. 2, 1
Continuous Glucose Monitoring
Real-time CGM in pregnancy complicated by type 1 diabetes demonstrated mild improvement in A1C without increased hypoglycemia and reductions in large-for-gestational-age births, length of stay, and neonatal hypoglycemia. 2 While this evidence is specific to type 1 diabetes, it supports the value of enhanced glucose monitoring in high-risk pregnancies.
Intrapartum Management
During labor, monitor maternal capillary glucose every 1-2 hours with a target range of 80-110 mg/dL to reduce the risk of fetal hypoxia and neonatal hypoglycemia. 1 If glucose exceeds 180 mg/dL, administer an insulin bolus. 1 If glucose exceeds 297 mg/dL, delay non-urgent procedures and give corrective insulin. 1
Delivery Timing
For women with diet-controlled GDM meeting glycemic targets: Delivery at 39-40 weeks of gestation is appropriate. 1
For women requiring insulin or with poor glycemic control: Delivery at 39 weeks of gestation (39⁰-39⁶ weeks) is recommended to balance maternal and fetal outcomes. 1 Postponing delivery beyond 40 weeks in this context increases perinatal mortality. 1
Postpartum Follow-Up
All women with GDM must be tested for persistent diabetes or prediabetes at 4-12 weeks postpartum using a 75-g oral glucose tolerance test with non-pregnancy diagnostic criteria. 1 Do NOT use HbA1c at this visit because the concentration may still be influenced by changes during pregnancy and/or peripartum blood loss. 1
Women with a history of GDM have a 50-70% risk of developing type 2 diabetes over 15-25 years. 1 Perform lifelong screening for diabetes at least every 3 years using standard non-pregnant criteria (annual HbA1c, annual fasting plasma glucose, or triennial 75-g OGTT). 1
Strongly encourage breastfeeding because it provides immediate nutritional and immunologic benefits and may confer longer-term metabolic advantages for both mother and child. 1
Common Pitfalls and How to Avoid Them
- Do not wait longer than 1-2 weeks to initiate insulin if lifestyle measures fail 1
- Do not start oral agents before attempting insulin - the safety concerns of placental transfer outweigh convenience 1
- Do not reduce carbohydrates below 175 g/day - this risks fetal compromise 1, 3
- Do not use hypocaloric diets <1,200 kcal/day - these cause ketonemia 3
- Discontinue metformin immediately if hypertension or preeclampsia develops - switch to insulin to prevent fetal growth restriction or acidosis 1
- Recognize that glyburide has the poorest safety profile among available agents, with the highest rates of neonatal hypoglycemia and macrosomia 1