Gestational Diabetes (Priscilla White Class A DM)
Updated July, 2023
Contributor: Division of Maternal-Fetal Medicine
Basics
Definition: insulin resistance arising during pregnancy that results in carbohydrate intolerance
Types: A1GDM (diet-controlled) and A2GDM (medication-controlled)
Prevalence: varies in direct proportion to the prevalence of T2DM in the population in a particular racial or ethnic group. Increasing globally with the increase in obesity and sedentary lifestyles in the U.S.
Screening
Universal screening for pregestational diabetes is recommended at the initial prenatal visit, in the form of a Hgb A1C (see algorithm for screening below). The goal of early screening is to identify women who have pregestational diabetes.
Institutionally, we utilize the Carpenter and Coustan threshold values for GDM diagnosis, as follows:
- Fasting >95
- 1 hr > 180
- 2 hr > 155
- 3 hr > 140
Monitoring and Treatment – SEE ATTACHED ALGORITHM FOR MANAGEMENT OF GDM and PGDM
All women diagnosed with GDM should receive lifestyle modification counseling, specifically nutrition and activity counseling
The actual dietary composition that maximizes perinatal outcomes is unknown, but the following breakdown of macronutrients is recommended:
- Carbohydrates: 33-40%, preferably complex carbohydrates; avoid sugar-sweetened beverages
- Protein: 20%
- Fat: 40%
Women should eat 3 meals and 2-3 snacks per day (one snack close to bedtime) to maintain stable plasma glucose levels. Meal/snack carbohydrate recommendations:
- Breakfast 15-30 grams of carbohydrate
- Lunch 30-60 grams of carbohydrate
- Dinner 30-60 grams of carbohydrates
- Snacks 15-30 gram of carbohydrate
Exercise/physical activity counseling
- 30 minutes of moderate aerobic exercise 5 days per week OR 150 minutes total per week is recommended to improve glycemic control
Glucose monitoring should occur 4 times daily: once fasting and again 2 hours after the first bite of each meal. “Fasting” is defined as nothing to eat or drink (with the exception of water) for the 8 hours preceding the check.
Target levels (per the American Diabetes Association 2024 Guidelines):
- Fasting < 95
- 2-hr post-prandial <120
Can consider continuous glucose monitor for patients who are not able to be compliant with fingersticks or for confirmation of glycemic control.
Patients should be seen in the office every 2-3 weeks to review logs. Logs should be reviewed at least weekly, either virtually or in the office, if glucose is poorly controlled or if patient is on medication
It is reasonable to allow a 1-2 week trial of dietary management before initiation of medication. Waiting longer does not increase the likelihood of good control after dietary and lifestyle adjustments have been made.
Insulin therapy is first-line pharmacologic treatment of A2GDM
Utilize the Diabetes in Pregnancy Smartset for prescribing
Long acting insulins: Glargine (Lantus, Semglee, Basaglar) and Degludec (Tresiba) will impact fasting and pre-prandial values (if checked)
- NPH is second line secondary to the higher risk of hypoglycemic episodes
Rapid acting insulins: Aspart (Novolog) and Lispro (Humalog or Admelog) impact post-prandial values. Avoid regular insulin.
Dosing: Weight-based dosing based on trimester using actual (current) body weight
TDI = Total Daily Insulin
- 1st trimester: TDI = 0.7 units/kg/day
- 2nd trimester: TDI = 0.8 units/kg/day
- 3rd trimester: TDI = 0.9 units/kg/day
Divide the TDI dose into 50% long-acting insulin and 50% rapid acting insulin
- Long-acting (basal) insulin glargine should be divided to be dosed every 12 hours OR decludec can be dosed once daily.
- Rapid-acting (bolus) insulin should be divided into TID with meals
Example: Patient weight 111kg at 32 weeks EGA.
111 x 0.9 = 100 (this is the TDI)
50% TDI long-acting (50units/2: 25 units every 12 hours)
50% TDI short-acting (50 units/3: 16 units with meals)
Individualize the patient’s regimen based on need (ie some patients may only need long-acting insulin)
Insulin should be adjusted in 10-20% increments every 3-7 days
Oral hypoglycemic agents are second-line treatment for GDM; however there is a use for them in women who decline insulin, who cannot afford insulin, or who cannot safely administer insulin
In these situations, patients must be counseled on the lack of safety data, particularly the lack of long-term neonatal follow-up, as well as high treatment failure requiring insulin administration
Metformin (preferred to glyburide)
- Dosing:
- Starting: Metformin 500 mg BID with breakfast and dinner OR Metformin XR 1000 mg daily with a meal (NOTE: there is currently a black box warning for certain versions of Metformin XR – do not use until this is resolved)
- Titrate slowly to minimize GI side effects
- Maximum dose: 2550 mg/day
Glyburide
- Dosing
- Starting: 2.5 mg PO BID with breakfast and dinner
- Major risk is hypoglycemia, especially if not taken with a meal
- Maximum dose: 20 mg per day
Two recent meta-analyses have demonstrated worse neonatal outcomes (RDS, hypoglycemia, macrosomia, birth injury) for glyburide compared to insulin despite no difference in overall glycemic control
Hypoglycemia is defined as blood glucose is ≤ 62 mg/dL
Treat with 15 g of rapid acting carbs (Dex4, 4 glucose tabs, or 4 oz juice)
Recheck glucose in 15 minutes
Repeat treatment until glucose > 62 mg/dL
Once adequately treated, eat meal or protein snack
Instruct patients not to operate a motorized vehicle until blood glucose is >70 mg/dL, without symptoms of hypoglycemia, and at least 30 minutes after hypoglycemic episode due to delayed recovery of cognitive function
Fetal risks
- Macrosomia
- Stillbirth
Neonatal risks
- LGA
- Neonatal hypoglycemia
- Hyperbilirubinemia
- Shoulder dystocia
- Birth trauma
- Childhood and adult risks of obesity and T2DM
Maternal risks
- Preeclampsia
- Cesarean delivery
- Development of T2DM outside of pregnancy
- Pelvic trauma
- Preterm delivery
Ultrasounds
Anatomic survey at 18-22 weeks
At least one additional growth scan in A1GDM
Serial growth scans at time of diagnosis of A2GDM
Antenatal testing
Risk of IUFD is increased with poor glycemic control during the pregnancy, and therefore antenatal testing is recommended in the setting of A2GDM. This includes patients who have declined recommended medication for glycemic control.
Institutionally, we initiate twice-weekly testing (once weekly NST, once weekly BPP) at 32 weeks (earlier if multiple comorbidities or poor control).
Delivery
Timing (in the absence of other comorbidities)
A1GDM: 39w0d- 40w6d (with appropriate antenatal testing)
A2GDM: depends on control
- Good control: 39w0d – 39w6d
- Poor control: 37w0d – 38w6d, only sooner with abnormal antenatal testing or failed in-hospital glycemic control attempts
Mode
Shared decision-making between patient and provider is essential in determining mode of delivery in patients with diabetes complicated by fetal macrosomia. Counseling regarding the risks and benefits of scheduled cesarean delivery when the EFW is >4500g is recommended
Intrapartum management
Discontinue entire home regimen if patient has A2GDM
Check blood sugars on admission and every 2 hours in active labor
Utilize IV insulin infusion (insulin drip) if glucose >120 mg/dL
Postpartum considerations
Check fasting and 2 hr postprandial blood sugars in the immediate postpartum period off of medications (for patients who are in-house longer than 2-3 days, individualize need for fingersticks).
Schedule a 2-hr GTT at 6-12 weeks postpartum
Patient needs a PCP referral placed in the third trimester, as ACOG and the ADA recommend repeat testing every 1-3 years if initial postpartum screening is normal
- Consider Access Health referral for patients who will not have insurance beyond the immediate postpartum period
- Utilize the Physician Finder referral for those patients who will remain insured beyond the immediate postpartum period
Up to 70% of women with GDM will develop diabetes within 22-28 years of pregnancy
Related Pages
- Adnexal Masses in Pregnancy
- Antenatal Testing
- Antenatal Testing
- Antenatal Guidelines for Narcotic Administration
- Assigning EDC
- Asthma During Pregnancy
- Cervical length screening in Pregnancy
- Condylomas in Pregnancy
- Depression in Pregnancy
- External Cephalic Version (ECV)
- Fetal Growth Restriction (FGR)
- Gestational Diabetes (Priscilla White Class A DM)
- Gestational Proteinuria
- Heparin Use in Pregnancy
- Hepatitis B in Pregnancy
- Hepatitis C in Pregnancy
- Herpes Simplex Virus
- Checklist for HIV Positive Patient
- HIV Screening and Management
- Hypertensive Disorders of Pregnancy
- Influenza in Pregnancy
- Intrahepatic Cholestasis of Pregnancy
- Low-Dose Aspirin for Prevention of Preeclampsia
- Lupus in Pregnancy
- Management of Cesarean Wound Disruption
- Management recommendations for pregnancies complicated by low fetal fractions on cell free DNA analysis
- Monoamniotic Twinning: Evaluation and Management
- Management of Monochorionic – Diamniotic Twins
- Nausea and Vomiting of Pregnancy (NVP)
- Obesity in Pregnancy
- Oligohydramnios in the Third Trimester
- Maternal Exposure to Parvovirus B1
- Placenta Previa
- Late-Term and Post-Term Pregnancy
- Pregestational Diabetes
- Research Studies
- Sickle Hemoglobinopathies in Pregnancy
- Syphilis in Pregnancy
- Thrombophilias During Pregnancy
- Thyroid Disease in Pregnancy
- Toxoplasmosis
- Urinary Tract Infection
- VBAC vs. Repeat Cesarean Policy
- Zika Virus in Pregnancy
- Chronic Hypertension in Pregnancy