1-hr GCT cutoff (mg/dL)
ACOG accepts any of the three; the choice is institutional.
Two accepted strategies, two different diagnostic philosophies. ACOG favors one; the ADA favors the other. Both are correct — and that is exactly the problem worth understanding.
This deck lays out the mechanics, thresholds, comparative outcomes, and practical tradeoffs of each strategy so the choice made at your institution is an informed one, not a default.
ACOG accepts any of the three; the choice is institutional.
Only those who screen positive need the longer, fasting test.
A separate fasting visit is required to complete the diagnosis.
| Timepoint | Carpenter–Coustan | NDDG |
|---|---|---|
| Fasting | ≥ 95 mg/dL | ≥ 105 mg/dL |
| 1 hour | ≥ 180 mg/dL | ≥ 190 mg/dL |
| 2 hour | ≥ 155 mg/dL | ≥ 165 mg/dL |
| 3 hour | ≥ 140 mg/dL | ≥ 145 mg/dL |
Diagnosis: ≥ 2 of 4 values met or exceeded. The ADA recommends the lower Carpenter–Coustan thresholds if the two-step approach is used.
ACOG notes a single elevated value may be used for diagnosis instead of two — but this would significantly increase GDM incidence and is not the default.
Performed once at 24–28 weeks. Any one of the following meets or exceeds threshold:
Set at the glucose level where the odds of adverse outcomes — LGA, neonatal hyperinsulinemia, excess adiposity — reached 1.75× estimated baseline odds.
These are the only GDM thresholds derived directly from pregnancy outcomes rather than prediction of later maternal diabetes.
| Timepoint | Carpenter–Coustan (two-step) | NDDG (two-step) | IADPSG (one-step) |
|---|---|---|---|
| Fasting | ≥ 95 mg/dL | ≥ 105 mg/dL | ≥ 92 mg/dL |
| 1 hour | ≥ 180 mg/dL | ≥ 190 mg/dL | ≥ 180 mg/dL |
| 2 hour | ≥ 155 mg/dL | ≥ 165 mg/dL | ≥ 153 mg/dL |
| 3 hour | ≥ 140 mg/dL | ≥ 145 mg/dL | — |
| # values required | ≥ 2 of 4 | ≥ 2 of 4 | ≥ 1 of 3 |
Sacks DB, et al. Guidelines and Recommendations for Laboratory Analysis in the Diagnosis and Management of Diabetes Mellitus. Diabetes Care. 2023. Table adapted per Will JS, Crellin H. Am Fam Physician. 2023.
8.9% vs. 9.2% — not significant
3.1% vs. 3.0% — not significant
13.6% vs. 13.5% — not significant
24.0% vs. 24.6% — not significant
One-step screening was associated with increased neonatal hypoglycemia — possibly reflecting heightened surveillance of infants born to mothers newly labeled with GDM, rather than a true biological difference.
Hillier TA, Pedula KL, Ogasawara KK, et al. A Pragmatic, Randomized Clinical Trial of Gestational Diabetes Screening. N Engl J Med. 2021.
Across the pooled evidence base, one-step screening consistently identifies roughly twice the number of GDM cases.
Despite the higher diagnosis rate, the review found no clear evidence that one-step screening improves short-term maternal or neonatal health outcomes.
Two independent, high-quality evidence sources — one pragmatic RCT, one systematic review — converge on the same conclusion: more diagnoses does not automatically mean better measured outcomes at delivery.
Pillay J, Donovan L, Guitard S, et al. Screening for Gestational Diabetes. JAMA. 2021.
Cites proven treatment benefit at the higher thresholds and concern about over-diagnosis and unproven benefit of treating milder hyperglycemia.
Favors thresholds derived directly from HAPO pregnancy-outcome data, arguing these best reflect the glucose levels that actually matter for the baby.
Both organizations acknowledge the need for further evidence, and either approach is considered acceptable. There is no professional or medico-legal expectation to pick one over the other.
Does not perform as well as the glucose load test for GDM screening. Not recommended as a standalone screening test.
Fasting ≥ 95, 1-hr postprandial ≥ 140, 2-hr postprandial ≥ 120 mg/dL — suggested when an OGTT can't be performed, but no consensus on how many abnormal values are required.
Used in some international settings (e.g., China: FPG ≥ 5.6 mmol/L as a first-trimester screen), but lacks the sensitivity of a full OGTT.
Recommended for women with risk factors, to identify pre-existing diabetes — managed as diabetes complicating pregnancy, not as GDM.
Minimizing the number of patients labeled and treated, at higher, outcome-validated-by-treatment-trial thresholds.
Capturing the broadest population linked to adverse pregnancy outcomes and later metabolic risk, in one encounter.
Practical rule: whichever strategy is adopted, apply it consistently, use the paired thresholds correctly (never mix Carpenter–Coustan cutoffs with IADPSG rules), and document the protocol in your practice's standing orders.
One-step screening identifies roughly twice as many GDM cases as two-step, replicated across a pragmatic RCT and a systematic review.
Whether treating the additional, milder hyperglycemia identified only by one-step criteria improves clinically meaningful short-term outcomes.
Whether IADPSG's outcome-derived thresholds or Carpenter–Coustan's treatment-trial-validated thresholds are the more appropriate diagnostic anchor.
Long-term, prospective comparisons of maternal and offspring metabolic outcomes under each diagnostic strategy, beyond the pregnancy episode itself.
Both ADA and ACOG acknowledge the evidence gaps and consider either approach acceptable.
Educational material for physicians and advanced practice providers. Apply current institutional protocols and individualized clinical judgment.