Know before delivery

Growth Intelligence takes the scans your sonographers already do and gives every pregnancy in your practice a projected weight at delivery, a flag if it needs a second look, and a plain statement of how much can be known at that point in the pregnancy.

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8141
pregnancies with recorded birth outcomes
79%1
of growth-restricted fetuses detected
81%1
of macrosomic fetuses detected
94%2
of Alert screens confirmed at birth

Internal validation, 814 pregnancies, August 2026.

Answers to three important questions

Which patients need attention today?

Growth Intelligence worklist: patients ranked by latest scan, with Alert and Watch flags and confidence.

The worklist ranks every active pregnancy by its latest scan. Each flag says what it found and how far to trust it.

How big will this baby be at delivery?

Growth chart: scans plotted on the INTERGROWTH-21st reference with the projected weight at term.

Every scan is placed on the INTERGROWTH-21st reference, with the projected weight at term and the range around it.

Why should I trust this flag?

How this was assessed panel: rule, threshold, scans, confidence, validation record, and a clinical note to copy.

Because it shows its work: the rule it crossed, the threshold, the scans it used, and how often that kind of flag was confirmed at birth. The clinical note is already written. Copy it.

Earned certainty

Patient screen for J. Nakamura at 27 weeks: Watch, large at target, Confidence: Early, with the validation line visible.

Two scans at 27 weeks is a signal. Four scans at 34 weeks is a finding. In validation, the first kind was confirmed at birth in 29 of 48 cases; the second in 66 of 69.²

Growth Intelligence knows the difference and shows it. The early flag is a Watch, with its own confirmation rate on the screen and what would raise it: a third scan, or 28 weeks. It becomes an Alert when the evidence supports one. Not before.

Patient screen at 36 weeks on three scans: Alert, large at target, Confidence: High.

The number drives the delivery

The estimated fetal weight decides who gets watched, who gets induced, and who gets a cesarean.³ It is least reliable at the extremes, where those decisions get made.

ACOG's own bulletin puts ultrasound sensitivity for a baby over 4,500 g at 10 to 45 percent, no better than a hand on the abdomen.⁴ One in four fetuses estimated at the 20th percentile is actually below the 10th.⁵

Run it on your own patients. Free.

You send.

A de-identified spreadsheet of past pregnancies. Abdominal circumference, gestational age at each scan, gestational age at delivery, and birth weight are all we need. Head circumference, biparietal diameter, and femur length are optional and improve the estimates. A formatting guide and a template are on the retrospective page.

We run.

Every pregnancy is assessed scan by scan, as it would have been at the time, and scored against the recorded birth weight.

You receive.

A written report on your population: what would have been flagged, how many weeks before delivery, and how that compares with the method you use today, on the same cases.

1. Validation cohort of 814 pregnancies with recorded birth outcomes, assessed against the INTERGROWTH-21st standard. The cohort is enriched for growth abnormality (14 percent small and 31 percent large for gestational age at birth), so confirmation rates run higher than in a general population. Growth restriction detected: 92 of 117. Macrosomia detected: 206 of 254. Data on file, August 2026.

2. Screens assessed as they would have appeared at each scan, 3,809 in total, scored against birth weight. Alert screens under the display rule, both tails: 235 of 249 confirmed (small for gestational age 48 of 52, large for gestational age 187 of 197). Data on file, September 2026.

3. Kadji et al., Am J Obstet Gynecol 2022.

4. ACOG Practice Bulletin 216, 2020.

5. Lappen & Myers, Am J Obstet Gynecol 2017.

6. Restatement (Third) of Torts: Medical Malpractice, American Law Institute, May 2024; summarized in Aaron et al., JAMA 2025.

7. Raposo v. United States, D. Alaska 2025.

Not an FDA-cleared device. Clinical decision support under the CDS exemption.