- Design
- Prospective multicentre cohort, four US programmes, 2016 to 2025
- Population
- 60 uterus transplant recipients, 42 living donors and the 48 neonates born
- Primary outcome
- Surgical complications, live birth or ongoing pregnancy, and child development
- Effect
- Live birth or ongoing pregnancy 70.0% (42/60); recipient reoperation 28.3% (17/60); preterm birth 58.3% of 48 neonates
A prospective cohort from the four US centres performing the procedure followed 60 uterus transplants between 2016 and 2025. Fifty-two recipients had Mayer-Rokitansky-Küster-Hauser syndrome, and 42 grafts came from living donors.
There were no deaths or life-threatening complications. Reoperation was needed in 17 of 60 recipients (28.3%), including graft loss from vascular thrombosis, and in 6 of 42 living donors (14.3%), with ureteral injury and vaginal cuff dehiscence among the causes. By December 2025, 42 recipients (70.0%) had a live birth or ongoing pregnancy and nine had two live births.
Among 48 neonates, median gestation at delivery was about 36.7 weeks and 58.3% were born preterm. Neurodevelopment was normal at discharge and six months. At three years (n = 29), two children had an autism diagnosis. The cohort is small and from high-volume research programmes, so these are not rates to quote for other settings.
- 70% of recipients reached a live birth or ongoing pregnancy.
- 28.3% of recipients and 14.3% of living donors needed reoperation.
- 58.3% of babies were born preterm, so obstetric care is high-risk.
- Three-year follow-up covers only 29 children.
- Counsel patients with absolute uterine factor infertility on surgical risk to the donor as well as the recipient.
Why it matters
Counselling can now draw on a decade of aggregate data rather than single-centre reports.
Don't overread it
These are results from a handful of experienced centres and say nothing about outcomes elsewhere or about availability in India.
The statistics, in plain English
With 60 transplants, a single event moves a percentage by nearly two points, so the rates are imprecise. Follow-up of the children is short and incomplete, so the absence of other diagnoses at three years does not exclude later problems.
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