# Prediction of survival after fetoscopic laser surgery for early‐onset twin‐to‐twin transfusion syndrome

**Authors:** S. Prasad, F. G. Sileo, J. Binder, E. Brunelli, N. Chianchiano, C. M. Coutinho, F. D'Antonio, M. Döbert, A. Fichera, Y. Gielchinsky, K. Hecher, C. Iacovella, S. Malone, A. Martinez‐Varea, L. N. Nørgaard, C. Rodo, T. Simões, F. Slaghekke, Y. Yinon, A. Khalil, F. Bahlmann, F. Bahlmann, E. Carreras, S. G. Alletti, O. Yaghi, E. Lopriore, M. M. Okido, A. Markovich, D. Mohammed, E. Moreno‐Perez, F. Prefumo, A. Queirós, J. M. Rosello, K. Sundberg, M. Yeoh, A. Youssef, C. O. Ulusoy

PMC · DOI: 10.1002/uog.70178 · Ultrasound in Obstetrics & Gynecology · 2026-02-15

## TL;DR

This study examines survival rates and predictors of survival after laser surgery for early-onset twin-to-twin transfusion syndrome.

## Contribution

The study identifies key predictors of dual-twin survival following fetoscopic laser surgery for early-onset TTTS.

## Key findings

- Dual-twin survival rate was 51.5% after fetoscopic laser surgery for early-onset TTTS.
- Absent or reversed end-diastolic flow in the donor umbilical artery and lower gestational age at birth were linked to lower survival rates.

## Abstract

Data on early‐onset twin‐to‐twin transfusion syndrome (TTTS) are scarce and, therefore, evidence‐based counseling and management of these pregnancies are challenging. This study aimed to investigate survival rates and establish predictors of survival after fetoscopic laser surgery (FLS) for early‐onset TTTS.

This was an international multicenter retrospective cohort study of monochorionic diamniotic twin pregnancies complicated by TTTS diagnosed before 18 + 0 weeks' gestation that underwent FLS. The primary outcome was dual‐twin survival at 28 days after birth. Secondary outcomes included survival of at least one twin and dual‐twin demise at 28 days after birth. Monoamniotic twin, triplet and higher‐order multiple pregnancies, pregnancies with chromosomal or structural fetal anomaly and TTTS cases not treated by FLS were excluded. Pre‐, intra‐ and postoperative characteristics were analyzed using multivariable logistic regression analysis. Discriminative performance was assessed using receiver‐operating‐characteristics‐curve analysis.

A total of 485 cases of early‐onset TTTS that underwent FLS were included. The rates of dual‐twin survival and survival of at least one twin at 28 days after birth were 51.5% (250/485) and 76.7% (372/485), respectively, while 23.3% (113/485) of cases resulted in dual‐twin demise. Multivariable logistic regression analysis showed that absent or reversed end‐diastolic flow (AREDF) in the donor umbilical artery (adjusted odds ratio (aOR), 0.487 (95% CI, 0.273–0.867)) and absent or reversed a‐wave in the donor ductus venosus (aOR, 0.299 (95% CI, 0.110–0.810)) at the time of TTTS diagnosis were associated independently with decreased odds of dual‐twin survival, while higher gestational age at birth was associated with increased odds of both dual‐twin survival (aOR, 1.172 (95% CI, 1.117–1.229)) and survival of at least one twin (aOR, 2.053 (95% CI, 1.699–2.481)). The model for dual‐twin survival showed modest discriminative performance with poor overall fit.

The presence of AREDF in the donor umbilical artery and absent or reversed a‐wave in the donor ductus venosus, at the time of diagnosis of TTTS, and lower gestational age at birth were independent adverse predictors for dual‐twin survival following FLS in cases of TTTS diagnosed before 18 weeks. Future studies should explore the impact of surgical technique on survival rates. © 2026 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

## Linked entities

- **Diseases:** twin-to-twin transfusion syndrome (MONDO:0019805), TTTS (MONDO:0019805)

## Full-text entities

- **Diseases:** PPROM (MESH:C563032), Twin-to- (MESH:D004200), bleeding (MESH:D006470), GA (MESH:D016640), polycythemia (MESH:D011086), fetal loss (MESH:D005315), transfusion syndrome (MESH:D065227), TTTS (MESH:D005330), oligohydramnios (MESH:D016104), Selective fetal growth restriction (MESH:D005317), chromosomal fetal anomaly (MESH:D000013), placental vascular occlusion (MESH:D008641), preterm labor (MESH:D007752), aneuploidy (MESH:D000782), functional impairment (MESH:D003072), tricuspid regurgitation (MESH:D014262), pregnancy loss (MESH:D000022), cardiac hypertrophy (MESH:D006332), IUFD (MESH:D005313), cardiac dysfunction (MESH:D006331), cardiovascular (MESH:D002318), preterm (MESH:D047928), fatality (MESH:C565541), prelabor rupture of membranes (MESH:D005322), ductus venosus (MESH:C562830), TAPS (MESH:D000740), polyhydramnios (MESH:D006831), FLS (MESH:D000267), NND (MESH:D066087)
- **Chemicals:** AREDF (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12951265/full.md

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Source: https://tomesphere.com/paper/PMC12951265