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Single intrauterine fetal death in monochorionic diamniotic twin pregnancies complicated by twin anemia polycythemia sequence leads to significant risks for the surviving co-twin

Single intrauterine fetal death in monochorionic diamniotic twin pregnancies complicated by twin…
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Key Takeaway
Single intrauterine fetal death in TAPS pregnancies carries high risks of preterm birth and cerebral anomalies for the surviving twin.

This systematic review and meta-analysis examined 83 monochorionic diamniotic twin pregnancies complicated by twin anemia polycythemia sequence where one fetus died in utero. The study aimed to determine the impact of this single intrauterine fetal death on the surviving co-twin's outcomes across multiple studies.

The analysis found that co-twin intrauterine fetal death occurred in 4.9% of cases, with a confidence interval ranging from 1.1% to 11.3%. Preterm birth before 34 weeks was highly prevalent, affecting 80.4% of the pregnancies, while 50% resulted in delivery before 28 weeks.

Neurological sequelae were also common, with cerebral abnormalities detected at follow-up ultrasound or fetal MRI in 15% of cases. Postnatal imaging identified anomalies in 9.4% of survivors. The review noted that meaningful pooled data synthesis was not possible due to variations in TAPS staging and donor-recipient classifications.

Further evidence is required to fully elucidate the long-term neurological and neurodevelopmental risks for these children. Clinicians must recognize the severe implications of single intrauterine fetal death in this specific population to guide appropriate counseling and management strategies.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
INTRODUCTION: Most of the studies reporting the outcome of the surviving twin after single intra-uterine fetal death (sIUFD) focused on uncomplicated pregnancies or those affected by twin-to-twin transfusion syndrome, while there is a paucity of data for those complicated by twin anemia polycythemia sequence (TAPS). The aim of this systematic review was to report perinatal outcomes in monochorionic diamniotic (MCDA) twin pregnancies complicated by TAPS after sIUFD, according to gestational age at fetal loss and the presence of pregnancy-related comorbidities. MATERIAL AND METHODS: MEDLINE, EMBASE, and The Cochrane Library were searched for studies reporting the outcome of monochorionic twin pregnancies complicated by TAPS experiencing single IUFD. The primary outcome was the occurrence of co-twin IUFD. Secondary outcomes were neonatal death (NND), preterm birth (PTB) <34, <32, and <28 weeks of gestation, cerebral abnormalities detected at follow-up prenatal ultrasound, fetal magnetic resonance imaging (MRI) or postnatal imaging (ultrasound or MRI), and adverse neurodevelopmental outcome. Random-effects meta-analysis of proportions was used to analyze the data, and results were reported as pooled proportions or odd ratios (OR) with 95% CI. RESULTS: Eleven studies (83 twin pregnancies affected by TAPS, either spontaneous or post-laser, and complicated by single IUFD) were included in the systematic review and 10 (78 pregnancies) in the meta-analysis. Co-twin IUFD occurred in 4.9% (95% CI 1.1-11.3) after a single IUFD in pregnancies affected by TAPS, while there was no case of NND. PTB, either spontaneous or iatrogenic, occurred in 80.4% (95% CI 44.3-99.5) <34 weeks, and 50.0% (95% CI 16.3-83.7) <28 weeks of cases. Intra-uterine transfusion was required in 8.0% (95% CI 0.9-38.3). Cerebral anomalies at follow-up ultrasound or fetal MRI were reported in 15.0% (95% CI 8.2-78.3) and 11.4% (95% CI 2.4-55.7) of cases, while anomalies at post-natal imaging in 9.4% (95% CI 5.6-57.6) of cases. It was not possible to perform a meaningful pooled data synthesis on the observed outcomes according to the type and staging of TAPS and according to the donor or recipient twin. CONCLUSIONS: The occurrence of co-twin death after single IUFD in pregnancies complicated by TAPS appears low, while cerebral abnormalities detected either pre- or post-natally occur in 10-15% of cases. Further evidence is needed to elucidate the long-term neurological and neurodevelopmental risk of these children.
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