SynthesisUltrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology2026
Multiple pregnancy with complete hydatidiform mole and coexisting normal fetus: systematic review and meta-analysis of clinical outcomes from non-randomized studies.
Synthesis in Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Article
- Complete hydatidiform mole with coexisting fetus: A case report.Case reports in women's health · 2026Article
- Complete hydatidiform mole in one twin after embryo transfer: a case report and literature review.Frontiers in medicine · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveComplete hydatidiform mole and coexisting normal fetus (CHMCF) is a rare condition for which there is significant heterogeneity in diagnosis, counseling and management of complications. The objective of this study was to summarize the prevalence of clinical outcomes in reported cases of CHMCF.
methodsA systematic literature search was conducted in PubMed, Embase and Scopus databases from inception until 1 October 2024. Case series and cohort studies including at least three cases of histologically confirmed CHMCF were included. A random-effects model was used for meta-analysis of proportions and heterogeneity was estimated using Higgins' I
resultsQuantitative synthesis included 19 studies and 417 cases of CHMCF. Diagnosis was made using ultrasound in 76.0% (95% CI, 58.5-90.6%) of cases and occurred in the first trimester in 52.7% (95% CI, 34.0-71.0%). Symptoms at diagnosis were present in 80.5% (95% CI, 66.1-92.3%) of cases, with vaginal bleeding being the most common symptom both at diagnosis and later in pregnancy. The pooled proportion of elective pregnancy termination was 48.8% (95% CI, 32.7-65.1%), with 6.2% (95% CI, 1.0-13.9%) due to maternal complications. The pooled proportion of live births was 46.5% (95% CI, 36.1-57.1%), with most being delivered by Cesarean section (71.2% (95% CI, 42.4-94.4%)). Preterm birth (< 37 weeks) occurred in 67.8% (95% CI, 44.7-88.1%) of cases, very preterm birth (< 32 weeks) in 12.4% (95% CI, 0.2-33.9%) and miscarriage (fetal death < 24 weeks) in 32.7% (95% CI, 26.1-39.6%). Pre-eclampsia was present in 17.8% (95% CI, 5.9-32.7%) of cases and postpartum hemorrhage occurred in 42.7% (95% CI, 5.1-84.8%). A small-for-gestational-age neonate (birth weight < 10
conclusionsPregnancies with CHMCF present a high risk of maternal, obstetric and neonatal complications, including miscarriage, pre-eclampsia, small-for-gestational age, postpartum hemorrhage and preterm birth. The risk of developing gestational trophoblastic neoplasia was not clearly mitigated by early pregnancy termination. Early diagnosis, referral to a maternal-fetal medicine unit with expertise in trophoblastic disorders and extensive implementation of screening protocols for preterm birth and pre-eclampsia are recommended to facilitate timely intervention aimed at outcome improvement. © 2025 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
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