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Published on: November 20, 2015
Etiology and perinatal outcome of polyhydramnios
M Kollmann1, J Voetsch1, C Koidl2
1Department of Obstetrics and Gynecology, Medical University of Graz.
Insights
Polyhydramnios in singleton pregnancies is often idiopathic but warrants investigation for maternal diabetes, congenital anomalies, and TORCH infections. Careful evaluation for fetal malformations is crucial, especially with co-existing maternal diabetes or small fetuses.
Area of Science:
- Perinatal Medicine
- Maternal-Fetal Medicine
- Obstetrics
Background:
- Polyhydramnios, characterized by excessive amniotic fluid, is a significant obstetric complication.
- Identifying the etiology of polyhydramnios is crucial for predicting perinatal outcomes.
- Previous studies have explored various causes and associations of polyhydramnios.
Purpose of the Study:
- To investigate the etiological factors contributing to polyhydramnios.
- To determine the perinatal outcomes associated with different causes of polyhydramnios.
Main Methods:
- Retrospective analysis of 860 singleton pregnancies diagnosed with polyhydramnios between 2003 and 2011.
- Inclusion criteria included amniotic fluid measurements (single deepest pocket ≥ 8 cm, amniotic fluid index ≥ 25 cm) or subjective assessment.
- Etiologies evaluated included TORCH infections, maternal diabetes, congenital malformations, and idiopathic causes.
Main Results:
- Idiopathic polyhydramnios accounted for 68.8% of cases.
- Maternal diabetes was present in 19.8%, congenital anomalies in 8.5%, and TORCH infections in 2.9%.
- Cardiac defects were the most common fetal anomaly (32.9%). Increased rates of elective cesarean sections were observed in pregnancies with malformations and maternal diabetes. Low birth weight combined with severe polyhydramnios or maternal diabetes correlated with malformations.
Conclusions:
- Diagnosis of polyhydramnios necessitates glucose tolerance testing, detailed sonography (including fetal echocardiography), and TORCH serology.
- Pregnancies with polyhydramnios, particularly those with small fetuses or maternal diabetes, require thorough evaluation for congenital malformations.
Purpose:
To determine causes of polyhydramnios and the respective perinatal outcome.
Materials And Methods:
We retrospectively analyzed cases with polyhydramnios at the Medical University Graz, Austria from 2003 - 2011. Inclusion criteria were single deepest pocket ≥ 8 cm, amniotic fluid index ≥ 25 cm, each of the latter parameters > 95th percentile or subjective impression. Etiologies, including TORCH infection, diabetes and congenital malformations, as well as perinatal outcome were evaluated.
Results:
Out of 860 singleton pregnancies with polyhydramnios, 2.9 % had positive TORCH serology, 8.5 % had congenital anomalies, 19.8 % had maternal diabetes, and 68.8 % were idiopathic. The most common fetal anomalies were cardiac defects (32.9 %). Elective caesarean sections were more common in the groups with malformations and maternal diabetes. Low birth weight combined with severe polyhydramnios or maternal diabetes was associated with malformations.
Conclusion:
Diagnosis of polyhydramnios should prompt glucose-tolerance testing, detailed sonography including fetal echocardiography, and TORCH serology. Especially pregnancies with polyhydramnios and small fetuses as well as those with maternal diabetes should be carefully evaluated for malformations.
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