Polyhydramnios
Roya Sohaey, MD
DIFFERENTIAL DIAGNOSIS
Common
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Idiopathic
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Macrosomia
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Diabetes
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Hydrops
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Twin-Twin Transfusion Syndrome
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Fetal Bowel Obstruction
Less Common
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Arthrogryposis, Akinesia Sequence
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Skeletal Dysplasia, Severe
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Chorioangioma
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Cystic Adenomatoid Malformation
Rare but Important
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Mesoblastic Nephroma
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Unilateral Ureteropelvic Junction Obstruction
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
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Amniotic fluid index (AFI)
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Divide uterus into 4 equal quadrants
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Measure maximum vertical pocket (MVP)
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Avoid fetal parts/cord in MVP
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Add the 4 MVPs to calculate AFI
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AFI/gestational age normogram tables available
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> 24 cm AFI = polyhydramnios
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Twin fluid assessment
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Measure MVP for each fetus
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≥ 8 cm = polyhydramnios
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Helpful Clues for Common Diagnoses
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Idiopathic
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Most common cause (2/3)
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Mild, stable finding
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Normal patient and fetus
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No diabetes or fetal anomalies
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28% with fetal macrosomia
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Macrosomia
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Estimated fetal weight > 90th percentile
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Large abdominal circumference is a hallmark finding
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↑ Truncal echogenic fat
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Causes
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Hereditary characteristics
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Maternal obesity
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Diabetes
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Beckwith-Wiedemann syndrome
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Diabetes
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Gestational diabetes (most common)
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Glucose intolerance during pregnancy
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Oral glucose tolerance test given between 24-28 wks
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Pregestational diabetes (type 1 or 2)
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Polyhydramnios associated with poor glucose control
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May be first finding in pregnancy
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Associated with macrosomia
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Hydrops
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Excessive fetal fluid accumulation (2 or more body cavities)
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Anasarca
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Pleural effusion (± pericardial)
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Ascites
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Amniotic fluid may be ↑ or ↓
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Immune hydrops (10%)
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Non-immune (90%)
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Infection
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Any cause of fetal anemia
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Any cause of fetal heart failure
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Lymphatic obstruction
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Aneuploidy associations
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Turner syndrome (cystic hygroma)
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Trisomy 21
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Trisomy 18
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Twin-Twin Transfusion Syndrome
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Monochorionic twinning
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Artery-to-vein anastomoses in shared placenta
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Donor twin partly perfuses recipient twin
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Fluid discrepancy may be 1st sign of developing twin-twin transfusion syndrome (need to follow carefully)
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Recipient twin with polyhydramnios
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Larger twin
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Donor twin with oligohydramnios
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Smaller “stuck” twin
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Fetal Bowel Obstruction
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Late polyhydramnios (> 24 wks)
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Esophageal atresia
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Absent or small stomach
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1/3 with trisomy 18 or 21
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Associated with VACTERL syndrome
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Duodenal atresia
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“Double-bubble” appearance
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1/3 with trisomy 21
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Jejunal, ileal atresia
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“Sausage-shaped” bowel loops
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Helpful Clues for Less Common Diagnoses
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Arthrogryposis, Akinesia Sequence
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Heterogeneous group of disorders
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Lack of extremity motion
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Contractures
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Polyhydramnios from ↓ fetal movement/swallowing
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Associations
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Trisomy 18
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Autosomal dominant and recessive syndromes
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Skeletal Dysplasia, Severe
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Common dysplasias
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Thanatophoric
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Achondroplasia
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Achondrogenesis
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Osteogenesis imperfecta
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Common skeletal findings
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Short limbs
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Poor ossification
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Bowed or broken bones
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Craniosynostosis
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Polyhydramnios common in 3rd trimester
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Chorioangioma
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Benign, vascular placental tumor
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Large masses (> 5 cm): ↑ Complications
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Polyhydramnios
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Transudate from leaky vessels
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Hydrops
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Arteriovenous shunting in mass
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Fetal anemia from hemolysis
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Cystic Adenomatoid Malformation
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Lung hamartoma
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Microcystic and macrocystic types
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Polyhydramnios etiology
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Esophagus compression
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Associated with hydrops
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Mass may make fluid
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Helpful Clues for Rare Diagnoses

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