Prenatal Diagnosis · 2012 · 54 citations · 19 references
MedicinePathologyPediatricsMaternal-fetal MedicinePediatric PathologyPrenatal DiagnosisFetal PathologyFirst-trimester UltrasoundPrenatal AssessmentPrenatal CarePrenatal ImagingAntenatal HydronephrosisFirst Trimester ImagingFirst-trimester Pregnancy UltrasoundPediatric Hydronephrosis EvaluationPrenatal Diagnostic PathologyPrenatal Hydronephrosis EvaluationPrenatal Vesicoureteral Reflux
OBJECTIVES: Clinical significance and management of prenatal hydronephrosis (PNH) are sources of debate. Existing studies are flawed with biased cohorts or inconsistent follow-up. We aimed to evaluate the incidence of pathology in a large cohort of PNH and assess the biases and outcomes of this population. METHODS: We reviewed 1034 charts of fetuses with PNH. Records of delivered offspring were reviewed at a pediatric center and analyzed with respect to prenatal and postnatal pathology and management. RESULTS: Prenatal resolution of hydronephrosis occurred in 24.7% of pregnancies. On first postnatal ultrasound, some degree of dilatation was present in 80%, 88% and 95% of mild, moderate and severe PNH cases, respectively. At the end of follow-up, hydronephrosis persisted in 10%, 25% and 72% of children, respectively. Incidence of vesicoureteral reflux did not correlate with severity of PNH. Children with postnatal workup had more severe PNH than those without. CONCLUSIONS: Despite prenatal resolution totalizing 25%, pelvic dilatation persisted on first postnatal imaging in most cases, thus justifying postnatal ultrasound evaluation. Whereas most mild cases resolved spontaneously, a quarter of moderate and more than half of severe cases required surgery. Patients with postnatal imaging and referral had more severe PNH, which could result in overestimation of pathology.
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Antenatal ultrasonography to detect fetal renal abnormalities: a prospective screening programme.
L. N. Livera, D S Brookfield, J. A. Egginton et al. · BMJ · 1989 · 227 citations · Full text