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Polyhydramnios and fetal intrauterine growth restriction: ominous combination

G K Sickler1, D A Nyberg, R Sohaey

  • 1Center for Perinatal Disease, Swedish Hospital Medical Center, Seattle, Washington, USA.

Insights

The combination of polyhydramnios and intrauterine growth restriction in fetuses is a serious condition. Most affected infants have major anomalies or chromosomal abnormalities, necessitating genetic evaluation.

Area of Science:

  • Perinatology
  • Medical Genetics
  • Prenatal Diagnosis

Background:

  • Polyhydramnios and intrauterine growth restriction (IUGR) are common prenatal findings.
  • The combined significance of these conditions requires further investigation.

Purpose of the Study:

  • To evaluate the prognostic significance of concurrent polyhydramnios and intrauterine growth restriction.
  • To determine the incidence of anomalies and mortality in affected fetuses.

Main Methods:

  • Retrospective review of 39 fetuses diagnosed with polyhydramnios and IUGR via prenatal sonography over 6 years.
  • Polyhydramnios defined as amniotic fluid index (AFI) ≥ 24; IUGR defined as estimated fetal weight < 10th percentile.
  • Postnatal evaluation for major anomalies and chromosomal abnormalities.

Main Results:

  • 92% of fetuses had major anomalies; 67% of those without prenatal sonographic anomalies had postnatal anomalies.
  • Chromosomal abnormalities were found in 38% of cases (including trisomy 18 and 13).
  • The overall mortality rate was 59%.

Conclusions:

  • The combination of polyhydramnios and IUGR is an ominous sign with a high rate of fetal anomalies and mortality.
  • Genetic analysis and thorough fetal assessment are crucial for fetuses diagnosed with both conditions.
  • Even in the absence of other sonographic findings, significant anomalies are common.

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