Thoracoamniotic Shunting for Fetal Hydrothorax: Predictors of Intrauterine Course and Postnatal Outcome

Fetal Diagn Ther. 2017;41(1):58-65. doi: 10.1159/000446110. Epub 2016 May 13.

Abstract

Objective: To assess predictors for survival and complications among a relatively large cohort of fetuses with hydrothorax treated by thoracoamniotic shunting.

Methods: All cases with hydrothorax treated by thoracoamniotic shunting in a 10-year period (2002-2011) in two centers were retrospectively reviewed.

Results: A total of 78 fetuses with hydrothorax treated with thoracoamniotic shunting were included in the study. Mean gestational age at diagnosis was 25.6 weeks (12-34 weeks). Initial thoracoamniotic shunting was performed at a mean gestational age of 26.5 weeks (16-33 weeks). A mean of 2.53 shunts (1-7) were inserted per fetus. Of the 78 fetuses, 9 (11.5%) died in utero, 69 (88.5%) were born alive and 46 (59%) survived. Prognostic markers significantly associated with nonsurvival were polyhydramnios, hydrops placentae and mediastinal shift at initial scan, onset of hydrops after first shunt placement, rupture of membranes, a shunt-birth interval <4 weeks and low gestational age at birth. In our cohort, fetuses with trisomy 21 had a significantly better survival than euploid fetuses.

Conclusions: Although associated with a significant rate of repeated interventions, thoracoamniotic shunting in fetuses with severe hydrothorax results in an overall survival rate of 59%. Fetuses with hydrothorax and trisomy 21 have a better survival when compared to euploid fetuses.

MeSH terms

  • Chylothorax / congenital*
  • Chylothorax / diagnostic imaging
  • Chylothorax / mortality
  • Chylothorax / surgery
  • Down Syndrome / complications
  • Female
  • Fetal Therapies / methods*
  • Gestational Age
  • Humans
  • Hydrops Fetalis / diagnostic imaging
  • Hydrops Fetalis / mortality
  • Polyhydramnios / diagnostic imaging
  • Polyhydramnios / mortality
  • Pregnancy
  • Prognosis
  • Retrospective Studies
  • Thoracostomy / methods
  • Treatment Outcome

Supplementary concepts

  • Chylothorax, congenital