Effect of single and multiple courses of maternal betamethasone on prenatal congenital lung lesion growth and fetal survival

J Pediatr Surg. 2016 Jan;51(1):28-32. doi: 10.1016/j.jpedsurg.2015.10.018. Epub 2015 Oct 23.

Abstract

Purpose: Administration of maternal betamethasone (BMZ) is a therapeutic option for fetuses with large microcystic congenital lung lesions at risk for, or causing, hydrops. Not all fetuses respond to a single course of BMZ. We review our experience with the use of single and multiple courses of maternal BMZ for the management of these patients.

Methods: A retrospective review of fetuses with congenital lung lesions managed with maternal BMZ from 2003 to 2014 was performed.

Results: Forty-three patients were managed with prenatal steroids (28 single course, 15 multiple courses). Single course recipients demonstrated a reduction in lesion size and resolution of hydrops in 82% and 88% of patients respectively compared to 47% and 56% in recipients of multiple steroid courses. Survival of multiple course patients (86%) was comparable to that of single course patients (93%) and improved compared to non-treated historical controls. Multiple course recipients demonstrated an increased need for open fetal surgery and postnatal surgery at a younger age.

Conclusion: Fetuses who fail to respond to a single course of BMZ may benefit, as indicated by hydrops resolution and improved survival, from additional courses. However, failure to respond is indicative of a lesion which may require fetal or immediate neonatal resection.

Keywords: Betamethasone; CCAM; Congenital lung lesion; Fetal surgery; Hydrops; Steroids.

MeSH terms

  • Adult
  • Anti-Inflammatory Agents / administration & dosage*
  • Anti-Inflammatory Agents / therapeutic use
  • Betamethasone / administration & dosage*
  • Betamethasone / therapeutic use
  • Cystic Adenomatoid Malformation of Lung, Congenital / complications
  • Cystic Adenomatoid Malformation of Lung, Congenital / drug therapy*
  • Cystic Adenomatoid Malformation of Lung, Congenital / mortality
  • Cystic Adenomatoid Malformation of Lung, Congenital / pathology
  • Drug Administration Schedule
  • Female
  • Fetal Therapies / methods*
  • Humans
  • Hydrops Fetalis / etiology
  • Infant, Newborn
  • Prenatal Care / methods*
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Anti-Inflammatory Agents
  • Betamethasone