Managing infants with craniofacial malformations - Where to go next?

Semin Fetal Neonatal Med. 2021 Dec;26(6):101289. doi: 10.1016/j.siny.2021.101289. Epub 2021 Sep 17.

Abstract

Treatment of infants with craniofacial malformations, e.g. Robin sequence, is characterized by considerable heterogeneity and a lack of randomized trials to identify an optimal approach. We propose to establish an international register using a common minimal dataset that will better allow for a comparison between key determinants and outcomes in these patients. In infants, this should include an assessment of mandibular micrognathia, glossoptosis, upper airway obstruction, weight gain and mode of feeding. Later on, neurocognition, speech development, hearing and quality of life should also be included. Together, these data will help better to advice parents on which treatment to choose for their baby with a craniofacial malformation.

Publication types

  • Review

MeSH terms

  • Airway Obstruction*
  • Humans
  • Infant
  • Pierre Robin Syndrome* / therapy
  • Quality of Life