EXIT (ex utero intrapartum treatment) in a growth restricted fetus with tracheal atresia. Gonzales, S., Goudy, S, Prickett, K, & Ellis, J Int J Pediatr Otorhinolaryngol, 105:72–74, February, 2018. Paper doi abstract bibtex Congenital high airway obstruction syndrome (CHAOS) encompasses a heterogeneous group of pathologies leading to poor lung development and difficulty oxygenating the newborn after delivery. While previously uniformly fatal, the ex utero intrapartum therapy (EXIT) procedure has provided a method to treat these patients and provide an airway to potentiate survival. We present a patient diagnosed prenatally with CHAOS secondary to tracheal atresia complicated by severe intra-uterine growth restriction (IUGR) who was successfully delivered via an EXIT procedure at 33-weeks. Multidisciplinary care and planning is paramount.
@article{gonzales_exit_2018,
title = {{EXIT} (ex utero intrapartum treatment) in a growth restricted fetus with tracheal atresia.},
volume = {105},
url = {https://www.ncbi.nlm.nih.gov/pubmed/29447823},
doi = {10.1016/j.ijporl.2017.12.010},
abstract = {Congenital high airway obstruction syndrome (CHAOS) encompasses a heterogeneous group of pathologies leading to poor lung development and difficulty oxygenating the newborn after delivery. While previously uniformly fatal, the ex utero intrapartum therapy (EXIT) procedure has provided a method to treat these patients and provide an airway to potentiate survival. We present a patient diagnosed prenatally with CHAOS secondary to tracheal atresia complicated by severe intra-uterine growth restriction (IUGR) who was successfully delivered via an EXIT procedure at 33-weeks. Multidisciplinary care and planning is paramount.},
language = {eng},
journal = {Int J Pediatr Otorhinolaryngol},
author = {Gonzales, SK and Goudy, S and Prickett, K and Ellis, J},
month = feb,
year = {2018},
keywords = {Young Adult},
pages = {72--74}
}
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