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Tracheal diameter at birth in severe congenital diaphragmatic hernia treated by fetal endoscopic tracheal occlusion
Author(s) -
Jani J.,
Valencia C.,
Cannie M.,
Vuckovic A.,
Sellars M.,
Nicolaides K.H.
Publication year - 2011
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.2806
Subject(s) - congenital diaphragmatic hernia , medicine , gestational age , diaphragmatic breathing , fetus , diaphragmatic hernia , occlusion , lung , hernia , surgery , anesthesia , pregnancy , pathology , genetics , alternative medicine , biology
Objective To investigate tracheal dimensional differences seen at birth following fetal endoscopic tracheal occlusion (FETO) in cases of severe congenital diaphragmatic hernia (CDH) and to report on their clinical follow‐up. Patients and Methods In chest X‐rays, taken within 48 h after birth, we measured the tracheal diameter at the level of the tracheal entry into the chest, 1 cm above the level of the carina and at middistance between these sites in 37 fetuses with severe CDH treated by FETO. These measurements were compared with those in 74 preterm and term neonates with no congenital lung abnormalities. Results In the CDH group, compared to the controls, the tracheal diameter corrected for gestational age was significantly larger at all three levels of the trachea. Regression analysis showed that significant predictors of the tracheal diameter at the level of tracheal entry into the chest were the observed to expected (o/e) lung area to head circumference ratio (LHR) and the duration of tracheal occlusion. In the CDH group, postnatal follow‐up until the age of 22 months (1–70) showed that 5 of 24 neonates had an effort‐induced barking cough. Conclusion A large number of infants with severe CDH surviving after FETO have a degree of tracheomegaly that is associated with the severity of CDH as assessed by pre‐FETO LHR. This tracheomegaly does not constitute an obvious clinical problem. Copyright © 2011 John Wiley & Sons, Ltd.