Link: http://www.ncbi.nlm.nih.gov/pubmed/26414203

J Matern Fetal Neonatal Med. 2015 Sep 28:1-8. [Epub ahead of print]
Patterns of fetal lung growth in fetuses with isolated left-sided congenital diaphragmatic hernia.
Antolin E1, Rodriguez R1, Encinas JL2, Herrero B1, Muner M1, Perez R3, Ortiz L3, Bartha JL1.
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Abstract
OBJECTIVE:
To evaluate right lung growth pattern in fetuses with isolated left-sided congenital diaphragmatic hernia (iL-CDH) and to analyze the pattern according to postnatal outcome.

METHODS:
Lung-to-head ratio (LHR) and observed-to-expected LHR (O/E LHR) were obtained in 58 cases. Correlation and regression analysis for the total number of measurements, general linear models for those cases with a least three serial measurements and linear mixed effect models were used to analyze the influence of gestational age on the right lung size. Cases expectantly managed and those with fetal endoscopic tracheal occlusion were analyzed separately.

RESULTS:
LHR, but not O/E LHR, increased significantly with gestational age (GA) (r = 0.43, p = 0.003 and r = -0.13, p = 0.30, respectively). According to neonatal mortality, in those fetuses that died, LHR remained unchanged and O/E LHR decreased significantly with GA (r = 0.07, p = 0.65 and r = -0.37, p = 0.02, respectively). In those cases with at least three serial measurements, the same two patterns were found. Similarly, in cases with expectant management, surviving fetuses showed a significantly higher weekly increase in LHR (p = 0.01) and a trend to a lower weekly decrease in O/E LHR (p = 0.17) than in those that died.

CONCLUSIONS:
Patterns of right lung growth in iL-CDH differ according to postnatal survival. Serial measurements, but not a single one, might increase the prediction of neonatal death.

KEYWORDS:
Congenital diaphragmatic hernia; fetal lung growth; prenatal prognosis; pulmonary hypertension; pulmonary hypoplasia