Literature DB >> 26563530

Risk-stratification of severity for infants with CDH: Prenatal versus postnatal predictors of outcome.

Adesola C Akinkuotu1, Stephanie M Cruz1, Paulette I Abbas1, Timothy C Lee1, Stephen E Welty2, Oluyinka O Olutoye3, Christopher I Cassady4, Amy R Mehollin-Ray4, Rodrigo Ruano5, Michael A Belfort5, Darrell L Cass6.   

Abstract

PURPOSE: The purpose of this study was to compare the predication accuracy of a newly described postnatally-based clinical prediction model to fetal imaging-based predictors of mortality for infants with CDH.
METHODS: We performed a retrospective review of all CDH patients treated at a comprehensive fetal care center from January 2004 to January 2014. Prenatal data reviewed included lung-to-head ratio (LHR), observed/expected-total fetal lung volume (O/E-TFLV), and percent liver herniation (%LH). Based on the postnatal prediction model, neonates were categorized as low, intermediate, and high risk of death. The primary outcome was 6-month mortality.
RESULTS: Of 176 CDH patients, 58 had a major cardiac anomaly, and 28 had a genetic anomaly. Patients with O/E-TFLV <35% and %LH >20% were at increased risk for mortality (44% and 36%, respectively). There was a significant difference in mortality between low, intermediate, and high-risk groups (4% vs. 22% vs. 51%; p<0.001). On multivariate regression, the O/E-TFLV and postnatal-based mortality risk score were the two independent predictors of 6-month mortality.
CONCLUSION: The CDH Study Group postnatal predictive model provides good discrimination among three risk groups in our patient cohort. The prenatal MRI-based O/E-TFLV is the strongest prenatal predictor of 6-month mortality in infants with CDH and will help guide prenatal counseling and discussions regarding fetal intervention and perinatal management.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CDH; Fetal lung volumes; Prenatal predictors; Risk stratification

Mesh:

Year:  2015        PMID: 26563530     DOI: 10.1016/j.jpedsurg.2015.10.009

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  8 in total

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8.  Changes in vasoactive pathways in congenital diaphragmatic hernia associated pulmonary hypertension explain unresponsiveness to pharmacotherapy.

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  8 in total

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