Title

Short-term weight gain velocity in infants with congenital diaphragmatic hernia (CDH).

Document Type

Article

Publication Date

3-1-2017

Identifier

DOI: 10.1016/j.earlhumdev.2017.01.010

Abstract

BACKGROUND: Appropriate post-natal growth remains a mainstay of therapeutic goals for infants with CDH, with the hypothesis that optimizing linear growth will improve survival through functional improvements in pulmonary hypoplasia. However, descriptions of growth and the effect on survival are limited in affected infants.

OBJECTIVE: Describe in-hospital weight gain related to survival among infants with CDH.

DESIGN/METHODS: Children's Hospitals Neonatal Database (CHND) identified infants with CDH born ≥34weeks' gestation (2010-14). Exclusion criteria were: admission age>7days, death/discharge age75%ile. Descriptive measures and unadjusted Kaplan-Meier analyses describe the implications of WGV on mortality/discharge.

RESULTS: In 630 eligible infants, median WGV was 4.6g/kg/day. After stratification by WGV [Q1: (n=156; <3.1g/kg/day); Q2-3 (n=316; 3.1-5.9g/kg/day), and Q4 (n=158, >5.9g/kg/day)] infants in Q1 had shortest median length of stay, less time on TPN and intervention for gastro-esophageal reflux relative to the other WGV strata (p<0.01 for all). Unadjusted survival estimates revealed that Q1 [hazard ratio (HR)=9.5, 95% CI: 5.7, 15.8] and Q4 [HR=2.9, 95% CI: 1.7, 5.1, p<0.001 for both] WGV were strongly associated with NICU mortality relative to Q2-3 WGV.

CONCLUSION: Variable WGV is evident in infants with CDH. Highest and lowest WGV appear to be related to adverse outcomes. Efforts are needed to develop nutritional strategies targeting optimal growth.

Journal Title

Early human development

Volume

106-107

First Page

7

Last Page

12

MeSH Keywords

Female; Hernias, Diaphragmatic, Congenital; Humans; Infant; Infant Mortality; Infant, Newborn; Length of Stay; Male; Survival Analysis; Weight Gain

Keywords

Congenital diaphragmatic hernia; NICU; Neonatal growth; Neonatal nutrition; Neonatology; Pulmonary hypertension; Pulmonary hypoplasia; Respiratory failure

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