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Short-term weight gain velocity in infants with congenital diaphragmatic hernia (CDH)
Jason Gien1, Karna Murthy2, Eugenia K Pallotto3
1Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, United States.
Insights
Infants with congenital diaphragmatic hernia (CDH) have variable weight gain velocity (WGV). Both very low and very high WGV are linked to increased NICU mortality, suggesting a need for targeted nutritional strategies.
Area of Science:
- Neonatalogy
- Pediatric Surgery
- Nutritional Science
Background:
- Optimizing post-natal growth is crucial for infants with congenital diaphragmatic hernia (CDH).
- The hypothesis is that improved linear growth enhances survival by addressing pulmonary hypoplasia.
- Limited data exist on growth patterns and their impact on survival in CDH infants.
Purpose of the Study:
- To investigate the relationship between in-hospital weight gain velocity (WGV) and survival in infants with CDH.
- To identify optimal WGV ranges associated with better outcomes in CDH patients.
Main Methods:
- Utilized the Children's Hospitals Neonatal Database (CHND) for infants with CDH born at ≥34 weeks gestation (2010-2014).
- Calculated Weight Gain Velocity (WGV) and stratified infants into quartiles (Q1, Q2-3, Q4).
- Employed descriptive statistics and unadjusted Kaplan-Meier analyses to assess WGV's impact on mortality and discharge.
Main Results:
- Median WGV was 4.6 g/kg/day in 630 eligible infants.
- Infants in the lowest WGV quartile (Q1) had shorter hospital stays and less need for TPN and GER interventions.
- Both the lowest (Q1) and highest (Q4) WGV quartiles were significantly associated with increased NICU mortality compared to the middle quartiles (Q2-3).
Conclusions:
- Weight gain velocity varies significantly among infants with CDH.
- Extremes in WGV (both very low and very high) are associated with adverse outcomes, including higher NICU mortality.
- Developing nutritional strategies to achieve optimal growth is essential for improving survival in CDH infants.
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 age<14days, or surgical CDH repair prior to admission. Weight gain velocity (WGV: g/kg/day) was calculated using an established exponential approximation and the cohort stratified by Q1: <25%ile, Q2-3: 25-75%ile, and Q4: >75%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.
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