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Markers of growth and nutrition in children with acquired chylothorax post CHD surgery
Kevin N Marzotto1, Karin R Videlefsky1, Meghan P Howell2
1Tulane University School of Medicine, New Orleans, LA, USA.
Insights
Chylothorax after congenital heart defect (CHD) surgery did not impact growth or nutrition markers in children. Further multi-site studies are needed to confirm these findings and guide clinical practice.
Area of Science:
- Pediatric Surgery
- Cardiology
- Critical Care Medicine
Background:
- Acquired chylothorax is a known complication following congenital heart defect (CHD) surgery, occurring in 2-9% of patients.
- Children with CHD are susceptible to failure to thrive, with chylothorax exacerbating this risk.
Purpose of the Study:
- To compare quantitative markers of nutrition and growth in pediatric patients who developed chylothorax after CHD surgery versus controls.
- To identify potential associations between chylous output and growth parameters in affected children.
Main Methods:
- Retrospective chart review of patients under 18 who underwent CHD surgery and developed chylothorax (2018-2022).
- Utilized electronic medical records (EPIC) and ICD-10 codes for subject identification.
- Matched 19 chylothorax cases with 19 controls based on procedure type and age; data analyzed using SPSS.
Main Results:
- No statistically significant differences were found in growth velocity, weight change, or Z-score changes between cases and controls.
- Serum protein and albumin levels showed no significant variation between the groups.
- Maximum chylous output did not correlate significantly with growth velocity or weight changes in the chylothorax group.
Conclusions:
- This study found no statistically significant differences in growth or nutritional markers between children with and without chylothorax post-CHD surgery.
- Larger, multi-site studies are recommended to better understand the clinical impact of chylothorax and inform clinical management.
Background:
Acquired chylothorax is an established complication of CHD surgery, affecting 2-9% of patients. CHD places a child at risk for failure to thrive, with subsequent chylothorax imposing additional risk.
Objective:
We conducted a retrospective chart review to ascertain quantitative markers of nutrition and growth in children affected by chylothorax following CHD surgery between 2018 and 2022 compared to controls.
Methods:
We utilised electronic medical record system, EPIC, at Children's Hospital, New Orleans, targeting subjects < 18 years old who underwent CHD surgery between 2018 and 2022 and developed a subsequent chylothorax. Study subjects were identified using the 10th revision of the International Classification of Diseases codes (ICD-10 codes: J94.0, I89.8, and J90.0). Each chylothorax case (n = 20) was matched by procedure type and age to a control with no chylothorax (n = 20). Data were recorded in REDCap and analysed using SPSS.
Results:
After removal of outliers, we analysed 19 total matched pairs. There was no statistical difference in growth velocity (p = 0.12), weight change (operation to discharge) (p = 0.95), weight change (admission to discharge) (p = 0.35), Z-score change (operation to discharge) (p = 0.90), Z-score change (admission to discharge) (p = 0.21), serum protein (p = 0.88), or serum albumin (p = 0.82). Among cases, linear regression demonstrated no significant association between maximum chylous output and growth velocity (p = 0.91), weight change (operation to discharge) (p = 0.15), or weight change (admission to discharge) (p = 0.98).
Conclusions:
We did not observe statistically significant markers of growth or nutrition in children with chylothorax post-CHD surgery compared to those without chylothorax. Multisite data collection and analysis is required to better ascertain clinical impact and guide clinical practice.
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