Impact of hernia sac in congenital diaphragmatic hernia: Associations with morbidity and mortality.

INTRODUCTION

The impact of hernia sac (HS+) on outcomes in congenital diaphragmatic hernia (CDH) when accounting for defect size is unknown. In a multicenter analysis, considering defect size, we aim to delineate the association of HS+ and morbidity and mortality.

METHODS

A retrospective analysis of CDH Study Group (2007-2024) data was performed. Demographics, defect characteristics, morbidity, and mortality were abstracted. Multilevel regression and parallel Bayesian analysis were performed on 80 % of the data, tested on 20 % hold-out data, and reported in area under the curve (AUC).

RESULTS

7828 operative CDH patients were included. HS+ in 20 %; most common in A and B defects (24 %, 25 %), decreasing in C and D defects (17 %, 7 %); present in a greater proportion of right-sided defects (30 % vs 18 %, p < 0.001). On multilevel logistic regression, with random effects for center, controlling for birth weight, major cardiac abnormalities, chromosomal anomaly, utilization of ECLS, side of the defect, CDHSG A-D, HS+ was not associated with survival (OR 1.19, 95 % CI 0.92-1.53). On Bayesian analysis the OR of HS+ on survival was 1.07 (95 % credible interval 0.87-1.36). HS+ was not associated with pulmonary hypertension (OR 0.97, 95 % CI 0.82-1.14) or cardiac dysfunction at birth. HS+ was associated with a reduction in ECLS utilization (OR 0.60, 95 % CI 0.48-0.74), oxygen status at 30 days (OR 0.56, 95 % CI 0.44-0.70), length of mechanical ventilation (IRR 0.84, 95 % CI 0.79-0.89), and length of hospital stay (IRR 0.92, 95 % CI 0.88-0.96).

CONCLUSION

HS+ is not associated with increased survival, with a neutral Bayesian probability of benefit. However, morbidity outcomes were improved in HS+ patients.