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Published on: September 11, 2021
One-year outcomes for congenital diaphragmatic hernia
Y Wang1, K Honeyford1, P Aylin1
1Dr Foster Unit, Department of Primary Care and Public Health, Imperial College London London UK.
Insights
Congenital diaphragmatic hernia (CDH) outcomes in England showed no significant time trends but high variation among specialist centers. Further investigation into care regionalization is recommended for this serious congenital anomaly.
Area of Science:
- Pediatric Surgery
- Neonatal Outcomes
- Public Health Surveillance
Background:
- Congenital diaphragmatic hernia (CDH) is a severe birth defect with significant mortality and long-term health issues.
- Benchmarking outcomes is crucial for improving care for infants with CDH.
Purpose of the Study:
- To analyze trends in 1-year survival and hospital volume outcomes for congenital diaphragmatic hernia (CDH) in England.
- To assess the association between hospital volume and patient outcomes in specialist pediatric surgery centers.
Main Methods:
- Retrospective analysis of 2336 infants with CDH in England (2003-2016) using Hospital Episode Statistics.
- Key outcomes measured: 1-year mortality, neonatal length of stay (nLOS), total bed-days, and readmission rates.
- Statistical analysis to determine associations between risk factors, interventions (e.g., ECMO), and outcomes, including hospital volume.
Main Results:
- 1-year mortality was 31.2%; no significant time trends in incidence or outcomes were observed.
- Higher mortality linked to low birthweight (<1kg), early gestational age (≤36 weeks), and Black ethnicity.
- Extracorporeal membrane oxygenation (ECMO) was associated with increased mortality and resource utilization; significant variation in outcomes and resource use existed among specialist centers without a clear volume-outcome relationship.
Conclusions:
- Congenital diaphragmatic hernia (CDH) outcomes in England are comparable to other developed nations.
- High variability in outcomes among specialist pediatric centers warrants further investigation, suggesting potential benefits of care regionalization.
Background:
Congenital diaphragmatic hernia (CDH) is a congenital anomaly with high mortality and long-term morbidity. The aim of this study was to benchmark trends in 1-year and hospital volume outcomes for this condition.
Methods:
This study included all infants born with CDH in England between 2003 and 2016. This was a retrospective analysis of the Hospital Episode Statistics database. The main outcomes were: 1-year mortality, neonatal length of hospital stay (nLOS), total bed-days at 1 year and readmission rate. The association between hospital volume and outcomes was assessed for specialist paediatric surgery centres.
Results:
A total of 2336 infants were included (incidence 2·5 per 10 000 live births). No significant time trends were found in incidence and main outcomes. Some 1491 infants (63·8 per cent) underwent surgical repair. The 1-year mortality rate was 31·2 per cent. Median nLOS and total bed-days were 17 and 19 days respectively. The readmission rate in specialist paediatric centres was 6·3 per cent. Higher mortality was associated with birthweight lower than 1 kg (OR 5·90, 95 per cent c.i. 1·03 to 33·75), gestational age of 36 weeks or less (OR 1·75, 1·12 to 2·75) and black ethnicity (OR 2·13, 1·03 to 4·48). Only 4·0 per cent had extracorporeal membrane oxygenation, which was associated with higher mortality (OR 5·34, 3·01 to 9·46), longer nLOS (OR 3·70, 2·14 to 6·14) and longer total bed-days (OR 3·87, 2·19 to 6·83). Specialist paediatric centres showed variation in 30-day mortality (4·6 per cent with 84 per cent coefficient of variation), nLOS (median 25 (i.q.r. 15-42) days) and total bed-days (median 28 (i.q.r. 16-51) days), but no significant volume-outcome relationship.
Conclusion:
Key outcomes for CDH were similar to those of other developed countries. High variation among specialist paediatric centres was found and should be investigated further to explore the value of regionalization of care.
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