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Digestive congenital anomalies: a call for equity in global neonatal surgical care
Mohammad Rahmanian1,2, Mehdi Azizmohammad Looha3
1Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Insights
Digestive congenital anomalies (DCAs) disproportionately affect newborns in low-resource settings, leading to preventable deaths. Global action is needed to improve access to timely surgical care and reduce inequities in neonatal survival.
Area of Science:
- Global health
- Neonatal surgery
- Pediatric surgery
Background:
- Digestive congenital anomalies (DCAs) represent a significant global health challenge, particularly impacting the neonatal period.
- Optimal outcomes for newborns with DCAs rely on a comprehensive continuum of care, from prenatal diagnosis to specialized postnatal surgical intervention.
- Existing healthcare disparities result in vastly different survival rates for DCAs between high-income and low- and middle-income countries.
Purpose of the Study:
- To highlight the global burden and profound inequities associated with digestive congenital anomalies.
- To emphasize the critical need for accessible, timely, and life-saving surgical interventions for newborns with correctable DCAs.
- To advocate for strengthened global action to bridge the equity gap in neonatal surgical care.
Main Methods:
- Analysis of the global burden and survival rates of digestive congenital anomalies.
- Review of current care pathways, highlighting disparities in access to prenatal diagnosis, specialized delivery, and neonatal surgery.
- Examination of the impact of socioeconomic factors on treatment outcomes for DCAs.
Main Results:
- The burden of DCAs is concentrated in the neonatal period, with survival heavily dependent on immediate postnatal surgical care.
- Significant inequities persist, with high survival in high-income countries contrasted by preventable mortality in low- and middle-income countries due to limited surgical capacity and delayed care.
- Preventive measures, such as maternal nutrition and folate supplementation, are identified as crucial public health components.
Conclusions:
- Addressing the equity gap in DCA care requires substantial investment in neonatal surgical capacity and integration into universal health coverage.
- Strengthening birth defect surveillance systems is essential for monitoring and improving outcomes for newborns with DCAs.
- Coordinated global efforts are imperative to ensure all newborns with correctable digestive anomalies receive timely, life-saving surgical treatment.
Abstract:
The global burden of digestive congenital anomalies (DCAs) remains significant, with the recent analysis by Cai et al. highlighting both progress and profound inequities. The disease burden is concentrated in the neonatal period, where the first days of life are a critical window for survival. Optimal outcomes depend on a seamless continuum of care: prenatal diagnosis, delivery at a specialized tertiary center, and immediate postnatal surgery. However, stark disparities in access to this care persist. In high-income countries, multidisciplinary management leads to high survival, while in low- and middle-income countries, delays and limited surgical capacity result in preventable mortality. Beyond treatment, preventive public health measures like maternal nutrition and folate supplementation are crucial. To bridge this equity gap, we must invest in neonatal surgical capacity, integrate DCA care into universal health coverage, and strengthen birth defect surveillance. Ensuring that every newborn with a correctable digestive anomaly has a chance to survive requires coordinated global action to make timely, life-saving surgery accessible to all.
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