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Impact of VACTERL Association and Chromosomal Anomalies on Outcomes After Esophageal Atresia Repair: Insights from the EUPSA Registry

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Topic overview

This registry study examines how VACTERL association and chromosomal anomalies affect surgical outcomes in esophageal atresia patients. Analysis of 372 cases from the EUPSA registry reveals that 22% had VACTERL-CA, with significantly lower gestational age and birth weight, providing evidence for improved risk stratification in this complex patient population.

Key takeaways

  • 22% of EA patients had VACTERL association or chromosomal anomalies, with lower gestational age and birth weight than isolated EA cases.
  • VACTERL-CA patients showed significantly different surgical outcomes, highlighting the need for tailored perioperative management strategies.
  • The EUPSA registry data (2014-2017) provides evidence-based risk stratification for EA repair based on associated anomalies.
  • Presence of VACTERL association or chromosomal anomalies should inform preoperative counseling and surgical planning in EA patients.

Keywords

Esophageal Atresia Vacterl Association Pediatric Surgery Chromosomal Anomalies Surgical Outcomes Congenital Malformations Risk Stratification

Hashtags

#EsophagealAtresia #VACTERLAssociation #PediatricSurgery #CongenitalAnomalies

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How to cite: GlobalCastMD. Impact of VACTERL Association and Chromosomal Anomalies on Outcomes After Esophageal Atresia Repair: Insights from the EUPSA Registry. GlobalCastMD Medical Library. 2025-10-15. https://library.globalcastmd.com/article/11119

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