Esophagic atresia type and its association with heart malformations in a Northern Mexico hospital

0Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Objective: To know the cardiac malformations frequency associated with esophageal atresia and its type in patients of the Children's Specialties Hospital of Chihuahua as well as related sociodemographic characteristics. Method: The epidemiology, clinic and evolution of patients with esophageal atresia diagnosis who were admitted to this hospital for a period of two years were studied. Variables such as sex, gestational age, birth weight, Apgar score, atresia type, associated congenital malformations, hospital complications and parental related aspects were analyzed. Results: Twelve patients were studied, 50% of them were male, most of them were products of term pregnancies with adequate birth weight. There were mestizo ethnicity prevalence, young mothers children with a medium socio-economic level, without geographical predominance. 82% of the cases corresponded to type III esophageal atresia, the most frequent congenital malformations associated were cardiac in 83% of which 90% corresponded to atrial septum defects. Conclusions: Esophageal atresia is a relatively common congenital malformation of multifactorial etiology. A complete approach to patients with this pathology is necessary to identify a concomitant illness and provide adequate treatment.

Cite

CITATION STYLE

APA

Chaparro-Escudero, J. A., García-González, Y., Cisneros-Castolo, M., Hernández-Vargas, O., & Rosas-Daher, D. (2022). Esophagic atresia type and its association with heart malformations in a Northern Mexico hospital. Cirugia y Cirujanos (English Edition), 90(1), 100–108. https://doi.org/10.24875/CIRU.20001125

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free