Abstract

Aim: To describe our experience of neonates with esophageal atresia with tracheo-esophageal fistula (EA with TEF) who presented after a week. Design: Retrospective study of the patients of EA with TEF who presented after a week. Study Setting: Department of Pediatric Surgery, Government Medical College Nagpur. Study Duration: Eight years. Materials and Methods: Demographic information, hematological, biochemical and radiological data were obtained from the patients' medical records. The gap between two ends of the esophagus, nature of upper pouch and lower esophagus were noted intra-operatively. Outcome in terms of mortality and surgical complications were noted. In operated group, babies who survived were compared with non-survivors with respect to various preoperative variables. Results: Of 52 patients, 27 babies expired during initial stabilisation period before surgery. The causes of mortality were severe pneumonitis and septicemia. One baby had associated cyanotic heart disease. Twenty-five patients with mean age of 8.28±1.21 days underwent surgery. Nearly two-third of them were male. All of them were born at full-term with mean birth weight of 2.47±0. 12 kg. More than 80% were previously hospitalised and nearly 70% babies were given feeds before present hospitalization. Mean Downe’s score for respiratory distress was 5.8±1.49. All patients were positive for septic profile. Associated congenital anomalies were present in ten patients. Intra-operatively, two ends of esophagus were either approximating or have short gap in 24 patients. All patients had well developed, thick and muscular upper oesophageal pouch. Lower esophagus at fistula was thin but dilated in 18 patients while thin and narrowed in 7 patients. However, esophageal anastomosis was possible with ease without any tension in all except one patient. There were 15 deaths in our study (13 due to pneumonitis and 2 during follow up due to aspiration). Three survivors required anti-reflux surgery. Comparison of preoperative variables of survivors and non-survivors showed a significant difference with respect to the variables like feedings, abdominal girth, immature band cells to neutrophil ratio and nature of pharyngeal or endotracheal aspirate. Conclusions: Late presentations in EA with TEF are associated with high mortality but less anastomotic complications after surgery. Preoperative factors like feedings, abdominal distension, immature band cells to neutrophil ratio and bilious pharyngeal or endotracheal aspirate are associated with high mortality.

Highlights

  • Esophageal atresia with tracheo-esophageal fistula (EA with TEF) is a well-known congenital anomaly with an incidence of 1 in 2,400–4,500 live births [1].The abnormality was uniformly fatal throughout the world in first half of the twentieth century

  • Late presentations in EA with TEF are associated with high mortality but less anastomotic complications after surgery

  • Waterston proposed a prognostic classification for EA with TEF in 1962 which included low birth weight, pneumonia and associated congenital anomalies as the risk factors [6]

Read more

Summary

Introduction

Esophageal atresia with tracheo-esophageal fistula (EA with TEF) is a well-known congenital anomaly with an incidence of 1 in 2,400–4,500 live births [1].The abnormality was uniformly fatal throughout the world in first half of the twentieth century. Esophageal atresia with tracheo-esophageal fistula (EA with TEF) is a well-known congenital anomaly with an incidence of 1 in 2,400–4,500 live births [1]. Ever since Cameron Haight’s first report of successful surgical correction in 1941, the survival of neonates with EA with TEF has dramatically improved [2]. Esophageal Atresia with Tracheo-Esophageal Fistula Presenting Beyond Seven Days anomaly is regarded as an eminently correctable congenital lesion with survival rates more than 90% [3,4,5]. The improvement in survival rate is multifactorial and is largely attributed to the advances in neonatal intensive care, anaesthetic management, ventilatory support and surgical techniques over the past decades. Waterston proposed a prognostic classification for EA with TEF in 1962 which included low birth weight, pneumonia and associated congenital anomalies as the risk factors [6]. Nowadays the survival can be achieved even in low birth weight babies [7], and the mortality is currently limited to those with coexistent severe life-threatening anomalies

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.