Welcome to Esophageal Atresia Care
Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a rare birth defect occurring in 1 in 2,500-4,000 babies where the esophagus fails to properly connect the mouth to the stomach. Babies with this condition must undergo surgical repair, usually shortly after birth. Without treatment, feeding may lead to milk and stomach acid getting into the airway (the trachea and lungs). This can affect the baby's ability to breathe or lea to infections like pneumonia.
Our team at Columbia University Irving Medical Center/NewYork-Presbyterian Morgan Stanley Children’s Hospital offers comprehensive care to children with EA/TEF.
- This process may begin during pregnancy, with prenatal counseling if the diagnosis can be made during an ultrasound.
- Patients born with EA/TEF frequently require immediate surgical intervention. Our surgeons offer minimally invasive surgical techniques whenever possible.
- Many children are born with other associated anomalies and our expert team offers multidisciplinary approaches to ensure delivery of the best possible care and outcome.
We are dedicated to improving care for children with EA/TEF through an evidence-based approach and offer many novel diagnostic and therapeutic options.
Please investigate our resources, including our specialty clinic, Researching Esophageal Atresia for Children's Health (REACH). Make an appointment or learn more about how we can help by calling (212) 342-8585.
Fall 2019: New EA/TEF Family Night coming up on Wednesday October 2, 2019. Please check back for more details. Email firstname.lastname@example.org for questions.
Esophageal atresia (EA) is a rare congenital condition (present at birth) in which the esophagus fails to connect to the stomach as it should and ends in a blind pouch instead. Some babies have a hole or connection between the trachea and esophagus, called a trachehoesophageal fistula, or TEF. These conditions can occur separately or together and may vary in severity, but babies with EA, TEF, or EA-TEF must undergo surgical repair soon after birth. Without a definitive repair, attempting to eat could lead to aspiration, a condition where formula or food escapes into the respiratory tree, causing respiratory illnesses.
Types of Esophageal Atresia
Types of EA/TEF based on Gross classification. The pink represents the esophagus (food tube) between the mouth and stomach. The blue structure is the trachea, or airway. The most common type of EA/TEF is type C (85%) followed by types A and E with which occur at about the same frequency (5–7%). Figure based on Singh et al. Surveillance in Patients with Esophageal Atresia. Curr Gastroenterol Rep (2017) 19: 4.
Causes of esophageal atresia are not fully understood. Some children are born with EA/TEF as part of a larger syndrome or associated anomalies of the heart, urinary or digestive tract, while others have EA/TEF without these additional problems.
Signs and Symptoms
Babies born with esophageal atresia may have symptoms including:
- Cyanosis – bluish tint to the skin – during attempted feeding
- Coughing and choking with attempted feeding
- Poor feeding
Suspected esophageal atresia may be diagnosed through several steps.
During pregnancy, excess amniotic fluid or small stomach on an ultrasound may signal EA/TEF. After birth, EA/TEF may be suspected if the baby chokes, coughs, and turns blue when attempting to feed. To diagnose EA/TEF, the baby’s physician will attempt to pass a feeding tube through the baby’s mouth or nose. X-ray imaging will show the feeding tube coiled in the upper esophagus, indicating EA/TEF.
Babies with EA/TEF must undergo surgical repair, often very soon after birth. Without treatment, attempting to eat could cause babies to aspirate milk and stomach contents into the trachea and lungs. This can cause symptoms such as coughing and choking, among others, and can also lead to lung infection. Surgery is successful in the vast majority of children.
The Researching Esophageal Atresia for Children's Health (REACH) Clinic uses a minimally invasive surgical approach for EA repair, using three small incisions in the chest, whenever possible. After surgery, the multidisciplinary team provides long-term follow-up in order to ensure optimal care as children mature into adulthood. For example, care is provided to prevent and treat acid reflux, assist with swallowing difficulties, and treat possible strictures (narrowing) all of which can affect children after EA/TEF surgery. Care is also coordinated for associated birth defects.
The collaborative format of the EA program also addresses an important need for patients and their families: the need to see multiple specialists for complicated, multi-system birth defects in the spectrum known as VACTERL (Vertebral anomalies, Anal atresia, Cardiac defects, Tracheoesophageal fistula and/or Esophageal atresia, Renal & Radial anomalies and Limb defects).
EA/TEF commonly appears with the following anomalies/ birth defects:
- Heart defects such as ventricular septal defects or Tetralogy of Fallot
- Defects with the gastrointestinal (digestive) system, like imperforate anus (incomplete or closed anal opening) or intestinal atresia (incomplete bowel formation)
- Defects in the urogenital tract, which can affect the production or release of urine
- Neurological and musculoskeletal defects
Elsewhere, parents must bring their children to individual specialists for care of these problems, but the collaborative team at Columbia/NYP Morgan Stanley Children’s Hospital includes a range of experts so that a child may see multiple specialists in a single visit, rather than making multiple separate trips.
William Middlesworth, MD
Surgical Director of the Esophageal Atresia Program
Julie Khlevner, MD
Medial Director of the Esophageal Atresia Program
Christina Carpenter, MD
Wendy K. Chung, MD, PhD
Clinical Genetics and Genomics
Sara Donnelly, MSN, CPNP
Pediatric Nurse Practitioner
Anne M. Ferris, MBBS
Eli Grunstein, MD
Christine Haro, MS, RD, CDN, CNSC, CSP
Pediatric Clinical Dietician
Carin I. Lamm, MD
Elle Quinn, MS, CF-SLP
Michael G. Vitale, MD, MPH
Jessica C. Price, MD, PhD
Clinical Research Assistant REACH Clinic
Priyanka Ahimaz, MS, CGC
Clinical Research Coordinator for Congenital Anomalies Research Exploration (CARE)
Make an appointment with our team by calling (212) 342-8585.
The Researching Esophageal Atresia for Children’s Health (REACH) Clinic at Columbia/NYP Morgan Stanley Children's Hospital was founded with the following goals in mind:
- Provide coordinated multidisciplinary care that addresses all facets of a child’s conditions
- Determine how to safely and effectively treat silent reflux and other complications associated with EA
- Help older patients transition to practitioners caring for adults who are well versed in the special needs associated with EA
- Conduct research to identify genetic abnormalities underlying EA and related anomalies
- Conduct longitudinal clinical research in order to develop best-practice treatment protocols.
Current Research Projects
Our ongoing research focuses on three main areas:
- To identify gene mutations that will help us better understand development of EA/TEF and its associated defects and serve as a target for future therapeutic modality.
- To identify the best practice guidelines for this patient population
- To identify the best treatment and surveillance plan that will optimize esophageal function, minimize esophageal injury and avoid unnecessary treatment using a multidisciplinary care approach.
- Singh A, Middlesworth W, Khlevner J. Surveillance in Patients with Esophageal Atresia. Curr Gastroenterol Rep. 2017 Jan;19(1):4
- Khlevner J, Middlesworth W, Wang J, et al. “Novel Candidate Genes in Esophageal Atresia/Tracheoesophageal Fistula Identified by Whole Exome Sequencing” Digestive Disease Week (DDW) June 2018, National Annual meeting. Washington DC
- Hawks C, Middlesworth W, Khlevner J. " Do Symptoms Reliably Identify Esophageal Stricture in Patients with Esophageal Atresia?” The North American Society of Pediatric Gastroenterology, Hepatology and Nutrition. National Annual Meeting. November 2017. Las Vegas, NV
- Suchy H, Middlesworth W, Khlevner J. “Correlation between multichannel intraluminal impedance/pH monitoring and esophageal biopsy for esophageal surveillance in children with esophageal atresia.” The North American Society of Pediatric Gastroenterology, Hepatology and Nutrition National Annual Meeting. October 2015. Washington, DC
For an initial consultation at our multidisciplinary EA/TEF clinic, please contact Amarilis Encarnacion at (212) 342-8585.
Stories & Perspectives
Learn how the REACH team helped transform the life of a girl born with esophageal atresia. Read more at the Daily News »
Please click to download our various educational resources for parents:
REACH Clinic Diagnostic Information Sheets:
- Upper Endoscopy Diagnostic Testing
- Impedance pH Probe Diagnostic Testing
- Esophageal Dilation Treatment
Our Educational Animations:
The following animations show the path of a food bolus, or mass of chewed food, during swallowing. The animations represent swallowing in a child without EA/TEF, and in a child with repaired EA/TEF. Patients with EA/TEF are prone to stricture, or narrowing, of the esophagus (food tube), as well as dysmotility, or poor forward movement through the esophagus coordinated by involuntary muscle contraction.
Food Path in non-EA Individual
Food Path in EA Individual with Stricture
Food Path in EA Individual with Esophageal Dysmotility
Please contact or visit the Family Resource Center at the NYP/Columbia Morgan Stanley Children’s Hospital for free assistance and additional resources.
Please consider giving a gift to support EA/TEF research and treatment. All proceeds from the Esophageal Atresia Clinic Fund go to the REACH Clinic and benefit patients with EA/TEF.
To donate today, please visit: The Esophageal Atresia Clinic Fund
All donation denominations are welcome. We appreciate your generous support!