Quality of Life after Surgical Treatment for Esophageal Atresia: Long-Term Outcome of 154 Patients

Alice Catherine Hölscher; Michael Laschat; Vera Choinitzki; Nadine Zwink; Ekkehart Jenetzky; Oliver Münsterer; Ralf Kurz; Marcus Pauly; Ulrike Brokmeier; Andreas Leutner; Benno Ure; Martin Lacher; Johannes Schumacher; Heiko Reutter; Thomas Michael Boemers

doi:10.1055/s-0036-1597956

European Journal of Pediatric Surgery, Inhaltsverzeichnis

Eur J Pediatr Surg 2017; 27(05): 443-448
DOI: 10.1055/s-0036-1597956

Original Article

Georg Thieme Verlag KG Stuttgart · New York

Quality of Life after Surgical Treatment for Esophageal Atresia: Long-Term Outcome of 154 Patients

Alice Catherine Hölscher

¹Department of Pediatric Surgery and Pediatric Urology, Children's Hospital, Cologne, Germany

,

Michael Laschat

²Division of Pediatric Anesthesiology, Children's Hospital, Cologne, NRW, Germany

,

Vera Choinitzki

³Institute of Human Genetics, Universitatsklinikum Bonn, Bonn, Nordrhein-Westfalen, Germany

,

Nadine Zwink

⁴Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany

,

Ekkehart Jenetzky

⁴Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany

⁵Department for Child and Adolescent Psychiatry, Johannes Gutenberg-University, Mainz, Germany

,

Oliver Münsterer

⁶Department of Pediatric Surgery, University Medicine of Mainz, Mainz, Germany

,

Ralf Kurz

⁷Department of General, Visceral, Thoracic and Vascular Surgery, University of Bonn, Bonn, Germany

,

Marcus Pauly

⁸Department of Pediatric Surgery, Asklepios Kinderklinik, Sankt Augustin, Germany

,

Ulrike Brokmeier

⁸Department of Pediatric Surgery, Asklepios Kinderklinik, Sankt Augustin, Germany

,

Andreas Leutner

⁹Department of Pediatric Surgery, Medical Center Dortmund, Dortmund, Germany

,

Benno Ure

¹⁰Department of Pediatric Surgery, Hannover Medical School, Hannover, Germany

,

Martin Lacher

¹⁰Department of Pediatric Surgery, Hannover Medical School, Hannover, Germany

¹¹Department of Pediatric Surgery, Universitat Leipzig Medizinische Fakultat, Leipzig, Sachsen, Germany

,

Johannes Schumacher

¹²Institute of Human Genetics, Rheinische Friedrich Wilhelms Universitat Bonn, Bonn, Nordrhein-Westfalen, Germany

,

Heiko Reutter

³Institute of Human Genetics, Universitatsklinikum Bonn, Bonn, Nordrhein-Westfalen, Germany

¹³Department of Neonatology, Children's Hospital, University of Bonn, Bonn, Germany

,

Thomas Michael Boemers

¹Department of Pediatric Surgery and Pediatric Urology, Children's Hospital, Cologne, Germany

› Institutsangaben

Abstract

Background The short- and long-term surgical results in patients with esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) have been described in depth from a physician's perspective. Contrarily, the perception and coping strategies of affected patients and their parents have rarely been reported. The aim of this study was to generate data on this matter.

Patients and Methods A total of 154 patients who had operative reconstruction for EA between 1971 and 2012 were evaluated for demographic data, surgical technique, affection of daily life, and coping strategies.

Results Gastroesophageal reflux (GER) symptoms were reported in 59% of cases with 33% requiring fundoplication. Regular bougienages of anastomotic strictures were necessary in 68% with 36% requiring repeated dilatations in the first postoperative year. Enteral nutrition via a nasogastric tube was performed in 66% after surgery. In 40%, the tube was needed until their sixth week of life. In 25%, nutritional support was necessary more than 1 year out of surgery. Quality of life in general was felt to be impaired according to the patients' parents in 50%. Regarding medical advice about long-term morbidities, more than 50% of the parents felt insufficiently advised. There were no statistical differences between the EA/TEF subtypes regarding GER symptoms, frequency of esophageal dilatations, eating behaviors, or support of the parents in feeding management.

Conclusion Our observations indicate that a high percentage of EA/TEF patients and families require more intensive aftercare and support during the first year following primary reconstruction than previously thought. We observed a higher need for adequate parental information on long-term complications of their children compared with current practice.

Keywords

esophageal atresia - tracheoesophageal fistula - quality of life

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Referenzen

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