Long-Term Management Challenges in Esophageal Atresia

Springer Science and Business Media LLC - Tập 15 - Trang 46-52 - 2017
Abby White1, Raphael Bueno1
1Division of Thoracic Surgery, Department of Surgery, Brigham and Women’s Hospital, Boston, USA

Tóm tắt

Esophageal atresia is a rare congenital anomaly, but improved surgical and critical care has resulted in survival rates exceeding 90%. Long-term survival is associated with numerous management challenges including chronic motility disorders, dysphagia, strictures, reflux, esophagitis and attendant complications, tracheomalacia and chronic restrictive lung disease, and recurrent pulmonary infections. No guidelines for adolescents and younger or older adults exist for the treatment and monitoring of this specialized patient population. As such, patients with esophageal atresia can experience life-long sequelae of their disease and are best served by intentional transition to adult care for surveillance and monitoring, specifically for chronic lung disease, reflux, and its complications. This is best accomplished in a multidisciplinary fashion at experienced esophageal and lung centers.

Tài liệu tham khảo

Wang B, Tashiro J, Allan BJ, et al. A nationwide analysis of clinical outcomes among newborns with esophageal atresia and tracheoesophageal fistulas in the United States. J Surg Res. 2014;190:604–12. Cassina M, Ruol M, Pertile R, et al. Prevalance, characteristics and survival of children with esophageal atresia: a 32-year population-based study including 1,417,724 consecutive newborns. Birth Defects Res A Clin Mol Teratol. 2016;106:542–8. Haight C. Congenital atresia of the esophagus with tracheoesophageal fistula: reconstruction of esophageal continuity by primary anastomosis. Ann Surg. 1944;120:623–52. Burge DM, Shah K, Spark P, Shenker N, et al. Contemporary management and outcomes for infants born with esophageal atresia. Br J Surg. 2013;100:515–21. Shulman A, Mazkereth R, Zalel Y, et al. Prenatal identification of esophageal atresia: the role of ultrasonography for evaluation of functional anatomy. Prenat Diagn. 2002;22(8):669. Petrosyan M, Estrada J, Hunter C, et al. Esophageal atresia/tracheoesophageal fistula in very low-birth-weight neonates: improved outcomes with staged repair. J Pediatr Surg. 2009;44(12):2278. Cowles RA, Coran AG. Gastric transposition in infants and children. Pediatr Surg Int. 2010;26:1129–34. Quality of life in adult survivors of correction of esophageal atresia. Arch Surg 2005;140:976–80. Esophageal morbidity and function in adults with repaired esophageal atresia with tracheoesophageal fistula. Ann Surg 2010;251:1167–73. Presse N, Taillefer J, Maynard S, Bouin M. Insufficient body weight of adults born with esophageal atresia. J Ped Gastroent Nut. 2016;62:469–73. Little DC, Rescorla JL, Grosfield KW, et al. Long-term analysis of children with esophageal atresia and tracheoesophageal fistula. J Pediatr Surg. 2003;38:852–6. Thyoka M, Barnacle A, Chippington S, et al. Fluoroscopic balloon dilation of esophageal atresia anastomotic strictures in children and young adults: single center study of 103 consecutive patients from 1999–2011. Radiology. 2014;271:596–601. Manfredi MA, Jennings RW, Anjum MW, et al. Externally removable stents in the treatment of benign recalcitrant strictures and esophageal perforations in pediatric patients with esophageal atresia. Gastrointest Endosc. 2014;80:246–52. Tan Y, Zhang J, Zhou J, et al. Endoscopic incision for the treatment of refractory anastomotic esophageal strictures in pediatric patients. J Pediatr Gastroent Nutr. 2015;61:319–22. • Sweed AS, Fawaz SA, Exxat WF, et al. A prospective randomized controlled study to assess the use of mitomycin C in improving the results of esophageal dilation in post corrosive esophageal stricture in children. Int J Pediatr Otorhinolaryngol. 2015;79:23–5. This study represents a prospective randomized trial evaluating mitomycin C injection, which was thought to mitigate fibrosis at the esophageal anastomosis Van der Zee D, Hulsker C. Indwelling esophageal balloon catheter for benign esophageal stenosis in infants and children. Surg Endosc. 2014;28:1126–30. Acher CW, Ostlie DJ, Leys CM, et al. Long-term outcomes of patients with tracheoesophageal fistula/esophageal atresia: survey results from tracheoesophageal fistula/esophageal atresia online communities. Eur J Pediatr Surg. 2015;2015:21. Duerloo JA, Ekkelkamp S, Bartelsman JF, et al. Gastroesophageal reflux: prevalence in adults older than 28 years after correction of esophageal atresia. Ann Surg. 2003;238:686–9. Jeurmink SM, van Herwaarden-Lindeboom MY, Siersema PD, et al. Barrett’s esophagus in children: does it need more attention? Dig Liver Dis. 2011;43:682–7. • Schneider A, Gottrand F, Bellaiche M, et al. Prevalence of Barrett’s esophagus in adolescents and young adults with esophageal atresia. Ann Surg. 2015; This thoughtful study highlights the inherent challenges in examining data for Barrett’s esophagus in patients with esophageal atresia Vergouwe FW, Ijsselstijn H, Wijnen R, et al. Screening and surveillance in esophageal atresia patients: current knowledge and future perspectives. Eur J Pediatr Surg. 2015;25:345–52. Jonsson L, Friberg LG, Gastzinsky V, et al. Treatment and follow-up of patients with long-gap esophageal atresia: 15 years of experience from the western region of Sweden. Eur J Pediatr Surg. 2016;26:150–9. Cartabuke RH, Lopez R, Prashanthi NT. Long-term esophageal and respiratory outcomes in children with esophageal atresia and tracheoesophageal fistula. Gastroenterology Report, 2015:1–5. DeBoer E, Prager J, Ruiz AG, et al. Multidisciplinary care of children with repaired esophageal atresia and tracheoesophageal fistula. Pediatr Pulmonol. 2016;51:576–81. Mirra V, Maglione M, DiMicco LL et al. Longitudinal follow-up of chronic pulmonary manifestations in esophageal atresia: a clinical algorithm and review of literature. Pediatrics and Neonatology. 2016. Gibreel W, Zendejas B, Antiel RM et al. Swallowing dysfunction and quality of life in adults with surgically corrected esophageal atresia/tracheoesophageal fistula as infants: forty years of follow-up. Ann Surg. 2016.