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Erschienen in: Journal of Gastrointestinal Surgery 6/2017

19.04.2017 | Original Article

Postoperative Complications and Functional Outcome after Esophageal Atresia Repair: Results from Longitudinal Single-Center Follow-Up

verfasst von: Florian Friedmacher, Birgit Kroneis, Andrea Huber-Zeyringer, Peter Schober, Holger Till, Hugo Sauer, Michael E. Höllwarth

Erschienen in: Journal of Gastrointestinal Surgery | Ausgabe 6/2017

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Abstract

Background

Esophageal atresia (EA) and tracheoesophageal fistula (TEF) represent major therapeutic challenges, frequently associated with serious morbidities following surgical repair. The aim of this longitudinal study was to assess temporal changes in morbidity and mortality of patients with EA/TEF treated in a tertiary-level center, focusing on postoperative complications and their impact on long-term gastroesophageal function.

Methods

One hundred nine consecutive patients with EA/TEF born between 1975 and 2011 were followed for a median of 9.6 years (range, 3–27 years). Comparative statistics were used to evaluate temporal changes between an early (1975–1989) and late (1990–2011) study period.

Results

Gross types of EA were A (n = 6), B (n = 5), C (n = 89), D (n = 7), and E (n = 2). Seventy (64.2%) patients had coexisting anomalies, 13 (11.9%) of whom died before EA correction was completed. In the remaining 96 infants, surgical repair was primary (n = 66) or delayed (n = 25) anastomosis, closure of TEF in EA type E (n = 2), and esophageal replacement with colon interposition (n=2) or gastric transposition (n=1). Long-gap EA was diagnosed in 23 (24.0%) cases. Postoperative mortality was 4/96 (4.2%). Overall survival increased significantly between the two study periods (42/55 vs. 50/54; P = 0.03). Sixty-nine (71.9%) patients presented postoperatively with anastomotic strictures requiring a median of 3 (range, 1–15) dilatations. Revisional surgery was required for anastomotic leakage (n = 5), recurrent TEF with (n = 1) or without (n=9) anastomotic stricture, undetected proximal TEF (n = 4), and refractory anastomotic strictures with (n = 1) or without (n = 2) fistula. Normal dietary intake was achieved in 89 (96.7%) patients, while 3 (3.3%) remained dependent on gastrostomy feedings. Manometry showed esophageal dysmotility in 78 (84.8%) infants at 1 year of age, increasing to 100% at 10-year follow-up. Fifty-six (60.9%) patients suffered from dysphagia with need for endoscopic foreign body removal in 12 (13.0%) cases. Anti-reflux medication was required in 43 (46.7%) children and 30 (32.6%) underwent fundoplication. The rate of gastroesophageal reflux increased significantly between the two study periods (29/42 vs. 44/50; P = 0.04). Twenty-two (23.9%) cases of endoscopic esophagitis and one Barrett’s esophagus were identified.

Conclusions

Postoperative complications after EA/TEF repair are common and should be expertly managed to reduce the risk of long-term morbidity. Regular multidisciplinary surveillance with transitional care into adulthood is recommended in all patients with EA/TEF.
Literatur
1.
Zurück zum Zitat Billmyre KK, Hutson M, Klingensmith J. One shall become two: separation of the esophagus and trachea from the common foregut tube. Dev Dyn 2015;244:277–88.CrossRefPubMed Billmyre KK, Hutson M, Klingensmith J. One shall become two: separation of the esophagus and trachea from the common foregut tube. Dev Dyn 2015;244:277–88.CrossRefPubMed
2.
Zurück zum Zitat Nassar N, Leoncini E, Amar E, et al. Prevalence of esophageal atresia among 18 international birth defects surveillance programs. Birth Defects Res A Clin Mol Teratol 2012;94:893–9.CrossRefPubMedPubMedCentral Nassar N, Leoncini E, Amar E, et al. Prevalence of esophageal atresia among 18 international birth defects surveillance programs. Birth Defects Res A Clin Mol Teratol 2012;94:893–9.CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat Oddsberg J, Lu Y, Lagergren J. Aspects of esophageal atresia in a population-based setting: incidence, mortality, and cancer risk. Pediatr Surg Int 2012;28:249–57.CrossRefPubMed Oddsberg J, Lu Y, Lagergren J. Aspects of esophageal atresia in a population-based setting: incidence, mortality, and cancer risk. Pediatr Surg Int 2012;28:249–57.CrossRefPubMed
4.
Zurück zum Zitat Pedersen RN, Calzolari E, Husby S, Garne E, EUROCAT Working group. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions. Arch Dis Child 2012;97:227–32.CrossRefPubMed Pedersen RN, Calzolari E, Husby S, Garne E, EUROCAT Working group. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions. Arch Dis Child 2012;97:227–32.CrossRefPubMed
5.
Zurück zum Zitat Conforti A, Morini F, Bagolan P. Difficult esophageal atresia: trick and treat. Semin Pediatr Surg 2014;23:261–9.CrossRefPubMed Conforti A, Morini F, Bagolan P. Difficult esophageal atresia: trick and treat. Semin Pediatr Surg 2014;23:261–9.CrossRefPubMed
6.
Zurück zum Zitat Zani A, Eaton S, Hoellwarth ME, et al. International survey on the management of esophageal atresia. Eur J Pediatr Surg 2014;24:3–8.CrossRefPubMed Zani A, Eaton S, Hoellwarth ME, et al. International survey on the management of esophageal atresia. Eur J Pediatr Surg 2014;24:3–8.CrossRefPubMed
7.
Zurück zum Zitat 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.CrossRefPubMed 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.CrossRefPubMed
9.
Zurück zum Zitat Sfeir R, Bonnard A, Khen-Dunlop N, et al. Esophageal atresia: data from a national cohort. J Pediatr Surg 2013;48:1664–9.CrossRefPubMed Sfeir R, Bonnard A, Khen-Dunlop N, et al. Esophageal atresia: data from a national cohort. J Pediatr Surg 2013;48:1664–9.CrossRefPubMed
10.
Zurück zum Zitat Koivusalo AI, Pakarinen MP, Rintala RJ. Modern outcomes of oesophageal atresia: single centre experience over the last twenty years. J Pediatr Surg 2013;48:297–303.CrossRefPubMed Koivusalo AI, Pakarinen MP, Rintala RJ. Modern outcomes of oesophageal atresia: single centre experience over the last twenty years. J Pediatr Surg 2013;48:297–303.CrossRefPubMed
11.
Zurück zum Zitat Malakounides G, Lyon P, Cross K, et al. Esophageal atresia: improved outcome in high-risk groups revisited. Eur J Pediatr Surg 2016;26:227–31.CrossRefPubMed Malakounides G, Lyon P, Cross K, et al. Esophageal atresia: improved outcome in high-risk groups revisited. Eur J Pediatr Surg 2016;26:227–31.CrossRefPubMed
12.
Zurück zum Zitat Orford J, Cass DT, Glasson MJ. Advances in the treatment of oesophageal atresia over three decades: the 1970s and the 1990s. Pediatr Surg Int 2004;20:402–7.CrossRefPubMed Orford J, Cass DT, Glasson MJ. Advances in the treatment of oesophageal atresia over three decades: the 1970s and the 1990s. Pediatr Surg Int 2004;20:402–7.CrossRefPubMed
13.
Zurück zum Zitat Dingemann C, Dietrich J, Zeidler J, et al. Early complications after esophageal atresia repair: analysis of a German health insurance database covering a population of 8 million. Dis Esophagus. 2016;29:780–6.CrossRefPubMed Dingemann C, Dietrich J, Zeidler J, et al. Early complications after esophageal atresia repair: analysis of a German health insurance database covering a population of 8 million. Dis Esophagus. 2016;29:780–6.CrossRefPubMed
14.
Zurück zum Zitat Schneider A, Blanc S, Bonnard A, et al. Results from the French National Esophageal Atresia register: one-year outcome. Orphanet J Rare Dis 2014;9:206.CrossRefPubMedPubMedCentral Schneider A, Blanc S, Bonnard A, et al. Results from the French National Esophageal Atresia register: one-year outcome. Orphanet J Rare Dis 2014;9:206.CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Alshehri A, Lo A, Baird R. An analysis of early nonmortality outcome prediction in esophageal atresia. J Pediatr Surg 2012;47:881–4.CrossRefPubMed Alshehri A, Lo A, Baird R. An analysis of early nonmortality outcome prediction in esophageal atresia. J Pediatr Surg 2012;47:881–4.CrossRefPubMed
16.
Zurück zum Zitat Rintala RJ, Pakarinen MP. Long-term outcome of esophageal anastomosis. Eur J Pediatr Surg 2013;23:219–25.CrossRefPubMed Rintala RJ, Pakarinen MP. Long-term outcome of esophageal anastomosis. Eur J Pediatr Surg 2013;23:219–25.CrossRefPubMed
17.
Zurück zum Zitat Ijsselstijn H, van Beelen NW, Wijnen RM. Esophageal atresia: long-term morbidities in adolescence and adulthood. Dis Esophagus 2013;26:417–21.CrossRefPubMed Ijsselstijn H, van Beelen NW, Wijnen RM. Esophageal atresia: long-term morbidities in adolescence and adulthood. Dis Esophagus 2013;26:417–21.CrossRefPubMed
18.
Zurück zum Zitat Legrand C, Michaud L, Salleron J, et al. Long-term outcome of children with oesophageal atresia type III. Arch Dis Child 2012;97:808–11.CrossRefPubMed Legrand C, Michaud L, Salleron J, et al. Long-term outcome of children with oesophageal atresia type III. Arch Dis Child 2012;97:808–11.CrossRefPubMed
19.
Zurück zum Zitat Connor MJ, Springford LR, Kapetanakis VV, Giuliani S. Esophageal atresia and transitional care—step 1: a systematic review and meta-analysis of the literature to define the prevalence of chronic long-term problems. Am J Surg 2015;209:747–59.CrossRefPubMed Connor MJ, Springford LR, Kapetanakis VV, Giuliani S. Esophageal atresia and transitional care—step 1: a systematic review and meta-analysis of the literature to define the prevalence of chronic long-term problems. Am J Surg 2015;209:747–59.CrossRefPubMed
20.
Zurück zum Zitat Shah R, Varjavandi V, Krishnan U. Predictive factors for complications in children with esophageal atresia and tracheoesophageal fistula. Dis Esophagus 2015;28:216–23.CrossRefPubMed Shah R, Varjavandi V, Krishnan U. Predictive factors for complications in children with esophageal atresia and tracheoesophageal fistula. Dis Esophagus 2015;28:216–23.CrossRefPubMed
21.
Zurück zum Zitat Pedersen RN, Markøw S, Kruse-Andersen S, et al. Esophageal atresia: gastroesophageal functional follow-up in 5–15 year old children. J Pediatr Surg 2013;48:2487–95.CrossRefPubMed Pedersen RN, Markøw S, Kruse-Andersen S, et al. Esophageal atresia: gastroesophageal functional follow-up in 5–15 year old children. J Pediatr Surg 2013;48:2487–95.CrossRefPubMed
22.
Zurück zum Zitat Castilloux J, Noble AJ, Faure C. Risk factors for short- and long-term morbidity in children with esophageal atresia. J Pediatr 2010;156:755–60.CrossRefPubMed Castilloux J, Noble AJ, Faure C. Risk factors for short- and long-term morbidity in children with esophageal atresia. J Pediatr 2010;156:755–60.CrossRefPubMed
23.
Zurück zum Zitat Höllwarth ME, Zaupa P. Oesophageal atresia. In Puri P, Höllwarth ME (eds.). Pediatric surgery. 1st edn. Heidelberg, Berlin, New York: Springer; 2006:29--48. Höllwarth ME, Zaupa P. Oesophageal atresia. In Puri P, Höllwarth ME (eds.). Pediatric surgery. 1st edn. Heidelberg, Berlin, New York: Springer; 2006:29--48.
24.
Zurück zum Zitat Somppi E, Tammela O, Ruuska T, et al. Outcome of patients operated on for esophageal atresia: 30 years’ experience. J Pediatr Surg 1998;33:1341–6.CrossRefPubMed Somppi E, Tammela O, Ruuska T, et al. Outcome of patients operated on for esophageal atresia: 30 years’ experience. J Pediatr Surg 1998;33:1341–6.CrossRefPubMed
25.
Zurück zum Zitat Low DE, Alderson D, Cecconello I, et al. International Consensus on Standardization of Data Collection for Complications Associated With Esophagectomy: Esophagectomy Complications Consensus Group (ECCG). Ann Surg 2015;262:286–94.CrossRefPubMed Low DE, Alderson D, Cecconello I, et al. International Consensus on Standardization of Data Collection for Complications Associated With Esophagectomy: Esophagectomy Complications Consensus Group (ECCG). Ann Surg 2015;262:286–94.CrossRefPubMed
26.
Zurück zum Zitat Vandenplas Y, Rudolph CD, Di Lorenzo C, et al. Pediatric gastroesophageal reflux clinical practice guidelines: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). J Pediatr Gastroenterol Nutr 2009;49:498–547.CrossRefPubMed Vandenplas Y, Rudolph CD, Di Lorenzo C, et al. Pediatric gastroesophageal reflux clinical practice guidelines: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). J Pediatr Gastroenterol Nutr 2009;49:498–547.CrossRefPubMed
27.
Zurück zum Zitat Maynard S, Bouin M. Follow-up of adult patients with repaired esophageal atresia: how, when, and for how long? Dis Esophagus 2013;26:422–4.CrossRefPubMed Maynard S, Bouin M. Follow-up of adult patients with repaired esophageal atresia: how, when, and for how long? Dis Esophagus 2013;26:422–4.CrossRefPubMed
28.
Zurück zum Zitat Burge DM, Shah K, Spark P, et al. Contemporary management and outcomes for infants born with oesophageal atresia. Br J Surg 2013;100:515–21.CrossRefPubMed Burge DM, Shah K, Spark P, et al. Contemporary management and outcomes for infants born with oesophageal atresia. Br J Surg 2013;100:515–21.CrossRefPubMed
29.
Zurück zum Zitat Mortell AE, Azizkhan RG. Esophageal atresia repair with thoracotomy: the Cincinnati contemporary experience. Semin Pediatr Surg 2009;18:12–9.CrossRefPubMed Mortell AE, Azizkhan RG. Esophageal atresia repair with thoracotomy: the Cincinnati contemporary experience. Semin Pediatr Surg 2009;18:12–9.CrossRefPubMed
30.
Zurück zum Zitat Koivusalo AI, Pakarinen MP, Lindahl HG, Rintala RJ. Revisional surgery for recurrent tracheoesophageal fistula and anastomotic complications after repair of esophageal atresia in 258 infants. J Pediatr Surg 2015;50:250–4.CrossRefPubMed Koivusalo AI, Pakarinen MP, Lindahl HG, Rintala RJ. Revisional surgery for recurrent tracheoesophageal fistula and anastomotic complications after repair of esophageal atresia in 258 infants. J Pediatr Surg 2015;50:250–4.CrossRefPubMed
31.
Zurück zum Zitat Coran AG. Diagnosis and surgical management of recurrent tracheoesophageal fistula. Dis Esophagus 2013;26:380–1.CrossRefPubMed Coran AG. Diagnosis and surgical management of recurrent tracheoesophageal fistula. Dis Esophagus 2013;26:380–1.CrossRefPubMed
32.
Zurück zum Zitat Zhu H, Shen C, Xiao X, Dong K, Zheng S. Reoperation for anastomotic complications of esophageal atresia and tracheoesophageal fistula. J Pediatr Surg 2015,50:2012–5.CrossRefPubMed Zhu H, Shen C, Xiao X, Dong K, Zheng S. Reoperation for anastomotic complications of esophageal atresia and tracheoesophageal fistula. J Pediatr Surg 2015,50:2012–5.CrossRefPubMed
33.
Zurück zum Zitat Guo W, Li Y, Jiao A, Peng Y, Hou D, Chen Y. Tracheoesophageal fistula after primary repair of type C esophageal atresia in the neonatal period: recurrent or missed second congenital fistula. J Pediatr Surg 2010;45:2351–5.CrossRefPubMed Guo W, Li Y, Jiao A, Peng Y, Hou D, Chen Y. Tracheoesophageal fistula after primary repair of type C esophageal atresia in the neonatal period: recurrent or missed second congenital fistula. J Pediatr Surg 2010;45:2351–5.CrossRefPubMed
34.
Zurück zum Zitat Lévesque D, Baird R, Laberge JM. Refractory strictures post-esophageal atresia repair: what are the alternatives? Dis Esophagus 2013;26:382–7.CrossRefPubMed Lévesque D, Baird R, Laberge JM. Refractory strictures post-esophageal atresia repair: what are the alternatives? Dis Esophagus 2013;26:382–7.CrossRefPubMed
35.
Zurück zum Zitat 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 to 2011. Radiology 2014;271:596–601.CrossRefPubMed 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 to 2011. Radiology 2014;271:596–601.CrossRefPubMed
36.
Zurück zum Zitat Höllwarth ME. Gastroesophageal reflux disease. In: Coran AG, Adzick NS, Krummel TM, Laberge JM, Shamberger R, Caldamone AA (eds.). Pediatric surgery. Vol. 2, 7th edn. Philadelphia: Elsevier Sauders; 2012:947–58.CrossRef Höllwarth ME. Gastroesophageal reflux disease. In: Coran AG, Adzick NS, Krummel TM, Laberge JM, Shamberger R, Caldamone AA (eds.). Pediatric surgery. Vol. 2, 7th edn. Philadelphia: Elsevier Sauders; 2012:947–58.CrossRef
37.
Zurück zum Zitat Pini Prato A, Carlucci M, Bagolan P, et al. A cross-sectional nationwide survey on esophageal atresia and tracheoesophageal fistula. J Pediatr Surg 2015;50:1441–56.CrossRefPubMed Pini Prato A, Carlucci M, Bagolan P, et al. A cross-sectional nationwide survey on esophageal atresia and tracheoesophageal fistula. J Pediatr Surg 2015;50:1441–56.CrossRefPubMed
38.
Zurück zum Zitat Koivusalo AI, Pakarinen MP, Lindahl HG, Rintala RJ. Endoscopic surveillance after repair of oesophageal atresia—longitudinal study in 209 patients. J Pediatr Gastroenterol Nutr 2016;62:562–6.CrossRefPubMed Koivusalo AI, Pakarinen MP, Lindahl HG, Rintala RJ. Endoscopic surveillance after repair of oesophageal atresia—longitudinal study in 209 patients. J Pediatr Gastroenterol Nutr 2016;62:562–6.CrossRefPubMed
39.
Zurück zum Zitat Sistonen SJ, Koivusalo A, Nieminen U, et al. Esophageal morbidity and function in adults with repaired esophageal atresia with tracheoesophageal fistula: a population-based long-term follow-up. Ann Surg 2010;251:1167–73.CrossRefPubMed Sistonen SJ, Koivusalo A, Nieminen U, et al. Esophageal morbidity and function in adults with repaired esophageal atresia with tracheoesophageal fistula: a population-based long-term follow-up. Ann Surg 2010;251:1167–73.CrossRefPubMed
40.
Zurück zum Zitat Zamiara P, Thomas KE, Connolly BL, Lane H, Marcon MA, Chiu PP. Long-term burden of care and radiation exposure in survivors of esophageal atresia. J Pediatr Surg 2015;50:1686–90.CrossRefPubMed Zamiara P, Thomas KE, Connolly BL, Lane H, Marcon MA, Chiu PP. Long-term burden of care and radiation exposure in survivors of esophageal atresia. J Pediatr Surg 2015;50:1686–90.CrossRefPubMed
41.
Zurück zum Zitat Lacher M, Froehlich S, von Schweinitz D, Dietz HG. Early and long term outcome in children with esophageal atresia treated over the last 22 years. Klin Padiatr 2010;222:296–301.CrossRefPubMed Lacher M, Froehlich S, von Schweinitz D, Dietz HG. Early and long term outcome in children with esophageal atresia treated over the last 22 years. Klin Padiatr 2010;222:296–301.CrossRefPubMed
42.
Zurück zum Zitat Friedmacher F, Puri P. Delayed primary anastomosis for management of long-gap esophageal atresia: a meta-analysis of complications and long-term outcome. Pediatr Surg Int 2012;28:899–906.CrossRefPubMed Friedmacher F, Puri P. Delayed primary anastomosis for management of long-gap esophageal atresia: a meta-analysis of complications and long-term outcome. Pediatr Surg Int 2012;28:899–906.CrossRefPubMed
43.
Zurück zum Zitat Dingemann C, Meyer A, Kircher G, et al. Long-term health-related quality of life after complex and/or complicated esophageal atresia in adults and children registered in a German patient support group. J Pediatr Surg 2014;49:631–8.CrossRefPubMed Dingemann C, Meyer A, Kircher G, et al. Long-term health-related quality of life after complex and/or complicated esophageal atresia in adults and children registered in a German patient support group. J Pediatr Surg 2014;49:631–8.CrossRefPubMed
44.
Zurück zum Zitat Burford JM, Dassinger MS, Copeland DR, Keller JE, Smith SD. Repair of esophageal atresia with tracheoesophageal fistula via thoracotomy: a contemporary series. Am J Surg 2011;202:203–6.CrossRefPubMed Burford JM, Dassinger MS, Copeland DR, Keller JE, Smith SD. Repair of esophageal atresia with tracheoesophageal fistula via thoracotomy: a contemporary series. Am J Surg 2011;202:203–6.CrossRefPubMed
45.
Zurück zum Zitat Laberge JM, Blair GK. Thoracotomy for repair of esophageal atresia: not as bad as they want you to think! Dis Esophagus 2013;26:365–71.CrossRefPubMed Laberge JM, Blair GK. Thoracotomy for repair of esophageal atresia: not as bad as they want you to think! Dis Esophagus 2013;26:365–71.CrossRefPubMed
46.
Zurück zum Zitat Pierro A. Hypercapnia and acidosis during the thoracoscopic repair of oesophageal atresia and congenital diaphragmatic hernia. J Pediatr Surg 2015;50:247–9.CrossRefPubMed Pierro A. Hypercapnia and acidosis during the thoracoscopic repair of oesophageal atresia and congenital diaphragmatic hernia. J Pediatr Surg 2015;50:247–9.CrossRefPubMed
Metadaten
Titel
Postoperative Complications and Functional Outcome after Esophageal Atresia Repair: Results from Longitudinal Single-Center Follow-Up
verfasst von
Florian Friedmacher
Birgit Kroneis
Andrea Huber-Zeyringer
Peter Schober
Holger Till
Hugo Sauer
Michael E. Höllwarth
Publikationsdatum
19.04.2017
Verlag
Springer US
Erschienen in
Journal of Gastrointestinal Surgery / Ausgabe 6/2017
Print ISSN: 1091-255X
Elektronische ISSN: 1873-4626
DOI
https://doi.org/10.1007/s11605-017-3423-0

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