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Published on: April 17, 2020
What Proportion of Children With Complex Oesophageal Atresia Require Oesophageal Lengthening Procedures?
Laura Phillips1, Bruce Jaffray1
1The Great North Children's Hospital, Queen Victoria Road, Newcastle upon Tyne, United Kingdom.
Insights
Management of complex esophageal atresia (OA) without lengthening procedures maintains the native esophagus with less morbidity. This study suggests lengthening is rarely needed for complex OA cases.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Congenital Anomalies
Background:
- Complex esophageal atresia (OA) cases often require surgical intervention beyond primary anastomosis.
- Oesophageal lengthening techniques have been employed for complex OA, but outcomes require further evaluation.
Purpose of the Study:
- To compare the outcomes of managing complex OA with and without oesophageal lengthening procedures.
- To assess the rate of native oesophagus retention and associated morbidities.
Main Methods:
- A consecutive series of complex OA patients treated in a regional center was analyzed.
- Outcomes including native oesophagus retention, complications (thoracotomy, anastomotic leak, stricture), and mortality were recorded.
- Surgical techniques, specifically oesophageal lengthening versus non-lengthening approaches, were examined as explanatory variables.
Main Results:
- Of 215 OA cases, 29 (13%) were complex; 25 survived to repair.
- The native oesophagus was retained in 97% of all OA cases without lengthening.
- Among complex OA cases not treated with lengthening, 78% retained their native oesophagus with significantly less morbidity compared to lengthening procedures.
Conclusions:
- Managing complex OA without oesophageal lengthening yields similar native oesophagus retention rates as lengthening techniques.
- Non-lengthening management of complex OA is associated with significantly reduced morbidity.
- Oesophageal lengthening procedures appear to have limited applicability in the current management of complex OA.
Introduction:
Babies with oesophageal atresia (OA) who cannot achieve a primary anastomosis (complex OA) may be treated by attempted oesophageal lengthening. We contrast reported outcomes of lengthening with our experience of managing complex OA.
Patients And Methods:
A consecutive series treated in an English regional centre was completed. Outcomes of interest were the rate of retention of the native oesophagus, complications requiring thoracotomy, rates of anastomotic leak, stricture, fundoplication, and mortality. Possible explanatory variables were the surgical techniques applied.
Results:
29/215 (13%) OA were complex, and 25/207 survived to repair. 14/25 (56%) had no distal fistula, pure OA, while 11/25 (44%) had a long gap with distal fistula. 18/25 (72%) had delayed primary anastomosis, while 7/25 (28%) required oesophageal replacement. However, 2 of the replacements were salvage procedures following failed traction. Only 4/207 (2%) of OA were potentially treatable by traction. Salvage surgery was required in 2/23 (9%) complex OA not subjected to lengthening. The native oesophagus was retained without utilising lengthening in 200/207 (97%). Amongst complex OA where traction techniques had not been attempted, the native oesophagus was retained in 18/23 (78%) of cases, with median time to oesophageal continuity of 77 days. There was no in hospital mortality following treatment of complex OA, and overall survival was identical to non-complex OA among cases surviving to anastomosis.
Discussion:
Management of complex OA without lengthening procedures leads a similar rate of retention of the native oesophagus as reports describing lengthening, but with significantly less morbidity. We see little need for oesophageal lengthening in the management of complex OA.
Level Of Evidence:
IV.
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