Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort.
<h4>Purpose</h4> <p>To describe the incidence and outcomes to one-year in infants born with oesophageal atresia (OA) with no distal tracheoesophageal fistula within a population cohort.</p> <h4>Method</h4> <p>A prospective multicentre population cohort stud...
| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Journal article |
| Dil: | English |
| Baskı/Yayın Bilgisi: |
Elsevier
2016
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| _version_ | 1826288705471512576 |
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| author | Long, A Tyraskis, A Allin, B Burge, D Knight, M |
| author_facet | Long, A Tyraskis, A Allin, B Burge, D Knight, M |
| author_sort | Long, A |
| collection | OXFORD |
| description | <h4>Purpose</h4> <p>To describe the incidence and outcomes to one-year in infants born with oesophageal atresia (OA) with no distal tracheoesophageal fistula within a population cohort.</p> <h4>Method</h4> <p>A prospective multicentre population cohort study was undertaken of all infants born with OA investigating clinical outcomes up to one year following initial surgery. Outcomes of infants with OA and a lower pouch fistula have previously been reported. A subgroup analysis describing the outcomes of infants with OA and no tracheoesophageal fistula, (Type A) and those with only an upper pouch fistula, (Type B) was performed.</p> <h4>Main Results</h4> <p>Twenty-one of 151 infants were diagnosed with Type A or B oesophageal atresia (14%). Fifteen were Type A (71%) and 6 Type B (29%). With the exception of an infant with Type A, who died before reconstruction; all but four infants (all Type B) underwent more than one operation. Median time to delayed primary anastomosis in infants with Type A and Type B was 82 days (75-89 days) (n=7). The median time to oesophageal replacement was 94 days (89-147 days) (n=8). Median length of stay for infants with Type A or B OA from first operation to first discharge was 101 days (31-123 days).</p> <h4>Conclusions</h4> <p>Oesophageal atresia with no distal tracheoesophageal fistula is uncommon. Infants with</p> |
| first_indexed | 2024-03-07T02:17:44Z |
| format | Journal article |
| id | oxford-uuid:a2d8aa4f-1202-45b7-82bd-6d5008bbcb01 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T02:17:44Z |
| publishDate | 2016 |
| publisher | Elsevier |
| record_format | dspace |
| spelling | oxford-uuid:a2d8aa4f-1202-45b7-82bd-6d5008bbcb012022-03-27T02:22:47ZOesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a2d8aa4f-1202-45b7-82bd-6d5008bbcb01EnglishSymplectic Elements at OxfordElsevier2016Long, ATyraskis, AAllin, BBurge, DKnight, M <h4>Purpose</h4> <p>To describe the incidence and outcomes to one-year in infants born with oesophageal atresia (OA) with no distal tracheoesophageal fistula within a population cohort.</p> <h4>Method</h4> <p>A prospective multicentre population cohort study was undertaken of all infants born with OA investigating clinical outcomes up to one year following initial surgery. Outcomes of infants with OA and a lower pouch fistula have previously been reported. A subgroup analysis describing the outcomes of infants with OA and no tracheoesophageal fistula, (Type A) and those with only an upper pouch fistula, (Type B) was performed.</p> <h4>Main Results</h4> <p>Twenty-one of 151 infants were diagnosed with Type A or B oesophageal atresia (14%). Fifteen were Type A (71%) and 6 Type B (29%). With the exception of an infant with Type A, who died before reconstruction; all but four infants (all Type B) underwent more than one operation. Median time to delayed primary anastomosis in infants with Type A and Type B was 82 days (75-89 days) (n=7). The median time to oesophageal replacement was 94 days (89-147 days) (n=8). Median length of stay for infants with Type A or B OA from first operation to first discharge was 101 days (31-123 days).</p> <h4>Conclusions</h4> <p>Oesophageal atresia with no distal tracheoesophageal fistula is uncommon. Infants with</p> |
| spellingShingle | Long, A Tyraskis, A Allin, B Burge, D Knight, M Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title | Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title_full | Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title_fullStr | Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title_full_unstemmed | Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title_short | Oesophageal atresia with no distal tracheoesophageal fistula: Management and outcomes from a population-based cohort. |
| title_sort | oesophageal atresia with no distal tracheoesophageal fistula management and outcomes from a population based cohort |
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