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Article: Clinical outcomes of primary thoracoscopic repair in patients with esophageal atresia and tracheoesophageal fistula: A multicenter study from the East Asia pediatric surgery research consortium

TitleClinical outcomes of primary thoracoscopic repair in patients with esophageal atresia and tracheoesophageal fistula: A multicenter study from the East Asia pediatric surgery research consortium
Authors
KeywordsEast Asia
Esophageal atresia
Thoracoscopic repair
Tracheoesophageal fistula
Issue Date16-Jul-2025
PublisherElsevier
Citation
Journal of Pediatric Surgery, 2025 How to Cite?
Abstract

Purpose: Thoracoscopic repair for esophageal atresia/tracheoesophageal fistula (EA/TEF) has not been widely adopted despite its introduction nearly 25 years ago. We reviewed the clinical outcomes of primary thoracoscopic EA/TEF repair performed at 5 leading centers for minimally invasive pediatric surgery in East Asia.

Methods: A retrospective review was conducted of patients with EA/TEF (Gross type C) who underwent primary thoracoscopic repair between 2008 and 2024. Patients with Gross type A/B/D/E, long-gap EA requiring staged repair, or trisomy18 were excluded. Collected data included demographics, surgical outcomes, and long-term outcomes.

Results: A total of 127 patients underwent thoracoscopic repair for EA/TEF during the study period. The mean gestational age, birth weight, and age at surgery were 38 ± 2.1 weeks, 2540 ± 487 g, and 3.0 ± 7.5 days, respectively. Thirty patients (23.6 %) had cardiac anomalies, and 8 (6.3 %) had chromosomal anomalies (excluding trisomy18). The mean operative time and intraoperative blood loss were 191 ± 67 min and 4.3 ± 8.7 mL, respectively. Nine patients (7.1 %) required conversion to open surgery and 10 (7.9 %) required blood transfusions. The mean length of hospitalization was 74 ± 73 days. Postoperative complications included anastomotic leak in 8 (6.3 %) patients and chylothorax in 9 (7.1 %). The long-term outcomes included anastomotic stenosis requiring dilatation in 52 patients (41.6 %), gastroesophageal reflux (GER) in 49 patients (39.2 %), and recurrent TEF in 3 (2.4 %). Mortality case was recognized in 2 (1.6 %).

Conclusion: The results of this study indicate that thoracoscopic repair for EA/TEF is a safe procedure when performed on selected patients and in centers with suitable thoracoscopic experience.


Persistent Identifierhttp://hdl.handle.net/10722/366842
ISSN
2023 Impact Factor: 2.4
2023 SCImago Journal Rankings: 0.949

 

DC FieldValueLanguage
dc.contributor.authorTsuruno, Yudai-
dc.contributor.authorSugita, Koshiro-
dc.contributor.authorOta, Kazuki-
dc.contributor.authorFung, Adrian Chi Heng-
dc.contributor.authorShigeta, Yusuke-
dc.contributor.authorDeie, Kyoichi-
dc.contributor.authorOnishi, Shun-
dc.contributor.authorChan, Ivy Hau Yee-
dc.contributor.authorTakezoe, Toshiko-
dc.contributor.authorMiyake, Yuichiro-
dc.contributor.authorTsutsuno, Takashi-
dc.contributor.authorShibuya, Soichi-
dc.contributor.authorChung, Patrick Ho Yu-
dc.contributor.authorShirota, Chiyoe-
dc.contributor.authorTainaka, Takahisa-
dc.contributor.authorMiyano, Go-
dc.contributor.authorKawashima, Hiroshi-
dc.contributor.authorWong, Kenneth Kak Yuen-
dc.contributor.authorUchida, Hiroo-
dc.contributor.authorIeiri, Satoshi-
dc.date.accessioned2025-11-26T02:50:28Z-
dc.date.available2025-11-26T02:50:28Z-
dc.date.issued2025-07-16-
dc.identifier.citationJournal of Pediatric Surgery, 2025-
dc.identifier.issn0022-3468-
dc.identifier.urihttp://hdl.handle.net/10722/366842-
dc.description.abstract<p><b>Purpose:</b> Thoracoscopic repair for esophageal atresia/tracheoesophageal fistula (EA/TEF) has not been widely adopted despite its introduction nearly 25 years ago. We reviewed the clinical outcomes of primary thoracoscopic EA/TEF repair performed at 5 leading centers for minimally invasive pediatric surgery in East Asia. <br></p><p><b>Methods:</b> A retrospective review was conducted of patients with EA/TEF (Gross type C) who underwent primary thoracoscopic repair between 2008 and 2024. Patients with Gross type A/B/D/E, long-gap EA requiring staged repair, or trisomy18 were excluded. Collected data included demographics, surgical outcomes, and long-term outcomes. <br></p><p><b>Results: </b>A total of 127 patients underwent thoracoscopic repair for EA/TEF during the study period. The mean gestational age, birth weight, and age at surgery were 38 ± 2.1 weeks, 2540 ± 487 g, and 3.0 ± 7.5 days, respectively. Thirty patients (23.6 %) had cardiac anomalies, and 8 (6.3 %) had chromosomal anomalies (excluding trisomy18). The mean operative time and intraoperative blood loss were 191 ± 67 min and 4.3 ± 8.7 mL, respectively. Nine patients (7.1 %) required conversion to open surgery and 10 (7.9 %) required blood transfusions. The mean length of hospitalization was 74 ± 73 days. Postoperative complications included anastomotic leak in 8 (6.3 %) patients and chylothorax in 9 (7.1 %). The long-term outcomes included anastomotic stenosis requiring dilatation in 52 patients (41.6 %), gastroesophageal reflux (GER) in 49 patients (39.2 %), and recurrent TEF in 3 (2.4 %). Mortality case was recognized in 2 (1.6 %). <br></p><p><b>Conclusion:</b> The results of this study indicate that thoracoscopic repair for EA/TEF is a safe procedure when performed on selected patients and in centers with suitable thoracoscopic experience.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofJournal of Pediatric Surgery-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectEast Asia-
dc.subjectEsophageal atresia-
dc.subjectThoracoscopic repair-
dc.subjectTracheoesophageal fistula-
dc.titleClinical outcomes of primary thoracoscopic repair in patients with esophageal atresia and tracheoesophageal fistula: A multicenter study from the East Asia pediatric surgery research consortium-
dc.typeArticle-
dc.identifier.doi10.1016/j.jpedsurg.2025.162470-
dc.identifier.scopuseid_2-s2.0-105011642039-
dc.identifier.issnl0022-3468-

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