Thoracoscopic management of recurrent tracheoesophageal fistula: a single-center outcome analysis
Feng et al. BMC Surgery
(2025) 25:548
https://doi.org/10.1186/s12893-025-03292-y
BMC Surgery
Open Access
RESEARCH
Thoracoscopic management of recurrent
tracheoesophageal fistula: a single-center
outcome analysis
Cuizhu Feng1,2*, Long Li1,2, Xiang Li2, Yanxia Zhang2, Haibin Yu3, Mao Ye2 and Zhen Chen2
Abstract
Background Although thoracoscopic treatment of congenital esophageal atresia is widely accepted among
pediatric surgeons, its application in recurrent tracheoesophageal fistula (RTEF) remains rare because of its technical
difficulty. This study retrospectively analyzed thoracoscopic RTEF repairs at a single center to evaluate the safety,
feasibility, and outcomes of this approach, providing a clinical reference.
Methods We retrospectively reviewed 22 patients with RTEF who underwent thoracoscopic repair at the Capital
Center for Children's Health between October 2020 and July 2024. All patients had a history of type III esophageal
atresia repair, including 13 cases of type IIIa and 9 cases of type IIIb (Gross classification). The cohort included 8 male
and 14 female patients, with an admission age of 2 to 30 months (mean: 8.0 ± 7.2) and weight of 2.3 to 11.0 kg (mean:
5.5 ± 2.4). There were 16 first recurrences, 5 s recurrences, and 1 fourth recurrence. Five patients had failed previous
endoscopic fistula ligation, and 9 had a history of open thoracotomy. All 22 underwent thoracoscopic repair.
Results Thoracoscopic RTEF repair was successfully completed in all 22 patients (100%). The operation time ranged
from 136 to 420 min (mean: 288.5 ± 93.1), hospitalization ranged from 15 to 124 days (median: 24), and postoperative
invasive ventilator support lasted 0 to 480 h (median: 20). Esophageal leakage occurred in 6 patients (27.3%), all of
whom recovered with 1 to 8 weeks of conservative treatment. Esophageal stenosis developed in 8 patients (36.4%),
including 6 pre-existing and 2 new-onset cases; all improved after 1 to 6 sessions of endoscopic balloon dilation.
During follow-up (0.5–4 years), only 1 patient (4.5%) experienced re-recurrence; the remaining patients showed good
growth and development.
Conclusion Thoracoscopic treatment of RTEF following esophageal atresia is safe, feasible, and yields satisfactory
clinical outcomes.
Keywords Recurrent tracheoesophageal fistula, Esophageal atresia, Thoracoscopic treatment
*Correspondence:
Cuizhu Feng
1
Department of General Surgery, Capital Institute of Pediatrics, Chinese
Academy of Medical Sciences & Peking Union Medical College, Beijing,
People’s Republic of China
2
Department of General Surgery, Capital Center for Children’s Health,
Capital Medical University, Beijing, People’s Republic of China
3
Department of Pediatric Surgery, Inner Mongolia Maternal and Child
Health Care Hospital, Inner Mongolia, People’s Republic of China
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Feng et al. BMC Surgery
(2025) 25:548
Background
Recurrent tracheoesophageal fistula (RTEF) is a serious
complication following congenital esophageal atresia repair
and often requires reoperation. Although endoscopic techniques—such as fistula ligation, drug injection, and covered
stent placement—have been reported in the literature [1–4],
their use remains limited because of small case numbers,
high recurrence rates, and the need for multiple interventions. As such, these methods are still considered exploratory. Surgical repair remains the most definitive treatment
[5–8]. Reoperations are typically performed via thoracotomy because of severe thoracic adhesions and unclear
anatomical structures, with only a few pediatric surgical
centers adopting thoracoscopic techniques for RTEF repair.
Since 2020, the Capital Institute of Pediatrics has routinely
employed thoracoscopy for RTEF treatment, achieving satisfactory outcomes. This study retrospectively analyzed 22
patients with RTEF treated thoracoscopically at our institute to evaluate the safety, feasibility, and outcomes of this
approach, aiming to provide a reference for thoracoscopic
management of RTEF.
Materials and methods
Patients
We retrospectively analyzed 22 patients with RTEF who
underwent thoracoscopic repair at the Capital Institute of
Pediatrics between October 2020 and July 2024. Among
them, 13 were classified as type IIIa and 9 as type IIIb (Gross
classification). The cohort included 8 male and 14 female
patients, with a mean age at admission of 8.0 ± 7.2 months
(range: 2–30 months) and a mean weight of 5.5 ± 2.4 kg
(range: 2.3–11.0 kg). Recurrence details included 16 first
recurrences, 5 s recurrences, and 1 fourth recurrence. Five
patients had previously failed endoscopic fistula ligation,
and 9 had a history of open thoracotomy. Among the children included, two were from our center; the remaining
were referred from other institutions. This study did not
include cases of missed proximal tracheoesophageal fistula.
All 22 patients underwent thoracoscopic tracheoesophageal
fistula repair.
Diagnostic methods
Diagnostic methods included gastroenterography (using a
water-soluble contrast medium), bronchoscopy, gastroscopy, and chest computed tomography (CT). These preoperative examinations were used to comprehensively evaluate
the esophagus, trachea, and lungs to aid surgical planning.
In this study, all 22 patients underwent gastroenterography;
19 underwent bronchoscopy, 18 underwent gastroscopy,
and 19 underwent chest CT.
Surgical methods
The patients were positioned in the left lateral decubitus
position with the right arm elevated. A 5-mm trocar was
Page 2 of 5
inserted at the subscapular angle as the thoracoscopic port.
Two 3-mm trocars were placed at the third and sixth intercostal spaces along the mid-axillary line as the main operating ports, and a 5-mm trocar was inserted at the seventh
intercostal space near the spine as an assistant port. After
successful trocar placement, pleural adhesions were dissected using an electric hook to expose the posterior mediastinum. Esophageal dissec (...truncated)