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Comparison of Endoscopy and Esophagram for the Routine Evaluation of Anastomosis After McKeown Esophagectomy

Comparison of Endoscopy and Esophagram for the Routine Evaluation of Anastomosis After McKeown Esophagectomy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07043491
Enrollment
2
Registered
2025-06-29
Start date
2024-11-04
Completion date
2025-12-01
Last updated
2025-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer, Surgery-Complications

Keywords

Esophageal cancer, Endoscopy, Esophagram, McKeown esophagectomy

Brief summary

This retrospective cohort study reviewed patients who underwent McKeown esophagectomy. All patients routinely underwent either endoscopy or esophagram for the evaluation of anastomosis on postoperative day 7. The initiation of oral intake depended on the status of anastomosis according to the assessment result of endoscopy or esophagram. All patients were followed up for six months after the assessment of anastomosis.

Detailed description

This retrospective cohort study reviewed patients who underwent McKeown esophagectomy. All patients routinely underwent either endoscopy or esophagram for the evaluation of anastomosis on postoperative day 7. The initiation of oral intake depended on the status of anastomosis according to the assessment result of endoscopy or esophagram. The patients whose esophagram indicated an intact anastomosis or whose endoscopy revealed a good healing anastomosis were allowed to initiate oral intake. While the patients whose endoscopy revealed a poor healing anastomosis were monitored with a repeat endoscopy weekly and these patients were delayed for oral intake until the repeat endoscopy revealed a good healing anastomosis. All patients were followed up for six months after the assessment of anastomosis. The primary endpoints were the efficacy of the evaluation of anastomosis, which included the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for AL, the accuracy of the evaluation of anastomosis, and the incidence of AL after oral intake. Cases of AL that were found after the previous assessment were regarded as missed diagnoses when the sensitivity was calculated. The secondary endpoints included the time from surgery to AL diagnosis, the time required for AL healing, and safety profile.

Interventions

DIAGNOSTIC_TESTEndoscopy

We first observed the residual esophagus to evaluate the mucosal color. We then reached the top of the anastomosis to obtain a full view of the anastomosis to exclude obvious leakage around that site. We next conducted a more detailed endoscopic examination at a close focal distance, circumferentially around the anastomosis. During this process, we utilized saline solution to meticulously remove white fibrin coverings and bloodstains to the greatest extent possible to ensure a thorough evaluation of anastomotic integrity. Finally, we inspected the staple line of the tubularized stomach to exclude gastric fistula and assessed the perfusion of the gastric graft. Endoscopic findings were assessed by an additional endoscopist and 3 esophageal surgeons during the examination, as well as by reviewing captured images or videos after endoscopy.

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

The inclusion criteria required patients to have routinely undergone either endoscopy or an esophagram for the postoperative evaluation of anastomosis.

Exclusion criteria

We excluded the patient with histologically confirmed benign tumors of the esophagus or esophagogastric junction and the patient who had incomplete data.

Design outcomes

Primary

MeasureTime frameDescription
The specificity for detecting ALFrom January 1, 2022 to July 9, 2023The number of the patients who is true negative for AL/ The total number of the patients who did not develop AL
Predictive negative value for ALFrom January 1, 2022 to July 9, 2023The number of the patients who is true negative for AL/ The number of the patients who is determined to have an intact anastomosis
The incidence of AL after oral intakeFrom January 1, 2022 to July 9, 2023The number of the AL that occurs after oral intake/ The number of the patients who were determined to have an intact anastomosis
The sensitivity for detecting ALFrom January 1, 2022 to July 9, 2023The number of the patients who is true positive for AL/ The total number of AL
Predictive positive value for ALFrom January 1, 2022 to July 9, 2023The number of the patients who is true positive for AL/ The number of the patients who is evaluated as AL

Secondary

MeasureTime frameDescription
The time required for the healing of ALFrom January 1, 2022 to July 9, 2023The degree of AL healing was determined on the basis of the evidence that no swallowed liquid flowed out of the anastomosis, accompanied by a repeat examination with a normal result and disappearance of clinical manifestations
The time from surgery to the diagnosis of ALFrom January 1, 2022 to July 9, 2023The time from surgery to the diagnosis of AL

Countries

China

Contacts

Primary ContactHong Yang, PhD.
yanghong@wy.sysucc.org.cn13560405144

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026