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Evaluation of the Respiratory Impact After Conventional or Minimally Invasive Esophageal Atresia Surgery

Conditions
Restrictive Lung Disease
Chest Wall Anomaly
Esophageal Atresia
Oesophageal Atresia
Registration Number
NCT04136795
Lead Sponsor
University Hospital, Angers
Brief Summary

Right thoracotomy, conventional approach to esophageal atresia repair, leads to up to 60% radiological chest wall sequelae anomalies. The impact of these anomalies on the patient's respiratory function remains unknown. Minimally invasive thoracic surgery considerably reduces this rate.

The primary objective of this study is to assess the occurrence of restrictive lung disease in patients with type III esophageal atresia depending on the type of surgical approach (Conventional or minimally invasive).

The primary endpoint will be he occurrence of restrictive lung disease , objectified by pulmonary function tests (PFTs), carried out according to the current national guidelines (PNDS = protocole national de diagnostic et de soins).

Detailed Description

Right thoracotomy, conventional approach to esophageal atresia repair, leads to up to 60% radiological chest wall sequelae anomalies. The impact of these anomalies on the patient's respiratory function remains unknown. Minimally invasive thoracic surgery considerably reduces this rate.

The primary objective of this study is to assess the occurrence of restrictive lung disease in patients with type III esophageal atresia depending on the type of surgical approach (Conventional or minimally invasive).

The primary endpoint will be the occurrence of restrictive lung disease, as assessed by pulmonary function tests (PFTs), carried out according to the current national guidelines (PNDS = protocole national de diagnostic et de soins).

The secondary endpoints will be to measure the severity of the restrictive disease, to look for other respiratory alterations, to correlate radiological chest wall sequelae anomalies with the impact on respiratory function and to look for a causal relationship between the surgical technique used and the respiratory impact.

The methodology used will be a retrospective non interventional study on the cohort of patients included in the national esophageal atresia registry (CRACMO, Lille University Hospital) between the 1st of january 2008 and the 31st of December 2013.

All the patients included in the national esophageal atresia registry (CRACMO) having had an operation for type III esophageal atresia (long gap esophageal atresia excluded), as defined by the Ladd Classification, will be included in this study.

The exclusion criterion will be patients lost to follow up or deceased, patients having had no pulmonary function tests (PFTs) or no thoracic X-Ray during the first 6 to 9 years of follow up and patients having had thoracic surgery before the esophageal atresia repair.

The number of patients expected in the national esophageal atresia registry over the 6 years excedes 500. The number of thoracoscopy repairs should be about 50.

This study should allow us to determine if minimally invasive surgery is beneficial on mid-term respiratory function in children, related to possible post-operative chest wall sequelae.

The results obtained from this study should lead to recommendations concerning the surgical approach to esophageal atresia repair to improve the prognosis of chest wall anomalies and respiratory function in these patients. It should also help to identify patient subgroups which would benefit from a reinforced respiratory follow up. This could then lead to a hospital clinical research program (PHRC)

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Patients included in the national esophageal atresia registry (CRACMO)
  • Operation for type III esophageal atresia (Ladd classification)
  • Between 01/01/2008 and 31/12/2013.
Exclusion Criteria
  • Long gap esophageal atresia
  • Patients lost to follow up
  • Deceased
  • No PFTs or X-rays between 6 and 9 years of follow up
  • Patients having had thoracic surgery before the esophageal atresia repair

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the occurrence of restrictive lung disease in patients with type III esophageal atresia depending on the type of surgical approach (Conventional or minimally invasive).6 to 9 years of age.

Objectified by pulmonary function tests (PFTs), carried out according to the current national guidelines. Restrictive lung disease defined by: FEV1/FVC ratio \> -1.64 Z-score and CVF \< -1.64 Z-score according to ATS/ERS-GLI (American Thoracic Society \& European Respiratory Society - Global Lungs Initiative) recommendations.

Secondary Outcome Measures
NameTimeMethod
Percentage of post-operative complications depending on the type of surgeryTime of surgery to 6 to 9 years consultation

Bleeding, infection, anastomotic stenosis, anastomotic leak

Severity of restrictive lung disease6 to 9 years of age

Depending on Z-score value

Assesse the occurrence of obstructive or mixed lung disease6 to 9 years

Objectified by pulmonary function tests (PFTs), carried out according to the current national guidelines. Mixed lung disease defined by: FEV1/FVC ratio \< -1.64 Z-score and CVF \< -1.64 Z-score and obstructive lung disease

Mortality rateTime of surgery to 6 to 9 years consultation

Percentage of mortality in each group, cause of death linked directly to surgery or not

Chest wall anomalies detected on thoracic X-rays6 to 9 years of age

Hemivertebra, rib fusion, intercostal abnormalities, scoliosis

Correlation between post-operative chest wall anomalies and restrictive lung disease6 to 9 years of age

In each group, comparison of the percentage of chest wall anomalies detected on the X-rays and the percentage of restrictive lung disease cases

Trial Locations

Locations (1)

CRACMO - centre de référence des atrésies de l'oesophage

🇫🇷

Lille, France

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