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Updated: Jul 11, 2026

Murine Intrapulmonary Tracheal Transplantation: A Model for Investigating Obliterative Airway Disease After Lung Transplantation
Published on: November 10, 2023
[Gastroesophageal reflux as a cause of pulmonary dysfunction after lung transplantation]
Masanori Tsuchida1, T Hashimoto, H Shinohara
1Division of Thoracic and Cardiovascular Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Insights
Gastroesophageal reflux can impair lung transplant outcomes. Surgical correction via fundoplication improved lung function in a teenage patient with interstitial lung disease post-transplant.
Area of Science:
- Transplantation immunology
- Gastroenterology
- Pulmonary medicine
Background:
- Gastroesophageal reflux (GER) is a known risk factor for allograft dysfunction in lung transplant recipients.
- Microaspiration, inflammation, and obliterative bronchiolitis are potential consequences of GER post-lung transplant.
Observation:
- A 16-year-old male with interstitial lung disease underwent bilateral lung transplantation.
- Post-transplant, the patient exhibited significantly reduced lung function (FVC 33%, FEV1 28% predicted).
- Gastroesophageal reflux was identified as the sole positive finding after extensive investigation.
Findings:
- Initial pyeloplasty failed to improve lung function, with persistent GER confirmed by pH monitoring.
- Laparoscopic fundoplication 9 months post-transplant led to gradual improvement in lung function (FVC 44%, FEV1 33% predicted).
Implications:
- This case highlights the critical role of managing gastroesophageal reflux in lung transplant recipients.
- Surgical intervention, specifically fundoplication, can be effective in improving allograft function when GER is a contributing factor.
- Early identification and management of GER may improve long-term outcomes for lung transplant patients.
Abstract:
Gastroesophageal reflux is a potential cause of allograft dysfunction after lung transplantation due to microaspiration, lung inflammation, and development of bronchitis obliterans. A 16-year-old Japanese boy who had been suffering from interstitial lung disease received bilateral lung transplant from a braindead donor in the United States. Three months after lung transplantation, his lung function has not increased as expected. Spirometory revealed forced vital capacity (FVC) of 1.11 l (33% of predicted) and forced expiratory volume in one second (FEV1.0) of 0.81 l (28% of predicted). All possible etiologies, including infection, acute and chronic rejection, and other abnormalities were investigated. The only positive finding was the presence of gastroesophageal reflux. He first underwent pyroloplasty which did not improve lung function. Twenty-four-hour pH monitor performed after surgery revealed frequent gastroesophageal reflux. He eventually underwent laparoscopic fundoplication 9 months after initial lung transplantation. His lung function gradually improving after fundoplication, an FVC was 1.56 l (44% of predicted) and FEV1 was 1.25 l (33% of predicted).
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