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Updated: Jun 21, 2026

Murine Intrapulmonary Tracheal Transplantation: A Model for Investigating Obliterative Airway Disease After Lung Transplantation
Published on: November 10, 2023
[Invasive mechanical ventilation in cystic fibrosis: Influence in lung transplant]
M A Frías Pérez1, I Ibarra de la Rosa, E García Menor
1Unidad de Cuidados Intensivos Pediátricos, Servicio de Pediatría, Hospital Universitario Reina Sofía, Córdoba, España.
Insights
Lung transplantation in children with cystic fibrosis (CF) on invasive mechanical ventilation (IMV) leads to a more complex surgery and immediate recovery. While short-term survival is encouraging, long-term outcomes are significantly poorer.
Area of Science:
- Pediatric Pulmonology
- Transplant Surgery
- Critical Care Medicine
Background:
- Invasive mechanical ventilation (IMV) is a relative contraindication for lung transplantation (LT) in adult cystic fibrosis (CF) patients.
- Limited data exists regarding the outcomes of LT in pediatric CF patients requiring IMV.
Purpose of the Study:
- To evaluate the impact of pre-transplant IMV on the surgical outcomes and survival of pediatric CF patients undergoing LT.
- To compare the postoperative course and survival rates between pediatric CF patients with and without pre-transplant IMV.
Main Methods:
- Retrospective study of 21 pediatric CF patients who underwent LT over 8 years.
- Comparison of demographic, surgical, and postoperative data between patients on IMV (n=8) and those not on IMV (n=13).
- Analysis of graft function, rejection episodes, multiorgan failure, and survival (immediate, 1-year, and long-term).
Main Results:
- Patients on IMV experienced longer bypass times, higher rates of tracheotomy, more rejection episodes, and multiorgan failure.
- No significant differences in graft function or immediate/1-year survival were observed between groups.
- Long-term survival was significantly lower in the IMV group compared to the non-IMV group.
Conclusions:
- Pediatric CF patients on IMV undergoing LT face more complex surgery and immediate postoperative challenges.
- While immediate and 1-year survival may be acceptable, the long-term prognosis for these patients is significantly worse.
Introduction:
Invasive mechanical ventilation (IMV) in patients with advanced cystic fibrosis (CF) is a relative contraindication for lung transplant (LT) in adults, although there is currently no data on children.
Patients And Methods:
An 8-year retrospective study on 21 children with CF who underwent LT was performed, analysing their results as they were receiving (n = 8) or not (n = 13) IMV pretransplant. Demographic and surgical data, postoperative course, lung function and survival (immediate and 1-year) were compared between both groups. The role of the IMV pretransplant as a postoperative risk factor was estimated (odds ratio) and Kaplan Meier survival study was performed in both groups.
Results:
No differences in patient age, sex and nutritional parameters were observed between both groups. Those on IMV who received LT required more frequent and longer bypass, more need for tracheotomy, a higher number of rejection episodes per patient and multiorgan failure, longer PICU stay and longer time on IMV than those who were not on IMV when LT was received. Nevertheless, no differences could be found regarding graft function and immediate and 1-year survivals (62.5% vs. 92.3% with and without IMV respectively). On the other hand, long-term survival was significantly lower than in patients on IMV.
Conclusions:
In our experience, children with CF on IMV who receive LT have more complicated surgery and immediate postoperative course. Though immediate and 1-year results and survivals may be encouraging, medium and long-term ones are significantly lower.
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