Lung Transplantation
Conditions
Keywords
Lung transplantation, Cyclosporine, Postconditioning
Brief summary
The morbidity and mortality of patients undergoing lung transplantation in the acute phase following surgical intervention is mainly due to the primary graft failure (PGF). The occurrence of PGF is multi factorial but is mainly caused by ischemia-reperfusion injury. The pulmonary graft suffers two periods of ischemia one when it is explanted from the donor (cold ischemia) followed by another when it is grafted into the recipient's thoracic cavity (warm ischemia). The brutal reperfusion of the graft exposes it to reperfusion injury that causes PGF. PGF occurs in up to 20% of transplanted patients and is associated with significantly higher levels of 30-days all-cause mortality. Patients with PGF have a 40% mortality at 30-days versus a 6% mortality in patients without PGF. Ischemic postconditioning, has recently been described in experimental models of ischemia-reperfusion injury in the heart, and although not yet fully understood. Several studies suggest that the mitochondria play a central role in cellular survival mechanisms after a prolonged period of ischemia-reperfusion (with the mitochondrial permeability transition pore (mPTP)). Experimental studies have shown that cyclosporin A (CsA) administered prior to reperfusion binds to cyclophilin D and blocks the opening of mPTP after reperfusion. This protective effect of ischemia-reperfusion injury by CsA has been shown in experimental studies and in clinical phase II trials in reperfused myocardial infarction patients. The hypothesis of this study is that the administration of CsA in transplanted patients (before re-opening of the first pulmonary graft vessels) protects the transplanted lung(s) from the deleterious effects of ischemia-reperfusion injury and thus reduce the frequency and severity of PGF.
Interventions
DRUGCyclosporine A
a pharmacological postconditioned group with IV administration of 2.5 mg/kg of CsA prior to first graft reperfusion
DRUGPlacebo
a control group with IV administration of 2.5 mg/kg of placebo prior to first graft reperfusion
Sponsors
Hospices Civils de Lyon
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* All patients over 18 years old, man or woman, who are listed for pulmonary transplantation either mono or double lung transplantation.
Exclusion criteria
* No contra-indication to CsA administration.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PaO2/FiO2 ratio (ratio of arterial oxygen partial pressure to fractional inspired oxygen) | 2 hours post-lung transplantation |
| PaO2/FiO2 ratio | 6 hours post-lung transplantation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| primary graft failure grade | 72 hours | clinical status of primary graft failure at 72 hours |
Countries
France
Outcome results
None listed