MUCO TRANSPLAN: Non-respiratory Comorbidities Observed in Pulmonary French Transplant Patients With Cystic Fibrosis
Study Details
Study Description
Brief Summary
Pulmonary transplantation is the reference treatment for chronic terminal respiratory failure in patients with cystic fibrosis. These are mainly bi-pulmonary transplants (cardiopulmonary transplants are exceptional). The annual number of pulmonary transplants in France for cystic fibrosis is about 90. In 2013, the transplant involves a total of more than 600 patients with cystic fibrosis. The average age at the time of the transplant is 28.5 years (2013 data, French cystic fibrosis register), compared to 58 years for patients transplanted to all pathologies. Cystic fibrosis accounts for 25% of adult bi-pulmonary grafts. Pediatric transplants are currently very rare.
The median survival after pulmonary transplantation in cystic fibrosis is currently 8.5 years (and 10 years when considering patients surviving 3 months, ie excluding early mortality). Cystic fibrosis is the pathology associated with better survival after pulmonary transplantation given the young age of patients (28.5 years on average).
The non-respiratory comorbidities associated with transplantation, all underlying pathologies combined, and referenced in the Registry of the International Society for Heart and Lung Transplantation (ISHLT) are: hypertension, diabetes, renal insufficiency, Dyslipidemia, cancers. Their frequency increases with the survival time of transplanted patients. Cystic fibrosis is associated with non-respiratory comorbidities, the frequency of which increases with age - diabetes, osteoporosis, renal insufficiency, hepatopathy, neoplastic pathologies - and may become worse after transplantation.
The main objective is to estimate the incidence of non-respiratory co-morbidities after lung transplantation in the cohort of patients with cystic fibrosis grafted in the Rhône-Alpes region.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Co morbidities after lung transplantation in cystic fibrosis The population studied is the cohort of cystic fibrosis patients who received a bipulmonary transplant between 2004 and 2014 in one of the two transplantation centers in the Rhône-Alpes region. |
Other: Lung transplantation
To estimate the incidence of non-respiratory co-morbidities after lung transplantation between 2004 and 2014 in the cohort of patients with cystic fibrosis grafted in the Rhône-Alpes region
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Outcome Measures
Primary Outcome Measures
- Incidence of co-morbidities after lung transplantation [1 year]
The incidence rate will be calculated at 1 year follow-up after lung transplantation. The comorbidities studied will be: diabetes kidney failure high blood pressure hepatopathies undernutrition osteoporosis neoplasms, and in particular colon cancer gynecological complications (viral and neoplastic)
- Incidence of co-morbidities after lung transplantation [2 years]
The incidence rate will be calculated at 2 years follow-up after lung transplantation. The comorbidities studied will be: diabetes kidney failure high blood pressure hepatopathies undernutrition osteoporosis neoplasms, and in particular colon cancer gynecological complications (viral and neoplastic)
- Incidence of co-morbidities after lung transplantation [5 years]
The incidence rate will be calculated at 5 years follow-up after lung transplantation. The comorbidities studied will be: diabetes kidney failure high blood pressure hepatopathies undernutrition osteoporosis neoplasms, and in particular colon cancer gynecological complications (viral and neoplastic)
- Incidence of co-morbidities after lung transplantation [10 years]
The incidence rate will be calculated at 10 years follow-up after lung transplantation. The comorbidities studied will be: diabetes kidney failure high blood pressure hepatopathies undernutrition osteoporosis neoplasms, and in particular colon cancer gynecological complications (viral and neoplastic)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patients with clinical diagnosis of cystic fibrosis
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Patients with Pulmonary transplant between 01/01/2004 and 31/12/2014
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Patients followed-up in one of the two pulmonary transplantation centers in the Rhône-Alpes region (Lyon, Grenoble)
Exclusion Criteria:
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Patients followed in Rhône Alpes but transplanted elsewhere in France will not be included.
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Patient refusing to participate in the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Service de médecine interne Centre Hospitalier Lyon Sud, Hospices Civils de Lyon | Pierre-Bénite | France | 69495 |
Sponsors and Collaborators
- Hospices Civils de Lyon
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MUCO TRANSPLAN