Survival After Lung Transplant for Cystic Fibrosis in Italy: A Single Center Experience With 20 Years of Follow-up
Lung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively analyzed our experience since the start of the transplantation program in 1996 with focus on survival analysis. All patients with CF who unde...
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Published in | Transplantation proceedings Vol. 50; no. 10; pp. 3732 - 3738 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.12.2018
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Abstract | Lung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively analyzed our experience since the start of the transplantation program in 1996 with focus on survival analysis.
All patients with CF who underwent lung transplant at our center were included (1996–2016). Survival analysis after lung transplant was performed using the Kaplan-Meier estimate, comparing by sex and by 4 eras (1996–2000, 2001–2005, 2006–2010, and 2011–2016).
In a 20-year period, 243 patients with CF were listed for lung transplant; 123 patients (61 male, 62 female) underwent transplant, and 85 died while waiting for donor organs. The mean (SD) and median age at transplant was 27.7 (8.7) years and 26.9 years (range, 9.1 – 52.1 years), respectively. Mean (SD) forced expiratory volume in the first second was 27.6 (9.7)% predicted; 115 patients (92.0%) were pancreatic insufficient, and 43 patients (34.0%) had CF-related diabetes. Removing patients with CF who died within the first 3 postoperative months, the mean (SD) and median survival after transplant were 8.2 (5.7) years and 7.5 years (range, 3 months-20 years), respectively.
Overall post–lung transplant 1-year survival was 93.6%, 5-year survival was 71.4%, 10-year survival was 53.6%, 15-year survival was 36.7%, and 20-year survival was 31.6%. We found no difference in survival between sex (P = .22) and among the 4 eras (P = .56).
Survival after lung transplant in our single center is similar to international data. |
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AbstractList | Lung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively analyzed our experience since the start of the transplantation program in 1996 with focus on survival analysis.
All patients with CF who underwent lung transplant at our center were included (1996-2016). Survival analysis after lung transplant was performed using the Kaplan-Meier estimate, comparing by sex and by 4 eras (1996-2000, 2001-2005, 2006-2010, and 2011-2016).
In a 20-year period, 243 patients with CF were listed for lung transplant; 123 patients (61 male, 62 female) underwent transplant, and 85 died while waiting for donor organs. The mean (SD) and median age at transplant was 27.7 (8.7) years and 26.9 years (range, 9.1 - 52.1 years), respectively. Mean (SD) forced expiratory volume in the first second was 27.6 (9.7)% predicted; 115 patients (92.0%) were pancreatic insufficient, and 43 patients (34.0%) had CF-related diabetes. Removing patients with CF who died within the first 3 postoperative months, the mean (SD) and median survival after transplant were 8.2 (5.7) years and 7.5 years (range, 3 months-20 years), respectively. Overall post-lung transplant 1-year survival was 93.6%, 5-year survival was 71.4%, 10-year survival was 53.6%, 15-year survival was 36.7%, and 20-year survival was 31.6%. We found no difference in survival between sex (P = .22) and among the 4 eras (P = .56).
Survival after lung transplant in our single center is similar to international data. Lung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively analyzed our experience since the start of the transplantation program in 1996 with focus on survival analysis. All patients with CF who underwent lung transplant at our center were included (1996–2016). Survival analysis after lung transplant was performed using the Kaplan-Meier estimate, comparing by sex and by 4 eras (1996–2000, 2001–2005, 2006–2010, and 2011–2016). In a 20-year period, 243 patients with CF were listed for lung transplant; 123 patients (61 male, 62 female) underwent transplant, and 85 died while waiting for donor organs. The mean (SD) and median age at transplant was 27.7 (8.7) years and 26.9 years (range, 9.1 – 52.1 years), respectively. Mean (SD) forced expiratory volume in the first second was 27.6 (9.7)% predicted; 115 patients (92.0%) were pancreatic insufficient, and 43 patients (34.0%) had CF-related diabetes. Removing patients with CF who died within the first 3 postoperative months, the mean (SD) and median survival after transplant were 8.2 (5.7) years and 7.5 years (range, 3 months-20 years), respectively. Overall post–lung transplant 1-year survival was 93.6%, 5-year survival was 71.4%, 10-year survival was 53.6%, 15-year survival was 36.7%, and 20-year survival was 31.6%. We found no difference in survival between sex (P = .22) and among the 4 eras (P = .56). Survival after lung transplant in our single center is similar to international data. OBJECTIVESLung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively analyzed our experience since the start of the transplantation program in 1996 with focus on survival analysis.METHODSAll patients with CF who underwent lung transplant at our center were included (1996-2016). Survival analysis after lung transplant was performed using the Kaplan-Meier estimate, comparing by sex and by 4 eras (1996-2000, 2001-2005, 2006-2010, and 2011-2016).RESULTSIn a 20-year period, 243 patients with CF were listed for lung transplant; 123 patients (61 male, 62 female) underwent transplant, and 85 died while waiting for donor organs. The mean (SD) and median age at transplant was 27.7 (8.7) years and 26.9 years (range, 9.1 - 52.1 years), respectively. Mean (SD) forced expiratory volume in the first second was 27.6 (9.7)% predicted; 115 patients (92.0%) were pancreatic insufficient, and 43 patients (34.0%) had CF-related diabetes. Removing patients with CF who died within the first 3 postoperative months, the mean (SD) and median survival after transplant were 8.2 (5.7) years and 7.5 years (range, 3 months-20 years), respectively. Overall post-lung transplant 1-year survival was 93.6%, 5-year survival was 71.4%, 10-year survival was 53.6%, 15-year survival was 36.7%, and 20-year survival was 31.6%. We found no difference in survival between sex (P = .22) and among the 4 eras (P = .56).CONCLUSIONSSurvival after lung transplant in our single center is similar to international data. |
Author | Cimino, G. Troiani, P. Bonci, E. D’Alù, V. Bertasi, S. Quattrucci, S. Palange, P. Savi, D. Rossi, P. Giordani, B. Mordenti, M. Poggi, C. |
Author_xml | – sequence: 1 givenname: D. surname: Savi fullname: Savi, D. email: danielasavi1@virgilio.it organization: Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 2 givenname: M. surname: Mordenti fullname: Mordenti, M. organization: Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 3 givenname: E. surname: Bonci fullname: Bonci, E. organization: Department of Experimental Medicine, Sapienza University of Rome, Italy – sequence: 4 givenname: P. surname: Troiani fullname: Troiani, P. organization: Department of Pediatrics, Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 5 givenname: B. surname: Giordani fullname: Giordani, B. organization: Lega Italiana Fibrosi Cistica ONLUS-LIFC, Rome, Italy – sequence: 6 givenname: V. surname: D’Alù fullname: D’Alù, V. organization: Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 7 givenname: S. surname: Bertasi fullname: Bertasi, S. organization: Department of Pediatrics, Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 8 givenname: G. surname: Cimino fullname: Cimino, G. organization: Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 9 givenname: P. surname: Rossi fullname: Rossi, P. organization: Department of Pediatrics, Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 10 givenname: C. surname: Poggi fullname: Poggi, C. organization: Department of General Surgery and Organ Transplant, Division of Thoracic Surgery, Sapienza University of Rome, Italy – sequence: 11 givenname: P. surname: Palange fullname: Palange, P. organization: Department of Public Health and Infectious Diseases, Adult Cystic Fibrosis Center, Sapienza University of Rome, Italy – sequence: 12 givenname: S. surname: Quattrucci fullname: Quattrucci, S. organization: Department of Pediatrics, Cystic Fibrosis Center, Sapienza University of Rome, Italy |
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CitedBy_id | crossref_primary_10_1016_j_transproceed_2019_08_011 crossref_primary_10_1016_j_pcl_2020_09_017 crossref_primary_10_1016_j_clinsp_2023_100274 crossref_primary_10_1097_MOT_0000000000000753 crossref_primary_10_1016_j_transproceed_2020_02_051 |
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Snippet | Lung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we retrospectively... OBJECTIVESLung transplantation is currently the only treatment for end-stage respiratory failure in patients with cystic fibrosis (CF). In this study we... |
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SubjectTerms | Adolescent Adult Child Cystic Fibrosis - mortality Cystic Fibrosis - surgery Female Follow-Up Studies Humans Italy Kaplan-Meier Estimate Lung Transplantation - methods Lung Transplantation - mortality Male Middle Aged Retrospective Studies Young Adult |
Title | Survival After Lung Transplant for Cystic Fibrosis in Italy: A Single Center Experience With 20 Years of Follow-up |
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