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1.
Transplant Proc ; 40(6): 2003-5, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18675114

RESUMEN

Lung transplantation (LT) is the only effective form of therapy for cystic fibrosis (CF) associated with end-stage pulmonary failure. In Italy, the management of CF is regulated by national law, which has instituted regional centers for care and follow-up of all CF patients. LT has been performed since 1992 in only nine LT certified centers. The structured national organization has led to a unified database for LT for CF. As of December 2006, 197 bilateral LT (96 male and 94 female patients; 7 retransplants) have been performed. Of these, four had also liver or heart and liver transplantation, and three are long-term survivors. Overall median survival is 7 years. Mean age at transplantation is 26.5 years, and the mortality on the waiting list is 33.6%. Patients listed for transplant either received a suitable donor within a mean of 10 months or died within a mean of 5.5 months. The most frequent cause of death is bronchiolitis obliterans syndrome (BOS). Our nationwide database indicates the excellent results obtained by LT in FC. Still, mortality on the waiting list remains a challenge and long-term outcome is limited by BOS.


Asunto(s)
Fibrosis Quística/cirugía , Trasplante de Pulmón/estadística & datos numéricos , Bronquiolitis Obliterante/epidemiología , Fibrosis Quística/complicaciones , Femenino , Humanos , Italia , Masculino , Complicaciones Posoperatorias/clasificación , Complicaciones Posoperatorias/epidemiología , Reoperación/estadística & datos numéricos , Insuficiencia Respiratoria/etiología , Insuficiencia Respiratoria/cirugía , Estudios Retrospectivos , Resultado del Tratamiento
2.
Transplant Proc ; 50(10): 3732-3738, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30577264

RESUMEN

OBJECTIVES: 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. METHODS: 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). RESULTS: 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). CONCLUSIONS: Survival after lung transplant in our single center is similar to international data.


Asunto(s)
Fibrosis Quística/mortalidad , Fibrosis Quística/cirugía , Trasplante de Pulmón/mortalidad , Adolescente , Adulto , Niño , Femenino , Estudios de Seguimiento , Humanos , Italia , Estimación de Kaplan-Meier , Trasplante de Pulmón/métodos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Adulto Joven
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