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Lung transplant in patients with familial pulmonary fibrosis. / Transplante pulmonar em pacientes com fibrose pulmonar familiar.
Bennett, David; Fossi, Antonella; Lanzarone, Nicola; Vita, Elda De; Luzzi, Luca; Paladini, Piero; Bargagli, Elena; Rottoli, Paola; Sestini, Piersante.
Afiliação
  • Bennett D; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Fossi A; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Lanzarone N; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Vita E; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Luzzi L; Chirurgia Toracica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Paladini P; Chirurgia Toracica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Bargagli E; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Rottoli P; Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze, Università di Siena, Siena, Italy.
  • Sestini P; Malattie dell'Apparato Respiratorio, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
J Bras Pneumol ; 46(6): e20200032, 2020.
Article em En, Pt | MEDLINE | ID: mdl-32725047
Objective Familial pulmonary fibrosis (FPF) is defined as an idiopathic interstitial lung disease affecting two or more members of the same family; poor outcome with high risk of death and chronic lung allograft dysfunction (CLAD) after lung transplant has been reported in these patients. The present study aimed to compare the short- and long-term outcome of lung transplants in patients with FPF and patients transplanted because of other interstitial lung diseases. Method Clinical pre- and post-transplant data from 83 consecutive patients with pulmonary fibrosis who underwent lung transplant at our centre were collected retrospectively. Patients were divided into those with familial (n=9 FPF group) and those with non-familial pulmonary fibrosis (n=74 controls). Results The FPF group was composed of 4 females and 5 males; 44.5% were ex-smokers. The majority presented their CT scan and pathology evidence of usual interstitial pneumonia. Patients with FPF had significantly lower pre-transplant levels of haemoglobin and haematocrit. No other differences in pre- and post-transplant characteristics were observed concerning controls. The clinical post-operative course was similar in the two groups. No significant difference in one-year CLAD-free survival and overall survival was observed. Conclusion The post-transplant course of patients with FPF was similar to patients with non-familial pulmonary fibrosis, although more patients with FPF had pre-transplant anaemia. Short- and long-term outcome was comparable in both groups. Lung transplant proved to be a valid option for patients with FPF as it was for patients with other types of pulmonary fibrosis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Pulmão / Fibrose Pulmonar Idiopática / Pulmão Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En / Pt Revista: J Bras Pneumol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Pulmão / Fibrose Pulmonar Idiopática / Pulmão Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En / Pt Revista: J Bras Pneumol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália País de publicação: Brasil