Between November 1996 and November 1997 we have transplanted 13 patients with Cystic Fibrosis (CF). Bilateral Sequential Lung Transplantation (BSLT) was successfully performed in all patients; one patient died from pneumonia and sepsis in the postoperative period and 12 are alive and well after a follow-up ranging between 1 and 13 months. Blood gas analysis improved from mean values of PaO2: 56 mm/Hg (with oxygen) and PaCO2: 43 mm/Hg to mean values of PaO2: 85 mm/Hg and PaCO2: 37 mm/Hg. Pulmonary function tests also improved dramatically: FEV1 improved from 20% predicted to 98% predicted. FVC also improved from 39% to 100%. The quality of life markedly improved: the ideal body weight moved from about 84% to normal values within nine months, and the 6-minute walk-test improved after transplantation from a preoperative distance of 325 meters, to 600 meters after 6 months. In conclusion, our favorable experience with BSLT in CF patients emphasizes the importance of lung transplantation in these patients. Carefully selected and properly managed patients may benefit from transplantation in terms of quality and duration of life.

Lung transplantation for cystic fibrosis / Rendina, Erino Angelo; Venuta, Federico; DE GIACOMO, Tiziano; E., Guarino; Annamaria, Ciccone; Serena, Quattrucci; G., Della Rocca; Antonelli, Mariano; Costante, Ricci; Coloni, Giorgio Furio. - In: EUROPEAN JOURNAL OF PEDIATRIC SURGERY. - ISSN 0939-7248. - STAMPA. - 8:4(1998), pp. 208-211. (Intervento presentato al convegno 10th International Symposium on Pediatric Surgical Research tenutosi a ZURICH, SWITZERLAND nel OCT 16-17, 1997) [10.1055/s-2008-1071155].

Lung transplantation for cystic fibrosis

RENDINA, Erino Angelo;VENUTA, Federico;DE GIACOMO, Tiziano;ANTONELLI, Mariano;COLONI, Giorgio Furio
1998

Abstract

Between November 1996 and November 1997 we have transplanted 13 patients with Cystic Fibrosis (CF). Bilateral Sequential Lung Transplantation (BSLT) was successfully performed in all patients; one patient died from pneumonia and sepsis in the postoperative period and 12 are alive and well after a follow-up ranging between 1 and 13 months. Blood gas analysis improved from mean values of PaO2: 56 mm/Hg (with oxygen) and PaCO2: 43 mm/Hg to mean values of PaO2: 85 mm/Hg and PaCO2: 37 mm/Hg. Pulmonary function tests also improved dramatically: FEV1 improved from 20% predicted to 98% predicted. FVC also improved from 39% to 100%. The quality of life markedly improved: the ideal body weight moved from about 84% to normal values within nine months, and the 6-minute walk-test improved after transplantation from a preoperative distance of 325 meters, to 600 meters after 6 months. In conclusion, our favorable experience with BSLT in CF patients emphasizes the importance of lung transplantation in these patients. Carefully selected and properly managed patients may benefit from transplantation in terms of quality and duration of life.
1998
cystic fibrosis; lung transplantation; postoperative results
01 Pubblicazione su rivista::01a Articolo in rivista
Lung transplantation for cystic fibrosis / Rendina, Erino Angelo; Venuta, Federico; DE GIACOMO, Tiziano; E., Guarino; Annamaria, Ciccone; Serena, Quattrucci; G., Della Rocca; Antonelli, Mariano; Costante, Ricci; Coloni, Giorgio Furio. - In: EUROPEAN JOURNAL OF PEDIATRIC SURGERY. - ISSN 0939-7248. - STAMPA. - 8:4(1998), pp. 208-211. (Intervento presentato al convegno 10th International Symposium on Pediatric Surgical Research tenutosi a ZURICH, SWITZERLAND nel OCT 16-17, 1997) [10.1055/s-2008-1071155].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/243752
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