Lung transplantation has become a valid therapeutic option for cystic fibro
sis patients with end-stage lung disease. The indication for transplantatio
n does not rely on strict criteria only but must be evaluated case by case.
In particular, the dynamics of the clinical course need to be considered w
ith regard to impaired physical performance, recurrent infections, decline
ill pulmonary function and weight loss. Important risk factors are a poor n
utritional status, osteoporosis, liver involvement, previous pleurodesis an
d the occurrence of multiresistant bacteria. Management and assessment of c
ystic fibrosis patients fur lung transplantation is complex. Therefore pati
ents should be referred to specialised centres at an early stage.