Patients with Cystic Fibrosis (CF) are in some respect potentially ide
al candidates for lung transplantation. However the transplantation su
rgeon has to face same complex specific problems typical of CF patient
s, which may cause increased complications and mortality. Consciousnes
s and prevention of these problems, as well as timely treatment, is th
e key for success. For this reason we have reviewed the postoperative
complications which occurred in our experience with 13 patients underg
oing bilateral sequential double lung transplantation, followed for 5
to 16 months. One patient died in the 15th postoperative day for pneum
onia and sepsis. Another patient died 45 days postoperatively for rena
l and cardiac failure associated with pneumonia and sepsis. Eleven pat
ients left the hospital without oxygen after 19 to 36 days and live cu
rrently a normal life. One patient had phrenic nerve palsy which solve
d spontaneously two months after the transplant. Three patients had a
partial dehiscence of the surgical wound which required reclosure. Two
patients had osteomielitis of the sternum which required surgical man
agement. Out of 26 brochial anastomoses, 3 (in 2 patients) developed a
stenosis which required Laser treatment. In one case the problem was
permanently solved, while in the other patient the stenosis recurred f
or over 4 months with mucosal hyperplasia and was successfully treated
by increased in steroid dosage. Eight patients had pneumonia which wa
s successfully treated, and 10 had CMV infection. In conclusion, patie
nts with FC have an increased risk for postransplant complications. Th
ese can however be successfully treated without jeopardizing lung term
results.