Objective: Living-donor lobar lung transplantation offers an alternati
ve for patients with a life expectancy of less than a few months. We r
eport on our intermediate results with respect to recipient survival,
complications, pulmonary function, and hemodynamic reserve. Methods: T
hirty-eight living-donor lobar lung transplants were performed in 27 a
dult and 10 pediatric patients for cystic fibrosis (32), pulmonary hyp
ertension (two), pulmonary fibrosis (one), viral bronchiolitis (one),
bronchopulmonary dysplasia (one), and posttransplantation obliterative
bronchiolitis (one). Seventy-six donors underwent donor lobectomies.
Results: There were 14 deaths among the 37 patients, with an average f
ollow-up of 14 months. Predominant cause of death,vas infection, consi
stent with the large percentage of patients with cystic fibrosis in ou
r population. The overall incidence of rejection was 0.07 episodes/pat
ient-month, representing 0.8 episodes/patient. Postoperative pulmonary
function testing generally showed a steady improvement that plateaued
by postoperative months 9 to 12. Fourteen patients who were followed
up for at least 1 year underwent right heart catheterization; pressure
s and pulmonary vascular resistances were within normal ranges. Bronch
iolitis obliterans was definitively diagnosed in three patients. Among
the 76 donors, complications in the postoperative period included pos
tpericardiotomy syndrome (three), atrial fibrillation (one), and surgi
cal reexploration (three). Conclusions: We believe that these data sup
port an expanded role for living-donor lobar lung transplantation. Our
intermediate data are encouraging with respect to the functional outc
ome and survival of these critically ill patients, who would have died
without this option.