Obstructive lung disease (OLD) has been described as a significant com
plication after allogeneic bone marrow transplantation (BMT). The inci
dence of OLD in adults appears to be low (similar to 3%), but there is
little data for children. We analyzed 89 consecutive pediatric alloge
neic BMTs, greater than or equal to 1.5 years post-BMT, performed at B
ritish Columbia's Children's Hospital from 1980 to 1992 for evidence o
f OLD. Diagnosis of OLD was based on clinical findings (nonproductive
cough, wheezing, and dyspnea with no evidence of infection), pulmonary
function tests (FEV, < 80% and FEF(25-75%) < 60% predicted), lung bio
psy, and computed tomography scan. Sixty-seven of the 89 children eval
uated survived greater than or equal to 90 days and were classified as
at risk for OLD. Thirteen of 67 (19.4%), developed OLD, 3 of which we
re transient. The development of OLD was strongly associated with the
following high-risk groups: chronic graft-versus-host disease (GVHD) (
37.1% OLD), increased donor age, acute GVHD, and either mismatched rel
ated or matched unrelated donor transplants. No correlation was found
with methotrexate prophylaxis for GVHD, total body irradiation, or cyt
omegalovirus reactivity in either donor or recipient and the developme
nt of OLD. Further analysis of only children with chronic GVHD showed
that liver involvement by GVHD before the onset of OLD (57.9%) was the
only other significant predictive factor. We observed an overall incr
eased prevalence of OLD in children compared with that previously repo
rted in adults. Further studies are required to confirm whether age is
a risk factor for development of OLD after allogeneic BMT. (C) 1994 b
y The American Society of Hematology.