Summary:We studied long-term pulmonary function testing (PFT) in a retrospective cohort of 6-month survivors of allogeneic marrow transplant (BMT) between 1980 and 1997. Of 593 patients, 73, 71 and 65% had adequate data to assess for obstruction, restriction and diffusion impairments respectively. Over 5 years, mean declines in 1-s forced expiratory volume/forced vital capacity (FEV1/FVC), total lung capacity (TLC) and diffusion were 4, 7 and 17%, respectively. TLC and diffusion tended to subsequently increase. In all, 6, 12 and 35% of patients met criteria for obstruction, restriction and impaired diffusion, respectively. Obstruction was less common in recent transplants (5 vs 15%, P ¼ 0.004), while restriction and diffusion impairment rates remained stable. There was significantly greater mortality with obstruction (HR 2.0 (1.04-3.95)), and a nonstatistically significant higher mortality rate with restriction (HR 1.6 (0.95-2.75)), but not with impaired diffusion (HR ¼ 0.99 (0.65-1.50)). cGVHD ) and busulfan (OR 2.9 (1.01-8.24)) were associated with obstruction. Marrow from nonsibling or mismatched donors (OR 4.9 (2.2-10.7)) was associated with restriction. In summary, after BMT, decreased diffusion capacity is common and benign; obstruction has decreased in frequency, is rare without cGVHD, and is associated with mortality; nonsibling and mismatched donor are risk factors for restriction. The lung is often a target organ for complications after allogeneic marrow transplantation (BMT), 1,2 with pulmonary complications including infection, neoplasia, and idiopathic and iatrogenic disorders. The latter group includes pulmonary edema, peri-engraftment respiratory distress syndrome, diffuse alveolar hemorrhage, idiopathic pneumonia syndrome and obliterative bronchiolitis (OB). 3 Pulmonary function testing (PFT) after BMT is useful for predicting survival, given that PFT abnormalities correlate with nonrelapse mortality, 4 and the diagnosis of BMT complications, where PFT abnormalities make up some of the diagnostic criteria. 3,5 There are three main categories of PFT abnormalities. Obstructive defects occur when there is small airway closure or obstruction on expiration, leading to diminished forced expiratory volumes (1-s forced expiratory volume -FEV1), classically with a preserved forced vital capacity (FVC), resulting in a decrease in FEV1/FVC ratio. In the BMT population, the prototypical cause of obstruction is OB. Its occurrence has been linked to cGVHD. 6 Restriction is a pattern of decreased lung volumes (including the total lung capacity -TLC) with a preserved FEV1/FVC ratio. Idiopathic pneumonia syndrome, a diffuse noninfectious pneumonitis is a prototypical cause of restriction and may be due to thoracic irradiation, chemotherapy or other causes. Pulmonary edema, infectious pneumonitis and bronchiolitis obliterans organizing pneumonia (BOOP) may also cause restriction post-BMT. The final PFT derangement is one of diminished diffusion capacity for carbon monoxide (DCO). A low DCO often reflects thickenin...