Hemorrhagic cystitis (HC) is a major cause of morbidity after BMT; we
have analyzed its incidence, risk factors, and complications in 977 pa
tients undergoing BMT between 1974 and 1988. Despite vigorous hydratio
n and frequent voiding in all patients receiving cyclophosphamide, 135
/977 (15% by Kaplan-Meier projection) developed HC (micro- or gross he
maturia, dysuria, bladder pain) between -11 and +100 days (median +22)
after BMT. Of these, 60 had severe HC, including major urinary obstru
ction (4/60), renal failure (13/60), or need for surgical or chemical
bladder cauterization (16/60). By univariate analysis, allogeneic BMT
recipients had more frequent HC than autologous patients (17% vs. 9%,
P=0.002). In addition, allogeneic patients with adenoviruria were at i
ncreased risk for the development of HC. Patients with aplastic anemia
conditioned with high dose cyclophosphamide and total lymphoid irradi
ation had the highest rate of HC (22%) versus those with hematologic m
alignancies (15%, P=0.03). A Cox proportional hazards regression model
was used to further identify those factors independently associated w
ith HC. In all regression models, the factor most highly associated wi
th the development of HC was the finding of adenovirus in the urine pr
eceding the onset of hematuria. HC-related morbidity, and its associat
ed increased hospitalization costs, frequently complicates BMT. Improv
ed prophylactic measures, perhaps including the use of 2-mercaptoethan
e sulfonate, are needed, at least for allogeneic BMT patients with the
ir attendant risk of adenovirus infection.