Seven of 21 patients with sickle cell anemia developed neurologic comp
lications 5 to 243 days (median, 33 days) after allogeneic marrow tran
splantation. Among these 7 patients, indications for transplantation i
ncluded either a past history of stroke (4 patients) or recurrent seve
re vaso-occlusive events (3 patients). All received marrow from an HLA
-identical sibling after preparation with busulfan and cyclophosphamid
e, and in 4 patients with antithymocyte globulin. Five of 6 patients d
eveloping seizures received anticonvulsant and supportive treatment wi
th resolution of neurologic abnormalities. Three patients experienced
intracranial bleeding, which was fatal in two. Of the 14 patients free
of neurologic complications, 4 patients had experienced stroke before
transplantation. However, among all patients with prior stroke, the i
ncidence of intracranial hemorrhage was 38% (3/8), whereas none of the
13 patients without prior stroke developed posttransplant intracrania
l bleeding (P = .026). We conclude that patients with sickle cell anem
ia are at increased risk for neurologic complications after marrow abl
ative therapy and that patients with prior stroke are at increased ris
k for intracranial hemorrhage. Transplantation of patients before the
onset of overt stroke may reduce this risk. (C) 1995 by The American S
ociety of Hematology.