Vr. Arruda et Jm. Annichinobizzacchi, HIGH-DOSE DEXAMETHASONE THERAPY IN CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA, Annals of hematology, 73(4), 1996, pp. 175-177
A high-dose pulse of dexamethasone has been described as a current opt
ion for the treatment of refractory idiopathic thrombocytopenic purpur
a (ITP), but the results are controversial. Here we describe the use o
f a high dose of dexamethasone (40 mg per day for 4 days every month)
in 18 patients with chronic ITP. The median age of the patients was 42
.5 years (range, 16-77 years); 13 were female and five male. The durat
ion of the disease ranged from 5 to 480 months, and splenectomy was ca
rried out in six of the 18 patients. The overall results obtained reve
aled a satisfactory response (platelet counts higher than 50 x 10(9)/l
) in eight of the 18 patients. However, a long-term remisson was achie
ved in only three of the eight patients with a follow up of 7-16 month
s. We were not able to identify any clinical or laboratory prognostic
parameters or previous treatment which would allow one to predict a su
ccessful outcome of this treatment. These results suggest that a high
dose of dexamethasone may provide an alternative, be it a poor one, fo
r the treatment of refractory IPT, in which the use of a low-cost drug
with limited side effects is an important consideration.