Intravenous immunoglobulin for adults with autoimmune thrombocytopenic purpura: results of a randomized trial comparing 0 center dot 5 and 1 g/kg bw

Citation
B. Godeau et al., Intravenous immunoglobulin for adults with autoimmune thrombocytopenic purpura: results of a randomized trial comparing 0 center dot 5 and 1 g/kg bw, BR J HAEM, 107(4), 1999, pp. 716-719
Citations number
12
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BRITISH JOURNAL OF HAEMATOLOGY
ISSN journal
00071048 → ACNP
Volume
107
Issue
4
Year of publication
1999
Pages
716 - 719
Database
ISI
SICI code
0007-1048(199912)107:4<716:IIFAWA>2.0.ZU;2-U
Abstract
Since the first reports demonstrating the ability of a total dose of 2g/kg body weight (b.w.)of intravenous immunoglobulin (IVIg) to increase the plat elet count in patients with autoimmune thrombocytopenic purpura (AITP), the optimal dose has remained controversial. We report the results of a random ized study which compared two low doses of IVIg (0.5 g/kg b.w., group A, n = 19, and 1 g/kg b.w.. group B, n = 18) in 37 adults with AITP and platelet count <50 x 10(9)/l, in preparation for surgery or in a situation with a r isk of bleeding. On day 4 the proportion of responses, defined by a platele t count >80 x 10(9)/l and at least twice the initial platelet count, was si gnificantly higher in the group receiving 1 g/kg b.w. (12/18 in group B Ver sus 4/19 in group A, P = 0.005), All but one of the day 4 responders had al ready responded on day 3, The daily changes in the platelet count from the beginning of IVIg treatment were larger in group 13, with a significant dif ference relative to group A on day 3 (92 x 10(9)/l in group 13 versus 50 x 10(9)/l in group A, P = 0.03) and on day 4 (106 x 10(9)/l in group B versus 55 x 10(9)/l in group A, P = 0.03). Patients who had not responded by day 4 subsequently received 1.5g IVIg/kg b.w. (group A) or 1 g IVIg/kg b.w. (gr oup B). A response was observed in 11/13 initial non-responders in group A, and in 2/6 initial nonresponders in group a. Finally on day 8, the proport ion of responders was 78% (29/37) in the entire group and was similar in th e two subgroups. In conclusion, (1) initial treatment with 1 g/kg b.w. of I VIg appeared to be more effective than 0.5 g/kg b.w. in adults with AITP; ( 2) infusion of a low dose of IVIg did not jeopardize the efficacy of IVIg r einfusion: (3) some adults who did not respond to Ig IVlg/ kg b.w, responde d to a higher dose.