To establish the efficacy of intravenous immunoglobulins (IVIG) in the
treatment of acute Guillain-Barre syndrome (GBS), we treated nine con
secutive pediatric cases (age 2.5-13.5 years) fulfilling the criteria
for GBS with a single dose of IVIG (Sandoglobulin; 2 g/kg/BW). None of
the patients experienced any IVIG related side-effects, The mean time
required to improve by at least one grade on the functional GBS scale
after IVIG treatment was 3.5 days, while the mean period to regain am
bulation was 11.2 days. Full mobilization without evidence of relapse
in the follow-up period (mean 14.5 months) was noted in all but one pa
tient who relapsed after 5 months. We conclude that the early use of a
single IVIG dose may prevent further progression of the disease, thus
shortening the clinical course of childhood GBS. The most beneficial
IVIG dose regimen remains to be determined by controlled trials. (C) 1
997 Elsevier Science B.V.