PROSPECTIVE, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY ON THE EFFECT OF HIGH-DOSE, INTRAVENOUS IMMUNOGLOBULIN IN CHILDREN AND ADOLESCENTS WITH SEVERE BRONCHIAL-ASTHMA
B. Niggemann et al., PROSPECTIVE, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY ON THE EFFECT OF HIGH-DOSE, INTRAVENOUS IMMUNOGLOBULIN IN CHILDREN AND ADOLESCENTS WITH SEVERE BRONCHIAL-ASTHMA, Clinical and experimental allergy, 28(2), 1998, pp. 205-210
Objective In order to study the effect of high-dose, intravenous immun
oglobulin (IVIG) in severe childhood asthma, we investigated 31 childr
en and adolescents (15 girls, 16 boys) aged 9-22 years (median age of
14 years) suffering from severe bronchial asthma. Methods In a prospec
tive, double-blind fashion, patients received either four doses of IVI
G (1 g/kg body weight) or identical doses of intravenous human serum a
lbumin. The first two doses were given on two consecutive days, follow
ed by two further doses at 4 week intervals. Results There was no stat
istical difference in the actively treated group when compared with th
e placebo group in symptom-score, bronchial hyperreactivity or peak-fl
ow-variability. There was a trend for fewer total days of upper respir
atory tract infections and also symptom-scores in the IVIG group but t
hese did not reach statistical significance. Conclusion Our data indic
ate that treatment with IVIG in asthmatic children did not show a sign
ificant reduction in the incidence of upper respiratory tract infectio
ns, but the patients who did have upper respiratory infections in the
IVIG-group appear to have less protracted infections. Severity and bro
nchial hyperreactivity do not seem to be affected by the treatment as
performed in our study.