The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia - A randomized, double-blind, multicenter crossover trial

Citation
Hw. Eijkhout et al., The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia - A randomized, double-blind, multicenter crossover trial, ANN INT MED, 135(3), 2001, pp. 165-174
Citations number
21
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
ANNALS OF INTERNAL MEDICINE
ISSN journal
00034819 → ACNP
Volume
135
Issue
3
Year of publication
2001
Pages
165 - 174
Database
ISI
SICI code
0003-4819(20010807)135:3<165:TEOTDD>2.0.ZU;2-6
Abstract
Background: In patients with hypogammaglobulinemia, substitution with immun oglobulin is the treatment of choice to reduce both frequency and severity of bacterial infections. Even with treatment, however, infections still occ ur in these patients. Objective: To determine whether doubling the standard dose of intravenous i mmunoglobulin would affect the incidence and duration of infections. Design: Multicenter, double-blind, randomized, crossover study. Setting: 15 outpatient clinics in the Netherlands. Patients: 43 patients with primary hypogammaglobulinemia, 41 of whom comple ted the protocol. Intervention: Patients received standard-dose immunoglobulin therapy for 9 months, followed by a 3-month washout period, and high-dose intravenous imm unoglobulin therapy for 9 months, or vice versa. Measurements: The primary outcome measures were total number and duration o f infections. Other measures were periods of fever, hospital admissions, us e of antiboditics, absence from school or work, and trough levels of serum immunoglobulin. Side effects from the study medication were also recorded. Results: Compared with the standard dose of intravenous immunoglobulin (adu lts, 300 mg/kg of body weight every 4 weeks; children, 400 mg/kg every 4 we eks), high-dose therapy (adults, 600 mg/kg every 4 weeks; children, 800 mg/ kg every 4 weeks) significantly reduced the number (3.5 vs. 2.5 per patient ; P = 0.004) and duration (median, 33 days vs. 21 days; P = 0.015) of infec tions. Trough levels of IgG increased significantly during high-dose therap y. The incidence and type of side effects did not differ significantly for the two dosages. Conclusion: in patients with hypogammaglobulinemia, doubling the standard d ose of intravenous immunoglobulin significantly reduced the number and dura tion of infections.