Intranasally administered immunoglobulin for the prevention of rhinitis in children

Pediatr Infect Dis J. 1998 May;17(5):367-72. doi: 10.1097/00006454-199805000-00004.

Abstract

Objective: To determine the efficacy of intranasally administered immunoglobulin in preventing symptoms of rhinitis in children.

Methods: Forty children ages 1 to 4 years who attended day-care centers in Turku, Finland, were enrolled in the double blind, placebo-controlled study. The children were randomly assigned to receive treatment with immunoglobulin, composed mainly of immunoglobulin A, or placebo, both administered as nasal sprays twice daily for 8 weeks. During this medication period and an additional 8-week follow-up period, the parents recorded the symptoms of the children daily in the diaries provided. One child who met an exclusion criterion was withdrawn from the study after a few days of medication.

Results: During the 8-week medication period the 19 children in the immunoglobulin group had 42% fewer days with rhinitis than the 20 children receiving placebo (mean, 10.8 vs. 18.7 days; P=0.004). The total numbers of episodes of rhinitis in the immunoglobulin and placebo groups were 33 and 51, respectively. No significant differences were observed between the groups during the postmedication follow-up period.

Conclusions: Intranasal administration of immunoglobulin appears to be an effective method to prevent symptoms of rhinitis in children, and further studies of this approach are needed.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Child, Preschool
  • Double-Blind Method
  • Female
  • Finland
  • Humans
  • Immunization, Passive / methods*
  • Immunoglobulin A / administration & dosage*
  • Immunoglobulin G / administration & dosage*
  • Infant
  • Male
  • Rhinitis / prevention & control*

Substances

  • Immunoglobulin A
  • Immunoglobulin G