Respiratory syncytial virus–enriched globulin for the prevention of acute otitis media in high-risk children - 12/10/17
Abstract |
Acute otitis media (AOM) has been associated with respiratory syncytial virus (RSV) infection; AOM develops in up to one third of children with RSV illness. A masked multicenter trial used an immune globulin enriched with RSV-neutralizing antibodies (RSVIG) to prevent RSV infection of the lower respiratory tract in 249 children with either bronchopulmonary dysplasia, congenital heart disease, or prematurity. To determine whether monthly RSVIG therapy might decrease the incidence of AOM, we retrospectively analyzed the records of 109 children in two of the centers. RSVIG was administered during RSV season at a high dose of 750 mg/kg monthly or a low dose of 150 mg/kg monthly; control children received no RSVIG. Children were examined for AOM by masked observers using pneumatic otoscopy. No difference in sex, race, underlying diagnosis, number of persons in the home, exposure to smoking, or atopy was found between groups studied. In recipients of high doses of RSVIG, significantly less AOM developed per season than in control children (mean episodes, 0.15 vs 0.78; p = 0.003), and fewer episodes of RSV-related AOM occurred (0 vs 5; p = 0.047). Low doses of RSVIG did not have a clinically significant impact. High doses of RSVIG appeared to have a significant impact on preventing AOM (both RSV- and non-RSV-related AOM) in these-high risk populations. This finding may have important implications in the development of improved preventive modalities for AOM. (J PEDIATR 1996;129:214-9)
Le texte complet de cet article est disponible en PDF.Abbreviations : AOM, BPIG, IVIG, RSV, RSVIG
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| From the Department of Pediatrics, Divisions of Infectious Diseases and Neonatology, the University of Colorado School of Medicine and Children's Hospital, Denver; the Department of Pediatrics, Division of Infectious Diseases, State University of New York Medical Centers Hospital, Buffalo; the Division of Infectious Diseases, Dana Farber Cancer Institute, Harvard Medical School and the Massachusetts Public Health Biologic Laboratories, Boston. |
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| Supported by National Institutes of Health/National Institute of Allergy and Infectious Diseases Contract No. 1A182520; General Clinical Research Center Program No. 5 MO1 RR00069, of the Division of Research Resources, National Institutes of Health (RR-69); and MedImmune, Inc. |
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| Reprint requests: Eric A.F. Simoes, MD, Children's Hospital, 1056 E. 19th Ave., B070, Denver, CO 80218. |
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| 0022-3476/96/$5.00 + 0 9/20/73293 |
Vol 129 - N° 2
P. 214-219 - août 1996 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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