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Pediatric Infectious Disease Journal:
doi: 10.1097/01.inf.0000202135.24485.f8
Original Studies

Hospitalization for Respiratory Syncytial Virus Infection in Young Children: Development of a Clinical Prediction Rule

Rietveld, Edwin MD, PhD*†§; Vergouwe, Yvonne PhD§; Steyerberg, Ewout W. PhD§; Huysman, Marianne W. A. MD, PhD‡; de Groot, Ronald MD, PhD†; Moll, Henriëtte A. MD, PhD; for the RSV Study Group Southwest Netherlands

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Abstract

Background: Because passive immunization against respiratory syncytial virus (RSV) is costly, its use should be restricted to well-defined groups of high risk children. We aimed to develop a clinical prediction rule that estimates the individual monthly risk of hospitalization for RSV infection in young children.

Methods: A retrospective cohort study was conducted in the southwestern part of the Netherlands. We included children born between January 1, 1996 and December 31, 1998. Children hospitalized for proven RSV infection were compared with children not hospitalized for RSV infection. The monthly risk was estimated with a logistic regression model including 5 clinical predictors (gender, gestational age, birth weight, presence of bronchopulmonary dysplasia and age) and the mean seasonal monthly pattern of RSV infections. We compared the predictive performance of the prediction rule with the guidelines of the American Academy of Pediatrics (AAP).

Findings: Information was collected on 2469 hospitalized children and 140,661 children who were 1,181,790 months at risk. All predictors were statistically significant, with age and the seasonal monthly RSV pattern having the strongest effects. The clinical prediction rule that included these predictors could better discriminate between high and low risk children than the AAP guidelines and would potentially reduce the number of immunizations by 20%.

Interpretation: The prediction rule reliably estimates individual monthly risks of hospitalization for RSV infection in the population studied. It provides an improved index for passive immunization but further validation in other populations is required.

© 2006 Lippincott Williams & Wilkins, Inc.

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