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Prediction model of RSV-hospitalization in late preterm infants: An update and validation study. | LitMetric

Prediction model of RSV-hospitalization in late preterm infants: An update and validation study.

Early Hum Dev

Division of Paediatric Immunology and Infectious Diseases, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address:

Published: April 2016

AI Article Synopsis

  • New vaccines and treatments for RSV have been created, prompting the need for a better prediction model to identify infants at risk for hospitalization due to RSV within their first year.
  • Two studies, RISK-I and RISK-II, analyzed data from over 4,000 infants to improve and validate this predictive model, which identified key factors like daycare attendance and maternal health that increase hospitalization risk.
  • The updated model proved to be more effective than the original, and a user-friendly nomogram was designed to help healthcare providers easily identify high-risk infants for targeted treatment.

Article Abstract

Background: New vaccines and RSV therapeutics have been developed in the past decade. With approval of these new pharmaceuticals on the horizon, new challenges lie ahead in selecting the appropriate target population. We aimed to improve a previously published prediction model for prediction of RSV-hospitalization within the first year of life.

Methods: Two consecutive prospective multicenter birth cohort studies were performed from June 2008 until February 2015. The first cohort (RISK-I, n=2524, 2008-2011) was used to update the existing model. The updated model was subsequently validated in the RISK-II cohort (n=1564, 2011-2015). We used the TRIPOD criteria for transparent reporting.

Results: 181 infants (n=127 in RISK-I, n=54 in RISK-II) were hospitalized for RSV within their first year of life. The updated model included the following predictors; day care attendance and/or siblings (OR: 5.3; 95% CI 2.8-10.1), birth between Aug. 14th and Dec. 1st (OR: 2.4; 1.8-3.2), neonatal respiratory support (OR 2.2; 1.6-3.0), breastfeeding ≤4 months (OR 1.6; 1.2-2.2) and maternal atopic constitution (OR 1.5; 1.1-2.1). The updated models' discrimination was superior to the original model in the RISK-II cohort (AUROC 0.72 95% CI 0.65-0.78 versus AUROC 0.66, 95% CI 0.60-0.73, respectively). The updated model was translated into a simple nomogram to be able to distinguish infants with high versus low risk of RSV-hospitalization.

Conclusion: We developed and validated a clinical prediction model to be able to predict RSV-hospitalization in preterm infants born within 32-35 weeks gestational age. A simple nomogram was developed to target RSV therapeutics to those children who will benefit the most.

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Source
http://dx.doi.org/10.1016/j.earlhumdev.2016.01.020DOI Listing

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