Respiratory Syncytial Virus-Load Kinetics and Clinical Course of Acute Bronchiolitis in Hospitalized Infants: Interim Results and Review of the Literature

Author:

Piccirilli Giulia1ORCID,Rocca Alessandro2,Borgatti Eva Caterina3,Gabrielli Liliana1ORCID,Zama Daniele23ORCID,Pierantoni Luca2ORCID,Leone Marta3,Totaro Camilla4,Pavoni Matteo1,Lazzarotto Tiziana13ORCID,Lanari Marcello23

Affiliation:

1. Microbiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via Massarenti 9, 40138 Bologna, Italy

2. Pediatric Emergency Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via Massarenti 9, 40138 Bologna, Italy

3. Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy

4. Specialty School of Pediatrics, Alma Mater Studiorum, University of Bologna, 40126 Bologna, Italy

Abstract

Respiratory Syncytial Virus (RSV) bronchiolitis is the leading cause of hospitalization in infants. The role of RSV load in disease severity is still debated. We present the interim results of a prospective monocentric study enrolling previously healthy infants hospitalized for RSV bronchiolitis, collecting nasopharyngeal aspirates every 48 h from admission to discharge, and evaluating RSV load dynamics in relation to clinical outcome measures of bronchiolitis severity, including: need, type and duration of oxygen therapy, length of hospitalization, and the bronchiolitis clinical score calculated at admission. The results showed that the highest viral replication occurs within the first 48 hours after admission, with a significant decrease at subsequent time points (p < 0.0001). Moreover, higher RSV-RNA values were associated with the need for oxygen therapy (p = 0.03), particularly high-flow nasal cannula type (p = 0.04), and longer duration of respiratory support (p = 0.04). Finally, higher RSV load values were correlated with lower white blood cells, especially lymphocyte counts and C-reactive protein levels (p = 0.03, p = 0.04, and p = 0.01, respectively), as well as with patients of a younger age (p = 0.02). These data suggest that RSV may actively contribute to the clinical severity of bronchiolitis, together with other potential non-viral factors.

Funder

EU funding

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference34 articles.

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3. (2023, January 22). National Institute for Health and Care Excellence: Bronchiolitis in Children. NG9. London: National Institute for Health and Clinical Excellence. Available online: https://www.nice.org.uk/guidance/ng9.

4. UPDATE—2022 Italian guidelines on the management of bronchiolitis in infants;Manti;Italy J. Pediatr.,2023

5. Nirsevimab: First Approval;Keam;Drugs,2023

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