Short‐ and mid‐term morbidity and primary‐care burden due to infant respiratory syncytial virus infection: A Spanish 6‐year population‐based longitudinal study

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia, e Pediatríaes_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicinaes_ES
dc.contributor.authorAres Gómez, Sonia
dc.contributor.authorMallah, Narmeen
dc.contributor.authorSalas Ellacuriaga, Antonio
dc.contributor.authorMartinón Torres, Federico
dc.date.accessioned2024-08-12T07:52:14Z
dc.date.available2024-08-12T07:52:14Z
dc.date.issued2024
dc.description.abstractBackground The morbidity burden of respiratory syncytial virus (RSV) in infants extends beyond hospitalization. Defining the RSV burden before implementing prophylaxis programs is essential for evaluating any potential impact on short- to mid-term morbidity and the utilization of primary healthcare (PHC) and emergency services (ES). We established this reference data using a population-based cohort approach. Methods Infants hospitalized for RSV from January 2016 to March 2023 were matched with non-hospitalized ones based on birthdate and sex. We defined the exposure as severe RSV hospitalization. The main study outcomes were as follows: (1) PHC and ES visits for RSV, categorized using the International Classification of Primary Care codes, (2) prescriptions for respiratory airway obstructive disease, and (3) antibacterial prescriptions. Participants were followed up from 30 days before hospitalization for severe RSV until the outcome occurrence or end of the study. Adjusted incidence rate ratios (IRRs) of the outcomes along with their 95% confidence intervals (CI) were estimated using Poisson regression models. Stratified analyses by type of PHC visit (nurse, pediatrician, or pharmacy) and follow-up period were undertaken. We defined mid-term outcomes as those taking place up to 24 months of follow-up period. Results The study included 6626 children (3313 RSV-hospitalized; 3313 non-hospitalized) with a median follow-up of 53.7 months (IQR = 27.9, 69.4). After a 3-month follow-up, severe RSV was associated with a considerable increase in PHC visits for wheezing/asthma (IRR = 4.31, 95% CI: 3.84–4.84), lower respiratory infections (IRR = 4.91, 95% CI: 4.34–5.58), and bronchiolitis (IRR = 4.68, 95% CI: 2.93–7.65). Severe RSV was also associated with more PHC visits for the pediatrician (IRR = 2.00, 95% CI: 1.96–2.05), nurse (IRR = 1.89, 95% CI: 1.75–1.92), hospital emergency (IRR = 2.39, 95% CI: 2.17–2.63), primary healthcare emergency (IRR: 1.54, 95% CI: 1.31–1.82), as well as with important increase in prescriptions for obstructive airway diseases (IRR = 5.98, 95% CI: 5.43–6.60) and antibacterials (IRR = 4.02, 95% CI: 3.38–4.81). All findings remained substantial until 2 years of post-infection. Conclusions Severe RSV infection in infants significantly increases short- to mid-term respiratory morbidity leading to an escalation in healthcare utilization (PHC/ES attendance) and medication prescriptions for up to 2 years afterward. Our approach could be useful in assessing the impact and cost-effectiveness of RSV prevention programs.es_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipThis work was supported by the Framework Partnership Agreementbetween the Consellería de Sanidad de la XUNTA de Galicia andGENVIP-IDIS-2021–2024 (SERGAS-IDIS March 2021; Spain). In ad-dition, it received support by (i) ISCIII: TRINEO: PI22/00162; DIAVIR:DTS19/00049; Resvi-Omics: PI19/01039 (to A.S.), ReSVinext: PI16/01569, Enterogen: PI19/01090, OMI-COVI-VAC: PI22/00406(to F.M.-T.), cofinanciados FEDER, (ii) GAIN: IN607B 2020/08and IN607A 2023/02 (to A.S.), GEN-COVID IN845D 2020/23 (toF.M.-T.), IIN607A2021/05 (to F.M.-T.); (iii) ACIS: BI-BACVIR (PRIS-3, to A.S.), CovidPhy (SA 304 C, to A.S.); and (iv) consorcio Centro de Investigación Biomédica en Red de Enfermedades Respiratorias(CB21/06/00103; to A.S. and F.M.-T.). The NIRSE-GAL study (CEIC2023–377) is funded by Sanofi Pasteur/AstraZeneca through a research grant to the Healthcare Research Institute of Santiago.es_ES
dc.identifier.citationAres-Gómez S, Mallah N, Pardo-Seco J, et al. Short- and mid-term morbidity and primary-care burden due to infant respiratory syncytial virus infection: A Spanish 6-year population-based longitudinal study. Pediatr Allergy Immunol. 2024; 0:e14131. doi:10.1111/pai.14131es_ES
dc.identifier.doi10.1111/pai.14131
dc.identifier.essn1399-3038
dc.identifier.urihttp://hdl.handle.net/10347/34649
dc.issue.number5
dc.journal.titlePediatric Allergy and Immunology
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights© 2024 The Authors. Pediatric Allergy and Immunology published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs Licensees_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleShort‐ and mid‐term morbidity and primary‐care burden due to infant respiratory syncytial virus infection: A Spanish 6‐year population‐based longitudinal studyes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dc.volume.number35
dspace.entity.typePublication
relation.isAuthorOfPublication7532a4d0-9488-4bc6-bf59-f432c9d4562b
relation.isAuthorOfPublication2badffc8-442d-4308-ab23-2eafbb77f6ba
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relation.isAuthorOfPublication.latestForDiscovery2badffc8-442d-4308-ab23-2eafbb77f6ba

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