Clinical manifestations, serotype distribution, and incidence of pediatric invasive pneumococcal disease in Catalonia (Spain), 2018-2022

Other authors

[de Sevilla MF] Servei de Pediatria, Hospital Sant Joan de Déu Barcelona, Esplugues de Llobregat, Barcelona, Spain. Institut de Recerca Sant Joan de Déu (IRSJD), Esplugues de Llobregat, Spain. Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. Universitat de Barcelona, Barcelona, Spain. [Alcaraz-Soler C] Servei de Pediatria, Hospital Sant Joan de Déu Barcelona, Esplugues de Llobregat, Barcelona, Spain. [Soldevila N] Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. Universitat de Barcelona, Barcelona, Spain. [Izquierdo C] Agència de Salut Pública de Catalunya (ASPCAT), Departament de Salut, Generalitat de Catalunya, Barcelona, Spain. [Esteva C, Ciruela P] Institut de Recerca Sant Joan de Déu (IRSJD), Esplugues de Llobregat, Spain. Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. Servei de Microbiologia, Hospital Sant Joan de Déu Barcelona, Esplugues de Llobregat, Spain. [Moraga-Llop F, González-Peris, S] Servei de Pediatria, Hospital Vall d'Hebron, Barcelona, Spain. [Viñado B] Servei de Microbiologia, Hospital Vall d'Hebron, Barcelona, Spain. [Muñoz-Almagro C] Institut de Recerca Sant Joan de Déu (IRSJD), Esplugues de Llobregat, Spain. Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. Servei de Microbiologia, Hospital Vall d'Hebron, Barcelona, Spain. Universitat Internacional de Catalunya (UIC), Barcelona, Spain

Departament de Salut

Publication date

2025-05-20T12:38:00Z

2025-05-20T12:38:00Z

2025-05-02



Abstract

Invasive pneumococcal disease; Pneumococcal conjugate vaccine; Pneumonia


Enfermedad neumocócica invasiva; Vacuna antineumocócica conjugada; Neumonía


Malaltia pneumocòcica invasiva; Vacuna conjugada contra el pneumocòccica; Pneumònia


The global incidence of invasive pneumococcal disease (IPD) decreased after the switch from PCV7 to PCV13 in 2010. However, serotype 3 remains the leading cause of IPD in Catalonia (Spain), due to the low effectiveness of PCV13 against it. This study aimed to analyze the clinical, epidemiological, and microbiological characteristics of IPD in children over 5 years and evaluate the potential impact of new vaccines (PCV15 and PCV20). A 5-year prospective observational study was conducted from 2018 to 2022, including children up to 18 hospitalized with IPD at three major children's hospitals in Catalonia. Data on clinical, epidemiological, and microbiological factors were collected. A total of 220 episodes were identified, with a median age of 33.0 months (range 0-209). Comparing pre-pandemic (2018-2019) to early pandemic years (2020-2021), the IPD rate in children < 18 years decreased by 60.6% (p < 0.001). However, no significant change was observed when comparing 2022 to 2018. The most common diagnoses were pneumonia (61.8%), meningitis (14.5%), and bacteremia without focus (13.2%). Serotype 3 was the leading cause (35.1%) of IPD and was associated with complicated pneumonia (84.7%) and vaccine failure (73.6%). Ninety-three IPD episodes (45.4%) were caused by PCV13 serotypes, 97 (47.3%) by PCV15 serotypes, and 132 (64.4%) by PCV20 serotypes. The incidence of IPD has remained stable, except for a decrease during the pandemic. Serotype 3 was the most common, often associated with vaccine failures and severe pneumonia. PCV15 and PCV20 vaccines could offer better coverage against circulating serotypes and further reduce IPD incidence in Catalonia. • Serotype 3 remains a leading cause of invasive pneumococcal disease (IPD) despite inclusion in PCV13 due to its limited vaccine effectiveness. • IPD incidence decreased globally during the COVID-19 pandemic, likely due to public health measures. • In Catalonia, serotype 3 continues to dominate pediatric IPD cases and is frequently associated with complicated pneumonia and vaccine failure. • PCV15 and PCV20 offer broader serotype coverage and may significantly improve IPD prevention in children.


Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This work was supported by the PI17/337 project, integrated in the Plan Nacional de I+ D + I, and funded by the ISCIII- Subdirección General de Evaluación y Fomento de la Investigación Sanitaria.

Document Type

Article


Published version

Language

English

Publisher

Springer

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European Journal of Pediatrics;184(5)

https://www.doi.org/10.1007/s00431-025-06137-1

info:eu-repo/grantAgreement/ES/PI17/337/

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Attribution-NonCommercial 4.0 International

https://creativecommons.org/licenses/by/4.0/

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