Association of clinical signs, host biomarkers and etiology with radiological pneumonia in bhutanese children
Autor/a
Data de publicació
2022ISSN
2333-794X
Resum
Diagnosing pneumonia and identifying those requiring antibiotherapy remain challenging. Chest radiographs (CXR) are often used as the reference standard. We aimed to describe clinical characteristics, host-response biomarkers and etiology, and assess their relationship to CXR findings in children with pneumonia in Thimphu, Bhutan. Children between 2 and 59 months hospitalized with WHO-defined pneumonia were prospectively enrolled and classified into radiological endpoint and non-endpoint pneumonia. Blood and nasopharyngeal washing were collected for microbiological analyses and plasma levels of 11 host-response biomarkers were measured. Among 149 children with readable CXR, 39 (26.2%) presented with endpoint pneumonia. Identification of respiratory viruses was common, with no significant differences by radiological outcomes. No clinical sign was suggestive of radiological pneumonia, but children with radiological pneumonia presented higher erythrocyte sedimentation rate, C-reactive protein and procalcitonin. Markers of endothelial and immune activation had little accuracy for the reliable identification of radiological pneumonia.
Tipus de document
Article
Versió del document
Versió publicada
Llengua
Anglès
Matèries (CDU)
61 - Medicina
Paraules clau
Pàgines
13
Publicat per
Sage Journals
Col·lecció
9;
Publicat a
Global Pediatric Health
Citació recomanada
Jullien, Sophie; Richard-Greenblatt, Melissa; Casellas, Aina [et al.]. Association of clinical signs, host biomarkers and etiology with radiological pneumonia in bhutanese children. Global Pediatric Health, 2022, 9, p. 1-13. Disponible en: <https://journals.sagepub.com/doi/full/10.1177/2333794X221078698>. Fecha de acceso: 21 mar. 2022. DOI: 10.1177/2333794X221078698
Nota
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: SJ reecived a pre-doctoral fellowhip from the Secretariat of Universities and Research, Ministry of Enterprise and Knowledge of the Government of Catalonia and co-funded by European Social Fund. This study received financial support from the Spanish Society of Paediatric Infectology (Sociedad Española de Infectología Pediátrica, SEIP), which contributed to the shipment and testing of biological samples [SJ]. ISGlobal receives support from the Spanish Ministry of Science and Innovation through the “Centro de Excelencia Severo Ochoa 2019-2023” Program (CEX2018-000806-S), and support from the Generalitat de Catalunya through the CERCA Program [SJ, AC, QB]. CISM is supported by the Government of Mozambique and the Spanish Agency for International Development (AECID) [QB]. This study was supported in part by the Canadian Institutes of Health Research (CIHR) Foundation grant FDN-148439 [KCK] and the Canada Research Chairs program [KCK]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Drets
Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
Excepte que s'indiqui una altra cosa, la llicència de l'ítem es descriu com https://creativecommons.org/licenses/by-nc/4.0/

