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Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study
INTRODUCTION: Clinically diagnosed pneumonia in children is a leading cause of paediatric hospitalisation and mortality. The aetiology is usually bacterial or viral, but malaria can cause a syndrome indistinguishable from clinical pneumonia. There is no method with high sensitivity to detect a bacte...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487183/ https://www.ncbi.nlm.nih.gov/pubmed/34593486 http://dx.doi.org/10.1136/bmjopen-2020-046590 |
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author | Valim, Clarissa Olatunji, Yekin Ajauoi Isa, Yasir Shitu Salaudeen, Rasheed Golam, Sarwar Knol, Edward F Kanyi, Sheriffo Jammeh, Abdoulie Bassat, Quique de Jager, Wilco Diaz, Alejandro A Wiegand, Roger C Ramirez, Julio Moses, Marsha A D’Alessandro, Umberto Hibberd, Patricia L Mackenzie, Grant A |
author_facet | Valim, Clarissa Olatunji, Yekin Ajauoi Isa, Yasir Shitu Salaudeen, Rasheed Golam, Sarwar Knol, Edward F Kanyi, Sheriffo Jammeh, Abdoulie Bassat, Quique de Jager, Wilco Diaz, Alejandro A Wiegand, Roger C Ramirez, Julio Moses, Marsha A D’Alessandro, Umberto Hibberd, Patricia L Mackenzie, Grant A |
author_sort | Valim, Clarissa |
collection | PubMed |
description | INTRODUCTION: Clinically diagnosed pneumonia in children is a leading cause of paediatric hospitalisation and mortality. The aetiology is usually bacterial or viral, but malaria can cause a syndrome indistinguishable from clinical pneumonia. There is no method with high sensitivity to detect a bacterial infection in these patients and, as result, antibiotics are frequently overprescribed. Conversely, unrecognised concomitant bacterial infection in patients with malarial infections occur with omission of antibiotic therapy from patients with bacterial infections. Previously, we identified two combinations of blood proteins with 96% sensitivity and 86% specificity for detecting bacterial disease. The current project aimed to validate and improve these combinations by evaluating additional biomarkers in paediatric patients with clinical pneumonia. Our goal was to describe combinations of a limited number of proteins with high sensitivity and specificity for bacterial infection to be incorporated in future point-of-care tests. Furthermore, we seek to explore signatures to prognosticate clinical pneumonia. METHODS AND ANALYSIS: Patients (n=900) aged 2–59 months presenting with clinical pneumonia at two Gambian hospitals will be enrolled and classified according to criteria for definitive bacterial aetiology (based on microbiological tests and chest radiographs). We will measure proteins at admission using Luminex-based immunoassays in 90 children with definitive and 160 with probable bacterial aetiology, and 160 children classified according to the prognosis of their disease. Previously identified diagnostic signatures will be assessed through accuracy measures. Moreover, we will seek new diagnostic and prognostic signatures through machine learning methods, including support vector machine, penalised regression and classification trees. ETHICS AND DISSEMINATION: Ethics approval has been obtained from the Gambia Government/Medical Research Council Unit The Gambia Joint Ethics Committee (protocol 1616) and the institutional review board of Boston University Medical Centre (STUDY00000958). Study results will be disseminated to the staff of the study hospitals, in scientific seminars and meetings, and in publications. TRIAL REGISTRATION NUMBER: H-38462. |
format | Online Article Text |
id | pubmed-8487183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-84871832021-10-13 Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study Valim, Clarissa Olatunji, Yekin Ajauoi Isa, Yasir Shitu Salaudeen, Rasheed Golam, Sarwar Knol, Edward F Kanyi, Sheriffo Jammeh, Abdoulie Bassat, Quique de Jager, Wilco Diaz, Alejandro A Wiegand, Roger C Ramirez, Julio Moses, Marsha A D’Alessandro, Umberto Hibberd, Patricia L Mackenzie, Grant A BMJ Open Diagnostics INTRODUCTION: Clinically diagnosed pneumonia in children is a leading cause of paediatric hospitalisation and mortality. The aetiology is usually bacterial or viral, but malaria can cause a syndrome indistinguishable from clinical pneumonia. There is no method with high sensitivity to detect a bacterial infection in these patients and, as result, antibiotics are frequently overprescribed. Conversely, unrecognised concomitant bacterial infection in patients with malarial infections occur with omission of antibiotic therapy from patients with bacterial infections. Previously, we identified two combinations of blood proteins with 96% sensitivity and 86% specificity for detecting bacterial disease. The current project aimed to validate and improve these combinations by evaluating additional biomarkers in paediatric patients with clinical pneumonia. Our goal was to describe combinations of a limited number of proteins with high sensitivity and specificity for bacterial infection to be incorporated in future point-of-care tests. Furthermore, we seek to explore signatures to prognosticate clinical pneumonia. METHODS AND ANALYSIS: Patients (n=900) aged 2–59 months presenting with clinical pneumonia at two Gambian hospitals will be enrolled and classified according to criteria for definitive bacterial aetiology (based on microbiological tests and chest radiographs). We will measure proteins at admission using Luminex-based immunoassays in 90 children with definitive and 160 with probable bacterial aetiology, and 160 children classified according to the prognosis of their disease. Previously identified diagnostic signatures will be assessed through accuracy measures. Moreover, we will seek new diagnostic and prognostic signatures through machine learning methods, including support vector machine, penalised regression and classification trees. ETHICS AND DISSEMINATION: Ethics approval has been obtained from the Gambia Government/Medical Research Council Unit The Gambia Joint Ethics Committee (protocol 1616) and the institutional review board of Boston University Medical Centre (STUDY00000958). Study results will be disseminated to the staff of the study hospitals, in scientific seminars and meetings, and in publications. TRIAL REGISTRATION NUMBER: H-38462. BMJ Publishing Group 2021-09-30 /pmc/articles/PMC8487183/ /pubmed/34593486 http://dx.doi.org/10.1136/bmjopen-2020-046590 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Diagnostics Valim, Clarissa Olatunji, Yekin Ajauoi Isa, Yasir Shitu Salaudeen, Rasheed Golam, Sarwar Knol, Edward F Kanyi, Sheriffo Jammeh, Abdoulie Bassat, Quique de Jager, Wilco Diaz, Alejandro A Wiegand, Roger C Ramirez, Julio Moses, Marsha A D’Alessandro, Umberto Hibberd, Patricia L Mackenzie, Grant A Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title | Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title_full | Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title_fullStr | Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title_full_unstemmed | Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title_short | Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study |
title_sort | seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-saharan africa: study protocol for an observational study |
topic | Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487183/ https://www.ncbi.nlm.nih.gov/pubmed/34593486 http://dx.doi.org/10.1136/bmjopen-2020-046590 |
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