Seeking diagnostic and prognostic biomarkers for childhood bacterial pneumonia in sub-Saharan Africa: study protocol for an observational study

• Published in: BMJ open 2021-09, Vol.11 (9), p.e046590-e046590
• Main Authors: 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
• Format: Article
• Language: English
• Subjects: Accuracy; Africa South of the Sahara; Anti-Bacterial Agents - therapeutic use; Antibiotics; Bacterial infections; Biomarkers; Child; Childhood; Classification; diagnostic microbiology; Diagnostics; Humans; Immunology; Infections; Laboratories; Machine learning; Malaria; Medical diagnosis; Medical prognosis; Observational studies; Observational Studies as Topic; paediatric infectious disease & immunisation; paediatric thoracic medicine; Pathogens; Pediatrics; Pneumonia; Pneumonia, Bacterial - diagnosis; Pneumonia, Bacterial - drug therapy; Population; Prognosis; Proteins; respiratory infections; Viral infections
• ISSN: 2044-6055; 2044-6055
• DOI: 10.1136/bmjopen-2020-046590

IntroductionClinically 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 analysisPatients (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 disseminationEthics 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 numberH-38462.