Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial
Background: A timely differential diagnostic is essential to identify the etiology of central nervous system (CNS) infections in children, in order to facilitate targeted treatment, manage patients, and improve clinical outcome. Objective: The Pediatric Infection-Point-of-Care (PI-POC) trial is inve...
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Science::Medicine Global Health Central Nervous System Infections Gaudenzi, Giulia Kumbakumba, Elias Rasti, Reza Nanjebe, Deborah Réu, Pedro Nyehangane, Dan Mårtensson, Andreas Nassejje, Milly Karlsson, Jens Mzee, John Nilsson, Peter Businge, Stephen Loh, Edmund Yap, Boum II Andersson-Svahn, Helene Gantelius, Jesper Mwanga-Amumpaire, Juliet Alfvén, Tobias Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
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Background: A timely differential diagnostic is essential to identify the etiology of central nervous system (CNS) infections in children, in order to facilitate targeted treatment, manage patients, and improve clinical outcome. Objective: The Pediatric Infection-Point-of-Care (PI-POC) trial is investigating novel methods to improve and strengthen the differential diagnostics of suspected childhood CNS infections in low-income health systems such as those in Southwestern Uganda. This will be achieved by evaluating (1) a novel DNA-based diagnostic assay for CNS infections, (2) a commercially available multiplex PCR-based meningitis/encephalitis (ME) panel for clinical use in a facility-limited laboratory setting, (3) proteomics profiling of blood from children with severe CNS infection as compared to outpatient controls with fever yet not severely ill, and (4) Myxovirus resistance protein A (MxA) as a biomarker in blood for viral CNS infection. Further changes in the etiology of childhood CNS infections after the introduction of the pneumococcal conjugate vaccine against Streptococcus pneumoniae will be investigated. In addition, the carriage and invasive rate of Neisseria meningitidis will be recorded and serotyped, and the expression of its major virulence factor (polysaccharide capsule) will be investigated. Methods: The PI-POC trial is a prospective observational study of children including newborns up to 12 years of age with clinical features of CNS infection, and age-/sex-matched outpatient controls with fever yet not severely ill. Participants are recruited at 2 Pediatric clinics in Mbarara, Uganda. Cerebrospinal fluid (for cases only), blood, and nasopharyngeal (NP) swabs (for both cases and controls) sampled at both clinics are analyzed at the Epicentre Research Laboratory through gold-standard methods for CNS infection diagnosis (microscopy, biochemistry, and culture) and a commercially available ME panel for multiplex PCR analyses of the cerebrospinal fluid. An additional blood sample from cases is collected on day 3 after admission. After initial clinical analyses in Mbarara, samples will be transported to Stockholm, Sweden for (1) validation analyses of a novel nucleic acid–based POC test, (2) biomarker research, and (3) serotyping and molecular characterization of S. pneumoniae and N. meningitidis. Results: A pilot study was performed from January to April 2019. The PI-POC trial enrollment of patients begun in April 2019 and will continue until September 2020, to include up to 300 cases and controls. Preliminary results from the PI-POC study are expected by the end of 2020. Conclusions: The findings from the PI-POC study can potentially facilitate rapid etiological diagnosis of CNS infections in low-resource settings and allow for novel methods for determination of the severity of CNS infection in such environment. |
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Singapore Centre for Environmental Life Sciences and Engineering |
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Singapore Centre for Environmental Life Sciences and Engineering Gaudenzi, Giulia Kumbakumba, Elias Rasti, Reza Nanjebe, Deborah Réu, Pedro Nyehangane, Dan Mårtensson, Andreas Nassejje, Milly Karlsson, Jens Mzee, John Nilsson, Peter Businge, Stephen Loh, Edmund Yap, Boum II Andersson-Svahn, Helene Gantelius, Jesper Mwanga-Amumpaire, Juliet Alfvén, Tobias |
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Article |
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Gaudenzi, Giulia Kumbakumba, Elias Rasti, Reza Nanjebe, Deborah Réu, Pedro Nyehangane, Dan Mårtensson, Andreas Nassejje, Milly Karlsson, Jens Mzee, John Nilsson, Peter Businge, Stephen Loh, Edmund Yap, Boum II Andersson-Svahn, Helene Gantelius, Jesper Mwanga-Amumpaire, Juliet Alfvén, Tobias |
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Gaudenzi, Giulia |
title |
Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
title_short |
Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
title_full |
Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
title_fullStr |
Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
title_full_unstemmed |
Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial |
title_sort |
point-of-care approaches for meningitis diagnosis in a low-resource setting (southwestern uganda) : observational cohort study protocol of the "pi-poc" trial |
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2021 |
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https://hdl.handle.net/10356/147053 |
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sg-ntu-dr.10356-1470532021-03-27T20:11:21Z Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial Gaudenzi, Giulia Kumbakumba, Elias Rasti, Reza Nanjebe, Deborah Réu, Pedro Nyehangane, Dan Mårtensson, Andreas Nassejje, Milly Karlsson, Jens Mzee, John Nilsson, Peter Businge, Stephen Loh, Edmund Yap, Boum II Andersson-Svahn, Helene Gantelius, Jesper Mwanga-Amumpaire, Juliet Alfvén, Tobias Singapore Centre for Environmental Life Sciences and Engineering Science::Medicine Global Health Central Nervous System Infections Background: A timely differential diagnostic is essential to identify the etiology of central nervous system (CNS) infections in children, in order to facilitate targeted treatment, manage patients, and improve clinical outcome. Objective: The Pediatric Infection-Point-of-Care (PI-POC) trial is investigating novel methods to improve and strengthen the differential diagnostics of suspected childhood CNS infections in low-income health systems such as those in Southwestern Uganda. This will be achieved by evaluating (1) a novel DNA-based diagnostic assay for CNS infections, (2) a commercially available multiplex PCR-based meningitis/encephalitis (ME) panel for clinical use in a facility-limited laboratory setting, (3) proteomics profiling of blood from children with severe CNS infection as compared to outpatient controls with fever yet not severely ill, and (4) Myxovirus resistance protein A (MxA) as a biomarker in blood for viral CNS infection. Further changes in the etiology of childhood CNS infections after the introduction of the pneumococcal conjugate vaccine against Streptococcus pneumoniae will be investigated. In addition, the carriage and invasive rate of Neisseria meningitidis will be recorded and serotyped, and the expression of its major virulence factor (polysaccharide capsule) will be investigated. Methods: The PI-POC trial is a prospective observational study of children including newborns up to 12 years of age with clinical features of CNS infection, and age-/sex-matched outpatient controls with fever yet not severely ill. Participants are recruited at 2 Pediatric clinics in Mbarara, Uganda. Cerebrospinal fluid (for cases only), blood, and nasopharyngeal (NP) swabs (for both cases and controls) sampled at both clinics are analyzed at the Epicentre Research Laboratory through gold-standard methods for CNS infection diagnosis (microscopy, biochemistry, and culture) and a commercially available ME panel for multiplex PCR analyses of the cerebrospinal fluid. An additional blood sample from cases is collected on day 3 after admission. After initial clinical analyses in Mbarara, samples will be transported to Stockholm, Sweden for (1) validation analyses of a novel nucleic acid–based POC test, (2) biomarker research, and (3) serotyping and molecular characterization of S. pneumoniae and N. meningitidis. Results: A pilot study was performed from January to April 2019. The PI-POC trial enrollment of patients begun in April 2019 and will continue until September 2020, to include up to 300 cases and controls. Preliminary results from the PI-POC study are expected by the end of 2020. Conclusions: The findings from the PI-POC study can potentially facilitate rapid etiological diagnosis of CNS infections in low-resource settings and allow for novel methods for determination of the severity of CNS infection in such environment. Published version 2021-03-24T05:22:52Z 2021-03-24T05:22:52Z 2020 Journal Article Gaudenzi, G., Kumbakumba, E., Rasti, R., Nanjebe, D., Réu, P., Nyehangane, D., Mårtensson, A., Nassejje, M., Karlsson, J., Mzee, J., Nilsson, P., Businge, S., Loh, E., Yap, B. I., Andersson-Svahn, H., Gantelius, J., Mwanga-Amumpaire, J. & Alfvén, T. (2020). Point-of-Care approaches for meningitis diagnosis in a low-resource setting (Southwestern Uganda) : observational cohort study protocol of the "PI-POC" trial. JMIR Research Protocols, 9(11). https://dx.doi.org/10.2196/21430 1929-0748 https://hdl.handle.net/10356/147053 10.2196/21430 33146628 2-s2.0-85096769705 11 9 en JMIR research protocols © 2020 The Author(s). Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 04.11.2020. This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included. application/pdf |