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Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis
BACKGROUND: Aetiology and outcomes of sepsis in sub-Saharan Africa (sSA) are poorly described; we performed a systematic review and meta-analysis to summarise the available data. METHODS: Systematic searches of PubMed and Scopus were undertaken to identify prospective studies recruiting adults (>...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558702/ https://www.ncbi.nlm.nih.gov/pubmed/31186062 http://dx.doi.org/10.1186/s13054-019-2501-y |
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author | Lewis, Joseph M. Feasey, Nicholas A. Rylance, Jamie |
author_facet | Lewis, Joseph M. Feasey, Nicholas A. Rylance, Jamie |
author_sort | Lewis, Joseph M. |
collection | PubMed |
description | BACKGROUND: Aetiology and outcomes of sepsis in sub-Saharan Africa (sSA) are poorly described; we performed a systematic review and meta-analysis to summarise the available data. METHODS: Systematic searches of PubMed and Scopus were undertaken to identify prospective studies recruiting adults (> 13 years) with community-acquired sepsis in sSA post-2000. Random effects meta-analysis of in-hospital and 30-day mortality was undertaken and available aetiology data also summarised by random effects meta-analysis. RESULTS: Fifteen studies of 2800 participants were identified. Inclusion criteria were heterogeneous. The majority of patients were HIV-infected, and Mycobacterium tuberculosis was the most common cause of blood stream infection where sought. Pooled in-hospital mortality for Sepsis-2-defined sepsis and severe sepsis was 19% (95% CI 12–29%) and 39% (95% CI 30–47%) respectively, and sepsis mortality was associated with the proportion of HIV-infected participants. Mortality and morbidity data beyond 30 days were absent. CONCLUSIONS: Sepsis in sSA is dominated by HIV and tuberculosis, with poor outcomes. Optimal antimicrobial strategies, including the role of tuberculosis treatment, are unclear. Long-term outcome data are lacking. Standardised sepsis diagnostic criteria that are easily applied in low-resource settings are needed to establish an evidence base for sepsis management in sSA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2501-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6558702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65587022019-06-13 Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis Lewis, Joseph M. Feasey, Nicholas A. Rylance, Jamie Crit Care Research BACKGROUND: Aetiology and outcomes of sepsis in sub-Saharan Africa (sSA) are poorly described; we performed a systematic review and meta-analysis to summarise the available data. METHODS: Systematic searches of PubMed and Scopus were undertaken to identify prospective studies recruiting adults (> 13 years) with community-acquired sepsis in sSA post-2000. Random effects meta-analysis of in-hospital and 30-day mortality was undertaken and available aetiology data also summarised by random effects meta-analysis. RESULTS: Fifteen studies of 2800 participants were identified. Inclusion criteria were heterogeneous. The majority of patients were HIV-infected, and Mycobacterium tuberculosis was the most common cause of blood stream infection where sought. Pooled in-hospital mortality for Sepsis-2-defined sepsis and severe sepsis was 19% (95% CI 12–29%) and 39% (95% CI 30–47%) respectively, and sepsis mortality was associated with the proportion of HIV-infected participants. Mortality and morbidity data beyond 30 days were absent. CONCLUSIONS: Sepsis in sSA is dominated by HIV and tuberculosis, with poor outcomes. Optimal antimicrobial strategies, including the role of tuberculosis treatment, are unclear. Long-term outcome data are lacking. Standardised sepsis diagnostic criteria that are easily applied in low-resource settings are needed to establish an evidence base for sepsis management in sSA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2501-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-11 /pmc/articles/PMC6558702/ /pubmed/31186062 http://dx.doi.org/10.1186/s13054-019-2501-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lewis, Joseph M. Feasey, Nicholas A. Rylance, Jamie Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title | Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title_full | Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title_fullStr | Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title_full_unstemmed | Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title_short | Aetiology and outcomes of sepsis in adults in sub-Saharan Africa: a systematic review and meta-analysis |
title_sort | aetiology and outcomes of sepsis in adults in sub-saharan africa: a systematic review and meta-analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558702/ https://www.ncbi.nlm.nih.gov/pubmed/31186062 http://dx.doi.org/10.1186/s13054-019-2501-y |
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