Evidence map›Paper›PMID 42010548›Full record

SynthesisBMC pediatrics2026

Prevalence and bacteriological profile of pathogens causing neonatal sepsis in Tanzania: a systematic review with meta-analysis.

Delfina R Msanga, Violet Dismas Kajogoo, Michaela Herz, Oliver Kurzai, Christoph Härtel, Stephen E Mshana

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Delfina R MsangaDepartment of Pediatrics and Child Health, Weill Bugando School of Medicine, Catholic University of Health and Allied Sciences, P.O. Box 1464, Mwanza, Tanzania. deromsah@gmail.com.
Violet Dismas KajogooTanzania Diabetes Association, Dar es Salaam, Tanzania.
Michaela HerzInstitute for Hygiene and Microbiology, University Würzburg, Würzburg, Germany.
Oliver KurzaiInstitute for Hygiene and Microbiology, University Würzburg, Würzburg, Germany.
Christoph HärtelDepartment of Pediatric and Child Health, University Würzburg, Würzburg, Germany.
Stephen E MshanaDepartment of Microbiology and Immunology, Weill Bugando School of Medicine, Catholic University of Health and Allied Sciences, P.O. Box 1464, Mwanza, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal sepsis is the significant cause of morbidity and mortality in low- and middle-income countries (LMICs) such as Tanzania, where 99% of global neonatal deaths occur. Epidemiological data regarding the causative agents and their resistance profiles can guide clinical practice and prevention strategies. A systematic review and meta-analysis was conducted to determine the prevalence, pathogens and the outcome of neonatal sepsis in Tanzania.

methodsWe conducted a systematic literature search using online databases such as PubMed/ Medline, Embase, Cochrane, Google Scholar, and Web of Science to identify peer-reviewed publications from January 2010 until May 2023. The data were analysed to determine the effect size using risk ratios (RR) and their 95% confidence interval (CI).

resultsWe included twelve hospital-based studies from 559 records, of which nine were prospective in design. The overall prevalence of microbiological confirmed neonatal sepsis in Tanzania was 33% (95% CI 22–44, p < 0.001). The most prevalent pathogen was Staphylococcus haemolyticus 23.7% (95% CI 20.57–27.02%) followed by Klebsiella spp. 19.3% (95% CI 9.2% to 32%, I2 98%). The resistance of pathogens to first-line (ampicillin plus gentamicin) and second-line (ceftriaxone) treatments were almost similar (RR:1.12 (95% CI: 1.09–1.16; I² = 79.5%, p < 0.001). The pathogens were more resistant to third-generation cephalosporins compared to meropenem with the overall pooled relative risk (RR) of 1.84 (95% CI: 1.77–1.91). Death occurred in 15.1% (95% CI 5.39–28.44) of the affected neonates. There was considerable heterogeneity among all analyses which may result from the different facilities where the studies were sampled. Furthermore, a sampling bias with the majority of studies being from tertiary hospital settings, may result in overestimating the burden of antimicrobial resistance (AMR).

conclusionsAMR and neonatal sepsis mortality remain a significant challenge. It is crucial to consider the early and optimal points for interventions to manage neonatal sepsis’s prevalence and outcomes. Revised recommendations for effective first-line antibiotics in the management of neonatal and infant sepsis in Tanzania are urgently needed. Further research is needed to come up with rapid and robust diagnostics to guide treatment and reduce unnecessary antibiotic use.

Indexed as

Neonatal SepsisAnti-Bacterial AgentsDrug Resistance, BacterialHumansInfant, NewbornPrevalenceTanzaniaAnti-Bacterial AgentsAntimicrobial resistanceMeta-analysisNeonatal sepsisPathogensPrevalenceSystematic review

Identifiers

PMID42010548
PMCPMC13231647

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.