Evidence map›Paper›PMID 40070697›Full record

ArticleOpen forum infectious diseases2024

Infectious Causes of Stillbirths: A Descriptive Etiological Study in Uganda.

Lauren Hookham, Valerie Tusubira, Amusa Wamawobe, Dan R Shelley, Caitlin Farley, Edward A R Portal, Simon Beach, Hannah G Davies, Konstantinos Karampatsas, Mary Kyohere and 7 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Lauren HookhamInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0000-0001-9703-655X
Valerie TusubiraMakerere University-Johns Hopkins University (MUJHU) Research Collaboration, Kampala, Uganda.ORCID https://orcid.org/0000-0002-3395-8755
Amusa WamawobeDepartment of Medical Microbiology, Makerere University, Kampala, Uganda.ORCID https://orcid.org/0000-0001-7503-6778
Dan R ShelleyDivision of Infection & Immunity, Cardiff University School of Medicine, Cardiff, UK.ORCID https://orcid.org/0009-0001-8195-1689
Caitlin FarleyDivision of Infection & Immunity, Cardiff University School of Medicine, Cardiff, UK.ORCID https://orcid.org/0009-0006-5309-2991
Edward A R PortalDivision of Infection & Immunity, Cardiff University School of Medicine, Cardiff, UK.
Simon BeachInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0009-0004-6234-6362
Hannah G DaviesInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0000-0002-9064-0874
Konstantinos KarampatsasInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0000-0002-5313-9482
Mary KyohereInstitute for Infection and Immunity, St George's University of London, London, UK.
Joseph PeacockInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0000-0002-8767-7377
Philippa MusokeMakerere University-Johns Hopkins University (MUJHU) Research Collaboration, Kampala, Uganda.
Owen B SpillerDivision of Infection & Immunity, Cardiff University School of Medicine, Cardiff, UK.ORCID https://orcid.org/0000-0002-9117-6911
Paul T HeathInstitute for Infection and Immunity, St George's, University of London, London, UK.
Musa SekikuboDepartment of Obstetrics and Gynaecology, Makerere University, Kampala, Uganda.ORCID https://orcid.org/0000-0002-7335-9650
Kirsty Le DoareInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID https://orcid.org/0000-0002-5104-085X
PROGRESS Study Author Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Every year an estimated 2-3 million babies are stillborn, with a high burden in Africa. Infection is an important driver of stillbirth. There is a lack of data on the bacterial causes of stillbirth in Uganda, contributing to a lack of interventions such as effective prophylaxis and development of maternal vaccine options against the most implicated pathogens. Methods: The PROGRESS study was an observational cohort study undertaken in Kampala, Uganda, between November 2018 and April 2021. If a woman delivered a stillborn baby, consent was sought for the collection of a heart-blood aspirate. One to three mL of blood was collected and sent for culture using the BD Bactec blood culture system. Organism identification was performed using biochemical testing and matrix-assisted laser desorption/ionization-time of flight mass spectrometry. Susceptibilities to appropriate panels of antimicrobials were determined by agar dilution. Results: Kawempe Hospital registered 34 517 births in the study period, of which 1717 (5.0%) were stillbirths. A total of 581 (33.8%) were recruited into the study, and heart blood aspirates were performed on 569 (97.9%). Blood samples were sufficient for analysis of 476, with a total of 108 positive cultures (22.7% of sampled stillbirths). Fifty-nine of 108 blood cultures contained organisms that were considered potential pathogens, giving a pathogen positivity rate of 12.4%. Common pathogens included Conclusions: The high proportion of stillbirths caused by likely pathogenic bacteria in Uganda highlights the potential for prevention with prophylaxis and stresses the need for further investment in this area.

Indexed as

antimicrobial resistanceinfectionpregnancysepsisstillbirth

Identifiers

PMID40070697
PMCPMC11891129

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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.