Evidence map›Paper›PMID 34407175›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

A Longitudinal, Observational Study of Etiology and Long-Term Outcomes of Sepsis in Malawi Revealing the Key Role of Disseminated Tuberculosis.

Joseph M Lewis, Madlitso Mphasa, Lucy Keyala, Rachel Banda, Emma L Smith, Jackie Duggan, Tim Brooks, Matthew Catton, Jane Mallewa, Grace Katha and 5 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 24% of its field
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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  5. Observational
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  7. Reply to Al-WardAmerican journal of respiratory and critical care medicine · 2025
    Article
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  10. Review
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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

15 authors at 4 institutions in 2 countries.

Joseph M LewisMalawi Liverpool Wellcome Programme, Blantyre, Malawi.ORCID 0000-0002-3837-5188
Madlitso MphasaMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Lucy KeyalaMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Rachel BandaMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Emma L SmithMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Jackie DugganRare and Imported Pathogens Laboratory, Public Health England, United Kingdom.
Tim BrooksRare and Imported Pathogens Laboratory, Public Health England, United Kingdom.
Matthew CattonRare and Imported Pathogens Laboratory, Public Health England, United Kingdom.
Jane MallewaCollege of Medicine, University of Malawi, Malawi.
Grace KathaCollege of Medicine, University of Malawi, Malawi.
Stephen B GordonMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Brian FaragherDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Melita A GordonMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Jamie RylanceMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
Nicholas A FeaseyMalawi Liverpool Wellcome Programme, Blantyre, Malawi.
University of Liverpool · GBPublic Health England · GBUniversity of Malawi · MWLiverpool School of Tropical Medicine · GB

Funding

Wellcome TrustWellcome Trust 109105z/15/aWellcome Trust 206545/Z/17/Z
6 · The paper itself

Abstract

backgroundSepsis protocols in sub-Saharan Africa are typically extrapolated from high-income settings, yet sepsis in sub-Saharan Africa is likely caused by distinct pathogens and may require novel treatment strategies. Data to guide such strategies are lacking. We aimed to define causes and modifiable factors associated with sepsis outcomes in Blantyre, Malawi, in order to inform the design of treatment strategies tailored to sub-Saharan Africa.

methodsWe recruited 225 adults who met a sepsis case definition defined by fever and organ dysfunction in an observational cohort study at a single tertiary center. Etiology was defined using culture, antigen detection, serology, and polymerase chain reaction. The effect of treatment on 28-day outcomes was assessed using Bayesian logistic regression.

resultsThere were 143 of 213 (67%) participants living with human immunodeficiency virus (HIV). We identified a diagnosis in 145 of 225 (64%) participants, most commonly tuberculosis (TB; 34%) followed by invasive bacterial infections (17%), arboviral infections (13%), and malaria (9%). TB was associated with HIV infection, whereas malaria and arboviruses with the absence of HIV infection. Antituberculous chemotherapy was associated with survival (adjusted odds ratio for 28-day death, 0.17; 95% credible interval, 0.05-0.49 for receipt of antituberculous therapy). Of those with confirmed etiology, 83% received the broad-spectrum antibacterial ceftriaxone, but it would be expected to be active in only 24%.

conclusionsSepsis in Blantyre, Malawi, is caused by a range of pathogens; the majority are not susceptible to the broad-spectrum antibacterials that most patients receive. HIV status is a key determinant of etiology. Novel antimicrobial strategies for sepsis tailored to sub-Saharan Africa, including consideration of empiric antituberculous therapy in individuals living with HIV, should be developed and trialed.

Indexed as

HIV InfectionsMalariaSepsisTuberculosisAdultAnti-Bacterial AgentsBayes TheoremHumansMalawiAnti-Bacterial AgentsAfrica south of the Saharaantimicrobial resistancecritical illnessHIVtuberculosis

Identifiers

PMID34407175
PMCPMC9155594
OpenAlexW3194208193

What OpenQuestion holds

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LicenceCC BY
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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.