Evidence map›Paper›PMID 40375337›Full record

ArticleVirology journal2025

Impact of most promising Ebola therapies on survival: a secondary analysis during the tenth outbreak in the Democratic Republic of Congo.

Esther Mamu Kikwango, Pierre Z Akilimali, Nguyen Toan Tran

Abstract read
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

3 authors.

Esther Mamu Kikwango *Field Epidemiology training program, Kinshasa School of Public Health, University of Kinshasa, P.O. Box 11850, Kinshasa, Democratic Republic of Congo.
Pierre Z Akilimali *Department of Nutrition, Kinshasa School of Public Health, University of Kinshasa, P.O. Box 11850, Kinshasa, Democratic Republic of Congo. pierre.akilimali@unikin.ac.cd.
Nguyen Toan TranAustralian Center for Public and Population Health Research, Faculty of Health, University of Technology, P.O. Box 123, Sydney, NSW, 2007, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMAb114, REGN-EB3, Remdesivir, and ZMapp, which are monoclonal antibody-based treatments, have been compared and shown to be promising therapies against the Ebola Virus Disease (EVD). There has been no comparison between these medications and standard treatment (without antiviral). Our study aimed to examine the contribution of each regimen compared to standard treatment on the survival of EVD patients and assess whether this association was modified by EVD vaccination (rVSV-ZEBOV Ebola vaccine) status. METHODOLOGY: We performed a secondary analysis study using retrospective cohort data obtained from four EVD treatment centers located in Katwa, Mangina, Butembo, and Beni in the North Kivu region. The main outcome measure was mortality within a 28-day period among 781 included patients. A Cox model was used to identify predictors of survival in hospitalized EVD patients.

resultsVaccinated EVD patients were 1.7 times less likely to die compared to unvaccinated patients (3.70 days vs. 5.00 days; p = 0.0002). Delaying care and treatment at EVD treatment centres increased mortality risk by 5% for each day following symptom onset. Compared to the standard treatment group, adjusted mortality rates were significantly reduced in the groups receiving MAb114 (0.27, p < 0.001), REGN-EB3 (0.26, p < 0.001), and Remdesivir (0.38, p = 0.005). ZMapp also showed a reduction, though with borderline statistical significance (0.47, p = 0.032).

conclusionsPrompt identification and treatment, along with enhanced supportive care (such as replenishing fluids and electrolytes and managing symptoms), significantly improve survival chances. Concurrently, administering vaccines and using mAb114, REGN-EB3, and, to some extent, Remdesivir further increase patient survival rates.

Indexed as

Antiviral AgentsDisease OutbreaksHemorrhagic Fever, EbolaAdenosine MonophosphateAdolescentAdultAlanineAntibodies, MonoclonalDemocratic Republic of the CongoEbola VaccinesEbolavirusFemaleHumansMaleMiddle AgedRetrospective StudiesAdenosine MonophosphateAlanineAntibodies, MonoclonalAntiviral AgentsEbola VaccinesremdesivirZMappEbola virus diseasemAb114Promising therapiesREGN EB3RemdesivirSecondary analysisSurvivalZMapp

Identifiers

PMID40375337
PMCPMC12079879

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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.