Evidence map›Paper›PMID 41809024›Full record

ArticleJournal of parasitology research2026

Control of Human African Trypanosomiasis in the Nola-Bilolo Focus, Central African Republic, 2020-2024: Outcome of Capacity Building, Improved Diagnosis and Treatment.

Pierre-Marie Douzima, Mireille Cornelia Ingrid Denissio Morissi Nalingbo, Yvon Andjingbopou, Veerle Lejon, Romaric Nzoumbou-Boko

Abstract read
In one paragraph

Article in Journal of parasitology research, 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

5 authors.

Pierre-Marie DouzimaNational Programme to Control Human African Trypanosomiasis, Ministry of Health, Bangui, Central African Republic, behdasht.gov.ir.ORCID https://orcid.org/0009-0006-5879-4140
Mireille Cornelia Ingrid Denissio Morissi NalingboLaboratoire de Parasitologie, Institut Pasteur de Bangui, Bangui, Central African Republic, pasteur-bangui.org.ORCID https://orcid.org/0009-0007-1061-8567
Yvon AndjingbopouFaculté des Sciences de la Santé, Université de Bangui, Bangui, Central African Republic.ORCID https://orcid.org/0009-0005-2997-6407
Veerle LejonInstitut de Recherche pour le Développement, UMR INTERTRYP, Université de Montpellier-IRD-CIRAD, Montpellier, France, ird.fr.ORCID https://orcid.org/0000-0002-6795-0962
Romaric Nzoumbou-BokoNational Programme to Control Human African Trypanosomiasis, Ministry of Health, Bangui, Central African Republic, behdasht.gov.ir.ORCID https://orcid.org/0000-0002-1603-258X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study is aimed at evaluating the inclusion of miniature anion-exchange centrifugation technique (mAECT) in the diagnosis and fexinidazole as treatment of gHAT in Central African Republic (CAR) after capacity building. A cross-sectional pilot study was conducted during a mass diagnostic campaign from 16 September to 22 October 2022 in Nola-Bilolo, a historic focus in CAR. The serological test, card agglutination test for trypanosomiasis (CATT), was performed on whole blood and diluted plasma to screen participants, followed by a confirmatory parasitological test by capillary tube centrifugation (CTC) and mAECT. Positive cases were treated mainly with fexinidazole. A total of 2070 participants were screened, out of an estimated population of 3584, representing a participation rate of 58%. The seroprevalence of HAT was 1.6% (CI 95%: 77%-99%) (33/2070) by the CATT plasma end-dilution titre ≥ 1:16. Blood from serological subjects was examined microscopically after concentration by CTC and mAECT was positive for trypanosomes in 48.48% (CI 95%: 31%-66%) (16/33) and 87.88% (CI 95%: 77%-99%) (29/33) of cases, respectively. The prevalence of microscopically confirmed HAT was 0.77% (CI 95%: 0.40%-1.15%) and 1.4% (CI 95%: 1%-2%) by CTC and mAECT, respectively. Twenty-one (72.41%) patients were treated with fexinidazole with a 0% interruption rate. The introduction of fexinidazole (2021) and mAECT (2022) likely contributed to the rise in reported cases (from 45 in 2021 to 111 in 2024) and improved screening coverage in the study area, reflecting enhanced case detection and access to care. There is a necessity to establish diagnostic quality assurance and to reinforce the other control measures including vector control.

Indexed as

diagnosisfexinidazolehuman African trypanosomiasismAECTNola-Bilolotreatment

Identifiers

PMID41809024
PMCPMC12968429

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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.