Evidence map›Paper›PMID 36780561›Full record

ArticlePLoS neglected tropical diseases2023

PCR for detection of Leishmania donovani from microscopically negative tissue smears of suspected patients in Gondar, Ethiopia.

Roma Melkamu, Nega Berhane, Bart K M Jacobs, Rezika Mohammed, Mekibib Kassa, Arega Yeshanew, Helina Fikre, Saba Atnafu, Saskia van Henten, Johan van Griensven and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Community Drivers ofTropical medicine and infectious disease · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

11 authors at 2 institutions in 2 countries.

Roma MelkamuLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.ORCID 0000-0002-5952-252X
Nega BerhaneInstitute of Biotechnology, University of Gondar, Gondar, Ethiopia.
Bart K M JacobsClinical Sciences Department, Institute of Tropical Medicine, Antwerp, Belgium.
Rezika MohammedLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.
Mekibib KassaLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.
Arega YeshanewLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.
Helina FikreLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.
Saba AtnafuLeishmaniasis Research and Treatment Center, University of Gondar, Gondar, Ethiopia.
Saskia van HentenClinical Sciences Department, Institute of Tropical Medicine, Antwerp, Belgium.
Johan van GriensvenClinical Sciences Department, Institute of Tropical Medicine, Antwerp, Belgium.
Myrthe PareynClinical Sciences Department, Institute of Tropical Medicine, Antwerp, Belgium.
University of Gondar · ETInstituut voor Tropische Geneeskunde · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs untreated visceral leishmaniasis (VL) is fatal, reliable diagnostics are pivotal for accurate treatment allocation. The current diagnostic algorithm for VL in Ethiopia, which is based on the rK39 rapid diagnostic test and microscopy of tissue smears, lacks sensitivity. This probably leads to missed cases and patients not receiving treatment. METHODOLOGY: We conducted a retrospective study on stored microscopically negative spleen and bone marrow smears from suspected VL patients collected at the Leishmaniasis Research and Treatment Center (LRTC) in Gondar, northern Ethiopia between June 2019 and November 2020. Sociodemographic, clinical and treatment data were collected and samples were tested by real-time PCR targeting kinetoplast DNA. PRINCIPLE

findingsAmong the 191 eligible samples (135 spleen and 56 bone marrow) with a microscopically negative and valid PCR result, 119 (62.3%) were positive by PCR, although Ct values for some were high (median 33.0). Approximately three quarters of these undiagnosed primary VL (77.3%) and relapse (69.6%) patients did not receive antileishmanial treatment. Of the 56 microscopically negative bone marrow samples, 46 (82.1%) were PCR positive, which is considerably higher compared to the microscopically negative spleen samples, for which 73 out of 135 (54.1%) were PCR positive. The odds of being PCR positive were significantly higher for bone marrow aspirates and higher when white blood cell values were lower and splenomegaly (in cm) was more pronounced.

conclusionsThis study demonstrates that a lot of suspected VL patients remain undiagnosed and untreated. This indicates the urgent need for better diagnostics for VL in the East-African region. The outcomes of PCR positive should be closely monitored and treatment should be provided if the patient deteriorates. In resource limited settings, implementation of PCR on bone marrow aspirate smears of patients with low WBC values and splenomegaly could lead to considerable improvements in patient management.

Indexed as

Leishmania donovaniLeishmaniasis, VisceralEthiopiaHumansReal-Time Polymerase Chain ReactionRetrospective StudiesSensitivity and SpecificitySplenomegaly

Identifiers

PMID36780561
PMCPMC9956792
OpenAlexW4320483339

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.