Evidence map›Paper›PMID 39802777›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Changes in susceptibility of

Martin Okitwi, Stephen Orena, Patrick K Tumwebaze, Thomas Katairo, Yoweri Taremwa, Oswald Byaruhanga, Stephen Tukwasibwe, Samuel L Nsobya, Jennifer Legac, Roland A Cooper and 2 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

5 · Who and what money

Authors and funding

12 authors.

Martin Okitwi
Stephen Orena
Patrick K Tumwebaze
Thomas Katairo
Yoweri Taremwa
Oswald Byaruhanga
Stephen Tukwasibwe
Samuel L Nsobya
Jennifer Legac
Roland A Cooper
Philip J RosenthalORCID 0000-0002-7953-7622

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The treatment and control of malaria in Africa is challenged by drug resistance, including Methods: We characterized ex vivo susceptibilities to nine drugs of isolates collected from individuals presenting with uncomplicated falciparum malaria in eastern (2019-2024) and northern (2021-2024) Uganda using a growth inhibition assay and the dihydroartemisinin (DHA) ring survival assay (RSA). Genetic polymorphisms were characterized by molecular inversion probe and dideoxy sequencing. We assessed drug susceptibilities over time and evaluated associations between susceptibilities and potential resistance markers for samples studied since 2016. Results: Of 1,297 collected, 724/828 eastern and 390/469 northern Uganda isolates were successfully evaluated for ex vivo drug susceptibilities. Median half-maximal inhibitory concentrations (IC Interpretation: Susceptibilities to antimalarial drugs were mostly excellent, but decreased activities of lumefantrine and DHA over time suggest potential loss of efficacies of leading regimens. Funding: National Institutes of Health, Medicines for Malaria Venture, Gates Foundation. Research in Context:

Identifiers

PMID39802777
PMCPMC11722467

What OpenQuestion holds

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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.