Evidence map›Paper›PMID 40554504›Full record

ArticlePloS one2025

Feasibility and acceptability of GeneXpert MTB/XDR implementation among healthcare workers in three low-middle income African countries.

Sara Keller, Kogieleum Naidoo, Medhane Zekarias, Sussan Israel-Isah, Mohammed Shaka, Gcinile Gule, Anushka Naidoo, Miriam Bathnna, Judith Nomthandazo Dlamini-Miti, Kalkidan Yae and 5 more

Abstract readMulticenter Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

15 authors.

Sara KellerKNCV Tuberculosis Foundation, Den Haag, The Netherlands.
Kogieleum NaidooCentre for the Aids Programme of Research in South Africa, Durban, KwaZulu-Natal, South Africa.ORCID https://orcid.org/0000-0002-8874-6661
Medhane ZekariasKNCV Tuberculosis Foundation, Ethiopia Office, Addis Ababa, Ethiopia.
Sussan Israel-IsahInternational Research Centre of Excellence- Institute of Human Virology, Abuja, Nigeria.
Mohammed ShakaKNCV Tuberculosis Foundation, Ethiopia Office, Addis Ababa, Ethiopia.
Gcinile GuleCentre for the Aids Programme of Research in South Africa, Durban, KwaZulu-Natal, South Africa.
Anushka NaidooCentre for the Aids Programme of Research in South Africa, Durban, KwaZulu-Natal, South Africa.
Miriam BathnnaInternational Research Centre of Excellence- Institute of Human Virology, Abuja, Nigeria.
Judith Nomthandazo Dlamini-MitiUniversity of the Witwatersrand, Johannesburg, South Africa.
Kalkidan YaeKNCV Tuberculosis Foundation, Ethiopia Office, Addis Ababa, Ethiopia.
Evaezi OkpokoroInternational Research Centre of Excellence- Institute of Human Virology, Abuja, Nigeria.
Alash'le AbimikuInternational Research Centre of Excellence- Institute of Human Virology, Abuja, Nigeria.
Ahmed BedruKNCV Tuberculosis Foundation, Ethiopia Office, Addis Ababa, Ethiopia.
Edine W TiemersmaKNCV Tuberculosis Foundation, Den Haag, The Netherlands.ORCID https://orcid.org/0000-0002-2071-3038
TRiAD Study Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundXpert MTB/XDR (Xpert-XDR) testing can significantly shorten time to initiating appropriate drug-resistant tuberculosis (DR-TB) treatment, but its introduction may impact laboratory workflow, especially in laboratories not currently performing drug susceptibility testing. This study evaluated the feasibility and acceptability of implementing the Xpert-XDR for rapid triage and selection of all-oral regimens for DR-TB.

methodThis was a multi-country, multi-site qualitative study conducted between July and November 2023, as part of the larger TriAD (Triage test for All oral DR TB drugs) study implemented in South Africa, Ethiopia, and Nigeria. We conducted semi-structured in-depth interviews with clinicians, nurses and laboratory staff at each study site until thematic saturation was achieved. Additionally, we interviewed policy makers (n = 9) and people with TB (PWTB) (n = 11), to provide additional insight on the implementation of this new diagnostic assay.

resultsHealthcare workers (n = 61) found the new workflow feasible and acceptable. It was the increased speed in which PWTB would receive a correct diagnosis and appropriate treatment that provided the biggest benefit to moving to Xpert-XDR for healthcare workers and PWTB. Laboratory staff mentioned that Xpert-XDR had expedited and simplified the laboratory workflows. Role-appropriate and ongoing training is a key factor in effective implementation as described by policy makers and healthcare workers alike. Barriers impacting the ability to perform Xpert-XDR included unstable power supply, internet, and temperature control. Additionally, the Xpert MTB/Rif Ultra test has higher sensitivity for the detection of TB than the Xpert-XDR test, leading to discordant test results.

conclusionThis study showed that implementation of Xpert-XDR in health facilities is both feasible and acceptable by all types of healthcare workers. Some barriers with Xpert-XDR are not exclusive to this particular diagnostic tool but are important to address when policy makers are deciding which tools to implement.

Indexed as

Health PersonnelMycobacterium tuberculosisTuberculosis, Multidrug-ResistantAdultEthiopiaFeasibility StudiesFemaleHumansMaleNigeriaSouth Africa

Identifiers

PMID40554504
PMCPMC12186877

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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.