Evidence map›Paper›PMID 34499665›Full record

Trial reportPLoS medicine2021

Computer-aided X-ray screening for tuberculosis and HIV testing among adults with cough in Malawi (the PROSPECT study): A randomised trial and cost-effectiveness analysis.

Peter MacPherson, Emily L Webb, Wala Kamchedzera, Elizabeth Joekes, Gugu Mjoli, David G Lalloo, Titus H Divala, Augustine T Choko, Rachael M Burke, Hendramoorthy Maheswaran and 4 more

Registry-linked trialAbstract readPragmatic Clinical Trial
In one paragraph

Trial report in PLoS medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03519425 (A Pragmatic Randomised Study to Optimise Screening, Prevention and Care for Tuberculosis in Malawi), which is not on this map. Cited by 42 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 3 pooled it
–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.

NCT03519425 naunknown statusnot on this map

A Pragmatic Randomised Study to Optimise Screening, Prevention and Care for Tuberculosis in Malawi

TypeinterventionalSponsorLiverpool School of Tropical MedicineRan2018 to 2020Enrolled1,455ConditionsTuberculosis, Hiv, Tuberculosis, PulmonaryArmsOptimised HIV screening and linkage to care, Optimised tuberculosis screening and linkage to care
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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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

14 authors.

Peter MacPhersonDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-0329-9613
Emily L WebbMRC Tropical Epidemiology Group, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-4019-7456
Wala KamchedzeraMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.ORCID 0000-0002-6709-4270
Elizabeth JoekesDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-5577-210X
Gugu MjoliDepartment of Radiology, Chris Hani Baragwanath Hospital, Soweto, South Africa.ORCID 0000-0002-6052-5859
David G LallooDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0001-7680-2200
Titus H DivalaMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.ORCID 0000-0003-3029-9579
Augustine T ChokoDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0001-6095-9430
Rachael M BurkeMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.ORCID 0000-0002-2156-5030
Hendramoorthy MaheswaranDepartment of Public Health and Policy, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0002-7375-4845
Madhukar PaiMcGill International TB Centre, McGill University, Montreal, Canada.ORCID 0000-0003-3667-4536
S Bertel SquireDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0001-7173-9038
Marriott NliwasaMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.ORCID 0000-0002-3100-5512
Elizabeth L CorbettMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

Funding

Medical Research Council MR/R010161/1Wellcome Trust 200901/Z/16/ZWellcome Trust 206575/Z/17/Z
6 · The paper itself

Abstract

backgroundSuboptimal tuberculosis (TB) diagnostics and HIV contribute to the high global burden of TB. We investigated costs and yield from systematic HIV-TB screening, including computer-aided digital chest X-ray (DCXR-CAD). METHODS AND

findingsIn this open, three-arm randomised trial, adults (≥18 years) with cough attending acute primary services in Malawi were randomised (1:1:1) to standard of care (SOC); oral HIV testing (HIV screening) and linkage to care; or HIV testing and linkage to care plus DCXR-CAD with sputum Xpert for high CAD4TBv5 scores (HIV-TB screening). Participants and study staff were not blinded to intervention allocation, but investigator blinding was maintained until final analysis. The primary outcome was time to TB treatment. Secondary outcomes included proportion with same-day TB treatment; prevalence of undiagnosed/untreated bacteriologically confirmed TB on day 56; and undiagnosed/untreated HIV. Analysis was done on an intention-to-treat basis. Cost-effectiveness analysis used a health-provider perspective. Between 15 November 2018 and 27 November 2019, 8,236 were screened for eligibility, with 473, 492, and 497 randomly allocated to SOC, HIV, and HIV-TB screening arms; 53 (11%), 52 (9%), and 47 (9%) were lost to follow-up, respectively. At 56 days, TB treatment had been started in 5 (1.1%) SOC, 8 (1.6%) HIV screening, and 15 (3.0%) HIV-TB screening participants. Median (IQR) time to TB treatment was 11 (6.5 to 38), 6 (1 to 22), and 1 (0 to 3) days (hazard ratio for HIV-TB versus SOC: 2.86, 1.04 to 7.87), with same-day treatment of 0/5 (0%) SOC, 1/8 (12.5%) HIV, and 6/15 (40.0%) HIV-TB screening arm TB patients (p = 0.03). At day 56, 2 SOC (0.5%), 4 HIV (1.0%), and 2 HIV-TB (0.5%) participants had undiagnosed microbiologically confirmed TB. HIV screening reduced the proportion with undiagnosed or untreated HIV from 10 (2.7%) in the SOC arm to 2 (0.5%) in the HIV screening arm (risk ratio [RR]: 0.18, 0.04 to 0.83), and 1 (0.2%) in the HIV-TB screening arm (RR: 0.09, 0.01 to 0.71). Incremental costs were US$3.58 and US$19.92 per participant screened for HIV and HIV-TB; the probability of cost-effectiveness at a US$1,200/quality-adjusted life year (QALY) threshold was 83.9% and 0%. Main limitations were the lower than anticipated prevalence of TB and short participant follow-up period; cost and quality of life benefits of this screening approach may accrue over a longer time horizon.

conclusionsDCXR-CAD with universal HIV screening significantly increased the timeliness and completeness of HIV and TB diagnosis. If implemented at scale, this has potential to rapidly and efficiently improve TB and HIV diagnosis and treatment.

trial registrationclinicaltrials.gov NCT03519425.

Indexed as

CoinfectionDiagnosis, Computer-AssistedHIV TestingRadiography, ThoracicAdultAnti-HIV AgentsAntitubercular AgentsCost-Benefit AnalysisCoughFemaleHealth Care CostsHealth Services AccessibilityHIV InfectionsHumansMalawiMaleAnti-HIV AgentsAntitubercular Agents

Identifiers

PMID34499665
PMCPMC8459969

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Registered trials

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.