Evidence map›Paper›PMID 29768503›Full record

ArticlePloS one2018

High uptake of antiretroviral therapy among HIV-positive TB patients receiving co-located services in Swaziland.

Ishani Pathmanathan, Munyaradzi Pasipamire, Sherri Pals, E Kainne Dokubo, Peter Preko, Trong Ao, Sikhathele Mazibuko, Janet Ongole, Themba Dhlamini, Samson Haumba

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Ishani PathmanathanDivision of Global HIV and TB, United States Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID 0000-0001-8815-2129
Munyaradzi PasipamireSwaziland National AIDS Programme, Ministry of Health, Mbabane, Swaziland.
Sherri PalsDivision of Global HIV and TB, United States Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
E Kainne DokuboDivision of Global HIV and TB, United States Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Peter PrekoDivision of Global HIV and TB, United States Centers for Disease Control and Prevention, Ezulwini, Swaziland.
Trong AoDivision of Global HIV and TB, United States Centers for Disease Control and Prevention, Ezulwini, Swaziland.
Sikhathele MazibukoSwaziland National AIDS Programme, Ministry of Health, Mbabane, Swaziland.
Janet OngoleUniversity Research Co., LLC, Mbabane, Swaziland.
Themba DhlaminiSwaziland National TB Control Program, Ministry of Health, Manzini, Swaziland.
Samson HaumbaUniversity Research Co., LLC, Mbabane, Swaziland.
Centers for Disease Control and Prevention · USMinistry of Health · SZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSwaziland has the highest adult HIV prevalence and second highest rate of TB/HIV coinfection globally. Recently, the Ministry of Health and partners have increased integration and co-location of TB/HIV services, but the timing of antiretroviral therapy (ART) relative to TB treatment-a marker of program quality and predictor of outcomes-is unknown.

methodsWe conducted a retrospective analysis of programmatic data from 11 purposefully-sampled facilities to evaluate timely ART provision for HIV-positive TB patients enrolled on TB treatment between July-November 2014. Timely ART was defined as within two weeks of TB treatment initiation for patients with CD4<50/μL or missing, and within eight weeks otherwise. Descriptive statistics were estimated and logistic regression used to assess factors independently associated with timely ART.

resultsOf 466 HIV-positive TB patients, 51.5% were male, median age was 35 (interquartile range [IQR]: 29-42), and median CD4 was 137/μL (IQR: 58-268). 189 (40.6%) were on ART prior to, and five (1.8%) did not receive ART within six months of TB treatment initiation. Median time to ART after TB treatment initiation was 15 days (IQR: 14-28). Almost 90% started ART within eight weeks, and 45.5% of those with CD4<50/μL started within two weeks. Using thresholds for "timely ART" according to baseline CD4 count, 73.3% of patients overall received timely ART after TB treatment initiation. Patients with CD4 50-200/μL or ≥200/μL had significantly higher odds of timely ART than patients with CD4<50/μL, with adjusted odds ratios of 11.5 (95% confidence interval [CI]: 5.0-26.6) and 9.6 (95% CI: 4.6-19.9), respectively. TB cure or treatment completion was achieved by 71.1% of patients at six months, but this was not associated with timely ART.

conclusionsThis study demonstrates the relative success of integrated and co-located TB/HIV services in Swaziland, and shows that timely ART uptake for HIV-positive TB patients can be achieved in resource-limited, but integrated settings. Gaps remain in getting patients with CD4<50/μL to receive ART within the recommended two weeks post TB treatment initiation.

Indexed as

Drug MonitoringAdolescentAdultAnti-HIV AgentsCoinfectionDelivery of Health CareEswatiniFemaleHIV InfectionsHumansMaleMiddle AgedRetrospective StudiesTuberculosis, PulmonaryYoung AdultAnti-HIV Agents

Identifiers

PMID29768503
PMCPMC5955520
OpenAlexW2804533871

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.