Evidence map›Paper›PMID 37967039›Full record

ArticlePloS one2023

Interruptions in treatment among adults on anti-retroviral therapy before and after test-and-treat policy in Tanzania.

Redempta J Mbatia, Expeditho L Mtisi, Abbas Ismail, Christopher V Henjewele, Sisty J Moshi, Alexander K Christopher, Noela W Nsanzugwanko, Appolinary G Bukuku, Rehema A Msimbe, Agnes R Kirato and 6 more

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. 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

16 authors.

Redempta J MbatiaTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.ORCID 0000-0003-0209-1690
Expeditho L MtisiDepartment of General Studies, Dar es Salaam Institute of Technology, Dar es Salaam, Tanzania.
Abbas IsmailUS Center for Disease Control and Prevention (CDC), Tanzania Country Office, Dar es Salaam, Tanzania.
Christopher V HenjeweleTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Sisty J MoshiTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Alexander K ChristopherTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Noela W NsanzugwankoTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Appolinary G BukukuTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Rehema A MsimbeTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Agnes R KiratoTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Francis S NyabukeneTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Eunice J MmariUS Center for Disease Control and Prevention (CDC), Tanzania Country Office, Dar es Salaam, Tanzania.
Anath A RwebemberaMinistry of Health, Community Development, Gender, Elderly and Children, Dodoma, Tanzania.
Benedicta N MasanjaTanzania Health Promotion Support (THPS), Dar es Salaam, Tanzania.
Alexander KailemboUS Center for Disease Control and Prevention (CDC), Tanzania Country Office, Dar es Salaam, Tanzania.
Eva J MatikoUS Center for Disease Control and Prevention (CDC), Tanzania Country Office, Dar es Salaam, Tanzania.ORCID 0000-0001-8887-9037

Funding

CGH CDC HHS U2G GH001068
6 · The paper itself

Abstract

introductionThe World Health Organization recommended the initiation of antiretroviral therapy (ART) for people living with HIV (PLHIV) regardless of CD4 cell counts. Tanzania adopted this recommendation known as test-and-treat policy in 2016. However, programmatic implementation of this policy has not been assessed since its initiation. The objective of the study was to assess the impact of this policy in Tanzania.

methodsThis was a cross-sectional study among PLHIV aged 15 years and older using routinely collected program data. The dependent variable was interruption in treatment (IIT), defined as no clinical contact for at least 90 days after the last clinical appointment. The main independent variable was test-and-treat policy status which categorized PLHIV into the before and after groups. Co-variates were age, sex, facility type, clinical stage, CD4 count, ART duration, and body mass index. The associations were assessed using the generalized estimating equation with inverse probability weighting.

resultsThe study involved 33,979 PLHIV-14,442 (42.5%) and 19,537 (57.5%) were in the before and after the policy groups, respectively. Among those who experienced IIT, 4,219 (29%) and 7,322 (38%) were in the before and after the policy groups respectively. Multivariable analysis showed PLHIV after the policy was instated had twice [AOR 2.03; 95%CI 1.74-2.38] the odds of experiencing IIT than those before the policy was adopted. Additionally, higher odds of experiencing IIT were observed among younger adults, males, and those with advanced HIV disease.

conclusionDemographic and clinical status variables were associated with IIT, as well as the test-and-treat policy. To achieve epidemic control, programmatic adjustments on continuity of treatment may are needed to complement the programmatic implementation of the policy.

Indexed as

Anti-HIV AgentsHIV InfectionsAdultCD4 Lymphocyte CountCross-Sectional StudiesHumansMaleTanzaniaWorld Health OrganizationAnti-HIV Agents

Identifiers

PMID37967039
PMCPMC10651022

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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.