Evidence map›Paper›PMID 42319224›Full record

Observational studyJournal of the International AIDS Society2026

Baseline Data on Viral Suppression, Treatment Adherence and Mental Health in Peripartum Girls and Young Women With HIV in Zimbabwe.

Tariro D Chawana-Mutingwende, Bernard Ngara, Leon-Say Mudadi, Thelma T Tauya, Marvelous Sibanda, Mercy Mutambanengwe-Jacob, Precious Andifasi, Bernadette Malunda, Tinashe Chidemo, Annie Mapfunde and 16 more

Abstract readObservational Study
In one paragraph

Observational study in Journal of the International AIDS Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Progress and Challenges in Elimination of Vertical HIV Transmission.Journal of the International AIDS Society · 2026
    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

26 authors.

Tariro D Chawana-MutingwendeUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.ORCID https://orcid.org/0000-0002-8754-331X
Bernard NgaraFaculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Leon-Say MudadiFaculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Thelma T TauyaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Marvelous SibandaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Mercy Mutambanengwe-JacobUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.ORCID https://orcid.org/0000-0002-5114-8449
Precious AndifasiMinistry of Health and Child Care, Harare, Zimbabwe.
Bernadette MalundaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Tinashe ChidemoUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Annie MapfundeUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Sandra NyakudyaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Anna Z MufumisiUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Thandiwe H ChirendaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Tobias ChitamboUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Walter T S NderechaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Constance MuranduUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Miriam GwandeUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Kudakwashe MuringayiUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Rhoda Micah BongoDivision of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, California, USA.
Hideaki OkochiDivision of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, California, USA.ORCID https://orcid.org/0000-0002-8519-7409
Karen KunczeDivision of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, California, USA.
Angela MushaviMinistry of Health and Child Care, Harare, Zimbabwe.
Nicola WillisZvandiri, Harare, Zimbabwe.
Karen WebbOrganization for Public Health Interventions and Development (OPHID), Harare, Zimbabwe.
Monica GandhiDivision of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, California, USA.
Lynda Stranix-ChibandaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.

Funding

Collaborative Initiative for Paediatric HIV Education and Research (CIPHER)
6 · The paper itself

Abstract

introductionPeripartum adolescent girls and young women (AGYW) with HIV have lower viral suppression compared to older women. But the recently introduced dolutegravir-based regimens and psychosocial peer motivation may improve viral control. We assessed viral suppression, adherence, drug exposure and mental health in a cohort of peripartum AGYW with HIV.

methodsWe present baseline data from an ongoing randomized controlled and observational cohort study. Peripartum (conception to 24 months postpartum) AGYW 15- to 24-year-old with HIV and >3 months on tenofovir-based antiretroviral therapy were enrolled between September 2024 and July 2025. Point-of-care viral load and urine tenofovir assays were performed at entry, as well as data on sociodemographic, HIV, treatment and mental health characteristics. Anxiety was assessed using the Generalized Anxiety Disorder-7, depression using the Patient Health Questionnaire-9, stigma using the Modified HIV Stigma Scale and post-traumatic stress disorder using the Primary Care Post Traumatic Stress Disorder 5 tools.

resultsWe enrolled 151 participants. Mean age was 21.1 years. All participants were receiving tenofovir, lamivudine and dolutegravir. Baseline mean viral load was 1133 copies/mL (cpm); 135 (89.4%) were virally suppressed (viral load <40 cpm). Mean self-reported adherence over the past 1 month was 97.5%. Tenofovir was detected in 141 (93.4%) participants at baseline. The following were significantly associated baseline with viral suppression (mean [SD]; 95% CI) or (n [%]): higher self-reported adherence (99.5 [1.7]; 99.2-99.8, p<0.001), detectable urine tenofovir (133 [94.3]; p<0.001), being married (79 [92.9]; p = 0.03), having food security (86 [95.6]; p = 0.004) and being financially secure (74 [96.1]; p = 0.02). Seven (4.6%) experienced post-traumatic stress disorder, 132 (88.0%) had minimal or no depression; 137 (92.0%) had minimal anxiety and 81 (53.6%) experienced moderate stigma. Participants without detectable tenofovir in urine were 0.05 times less likely to have baseline viral suppression, adjusted odds ratio (95% CI) (0.05 [0.006-0.4]; p = 0.004). Participants with higher self-reported adherence were 1.3 times more likely to have viral suppression (1.3 [1.1-1.6]; p = 0.008).

conclusionsWe found high viral suppression at enrolment into a cohort study in peripartum AGYW with HIV. Viral suppression was strongly associated with positive urine tenofovir assays and higher self-reported adherence. High mental wellness was demonstrated.

Indexed as

Anti-HIV AgentsHIV InfectionsMedication AdherenceMental HealthViral LoadAdolescentCohort StudiesDolutegravirFemaleHumansPeripartum PeriodPregnancyTenofovirYoung AdultZimbabweAnti-HIV AgentsDolutegravirTenofoviradherenceadolescent girls and young womenHIVperipartumurine tenofovir levelsvirological suppression

Identifiers

PMID42319224
PMCPMC13281420

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.