Evidence map›Paper›PMID 31242142›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2019

Extending Visit Intervals for Clinically Stable Patients on Antiretroviral Therapy: Multicohort Analysis of HIV Programs in Southern Africa.

Andreas D Haas, Leigh F Johnson, Anna Grimsrud, Nathan Ford, Catarina Mugglin, Matthew P Fox, Jonathan Euvrard, Monique van Lettow, Hans Prozesky, Izukanji Sikazwe and 5 more

Abstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

15 authors.

Andreas D HaasInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Leigh F JohnsonCentre for Infectious Disease Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
Anna GrimsrudInternational AIDS Society, Cape Town, South Africa.
Nathan FordDepartment of HIV/AIDS World Health Organization, Geneva, Switzerland.
Catarina MugglinInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Matthew P FoxDepartment of Internal Medicine, Health Economics and Epidemiology Research Office, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Jonathan EuvrardCentre for Infectious Disease Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
Monique van LettowDignitas International, Zomba, Malawi.
Hans ProzeskyDivision of Infectious Diseases, Department of Medicine, Tygerberg Academic Hospital, University of Stellenbosch, Cape Town, South Africa.
Izukanji SikazweCentre for Infectious Diseases Research in Zambia, Lusaka, Zambia.
Cleophas ChimbeteteNewlands Clinic, Harare, Zimbabwe.
Michael HobbinsSolidarMed, Lucerne, Switzerland.
Cordelia KunzekwenyikaSolidarMed, Masvingo, Zimbabwe.
Matthias EggerInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
for IeDEA Southern Africa

Funding

Observational Antiretroviral Studies In Southern Africa (OASIS) CollaborationU01AI069924 · NIAID · UNIVERSITAT BERN · PI Cleophas Chimbetete, Mary-Ann Davies · 2006 to 2026
$55.9M
NIAID NIH HHS U01 AI069924World Health Organization 001
6 · The paper itself

Abstract

backgroundThe World Health Organization recommends differentiated antiretroviral therapy (ART) delivery with longer visit intervals for clinically stable patients. We examined time trends in visit frequency and associations between criteria for clinical stability and visit frequency in ART programs in Southern Africa.

methodsWe included adults on ART from 4 programs with viral-load monitoring, 2 programs with CD4 monitoring, and 4 programs with clinical monitoring of ART. We classified patients as clinically stable based on virological (viral load <1000 copies/mL), immunological (CD4 >200 cells/µL), or clinical (no current tuberculosis) criteria. We used Poisson regression and survival models to examine associations between criteria for clinical stability and the rate of clinic visits.

resultsWe included 180,837 patients. There were trends toward fewer visits in more recent years and with longer ART duration. In all ART programs, clinically stable patients were seen less frequently than patients receiving failing ART, but the strength of the association varied. Adjusted incidence rate ratios comparing visit rates for stable patients with patients on failing ART were 0.82 (95% confidence interval: 0.73 to 0.90) for patients classified based on the virological criterion, 0.81 (0.69 to 0.93) for patients classified based on the clinical criterion, and 0.90 (0.85 to 0.96) for patients classified based on the immunological criterion for stability.

conclusionDifferences in visit rates between stable patients and patients failing ART were variable and modest overall. Larger differences were seen in programs using virological criteria for clinical stability than in programs using immunological criteria. Greater access to routine viral-load monitoring may increase scale-up of differentiated ART delivery.

Indexed as

Drug MonitoringAdolescentAdultAfrica, SouthernAnti-Retroviral AgentsCD4 Lymphocyte CountCohort StudiesDelivery of Health CareFemaleHIV InfectionsHumansMaleMiddle AgedRegression AnalysisSurvival AnalysisTreatment OutcomeAnti-Retroviral Agents

Identifiers

PMID31242142
PMCPMC6597180

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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.