Evidence map›Paper›PMID 29514235›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2018

Late Presentation With HIV in Africa: Phenotypes, Risk, and Risk Stratification in the REALITY Trial.

Abraham Siika, Leanne McCabe, Mutsa Bwakura-Dangarembizi, Cissy Kityo, Jane Mallewa, Jay Berkley, Kath Maitland, Anna Griffiths, Keith Baleeta, Shepherd Mudzingwa and 7 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Causes and Timing of Mortality and Morbidity Among Late Presenters Starting Antiretroviral Therapy in the REALITY Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018
    Trial
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  3. Review
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  5. Observational
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  11. CD4+ T-Cell Count at Antiretroviral Therapy Initiation in the "Treat-All" Era in Rural South Africa: An Interrupted Time Series Analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Inflammatory Phenotypes Predict Changes in Arterial Stiffness Following Antiretroviral Therapy Initiation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  16. Observational
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  18. Observational
  19. Article
  20. The Persistent Challenge of Advanced HIV Disease and AIDS in the Era of Antiretroviral Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018
    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

17 authors.

Abraham SiikaMoi University School of Medicine, Eldoret, Kenya.
Leanne McCabeMedical Research Council Clinical Trials Unit at University College London, United Kingdom.
Mutsa Bwakura-DangarembiziUniversity of Zimbabwe Clinical Research Centre, Harare.
Cissy KityoJoint Clinical Research Centre, Kampala, Uganda.
Jane MallewaDepartment/College of Medicine and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre.
Jay BerkleyKenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi.
Kath MaitlandKenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi.
Anna GriffithsMedical Research Council Clinical Trials Unit at University College London, United Kingdom.
Keith BaleetaJoint Clinical Research Centre, Mbale.
Shepherd MudzingwaUniversity of Zimbabwe Clinical Research Centre, Harare.
James AbachJoint Clinical Research Centre, Gulu, Uganda.
Kusum NathooUniversity of Zimbabwe Clinical Research Centre, Harare.
Margaret J ThomasonMedical Research Council Clinical Trials Unit at University College London, United Kingdom.
Andrew J PrendergastQueen Mary University of London, United Kingdom.
Ann Sarah WalkerMedical Research Council Clinical Trials Unit at University College London, United Kingdom.
Diana M GibbMedical Research Council Clinical Trials Unit at University College London, United Kingdom.
REALITY Trial Team

Funding

East Africa International Epidemiology Database to evaluate AIDS (IeDEA) Regional ConsortiumU01AI069911 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Leslie Anne Enane, AGGREY SEMWENDERO SEMEERE · 2006 to 2026
$57.7M
Medical Research Council G1100693Medical Research Council MC_EX_G1100693Medical Research Council MC_EX_UU_G1100693Medical Research Council MC_UU_12023/17Medical Research Council MC_UU_12023/23Medical Research Council MC_UU_12023/26Medical Research Council MR/M007367/1Medical Research Council MR/P022251/1NIAID NIH HHS U01 AI069911Wellcome TrustWellcome Trust 101113/Z/13/ZWellcome Trust 108065/Z/15/ZWellcome Trust 203077/Z/16/Z
6 · The paper itself

Abstract

Background: Severely immunocompromised human immunodeficiency virus (HIV)-infected individuals have high mortality shortly after starting antiretroviral therapy (ART). We investigated predictors of early mortality and "late presenter" phenotypes. Methods: The Reduction of EArly MortaLITY (REALITY) trial enrolled ART-naive adults and children ≥5 years of age with CD4 counts <100 cells/µL initiating ART in Uganda, Zimbabwe, Malawi, and Kenya. Baseline predictors of mortality through 48 weeks were identified using Cox regression with backwards elimination (exit P > .1). Results: Among 1711 included participants, 203 (12%) died. Mortality was independently higher with older age; lower CD4 count, albumin, hemoglobin, and grip strength; presence of World Health Organization stage 3/4 weight loss, fever, or vomiting; and problems with mobility or self-care at baseline (all P < .04). Receiving enhanced antimicrobial prophylaxis independently reduced mortality (P = .02). Of five late-presenter phenotypes, Group 1 (n = 355) had highest mortality (25%; median CD4 count, 28 cells/µL), with high symptom burden, weight loss, poor mobility, and low albumin and hemoglobin. Group 2 (n = 394; 11% mortality; 43 cells/µL) also had weight loss, with high white cell, platelet, and neutrophil counts suggesting underlying inflammation/infection. Group 3 (n = 218; 10% mortality) had low CD4 counts (27 cells/µL), but low symptom burden and maintained fat mass. The remaining groups had 4%-6% mortality. Conclusions: Clinical and laboratory features identified groups with highest mortality following ART initiation. A screening tool could identify patients with low CD4 counts for prioritizing same-day ART initiation, enhanced prophylaxis, and intensive follow-up. Clinical Trials Registration: ISRCTN43622374.

Indexed as

AdolescentAdultAfrica South of the SaharaAge FactorsAIDS-Related Opportunistic InfectionsAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountChildChild, PreschoolFemaleHIVHIV InfectionsHumansImmunocompromised HostMaleAnti-HIV Agents

Identifiers

PMID29514235
PMCPMC5850547

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.