Evidence map›Paper›PMID 40038791›Full record

Observational studyAIDS research and therapy2025

Temporal trends from HIV diagnosis to ART initiation among adults living with HIV in the Asia-Pacific (2013-2023).

Thinh Toan Vu, Dhanushi Rupasinghe, Vohith Khol, Romanee Chaiwarith, Junko Tanuma, Nagalingeswaran Kumarasamy, Suwimon Khusuwan, IKetut Agus Somia, Sanjay Pujari, Man Po Lee and 12 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in AIDS research and therapy, 2025. 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
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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

22 authors.

Thinh Toan VuDepartment of Community Health and Social Sciences, CUNY Graduate School of Public Health and Health Policy, New York, NY, USA. vutoanthinhph@gmail.com.
Dhanushi RupasingheThe Kirby Institute, UNSW Sydney, Sydney, Australia.
Vohith KholSocial Health Clinic, National Center for HIV/AIDS, Dermatology and STDs (NCHADS), Phnom Penh, Cambodia.
Romanee ChaiwarithDivision of Infectious Diseases and Tropical Medicine, Department of Medicine, Faculty of Medicine and Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Junko TanumaNational Center for Global Health and Medicine, Tokyo, Japan.
Nagalingeswaran KumarasamyCART CRS, Voluntary Health Services, Chennai, India.
Suwimon KhusuwanChiangrai Prachanukroh Hospital, Chiang Rai, Thailand.
IKetut Agus SomiaFaculty of Medicine, Udayana University - Prof. Dr. I.G.N.G. Ngoerah Hospital, Bali, Indonesia.
Sanjay PujariInstitute of Infectious Diseases, Pune, India.
Man Po LeeQueen Elizabeth Hospital, Hong Kong SAR, China.
Rohidas T BorseBJ Government Medical College and Sassoon General Hospitals, Pune, India.
Sasisopin KiertiburanakulFaculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Evy YunihastutiFaculty of Medicine Universitas Indonesia - Dr. Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.
Iskandar AzwaInfectious Diseases Unit, Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Jun Yong ChoiDivision of Infectious Diseases, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Hsin-Pai ChenTaipei Veterans General Hospital, Taipei, Taiwan.
Rossana DitangcoResearch Institute for Tropical Medicine, Muntinlupa City, Philippines.
Anchalee AvihingsanonHIV-NAT/ Thai Red Cross AIDS Research Centre, and Tuberculosis Research Unit, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Yasmin GaniHospital Sungai Buloh, Sungai Buloh, Malaysia.
Jeremy RossTREAT Asia, amfAR - The Foundation for AIDS Research, Bangkok, Thailand.
Awachana JiamsakulThe Kirby Institute, UNSW Sydney, Sydney, Australia.
IeDEA Asia-Pacific

Funding

The Asia-Pacific HIV Research CollaborationU01AI069907 · NIAID · FOUNDATION FOR AIDS RESEARCH · PI ANNETTE H SOHN · 2006 to 2026
$44.8M
NIAID NIH HHS U01 AI069907
6 · The paper itself

Abstract

introductionData on the impact of World Health Organization (WHO)'s guideline changes and COVID-19 on ART initiation in the Asia-Pacific remain scarce. This study described temporal trends from HIV diagnosis to ART initiation from 2013 to 2023 and its associated factors.

methodsAdults (≥ 18 years) diagnosed with HIV after 2013 in a regional observational cohort were included. Fine and Gray competing risk regression examined predictors of ART initiation (≥ 3 antiretroviral medications), accounting for those lost to follow-up or deceased before treatment considered as competing risks.

resultsAmong 14,968 participants, most were male (70.1%), with a median age of 36 years (interquartile range [IQR]: 28-44). At HIV diagnosis, median CD4 count was 208 cells/µL (IQR: 69-395), and median viral load was 86,296 copies/mL (IQR: 13,186-392,000). Over 85% of participants had initiated ART during the study period. Median time from HIV diagnosis to ART initiation differed across years of HIV diagnosis: 51 days (2013-2015), 28 days (2016-2019), and 26 days (≥ 2020). Factors associated with shorter time to ART initiation were higher country income-level (upper-middle: sub-distribution hazard ratio [SHR] = 1.34, 95% CI: 1.28, 1.40; high: SHR = 1.35, 95% CI: 1.28, 1.43; vs. lower-middle); HIV transmission via male-to-male contact (SHR = 1.06, 95% CI: 1.02, 1.11) or injection drug use (SHR = 1.23, 95% CI: 1.09, 1.38; vs. heterosexual contact); and later years of HIV diagnosis (2016-2019: SHR = 1.33, 95% CI: 1.28, 1.38; ≥ 2020: SHR = 1.40, 95% CI: 1.33, 1.48; vs. 2013-2015). Those with higher CD4 counts had longer time to ART start (350-499 cells/µL: SHR = 0.76, 95% CI: 0.67, 0.86; > 500 cells/µL: SHR = 0.55, 95% CI: 0.49, 0.61; vs. CD4 < 200 cells/µL).

conclusionTime to ART initiation from HIV diagnosis decreased after 2016, aligning with evolving WHO guidelines, and did not appear to be impacted by COVID-19. Optimizing treatment initiation during the treat-all era is crucial, especially among those with higher CD4 counts.

Indexed as

Anti-HIV AgentsHIV InfectionsAdultAsiaCD4 Lymphocyte CountCOVID-19FemaleHumansMaleMiddle AgedTime FactorsTime-to-TreatmentViral LoadAnti-HIV AgentsART initiationAsia–PacificCompeting risksCOVID-19WHO guidelines

Identifiers

PMID40038791
PMCPMC11881487

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.