Evidence map›Paper›PMID 33973874›Full record

ArticleAIDS (London, England)2021

Initiating antiretroviral treatment for newly diagnosed HIV patients in sexual health clinics greatly improves timeliness of viral suppression.

Preeti Pathela, Kelly Jamison, Sarah L Braunstein, Christine M Borges, Rachael Lazar, Tarek Mikati, Demetre Daskalakis, Susan Blank

Abstract read
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In one paragraph

Article in AIDS (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 13% of its field
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

11 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Preeti PathelaNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Kelly JamisonNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Sarah L BraunsteinNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Christine M BorgesNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Rachael LazarNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Tarek MikatiNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Demetre DaskalakisNew York City Department of Health and Mental Hygiene, Bureau of Sexually Transmitted Infections, New York, NY.
Susan BlankRetired (formerly with New York City Department of Health and Mental Hygiene and Centers for Disease Control and Prevention, Division of STD Prevention, Atlanta, GA, USA).
New York City Department of Health and Mental Hygiene · USGTx (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe 'JumpstART' program in New York City (NYC) public Sexual Health Clinics (SHC) provides patients newly diagnosed with human immunodeficiency virus (HIV) with antiretroviral medication (ART) (1-month supply) on day of diagnosis and active linkage to HIV care (LTC). We examined viral suppression (VS) among patients who did and did not receive JumpstART services.

designRetrospective cohort.

methodsAmong newly diagnosed SHC patients (23 November 2016-30 September 2018) who were matched to the NYC HIV surveillance registry to obtain HIV laboratory test results through 30 June 2019, we compared 230 JumpstART and 73 non-JumpstART patients regarding timely LTC (≤30 days), probability of VS (viral load < 200 copies/ml) by 3 months post-diagnosis, and time to and factors associated with achieving VS within the follow-up period.

resultsOf 303 patients, 76% (230/303) were JumpstART and the remaining were non-JumpstART patients; 36 (11%) had acute HIV infections. LTC ≤30 days was observed for 63% of JumpstART and 73% of non-JumpstART patients. By 3 months post-diagnosis, 83% of JumpstART versus 45% of non-JumpstART patients achieved VS (log-rank, P < .0001). Median times to VS among virally suppressed JumpstART and non-JumpstART patients were 31 (interquartile range [IQR]: 24-51) and 95 days (IQR: 52-153), respectively. For groups with and without timely LTC, JumpstART was associated with viral suppression within 3 months post-diagnosis, after adjusting for age and baseline viral load.

conclusionsPrompt ART initiation among SHC patients, some with acute HIV infections, resulted in markedly shortened intervals to VS. Immediate ART provision and active LTC can be key contributors to improved HIV treatment outcomes and the treatment-as-prevention paradigm, with potential for downstream, population-level benefit.

Indexed as

Anti-HIV AgentsHIV InfectionsSexual HealthAnti-Retroviral AgentsHumansRetrospective StudiesViral LoadAnti-HIV AgentsAnti-Retroviral Agents

Identifiers

PMID33973874
OpenAlexW3163382699

What OpenQuestion holds

Textmetadata
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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.