Evidence map›Paper›PMID 35120633›Full record

ReviewThe lancet. HIV2022

Use of integrase inhibitors in HIV-associated tuberculosis in high-burden settings: implementation challenges and research gaps.

Anushka Naidoo, Kogieleum Naidoo, Nesri Padayatchi, Kelly E Dooley

Open access · greenAbstract readReview
In one paragraph

Review in The lancet. HIV, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Observational
  8. Article
  9. Review
  10. Article
  11. 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

4 authors at 3 institutions in 2 countries.

Anushka NaidooCenter for the AIDS Program of Research in South Africa (CAPRISA), Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa. Electronic address: anushka.naidoo@caprisa.org.
Kogieleum NaidooCenter for the AIDS Program of Research in South Africa (CAPRISA), Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Nesri PadayatchiCenter for the AIDS Program of Research in South Africa (CAPRISA), Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Kelly E DooleyCenter for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Centre for the AIDS Programme of Research in South Africa · ZAJohns Hopkins Medicine · USUniversity of KwaZulu-Natal · ZA

Funding

Second Generation InSTIs for the Treatment of HIV-1 in patients with TB co-infection on Rifampicin-based Treatment in KwaZulu Natal, South AfricaR01AI152142 · NIAID · CENTRE/AIDS PROGRAMME/RES/SOUTH AFRICA · PI DOOLEY, KELLY E., NAIDOO, ANUSHKA · 2020 to 2024
$2.9M
Mentoring Investigators in HIV and Tuberculosis Therapeutics ResearchK24AI150349 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DOOLEY, KELLY E. · 2020 to 2025
$789k
Dolutegravir for the treatment of HIV in patients with Tuberculosis in KwaZulu-Natal South AfricaK43TW011437 · FIC · CENTRE/AIDS PROGRAMME/RES/SOUTH AFRICA · PI NAIDOO, ANUSHKA · 2019 to 2023
$616k
FIC NIH HHS K43 TW011437NIAID NIH HHS K24 AI150349NIAID NIH HHS R01 AI152142
6 · The paper itself

Abstract

People living with HIV have a higher risk of developing tuberculosis, and tuberculosis is one of the leading causes of death among people living with HIV globally. Treating HIV and tuberculosis concurrently has morbidity and mortality benefits. However, HIV and tuberculosis co-treatment is challenging due to drug-drug interactions, overlapping toxicities, tuberculosis-associated immune reconstitution syndrome, and concerns for treatment failure or drug resistance. Drug-drug interactions between antiretrovirals and tuberculosis drugs are driven mainly by the rifamycins (for example, the first-line tuberculosis drug rifampicin), and dose adjustments or drug switches during co-treatment are commonly required. Several implementation challenges and research gaps exist when combining the integrase strand transfer inhibitors (INSTIs), highly potent antiretroviral drugs recommended as first-line treatment of HIV, and drugs used for the treatment and prevention of tuberculosis. Ongoing and planned studies will address some critical questions on the use of INSTIs in settings with a high tuberculosis burden, including dosing of dolutegravir, bictegravir, and cabotegravir when used with the rifamycins for both tuberculosis treatment and prevention. Failure, in the past, to include people with tuberculosis in HIV clinical treatment trials has been responsible for some of the research gaps still evident for informing optimisation of HIV and tuberculosis co-treatment.

Indexed as

Anti-HIV AgentsHIV InfectionsHIV Integrase InhibitorsTuberculosisAnti-Retroviral AgentsDrug Resistance, ViralHeterocyclic Compounds, 3-RingHumansIntegrase InhibitorsAnti-HIV AgentsAnti-Retroviral AgentsHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsIntegrase Inhibitors

Identifiers

PMID35120633
PMCPMC8970050
OpenAlexW4210547859

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.