Evidence map›Paper›PMID 40275253›Full record

ArticleBMC health services research2025

Integrating HIV advanced disease management into a routine program setting: cohort from Mumbai, India.

Shrikala Acharya, Ramesh Reddy Allam, Vijay Kumar Karanjkar, Dhirubhai Rathod, Prashant Deshpande, Amol Palkar, Shashikant Todmal, Sagar Koli, Sachin Dhande, Nalini Chava and 5 more

Abstract read
In one paragraph

Article in BMC health services research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Shrikala AcharyaMumbai Districts AIDS Control Society, Acworth Complex, R.A. Kidwai Marg, Wadala West, Mumbai, Maharashtra, India.
Ramesh Reddy AllamU.S. Centers for Disease Control and Prevention, Division of Global HIV and Tuberculosis (DGHT), Panchsheel Marg, Shantipath, Chanakyapuri, New Delhi, Delhi, 110021, India. qdj4@cdc.gov.
Vijay Kumar KaranjkarMumbai Districts AIDS Control Society, Acworth Complex, R.A. Kidwai Marg, Wadala West, Mumbai, Maharashtra, India.
Dhirubhai RathodMumbai Districts AIDS Control Society, Acworth Complex, R.A. Kidwai Marg, Wadala West, Mumbai, Maharashtra, India.
Prashant DeshpandeInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Amol PalkarInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Shashikant TodmalInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Sagar KoliInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Sachin DhandeInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Nalini ChavaSociety for Health Allied Research and Education (SHARE INDIA), Ghanpur Village, Medchal Malkajgiri District, Hyderabad, Telangana State, India.
Vijay V YeldandiSociety for Health Allied Research and Education (SHARE INDIA), Ghanpur Village, Medchal Malkajgiri District, Hyderabad, Telangana State, India.
Amit HarshanaInternational Training and Education HIV (I-TECH), 808, 8th Floor, Ansal Bhawan, 16, Kasturba Gandhi Marg, Connaught Place, New Delhi, India.
Reshu AgarwalU.S. Centers for Disease Control and Prevention, Division of Global HIV and Tuberculosis (DGHT), Panchsheel Marg, Shantipath, Chanakyapuri, New Delhi, Delhi, 110021, India.
Sunita UpadhyayaU.S. Centers for Disease Control and Prevention, Division of Global HIV and Tuberculosis (DGHT), Panchsheel Marg, Shantipath, Chanakyapuri, New Delhi, Delhi, 110021, India.
Melissa NyendakU.S. Centers for Disease Control and Prevention, Division of Global HIV and Tuberculosis (DGHT), Panchsheel Marg, Shantipath, Chanakyapuri, New Delhi, Delhi, 110021, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe advanced disease management (ADM) package, which aims to reduce morbidity and mortality in people with Advanced HIV disease (AHD, WHO stage III/IV and/or CD4 count < 200 cells/mm

methodsWe implemented the ADM package (screening, treatment, and prophylaxis for major opportunistic infections, rapid ART initiation, and ART adherence support) in 17 ART centers from October 2020 to December 2021. Treatment naïve and experienced persons with AHD, including children, were enrolled. We assessed the feasibility through coverage of ADM package components and reported the proportion of rapid ART initiation (≤ 7 days), cotrimoxazole prophylaxis, TB preventive treatment (TPT) for those eligible [(excluded active TB disease (n = 280) and those completed TPT prior to enrolment (n = 1,186)], TB-LAM screening (excluded current TB disease), and cryptococcal antigen (CrAg) assay (excluded children < 10 years of age). We used a point of care test for TB (LAM) and cryptococcus (CrAg) screening. We followed the prospective cohort for one year (through 31 July 2022) to document outcomes for survival and lost to follow- up (LTFU).

resultsWe identified 4,334 PLHIV with AHD and provided the full ADM package to 64% (2,779/4,334); 297 did not receive ADM (146 died, 151 LTFU), and 1,258 received routine standard of care (587 had TB, 366 were at decentralized sites, and 305 LAM/CrAg kits were not available) with existing ART center staff. Nearly 78% (385/494) of treatment naïve were rapidly initiated on ART. Nearly 82% (1,129/1,383) and 99% (2,751/2,779) received TPT and cotrimoxazole prophylaxis, respectively. Of the eligible, 99% (2,508/2,524) and 98% (2,715/2,758) were screened for TB and cryptococcal infection, respectively. At the end of 12 months, 88% (2,458/2,779) were alive, 8% (210/2,779) died, and 4% (111/2,779) were LTFU. Mean survival time was significantly (p < 0.001) higher among treatment experienced people; 11.6 months (95% CI: 11.5,11.7) compared to treatment naïve people 10.8 months (95% CI: 10.5,11.0).

conclusionWith careful anticipatory planning, stakeholder engagement, and training, implementing the full ADM package is feasible in a routine program setting with existing human resources. Additional intensive case management may be necessary for the reduction of mortality among treatment naïve PLHIV.

Indexed as

Disease ManagementHIV InfectionsAdultAIDS-Related Opportunistic InfectionsAnti-HIV AgentsCD4 Lymphocyte CountChild, PreschoolCohort StudiesFemaleHumansIndiaMaleMiddle AgedTrimethoprim, Sulfamethoxazole Drug CombinationAnti-HIV AgentsTrimethoprim, Sulfamethoxazole Drug CombinationAdvanced disease managementAdvanced HIV diseaseHIV survivalMortality

Identifiers

PMID40275253
PMCPMC12023558

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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.