Evidence map›Paper›PMID 41126082›Full record

Observational studyBMC infectious diseases2025

Decline in estimated glomerular filtration rate following substitution of Nevirapine-based regimen with Tenofovir-based regimen in Indonesia.

Evy Yunihastuti, Pringgodigdo Nugroho, Muhammad Yusuf, Salfia Dian Lastari, Fadlika Harinda, Tiara Kumala Putri, Meivina Ramadhani Pane, Metra Adi Pratama, Mira Yulianti, Alvina Widhani and 5 more

Abstract readObservational Study
In one paragraph

Observational study in BMC infectious diseases, 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. Observational
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.

Evy YunihastutiDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia. evy.yunihastuti@gmail.com.ORCID http://orcid.org/0000-0001-6650-0559
Pringgodigdo NugrohoDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0002-5045-6562
Muhammad YusufHIV Integrated Unit, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0002-9599-1825
Salfia Dian LastariHIV Integrated Unit, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Fadlika HarindaHIV Integrated Unit, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Tiara Kumala PutriHIV Integrated Unit, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Meivina Ramadhani PaneDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Metra Adi PratamaDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Mira YuliantiDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Alvina WidhaniDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.
Suzy MariaDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0001-6951-1480
Anshari Saifuddin HasibuanDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0003-4331-2381
Maruhum Bonar Hasiholan MarbunDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0001-7505-0289
Sukamto KoesnoeDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.ORCID http://orcid.org/0000-0002-7941-7743
Teguh Harjono KarjadiDepartment of Internal Medicine, Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Diponegoro 71 Senen, Jakarta, 10430, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndonesia started transitioning people living with HIV (PLHIV) from Nevirapine (NVP)-based antiretroviral therapy to tenofovir (TDF)-lamivudine-dolutegravir fixed-dose combination (TLD) in 2023. We aimed to evaluate changes in estimated glomerular filtration rate (eGFR) and predictors of rapid eGFR decline within 6 months during this programmatic dolutegravir (DTG) transition.

methodsThis prospective observational study included all adult PLHIV (≥ 18 years old) who received an NVP-based regimen initially, had baseline eGFR of more than 60 mL/min/1.73m2 before the transition, and underwent the DTG transition program in Cipto Mangunkusumo Hospital from March 2023 to January 2024. Participants who did not have at least two eGFR measurements were not included in the study. The decline in the eGFR during the study period was defined by a minimum 25% eGFR decline from baseline, and multivariate regression was used for analysis.

resultsA total of 329 participants were transitioned to TLD. Of these patients, 242 (73.6%) transitioned from the zidovudine-lamivudine fixed-dose combination and NVP (AZT/3TC+NVP), and 87 (26.4%) transitioned from TDF+3TC+NVP. Within six months of observation, 87.2% of participants had eGFR decline. Sixty-one participants (18.5%) experienced rapid eGFR decline: 19.8% and 14.9% in those who had previously used AZT and TDF, respectively. Factors related to rapid eGFR decline were hypertension (aRR 1.87; 95% CI: 1.15 – 3.05) and longer usage of previous ART (aRR 1.05; 95% CI: 1.01 – 1.10).

conclusionRapid eGFR decline after transitioning from an NVP-based regimen to TLD warrants close monitoring, especially in patients with hypertension and longer use of ART.

Indexed as

Anti-HIV AgentsDrug SubstitutionGlomerular Filtration RateHIV InfectionsNevirapineTenofovirAdultDolutegravirDrug CombinationsFemaleHeterocyclic Compounds, 3-RingHumansIndonesiaLamivudineMaleMiddle AgedAnti-HIV AgentsDolutegravirDrug CombinationsHeterocyclic Compounds, 3-RingLamivudineNevirapineOxazinesPiperazinesPyridonesTenofovirZidovudineARTDolutegravirDrug substitutionHIVKidney functionNevirapineTenofovir

Identifiers

PMID41126082
PMCPMC12542238

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.