# Kidney disease screening at ART initiation among adults with HIV in Uganda: A missed priority for a high-risk population

**Authors:** Grace Kansiime, Joseph Baruch Baluku, Edwin Nuwagira, Michael Kanyesigye, Paul Stephen Obwoya, Rose Muhindo, Winnie R. Muyindike, Pliers Denis Tusingwire, Henry Mugerwa, Matthew Odera, Monday Busuulwa, Matthew Ssemakadde, Esther C. Atukunda, Francis Bajunirwe, Robert Kalyesubula, Mark J. Siedner

PMC · DOI: 10.1371/journal.pgph.0005106 · PLOS Global Public Health · 2026-02-02

## TL;DR

This study finds that kidney disease screening for people with HIV at the start of treatment is very low in Uganda, especially in rural areas, despite national guidelines.

## Contribution

The study provides new evidence on the poor adherence to kidney disease screening guidelines for HIV patients in Uganda, particularly in rural clinics.

## Key findings

- Only 22.4% of HIV patients were screened for kidney disease at ART initiation.
- Screening rates were significantly higher in urban clinics compared to rural clinics.
- Screening decreased over time in rural clinics despite updated national guidelines.

## Abstract

Kidney disease affects 850 million people worldwide, with Sub-Saharan Africa bearing a significant burden. People living with HIV (PWH) are at increased risk due to nephrotoxicity of antiretroviral therapy (ART), in part due to widespread use of tenofovir disoproxil fumarate. In response, Uganda recommends routine kidney disease screening by doing a serum creatinine test at ART initiation. However, the extent of adherence to these guidelines remains poorly understood. We extracted clinical data for adults initiating ART between 2017 and 2024 at three large-volume HIV clinics in Uganda. To determine if kidney disease screening rates had increased appropriately over time, we divided the observation period into three eras as per national guidelines: (1) Test and Treat (2017–2019), that recommended screening only PWH and diabetes or hypertension; (2) DTG rollout/COVID-19 (2020–2022); and (3) creatinine-for-all (2023–2024), recommending screening everyone initiating ART. Logistic regression models were fit to identify correlates of renal screening. Of the 17,485 participants, only 22.4% (3,909/17,485) were screened for kidney disease at ART initiation. Screening was more common at the urban site (54.2%) compared to rural sites (10.0%). At rural sites, screening declined over time and individuals were 83% less likely to be screened in the creatinine-for-all era compared to the baseline era (aOR 0.17, 95% CI: 0.13–0.22) while it increased at urban site (aOR 9.27, 95% CI: 7.37–11.66). Male sex (aOR 1.37, 95% CI: 1.20–1.57), older age (≥45 years), hypertension, and non–TDF-based ART regimens were associated with higher screening odds at rural sites. Diabetes, opportunistic infections, and TDF use were not significantly associated with screening likelihood at any site. Kidney disease screening for PWH at ART initiation remains poor in Uganda, even when using a single creatinine test, particularly in rural clinics, highlighting critical challenges in translating national guidelines into practice. Future research should focus on understanding multilevel barriers to screening and evaluating strategies to improve guideline uptake.

## Linked entities

- **Chemicals:** tenofovir disoproxil fumarate (PubChem CID 5486830)
- **Diseases:** kidney disease (MONDO:0001343), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, APOL1 (apolipoprotein L1) [NCBI Gene 8542] {aka APO-L, APOL, APOL-I, FSGS4}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** CKD (MESH:D051436), HIV-associated opportunistic infections (MESH:D017088), ISS (OMIM:146850), Kidney disease (MESH:D007674), dyslipidemia (MESH:D050171), sickle cell trait (MESH:D012805), bone disorders (MESH:D001847), COVID-19 (MESH:D000086382), opportunistic infections (MESH:D009894), Diabetes (MESH:D003920), DM (MESH:D009223), malaria (MESH:D008288), cardiovascular disease (MESH:D002318), cognitive decline (MESH:D003072), hepatitis B and C (MESH:D006509), TB (MESH:D014390), HIV (MESH:D015658), cryptococcal meningitis (MESH:D016919), tuberculosis (MESH:D014376), infections (MESH:D007239), PWH (MESH:C000719191), schistosomiasis (MESH:D012552), Kaposi sarcoma (MESH:D012514), hypertension (MESH:D006973)
- **Chemicals:** alcohol (MESH:D000438), DTG (MESH:C562325), Tenofovir Lamivudine (-), creatinine (MESH:D003404), TDF (MESH:D000068698), Efavirenz (MESH:C098320), lamivudine (MESH:D019259)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12863478/full.md

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Source: https://tomesphere.com/paper/PMC12863478