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Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana
OBJECTIVE: Tenofovir disoproxil fumarate (TDF) is a nucleotide analogue recommended in international HIV treatment guidelines. Purpose of this study was to estimate the long term effects of TDF on renal profile in a cohort of HIV patients in Ghana. Three hundred (300) consecutive HIV-positive patien...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647254/ https://www.ncbi.nlm.nih.gov/pubmed/31331365 http://dx.doi.org/10.1186/s13104-019-4454-2 |
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author | Nartey, Edmund T. Tetteh, Raymond A. Yankey, Barbara A. Mantel-Teeuwisse, Aukje K. Leufkens, Hubert G. M. Dodoo, Alexander N. O. Lartey, Margaret |
author_facet | Nartey, Edmund T. Tetteh, Raymond A. Yankey, Barbara A. Mantel-Teeuwisse, Aukje K. Leufkens, Hubert G. M. Dodoo, Alexander N. O. Lartey, Margaret |
author_sort | Nartey, Edmund T. |
collection | PubMed |
description | OBJECTIVE: Tenofovir disoproxil fumarate (TDF) is a nucleotide analogue recommended in international HIV treatment guidelines. Purpose of this study was to estimate the long term effects of TDF on renal profile in a cohort of HIV patients in Ghana. Three hundred (300) consecutive HIV-positive patients who initiated TDF-based antiretroviral treatment in 2008 at the Korle-Bu Teaching Hospital were sampled. Creatinine clearance (CrCl) was calculated using the Cockcroft-Gault equation at baseline and renal impairment was defined as CrCl values of 30.0–49.9 mL/min (moderate renal impairment) and < 30 mL/min (severe renal impairment) as per institutional guidelines for renal function test. RESULTS: Median follow up time was 2.9 years (IQR 2.3–3.4 years). At study endpoint, 63 participants (21.0% [95% CI 6.5–26.1]) recorded CrCl rate below 50 mL/min indicating incident renal impairment, made up of 18.3% moderate renal impairment and 2.3% severe renal impairment. Factors associated with incidence of renal impairment were increasing age, decrease in creatinine clearance rate at baseline, WHO HIV stage III/IV and participants with BMI of < 18.5 kg/m(2). Patients with identified renal impairment risk factors at ART initiation should be targeted and monitored effectively to prevent renal injury. |
format | Online Article Text |
id | pubmed-6647254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66472542019-07-31 Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana Nartey, Edmund T. Tetteh, Raymond A. Yankey, Barbara A. Mantel-Teeuwisse, Aukje K. Leufkens, Hubert G. M. Dodoo, Alexander N. O. Lartey, Margaret BMC Res Notes Research Note OBJECTIVE: Tenofovir disoproxil fumarate (TDF) is a nucleotide analogue recommended in international HIV treatment guidelines. Purpose of this study was to estimate the long term effects of TDF on renal profile in a cohort of HIV patients in Ghana. Three hundred (300) consecutive HIV-positive patients who initiated TDF-based antiretroviral treatment in 2008 at the Korle-Bu Teaching Hospital were sampled. Creatinine clearance (CrCl) was calculated using the Cockcroft-Gault equation at baseline and renal impairment was defined as CrCl values of 30.0–49.9 mL/min (moderate renal impairment) and < 30 mL/min (severe renal impairment) as per institutional guidelines for renal function test. RESULTS: Median follow up time was 2.9 years (IQR 2.3–3.4 years). At study endpoint, 63 participants (21.0% [95% CI 6.5–26.1]) recorded CrCl rate below 50 mL/min indicating incident renal impairment, made up of 18.3% moderate renal impairment and 2.3% severe renal impairment. Factors associated with incidence of renal impairment were increasing age, decrease in creatinine clearance rate at baseline, WHO HIV stage III/IV and participants with BMI of < 18.5 kg/m(2). Patients with identified renal impairment risk factors at ART initiation should be targeted and monitored effectively to prevent renal injury. BioMed Central 2019-07-22 /pmc/articles/PMC6647254/ /pubmed/31331365 http://dx.doi.org/10.1186/s13104-019-4454-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Nartey, Edmund T. Tetteh, Raymond A. Yankey, Barbara A. Mantel-Teeuwisse, Aukje K. Leufkens, Hubert G. M. Dodoo, Alexander N. O. Lartey, Margaret Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title | Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title_full | Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title_fullStr | Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title_full_unstemmed | Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title_short | Tenofovir-associated renal toxicity in a cohort of HIV infected patients in Ghana |
title_sort | tenofovir-associated renal toxicity in a cohort of hiv infected patients in ghana |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647254/ https://www.ncbi.nlm.nih.gov/pubmed/31331365 http://dx.doi.org/10.1186/s13104-019-4454-2 |
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