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Long-term treatment of patients with HIV-1: the role of atazanavir

BACKGROUND: The introduction of highly-active antiretroviral therapy (HAART) remains a major milestone in the management of HIV-infected patients. Protease inhibitors (PI) are commonly used as part of triple combinations, given that to antiviral potency, better tolerance and convenience has been ach...

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Autores principales: Artacho, Miguel Ángel, Barreiro, Pablo, Fernández-Montero, José Vicente
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218682/
https://www.ncbi.nlm.nih.gov/pubmed/22096394
http://dx.doi.org/10.2147/HIV.S5069
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author Artacho, Miguel Ángel
Barreiro, Pablo
Fernández-Montero, José Vicente
author_facet Artacho, Miguel Ángel
Barreiro, Pablo
Fernández-Montero, José Vicente
author_sort Artacho, Miguel Ángel
collection PubMed
description BACKGROUND: The introduction of highly-active antiretroviral therapy (HAART) remains a major milestone in the management of HIV-infected patients. Protease inhibitors (PI) are commonly used as part of triple combinations, given that to antiviral potency, better tolerance and convenience has been achieved in recent years. OBJECTIVE: To summarize and update evidence-based information about atazanavir (ATV) on initial, simplification, and rescue interventions in HIV patients. METHODS: Review of observational and randomized trials reported in medical conferences, peer-reviewed journals, and treatment guidelines. RESULTS: ATV is a second-generation PI, which has shown across studies potent antiviral activity and high genetic barrier, both in HAART-naïve patients or after virological failure. Indulgent metabolic profile, in terms of insulin glucose and lipid levels, adds value to this drug for the long-term management of HIV infection.
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spelling pubmed-32186822011-11-17 Long-term treatment of patients with HIV-1: the role of atazanavir Artacho, Miguel Ángel Barreiro, Pablo Fernández-Montero, José Vicente HIV AIDS (Auckl) Review BACKGROUND: The introduction of highly-active antiretroviral therapy (HAART) remains a major milestone in the management of HIV-infected patients. Protease inhibitors (PI) are commonly used as part of triple combinations, given that to antiviral potency, better tolerance and convenience has been achieved in recent years. OBJECTIVE: To summarize and update evidence-based information about atazanavir (ATV) on initial, simplification, and rescue interventions in HIV patients. METHODS: Review of observational and randomized trials reported in medical conferences, peer-reviewed journals, and treatment guidelines. RESULTS: ATV is a second-generation PI, which has shown across studies potent antiviral activity and high genetic barrier, both in HAART-naïve patients or after virological failure. Indulgent metabolic profile, in terms of insulin glucose and lipid levels, adds value to this drug for the long-term management of HIV infection. Dove Medical Press 2010-09-13 /pmc/articles/PMC3218682/ /pubmed/22096394 http://dx.doi.org/10.2147/HIV.S5069 Text en © 2010 Artacho et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Artacho, Miguel Ángel
Barreiro, Pablo
Fernández-Montero, José Vicente
Long-term treatment of patients with HIV-1: the role of atazanavir
title Long-term treatment of patients with HIV-1: the role of atazanavir
title_full Long-term treatment of patients with HIV-1: the role of atazanavir
title_fullStr Long-term treatment of patients with HIV-1: the role of atazanavir
title_full_unstemmed Long-term treatment of patients with HIV-1: the role of atazanavir
title_short Long-term treatment of patients with HIV-1: the role of atazanavir
title_sort long-term treatment of patients with hiv-1: the role of atazanavir
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218682/
https://www.ncbi.nlm.nih.gov/pubmed/22096394
http://dx.doi.org/10.2147/HIV.S5069
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