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Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients

BACKGROUND: Switch from first line antiretroviral therapy (ART) to second-line ART is common in clinical practice. However, there is limited knowledge of to which extent different reason for therapy switch are associated with differences in long-term consequences and sustainability of the second lin...

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Autores principales: Häggblom, Amanda, Santacatterina, Michele, Neogi, Ujjwal, Gisslen, Magnus, Hejdeman, Bo, Flamholc, Leo, Sönnerborg, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519043/
https://www.ncbi.nlm.nih.gov/pubmed/28727795
http://dx.doi.org/10.1371/journal.pone.0180140
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author Häggblom, Amanda
Santacatterina, Michele
Neogi, Ujjwal
Gisslen, Magnus
Hejdeman, Bo
Flamholc, Leo
Sönnerborg, Anders
author_facet Häggblom, Amanda
Santacatterina, Michele
Neogi, Ujjwal
Gisslen, Magnus
Hejdeman, Bo
Flamholc, Leo
Sönnerborg, Anders
author_sort Häggblom, Amanda
collection PubMed
description BACKGROUND: Switch from first line antiretroviral therapy (ART) to second-line ART is common in clinical practice. However, there is limited knowledge of to which extent different reason for therapy switch are associated with differences in long-term consequences and sustainability of the second line ART. MATERIAL AND METHODS: Data from 869 patients with 14601 clinical visits between 1999–2014 were derived from the national cohort database. Reason for therapy switch and viral load (VL) levels at first-line ART failure were compared with regard to outcome of second line ART. Using the Laplace regression model we analyzed the median, 10(th), 20(th), 30(th) and 40(th) percentile of time to viral failure (VF). RESULTS: Most patients (n = 495; 57.0%) switched from first-line to second-line ART without VF. Patients switching due to detectable VL with (n = 124; 14.2%) or without drug resistance mutations (DRM) (n = 250; 28.8%) experienced VF to their second line regimen sooner (median time, years: 3.43 (95% CI 2.90–3.96) and 3.20 (95% 2.65–3.75), respectively) compared with those who switched without VF (4.53 years). Furthermore level of VL at first-line ART failure had a significant impact on failure of second-line ART starting after 2.5 years of second-line ART. CONCLUSIONS: In the context of life-long therapy, a median time on second line ART of 4.53 years for these patients is short. To prolong time on second-line ART, further studies are needed on the reasons for therapy changes. Additionally patients with a high VL at first-line VF should be more frequently monitored the period after the therapy switch.
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spelling pubmed-55190432017-08-07 Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients Häggblom, Amanda Santacatterina, Michele Neogi, Ujjwal Gisslen, Magnus Hejdeman, Bo Flamholc, Leo Sönnerborg, Anders PLoS One Research Article BACKGROUND: Switch from first line antiretroviral therapy (ART) to second-line ART is common in clinical practice. However, there is limited knowledge of to which extent different reason for therapy switch are associated with differences in long-term consequences and sustainability of the second line ART. MATERIAL AND METHODS: Data from 869 patients with 14601 clinical visits between 1999–2014 were derived from the national cohort database. Reason for therapy switch and viral load (VL) levels at first-line ART failure were compared with regard to outcome of second line ART. Using the Laplace regression model we analyzed the median, 10(th), 20(th), 30(th) and 40(th) percentile of time to viral failure (VF). RESULTS: Most patients (n = 495; 57.0%) switched from first-line to second-line ART without VF. Patients switching due to detectable VL with (n = 124; 14.2%) or without drug resistance mutations (DRM) (n = 250; 28.8%) experienced VF to their second line regimen sooner (median time, years: 3.43 (95% CI 2.90–3.96) and 3.20 (95% 2.65–3.75), respectively) compared with those who switched without VF (4.53 years). Furthermore level of VL at first-line ART failure had a significant impact on failure of second-line ART starting after 2.5 years of second-line ART. CONCLUSIONS: In the context of life-long therapy, a median time on second line ART of 4.53 years for these patients is short. To prolong time on second-line ART, further studies are needed on the reasons for therapy changes. Additionally patients with a high VL at first-line VF should be more frequently monitored the period after the therapy switch. Public Library of Science 2017-07-20 /pmc/articles/PMC5519043/ /pubmed/28727795 http://dx.doi.org/10.1371/journal.pone.0180140 Text en © 2017 Häggblom et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Häggblom, Amanda
Santacatterina, Michele
Neogi, Ujjwal
Gisslen, Magnus
Hejdeman, Bo
Flamholc, Leo
Sönnerborg, Anders
Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title_full Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title_fullStr Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title_full_unstemmed Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title_short Effect of therapy switch on time to second-line antiretroviral treatment failure in HIV-infected patients
title_sort effect of therapy switch on time to second-line antiretroviral treatment failure in hiv-infected patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519043/
https://www.ncbi.nlm.nih.gov/pubmed/28727795
http://dx.doi.org/10.1371/journal.pone.0180140
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