Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment

Objectives: Virological failure on first-line nonnucleoside reverse transcriptase inhibitor (NNRTI)-based treatment regimens has become a problem in HIV-infected children on long-term antiretroviral therapy (ART). Protease inhibitor (PI)-based regimens are therefore often given to children failing N...

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Main Authors: N. Wattanutchariya, V. Sirisanthana, P. Oberdorfer
Format: Journal
Published: 2018
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874544986&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/48021
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spelling th-cmuir.6653943832-480212018-04-25T08:46:45Z Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment N. Wattanutchariya V. Sirisanthana P. Oberdorfer Objectives: Virological failure on first-line nonnucleoside reverse transcriptase inhibitor (NNRTI)-based treatment regimens has become a problem in HIV-infected children on long-term antiretroviral therapy (ART). Protease inhibitor (PI)-based regimens are therefore often given to children failing NNRTI-based regimens. The aim of the study was to assess the 48-week effectiveness, safety and predictive factors for viral suppression of PI-based regimens in HIV-infected Thai children who had failed NNRTI-based regimens. Methods: This study assessed 41 HIV-infected children who had failed first-line NNRTI-based regimens and were switched to PI-based regimens for at least 48 weeks. We assessed their CD4 cell counts, plasma HIV RNA levels, weight-for-age and height-for-age z-scores, and adverse events. Results: The children's median age was 9.5 years (range 1.5-15.8 years). At baseline, their median CD4 cell count was 276 cells/μL [interquartile range (IQR) 160-749 cells/μL], and their median plasma HIV RNA level was 4.5 log 10 HIV-1 RNA copies/mL (IQR 3.9-4.8 log 10 copies/mL). After 48 weeks of PI-based therapy, their CD4 cell counts increased to a median of 572 cells/μL (IQR 343-845 cells/μL) and in 73.2% plasma HIV RNA levels decreased to < 50 copies/mL. Their median weight-for-age and height-for-age z-scores were stable over the period of the study. Diarrhoea occurred in 29.3% of patients. Triglyceride levels were significantly higher at weeks 24 and 48 in comparison to baseline measurements. Conclusions: PI-based regimens are safe and effective for HIV-infected Thai children who have failed first-line NNRTI-based regimens. However, long-term follow-up is warranted in order to ascertain the feasibility and sustainability of these new regimens. © 2012 British HIV Association. 2018-04-25T08:46:45Z 2018-04-25T08:46:45Z 2013-04-01 Journal 14681293 14642662 2-s2.0-84874544986 10.1111/j.1468-1293.2012.01061.x https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874544986&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48021
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description Objectives: Virological failure on first-line nonnucleoside reverse transcriptase inhibitor (NNRTI)-based treatment regimens has become a problem in HIV-infected children on long-term antiretroviral therapy (ART). Protease inhibitor (PI)-based regimens are therefore often given to children failing NNRTI-based regimens. The aim of the study was to assess the 48-week effectiveness, safety and predictive factors for viral suppression of PI-based regimens in HIV-infected Thai children who had failed NNRTI-based regimens. Methods: This study assessed 41 HIV-infected children who had failed first-line NNRTI-based regimens and were switched to PI-based regimens for at least 48 weeks. We assessed their CD4 cell counts, plasma HIV RNA levels, weight-for-age and height-for-age z-scores, and adverse events. Results: The children's median age was 9.5 years (range 1.5-15.8 years). At baseline, their median CD4 cell count was 276 cells/μL [interquartile range (IQR) 160-749 cells/μL], and their median plasma HIV RNA level was 4.5 log 10 HIV-1 RNA copies/mL (IQR 3.9-4.8 log 10 copies/mL). After 48 weeks of PI-based therapy, their CD4 cell counts increased to a median of 572 cells/μL (IQR 343-845 cells/μL) and in 73.2% plasma HIV RNA levels decreased to < 50 copies/mL. Their median weight-for-age and height-for-age z-scores were stable over the period of the study. Diarrhoea occurred in 29.3% of patients. Triglyceride levels were significantly higher at weeks 24 and 48 in comparison to baseline measurements. Conclusions: PI-based regimens are safe and effective for HIV-infected Thai children who have failed first-line NNRTI-based regimens. However, long-term follow-up is warranted in order to ascertain the feasibility and sustainability of these new regimens. © 2012 British HIV Association.
format Journal
author N. Wattanutchariya
V. Sirisanthana
P. Oberdorfer
spellingShingle N. Wattanutchariya
V. Sirisanthana
P. Oberdorfer
Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
author_facet N. Wattanutchariya
V. Sirisanthana
P. Oberdorfer
author_sort N. Wattanutchariya
title Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
title_short Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
title_full Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
title_fullStr Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
title_full_unstemmed Effectiveness and safety of protease inhibitor-based regimens in HIV-infected Thai children failing first-line treatment
title_sort effectiveness and safety of protease inhibitor-based regimens in hiv-infected thai children failing first-line treatment
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874544986&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/48021
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