Long-term safety and effectiveness of lopinavir/ritonavir in antiretroviral-experienced HIV-1-infected children

Aim To evaluate the long-term safety and effectiveness of lopinavir/ritonavir (LPV/r) in a population-based cohort of HIV-1-infected children. Methods All children enrolled in the Swiss Mother and Child HIV Cohort Study, treated with LPV/r-based combination antiretroviral treatment (cART) between No...

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Veröffentlicht in:Archives of disease in childhood 2010-06, Vol.95 (6), p.478-481
Hauptverfasser: Rudin, Christoph, Wolbers, Marcel, Nadal, David, Rickenbach, Martin, Bucher, Heiner C
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container_end_page 481
container_issue 6
container_start_page 478
container_title Archives of disease in childhood
container_volume 95
creator Rudin, Christoph
Wolbers, Marcel
Nadal, David
Rickenbach, Martin
Bucher, Heiner C
description Aim To evaluate the long-term safety and effectiveness of lopinavir/ritonavir (LPV/r) in a population-based cohort of HIV-1-infected children. Methods All children enrolled in the Swiss Mother and Child HIV Cohort Study, treated with LPV/r-based combination antiretroviral treatment (cART) between November 2000 and October 2008, were included. Results 88 children (25 (28%) protease inhibitor (PI)-naive, 16 (18%) ART-naive) were analysed (251 patient-years on LPV/r). After 48 weeks on LPV/r, 70 children had a median (interquartile range (IQR)) decrease in HIV-1 viral load of 4.25 log (5.45–3.17; PI-naive, n=17) and 2.53 (3.68–1.38; PI-experienced, n=53). Median (IQR) increase in CD4 count was 429 (203–593; PI-naive) and 177 (21–331; PI-experienced) cells/µl. These effects remained stablethroughout 192 weeks for 25 children. Treatment was stopped for viral rebound in seven and suspected toxicity in 12 children. Conclusion Long-term treatment with LPV/r-based cART is safe and effective in HIV-1-infected children.
doi_str_mv 10.1136/adc.2009.169375
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Methods All children enrolled in the Swiss Mother and Child HIV Cohort Study, treated with LPV/r-based combination antiretroviral treatment (cART) between November 2000 and October 2008, were included. Results 88 children (25 (28%) protease inhibitor (PI)-naive, 16 (18%) ART-naive) were analysed (251 patient-years on LPV/r). After 48 weeks on LPV/r, 70 children had a median (interquartile range (IQR)) decrease in HIV-1 viral load of 4.25 log (5.45–3.17; PI-naive, n=17) and 2.53 (3.68–1.38; PI-experienced, n=53). Median (IQR) increase in CD4 count was 429 (203–593; PI-naive) and 177 (21–331; PI-experienced) cells/µl. These effects remained stablethroughout 192 weeks for 25 children. Treatment was stopped for viral rebound in seven and suspected toxicity in 12 children. Conclusion Long-term treatment with LPV/r-based cART is safe and effective in HIV-1-infected children.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/adc.2009.169375</identifier><identifier>PMID: 20501542</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Adolescent ; Antiretroviral agents ; Biological and medical sciences ; CD4 Lymphocyte Count ; Child ; Child, Preschool ; Children ; Data Analysis ; Diseases ; Drug therapy ; Drug Therapy, Combination ; Female ; Follow-Up Studies ; General aspects ; Health aspects ; HIV infection ; HIV infections ; HIV Infections - drug therapy ; HIV Infections - immunology ; HIV Infections - virology ; HIV Protease Inhibitors - adverse effects ; HIV Protease Inhibitors - therapeutic use ; HIV-1 - isolation &amp; purification ; Human viral diseases ; Humans ; Immunology ; Infectious diseases ; Lopinavir ; Male ; Medical sciences ; Miscellaneous ; Observation ; Patients ; Pediatric diseases ; Prevention and actions ; Prospective Studies ; Proteinase inhibitors ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Pyrimidinones - adverse effects ; Pyrimidinones - therapeutic use ; Ritonavir ; Ritonavir - adverse effects ; Ritonavir - therapeutic use ; Treatment Outcome ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral Load</subject><ispartof>Archives of disease in childhood, 2010-06, Vol.95 (6), p.478-481</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2010 Published by the BMJ Publishing Group Limited. 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Methods All children enrolled in the Swiss Mother and Child HIV Cohort Study, treated with LPV/r-based combination antiretroviral treatment (cART) between November 2000 and October 2008, were included. Results 88 children (25 (28%) protease inhibitor (PI)-naive, 16 (18%) ART-naive) were analysed (251 patient-years on LPV/r). After 48 weeks on LPV/r, 70 children had a median (interquartile range (IQR)) decrease in HIV-1 viral load of 4.25 log (5.45–3.17; PI-naive, n=17) and 2.53 (3.68–1.38; PI-experienced, n=53). Median (IQR) increase in CD4 count was 429 (203–593; PI-naive) and 177 (21–331; PI-experienced) cells/µl. These effects remained stablethroughout 192 weeks for 25 children. Treatment was stopped for viral rebound in seven and suspected toxicity in 12 children. Conclusion Long-term treatment with LPV/r-based cART is safe and effective in HIV-1-infected children.</description><subject>Adolescent</subject><subject>Antiretroviral agents</subject><subject>Biological and medical sciences</subject><subject>CD4 Lymphocyte Count</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Data Analysis</subject><subject>Diseases</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>General aspects</subject><subject>Health aspects</subject><subject>HIV infection</subject><subject>HIV infections</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - immunology</subject><subject>HIV Infections - virology</subject><subject>HIV Protease Inhibitors - adverse effects</subject><subject>HIV Protease Inhibitors - therapeutic use</subject><subject>HIV-1 - isolation &amp; purification</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infectious diseases</subject><subject>Lopinavir</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Observation</subject><subject>Patients</subject><subject>Pediatric diseases</subject><subject>Prevention and actions</subject><subject>Prospective Studies</subject><subject>Proteinase inhibitors</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Pyrimidinones - adverse effects</subject><subject>Pyrimidinones - therapeutic use</subject><subject>Ritonavir</subject><subject>Ritonavir - adverse effects</subject><subject>Ritonavir - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Methods All children enrolled in the Swiss Mother and Child HIV Cohort Study, treated with LPV/r-based combination antiretroviral treatment (cART) between November 2000 and October 2008, were included. Results 88 children (25 (28%) protease inhibitor (PI)-naive, 16 (18%) ART-naive) were analysed (251 patient-years on LPV/r). After 48 weeks on LPV/r, 70 children had a median (interquartile range (IQR)) decrease in HIV-1 viral load of 4.25 log (5.45–3.17; PI-naive, n=17) and 2.53 (3.68–1.38; PI-experienced, n=53). Median (IQR) increase in CD4 count was 429 (203–593; PI-naive) and 177 (21–331; PI-experienced) cells/µl. These effects remained stablethroughout 192 weeks for 25 children. Treatment was stopped for viral rebound in seven and suspected toxicity in 12 children. Conclusion Long-term treatment with LPV/r-based cART is safe and effective in HIV-1-infected children.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><pmid>20501542</pmid><doi>10.1136/adc.2009.169375</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Antiretroviral agents
Biological and medical sciences
CD4 Lymphocyte Count
Child
Child, Preschool
Children
Data Analysis
Diseases
Drug therapy
Drug Therapy, Combination
Female
Follow-Up Studies
General aspects
Health aspects
HIV infection
HIV infections
HIV Infections - drug therapy
HIV Infections - immunology
HIV Infections - virology
HIV Protease Inhibitors - adverse effects
HIV Protease Inhibitors - therapeutic use
HIV-1 - isolation & purification
Human viral diseases
Humans
Immunology
Infectious diseases
Lopinavir
Male
Medical sciences
Miscellaneous
Observation
Patients
Pediatric diseases
Prevention and actions
Prospective Studies
Proteinase inhibitors
Public health. Hygiene
Public health. Hygiene-occupational medicine
Pyrimidinones - adverse effects
Pyrimidinones - therapeutic use
Ritonavir
Ritonavir - adverse effects
Ritonavir - therapeutic use
Treatment Outcome
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral Load
title Long-term safety and effectiveness of lopinavir/ritonavir in antiretroviral-experienced HIV-1-infected children
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