Durability and Outcome of Initial Antiretroviral Treatments Received during 2000–2005 by Patients in the Swiss HIV Cohort Study

Background. Little is known about time trends, predictors, and consequences of changes made to antiretroviral therapy (ART) regimens early after patients initially start treatment. Methods. We compared the incidence of, reasons for, and predictors of treatment change within 1 year after starting com...

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Veröffentlicht in:The Journal of infectious diseases 2008-06, Vol.197 (12), p.1685-1694
Hauptverfasser: Vo, Thi Tuyet Nhung, Ledergerber, Bruno, Keiser, Olivia, Hirschel, Bernard, Furrer, Hansjakob, Battegay, Manuel, Cavassini, Matthias, Bernasconi, Enos, Vernazza, Pietro, Weber, Rainer
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container_end_page 1694
container_issue 12
container_start_page 1685
container_title The Journal of infectious diseases
container_volume 197
creator Vo, Thi Tuyet Nhung
Ledergerber, Bruno
Keiser, Olivia
Hirschel, Bernard
Furrer, Hansjakob
Battegay, Manuel
Cavassini, Matthias
Bernasconi, Enos
Vernazza, Pietro
Weber, Rainer
description Background. Little is known about time trends, predictors, and consequences of changes made to antiretroviral therapy (ART) regimens early after patients initially start treatment. Methods. We compared the incidence of, reasons for, and predictors of treatment change within 1 year after starting combination ART (cART), as well as virological and immunological outcomes at 1 year, among 1866 patients from the Swiss HIV Cohort Study who initiated cART during 2000–2001, 2002–2003, or 2004–2005. Results. The durability of initial regimens did not improve over time (P = .15): 48.8% of 625 patients during 2000–2001, 43.8% of 607 during 2002–2003, and 44.3% of 634 during 2004-2005 changed cART within 1 year; reasons for change included intolerance (51.1% of all patients), patient wish (15.4%), physician decision (14.8%), and virological failure (7.1%). An increased probability of treatment change was associated with larger CD4+ cell counts, larger human immunodeficiency virus type 1 (HIV-1) RNA loads, and receipt of regimens that contained stavudine or indinavir/ritonavir, but a decreased probability was associated with receipt of regimens that contained tenofovir. Treatment discontinuation was associated with larger CD4+ cell counts, current use of injection drugs, and receipt of regimens that contained nevirapine. One-year outcomes improved between 2000–2001 and 2004–2005: 84.5% and 92.7% of patients, respectively, reached HIV-1 RNA loads of
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Little is known about time trends, predictors, and consequences of changes made to antiretroviral therapy (ART) regimens early after patients initially start treatment. Methods. We compared the incidence of, reasons for, and predictors of treatment change within 1 year after starting combination ART (cART), as well as virological and immunological outcomes at 1 year, among 1866 patients from the Swiss HIV Cohort Study who initiated cART during 2000–2001, 2002–2003, or 2004–2005. Results. The durability of initial regimens did not improve over time (P = .15): 48.8% of 625 patients during 2000–2001, 43.8% of 607 during 2002–2003, and 44.3% of 634 during 2004-2005 changed cART within 1 year; reasons for change included intolerance (51.1% of all patients), patient wish (15.4%), physician decision (14.8%), and virological failure (7.1%). An increased probability of treatment change was associated with larger CD4+ cell counts, larger human immunodeficiency virus type 1 (HIV-1) RNA loads, and receipt of regimens that contained stavudine or indinavir/ritonavir, but a decreased probability was associated with receipt of regimens that contained tenofovir. Treatment discontinuation was associated with larger CD4+ cell counts, current use of injection drugs, and receipt of regimens that contained nevirapine. One-year outcomes improved between 2000–2001 and 2004–2005: 84.5% and 92.7% of patients, respectively, reached HIV-1 RNA loads of &lt;50 copies/mL and achieved median increases in CD4+ cell counts of 157.5 and 197.5 cells/µL, respectively (P &lt; .001 for all comparisons). Conclusions. Virological and immunological outcomes of initial treatments improved between 2000–2001 and 2004–2005, irrespective of uniformly high rates of early changes in treatment across the 3 study intervals.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/588141</identifier><identifier>PMID: 18513155</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Adult ; Anti-HIV Agents - administration &amp; dosage ; Anti-HIV Agents - therapeutic use ; Antiretrovirals ; Biological and medical sciences ; Carts ; Cohort Studies ; Drug Administration Schedule ; Durability ; Female ; Fundamental and applied biological sciences. Psychology ; Hepatitis B - complications ; Hepatitis B virus ; Hepatitis C - complications ; HIV ; HIV 1 ; HIV Infections - complications ; HIV Infections - drug therapy ; HIV/AIDS ; Human immunodeficiency virus 1 ; Human viral diseases ; Humans ; Immunology ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Middle Aged ; RNA ; Switzerland ; Time Factors ; Treatment Outcome ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. 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Little is known about time trends, predictors, and consequences of changes made to antiretroviral therapy (ART) regimens early after patients initially start treatment. Methods. We compared the incidence of, reasons for, and predictors of treatment change within 1 year after starting combination ART (cART), as well as virological and immunological outcomes at 1 year, among 1866 patients from the Swiss HIV Cohort Study who initiated cART during 2000–2001, 2002–2003, or 2004–2005. Results. The durability of initial regimens did not improve over time (P = .15): 48.8% of 625 patients during 2000–2001, 43.8% of 607 during 2002–2003, and 44.3% of 634 during 2004-2005 changed cART within 1 year; reasons for change included intolerance (51.1% of all patients), patient wish (15.4%), physician decision (14.8%), and virological failure (7.1%). An increased probability of treatment change was associated with larger CD4+ cell counts, larger human immunodeficiency virus type 1 (HIV-1) RNA loads, and receipt of regimens that contained stavudine or indinavir/ritonavir, but a decreased probability was associated with receipt of regimens that contained tenofovir. Treatment discontinuation was associated with larger CD4+ cell counts, current use of injection drugs, and receipt of regimens that contained nevirapine. One-year outcomes improved between 2000–2001 and 2004–2005: 84.5% and 92.7% of patients, respectively, reached HIV-1 RNA loads of &lt;50 copies/mL and achieved median increases in CD4+ cell counts of 157.5 and 197.5 cells/µL, respectively (P &lt; .001 for all comparisons). Conclusions. Virological and immunological outcomes of initial treatments improved between 2000–2001 and 2004–2005, irrespective of uniformly high rates of early changes in treatment across the 3 study intervals.</description><subject>Adult</subject><subject>Anti-HIV Agents - administration &amp; dosage</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Antiretrovirals</subject><subject>Biological and medical sciences</subject><subject>Carts</subject><subject>Cohort Studies</subject><subject>Drug Administration Schedule</subject><subject>Durability</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B virus</topic><topic>Hepatitis C - complications</topic><topic>HIV</topic><topic>HIV 1</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - drug therapy</topic><topic>HIV/AIDS</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunology</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>RNA</topic><topic>Switzerland</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vo, Thi Tuyet Nhung</creatorcontrib><creatorcontrib>Ledergerber, Bruno</creatorcontrib><creatorcontrib>Keiser, Olivia</creatorcontrib><creatorcontrib>Hirschel, Bernard</creatorcontrib><creatorcontrib>Furrer, Hansjakob</creatorcontrib><creatorcontrib>Battegay, Manuel</creatorcontrib><creatorcontrib>Cavassini, Matthias</creatorcontrib><creatorcontrib>Bernasconi, Enos</creatorcontrib><creatorcontrib>Vernazza, Pietro</creatorcontrib><creatorcontrib>Weber, Rainer</creatorcontrib><creatorcontrib>Swiss HIV Cohort Study</creatorcontrib><creatorcontrib>Swiss HIV Cohort Study</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vo, Thi Tuyet Nhung</au><au>Ledergerber, Bruno</au><au>Keiser, Olivia</au><au>Hirschel, Bernard</au><au>Furrer, Hansjakob</au><au>Battegay, Manuel</au><au>Cavassini, Matthias</au><au>Bernasconi, Enos</au><au>Vernazza, Pietro</au><au>Weber, Rainer</au><aucorp>Swiss HIV Cohort Study</aucorp><aucorp>Swiss HIV Cohort Study</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Durability and Outcome of Initial Antiretroviral Treatments Received during 2000–2005 by Patients in the Swiss HIV Cohort Study</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2008-06-15</date><risdate>2008</risdate><volume>197</volume><issue>12</issue><spage>1685</spage><epage>1694</epage><pages>1685-1694</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Background. Little is known about time trends, predictors, and consequences of changes made to antiretroviral therapy (ART) regimens early after patients initially start treatment. Methods. We compared the incidence of, reasons for, and predictors of treatment change within 1 year after starting combination ART (cART), as well as virological and immunological outcomes at 1 year, among 1866 patients from the Swiss HIV Cohort Study who initiated cART during 2000–2001, 2002–2003, or 2004–2005. Results. The durability of initial regimens did not improve over time (P = .15): 48.8% of 625 patients during 2000–2001, 43.8% of 607 during 2002–2003, and 44.3% of 634 during 2004-2005 changed cART within 1 year; reasons for change included intolerance (51.1% of all patients), patient wish (15.4%), physician decision (14.8%), and virological failure (7.1%). An increased probability of treatment change was associated with larger CD4+ cell counts, larger human immunodeficiency virus type 1 (HIV-1) RNA loads, and receipt of regimens that contained stavudine or indinavir/ritonavir, but a decreased probability was associated with receipt of regimens that contained tenofovir. Treatment discontinuation was associated with larger CD4+ cell counts, current use of injection drugs, and receipt of regimens that contained nevirapine. One-year outcomes improved between 2000–2001 and 2004–2005: 84.5% and 92.7% of patients, respectively, reached HIV-1 RNA loads of &lt;50 copies/mL and achieved median increases in CD4+ cell counts of 157.5 and 197.5 cells/µL, respectively (P &lt; .001 for all comparisons). Conclusions. Virological and immunological outcomes of initial treatments improved between 2000–2001 and 2004–2005, irrespective of uniformly high rates of early changes in treatment across the 3 study intervals.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>18513155</pmid><doi>10.1086/588141</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection
subjects Adult
Anti-HIV Agents - administration & dosage
Anti-HIV Agents - therapeutic use
Antiretrovirals
Biological and medical sciences
Carts
Cohort Studies
Drug Administration Schedule
Durability
Female
Fundamental and applied biological sciences. Psychology
Hepatitis B - complications
Hepatitis B virus
Hepatitis C - complications
HIV
HIV 1
HIV Infections - complications
HIV Infections - drug therapy
HIV/AIDS
Human immunodeficiency virus 1
Human viral diseases
Humans
Immunology
Infectious diseases
Male
Medical sciences
Microbiology
Middle Aged
RNA
Switzerland
Time Factors
Treatment Outcome
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Virology
title Durability and Outcome of Initial Antiretroviral Treatments Received during 2000–2005 by Patients in the Swiss HIV Cohort Study
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