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Second-line antiretroviral therapy in resource-limited settings: the experience of Médecins Sans Frontières

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dc.contributor Epicentre, Paris, France; Médecins Sans Frontières, Paris, France; Campaign for Access to Essential Medicines, Geneva, Switzerland
dc.creator Pujades-Rodriguez, M
dc.creator O'Brien, D
dc.creator Humblet, P
dc.creator Calmy, A
dc.date 2008-07-11
dc.date.accessioned 2017-01-31T07:11:42Z
dc.date.available 2017-01-31T07:11:42Z
dc.identifier AIDS 2008;22(11):1305-12
dc.identifier 1473-5571
dc.identifier 18580610
dc.identifier 10.1097/QAD.0b013e3282fa75b9
dc.identifier http://hdl.handle.net/10144/33194
dc.identifier http://fieldresearch.msf.org/msf/handle/10144/33194
dc.identifier AIDS (London, England)
dc.identifier.uri http://dspace.mediu.edu.my:8181/xmlui/handle/10144/33194
dc.description OBJECTIVES: To describe the use of second-line protease-inhibitor regimens in Médecins Sans Frontières HIV programmes, and determine switch rates, clinical outcomes, and factors associated with survival. DESIGN/METHODS: We used patient data from 62 Médecins Sans Frontières programmes and included all antiretroviral therapy-naive adults (> 15 years) at the start of antiretroviral therapy and switched to a protease inhibitor-containing regimen with at least one nucleoside reverse transcriptase inhibitor change after more than 6 months of nonnucleoside reverse transcriptase inhibitor first-line use. Cumulative switch rates and survival curves were estimated using Kaplan-Meier methods, and mortality predictors were investigated using Poisson regression. RESULTS: Of 48,338 adults followed on antiretroviral therapy, 370 switched to a second-line regimen after a median of 20 months (switch rate 4.8/1000 person-years). Median CD4 cell count at switch was 99 cells/microl (interquartile ratio 39-200; n = 244). A lopinavir/ritonavir-based regimen was given to 51% of patients and nelfinavir-based regimen to 43%; 29% changed one nucleoside reverse transcriptase inhibitor and 71% changed two nucleoside reverse transcriptase inhibitors. Median follow-up on second-line antiretroviral therapy was 8 months, and probability of remaining in care at 12 months was 0.86. Median CD4 gains were 90 at 6 months and 135 at 12 months. Death rates were higher in patients in World Health Organization stage 4 at antiretroviral therapy initiation and in those with CD4 nadir count less than 50 cells/microl. CONCLUSION: The rate of switch to second-line treatment in antiretroviral therapy-naive adults on non-nucleoside reverse transcriptase inhibitor-based first-line antiretroviral therapy was relatively low, with good early outcomes observed in protease inhibitor-based second-line regimens. Severe immunosuppression was associated with increased mortality on second-line treatment.
dc.language en
dc.rights Published by Wolters Kluwer Lippincott Williams & Wilkins - Archived on this site by kind permission Wolters Kluwer
dc.subject Second-line treatment
dc.title Second-line antiretroviral therapy in resource-limited settings: the experience of Médecins Sans Frontières
dc.type Article


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