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dc.contributor.authorBrennan, Alana T.en_US
dc.contributor.authorDavies, Mary-Annen_US
dc.contributor.authorBor, Jacoben_US
dc.contributor.authorWandelere, G.en_US
dc.contributor.authorStinson, K.en_US
dc.contributor.authorWood, R.en_US
dc.contributor.authorProzesky, H.en_US
dc.contributor.authorTanser, F.en_US
dc.contributor.authorFatii, G.en_US
dc.contributor.authorBoulle, A.en_US
dc.contributor.authorSikazwe, I.en_US
dc.contributor.authorWool-Kaloustian, K.en_US
dc.contributor.authorYuannoutsos, C.en_US
dc.contributor.authorLeroy, V.en_US
dc.contributor.authorde Rekeneire, N.en_US
dc.contributor.authorFox, M.P.en_US
dc.date.accessioned2018-08-30T19:20:18Z
dc.date.available2018-08-30T19:20:18Z
dc.date.copyright2017
dc.date.issued2017-01
dc.identifier.citationBrennan, A. T., Davies, M. A., Bor, J., Wandeler, G., Stinson, K., Wood, R., ... & Sikazwe, I. (2017). Has the phasing out of stavudine in accordance with changes in WHO guidelines led to a decrease in single-drug substitutions in first-line antiretroviral therapy for HIV in sub-Saharan Africa?. AIDS (London, England), 31(1), 147-157. https://doi.org/10.1097/QAD.0000000000001307.
dc.identifier.urihttps://hdl.handle.net/2144/31120
dc.descriptionThis version is the Accepted Manuscript and is published in final edited form as: AIDS. 2017 January 02; 31(1): 147–157. doi:10.1097/QAD.0000000000001307en_US
dc.description.abstractOBJECTIVE: We assessed the relationship between phasing out stavudine in first-line antiretroviral therapy (ART) in accordance with WHO 2010 policy and single-drug substitutions (SDS) (substituting the nucleoside reverse transcriptase inhibitor in first-line ART) in sub-Saharan Africa. DESIGN: Prospective cohort analysis (International epidemiological Databases to Evaluate AIDS-Multiregional) including ART-naive, HIV-infected patients aged at least 16 years, initiating ART between January 2005 and December 2012. Before April 2010 (July 2007 in Zambia) national guidelines called for patients to initiate stavudine-based or zidovudine-based regimen, whereas thereafter tenofovir or zidovudine replaced stavudine in first-line ART. METHODS: We evaluated the frequency of stavudine use and SDS by calendar year 2004-2014. Competing risk regression was used to assess the association between nucleoside reverse transcriptase inhibitor use and SDS in the first 24 months on ART. RESULTS: In all, 33 441 (8.9%; 95% confience interval 8.7-8.9%) SDS occurred among 377 656 patients in the first 24 months on ART, close to 40% of which were amongst patients on stavudine. The decrease in SDS corresponded with the phasing out of stavudine. Competing risks regression models showed that patients on tenofovir were 20-95% less likely to require a SDS than patients on stavudine, whereas patients on zidovudine had a 75-85% decrease in the hazards of SDS when compared to stavudine. CONCLUSION: The decline in SDS in the first 24 months on treatment appears to be associated with phasing out stavudine for zidovudine or tenofovir in first-line ART in our study. Further efforts to decrease the cost of tenofovir and zidovudine for use in this setting is warranted to substitute all patients still receiving stavudine.en_US
dc.language.isoen_US
dc.publisherAIDS.en_US
dc.subjectAIDS/HIVen_US
dc.subjectSub-Saharan Africaen_US
dc.subjectStavudineen_US
dc.subjectAntiretroviral therapyen_US
dc.titleHas the phasing out of stavudine in accordance with changes in WHO guidelines led to a decrease in single-drug substitutions in first-line antiretroviral therapy for HIV in sub-Saharan Africa?en_US
dc.typeArticleen_US
dc.identifier.doi10.1097/QAD.0000000000001307


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