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Seven-year experience of a primary care antiretroviral treatment programme in Khayelitsha, South Africa.

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dc.contributor School of Public Health and Family Medicine, University of Cape Town, Anzio Road, Cape Town, South Africa. andrew.boulle@uct.ac.za
dc.creator Boulle, Andrew
dc.creator Van Cutsem, Gilles
dc.creator Hilderbrand, Katherine
dc.creator Cragg, Carol
dc.creator Abrahams, Musaed
dc.creator Mathee, Shaheed
dc.creator Ford, Nathan
dc.creator Knight, Louise
dc.creator Osler, Meg
dc.creator Myers, Jonny
dc.creator Goemaere, Eric
dc.creator Coetzee, David
dc.creator Maartens, Gary
dc.date 2010-02-20
dc.date.accessioned 2017-01-31T07:16:32Z
dc.date.available 2017-01-31T07:16:32Z
dc.identifier Seven-year experience of a primary care antiretroviral treatment programme in Khayelitsha, South Africa. 2010, 24 (4):563-72 AIDS
dc.identifier 1473-5571
dc.identifier 20057311
dc.identifier 10.1097/QAD.0b013e328333bfb7
dc.identifier http://hdl.handle.net/10144/95573
dc.identifier http://fieldresearch.msf.org/msf/handle/10144/95573
dc.identifier AIDS (London, England)
dc.identifier.uri http://dspace.mediu.edu.my:8181/xmlui/handle/10144/95573
dc.description OBJECTIVES: We report on outcomes after 7 years of a community-based antiretroviral therapy (ART) programme in Khayelitsha, South Africa, with death registry linkages to correct for mortality under-ascertainment. DESIGN: This is an observational cohort study. METHODS: Since inception, patient-level clinical data have been prospectively captured on-site into an electronic patient information system. Patients with available civil identification numbers who were lost to follow-up were matched with the national death registry to ascertain their vital status. Corrected mortality estimates weighted these patients to represent all patients lost to follow-up. CD4 cell count outcomes were reported conditioned on continuous virological suppression. RESULTS: Seven thousand, three hundred and twenty-three treatment-naive adults (68% women) started ART between 2001 and 2007, with annual enrolment increasing from 80 in 2001 to 2087 in 2006. Of 9.8% of patients lost to follow-up for at least 6 months, 32.8% had died. Corrected mortality was 20.9% at 5 years (95% confidence interval 17.9-24.3). Mortality fell over time as patients accessed care earlier (median CD4 cell count at enrolment increased from 43 cells/microl in 2001 to 131 cells/microl in 2006). Patients who remained virologically suppressed continued to gain CD4 cells at 5 years (median 22 cells/microl per 6 months). By 5 years, 14.0% of patients had failed virologically and 12.2% had been switched to second-line therapy. CONCLUSION: At a time of considerable debate about future global funding of ART programmes in resource-poor settings, this study has demonstrated substantial and durable clinical benefits for those able to access ART throughout this period, in spite of increasing loss to follow-up.
dc.language en
dc.rights Published by Wolters Kluwer Lippincott Williams & Wilkins - Archived on this site by kind permission Wolters Kluwer
dc.title Seven-year experience of a primary care antiretroviral treatment programme in Khayelitsha, South Africa.


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