• Login
    View Item 
    •   Mak IR Home
    • College of Health Sciences (CHS)
    • Infectious Diseases Institute (IDI)
    • Infectious Diseases Institute (IDI) Collections
    • View Item
    •   Mak IR Home
    • College of Health Sciences (CHS)
    • Infectious Diseases Institute (IDI)
    • Infectious Diseases Institute (IDI) Collections
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Estimation of mortality among HIV-infected people on antiretroviral therapy treatment in East Africa: a sampling based approach in an observational, multisite, cohort study

    Thumbnail
    View/Open
    Research article (958.4Kb)
    Date
    2015
    Author
    Geng, Elvin H.
    Odeny, Thomas A.
    Lyamuya, Rita E.
    Nakiwogga Muwanga, Alice
    Diero, Lameck
    Bwana, Mwebesa
    Muyindike, Winnie
    Braitstein, Paula
    Somi, Geoffrey R.
    Kambugu, Andrew
    Bukusi, Elizabeth A.
    Wenger, Megan
    Wools-Kaloustian, Kara K.
    Glidden, David V.
    Yiannoutsos, Constantin T.
    Martin, Jeffrey
    Metadata
    Show full item record
    Abstract
    Background—Mortality after initiation of antiretroviral treatment (ART) among HIV-infected patients in resource limited settings is a critical measure of the effectiveness and comparative effectiveness of the global public health response. Unknown outcomes due to high loss to followup (LTFU) preclude accurate accounting of deaths and limit our understanding of effectiveness. Methods—We evaluated in HIV-infected adults on ART in 14 clinics in five settings in Kenya, Uganda and Tanzania using a sampling-based approach in which we intensively traced a random sample of lost patients (> 90 days late for last scheduled visit) and incorporated their vital status outcomes into analyses of the entire clinic population through probability-weighted survival analyses. Findings—We followed 34,277 adults on ART from Mbarara and Kampala, Uganda; Eldoret and Kisumu, Kenya; and Morogoro, Tanzania. The median age was 35 years, 34% were men, and median pre-therapy CD4 count was 154 cells/μl. Overall 5,780 (17%) were LTFU, 991 (17%) were randomly selected for tracing and vital status was ascertained in 860 of 991 (87%). Incorporating outcomes among the lost increased estimated 3-year mortality from 3.9% (95% CI: 3.6%-4.2%) to 12.5% (95% CI: 11.8%-13.3%). The sample-corrected, unadjusted 3-year mortality across settings ranged from 7.2% in Mbarara to 23.6% in Morogoro. After adjustment for age, sex, pre-therapy CD4 value, and WHO stage, the sample-corrected hazard ratio comparing the setting with highest vs. lowest mortality was 2.2 (95% CI: 1.5-3.4) and the risk difference for death at 3 years was 11% (95% CI: 5.0%-17.7%). Author Manuscript Author Manuscript Author Manuscript Interpretation—A sampling based approach is widely feasible and important for understanding mortality after starting ART. After adjustment for measured biological drivers, mortality differs substantially across settings despite delivery of a similar clinical package of treatment. Implementation research to understand the systems, community, and patient behaviors driving these differences is urgently needed.
    URI
    http://hdl.handle.net/10570/14547
    Collections
    • Infectious Diseases Institute (IDI) Collections

    DSpace 5.8 copyright © Makerere University 
    Contact Us | Send Feedback
    Theme by 
    Atmire NV
     

     

    Browse

    All of Mak IRCommunities & CollectionsTitlesAuthorsBy AdvisorBy Issue DateSubjectsBy TypeThis CollectionTitlesAuthorsBy AdvisorBy Issue DateSubjectsBy Type

    My Account

    LoginRegister

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    DSpace 5.8 copyright © Makerere University 
    Contact Us | Send Feedback
    Theme by 
    Atmire NV