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Evidence for optimizing highly active antiretroviral treatment (HAART) in Kenya Dr. Washingtone Ochieng CNHR RCDG Fellow returning from Harvard University,

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Presentation on theme: "Evidence for optimizing highly active antiretroviral treatment (HAART) in Kenya Dr. Washingtone Ochieng CNHR RCDG Fellow returning from Harvard University,"— Presentation transcript:

1 Evidence for optimizing highly active antiretroviral treatment (HAART) in Kenya Dr. Washingtone Ochieng CNHR RCDG Fellow returning from Harvard University, U.S.A Research Host: CREATES

2 Summary: HIV Prevalence & treatment Declining prevalence, rising numbers! Longevity- ART More PLWH TREATMENT ARV access improved Monitoring not so Adherence & failure Study sites

3 Relevance to Policy Great progress at controlling the HIV epidemic, but Exposure trends and sources are increasing Substance use, Commercial sex, same sex etc. Increased ARV access- likely to drive resistance and misuse Weak monitoring structures- need evidence-backed guidance

4 Treatment failure and underlying influencers Overall, 35.9% of all patients failed treatment Failure highest among Patients receiving D4T(stavudine) regimen First-line D4T discontinued elsewhere but still widely used in Kenya 33.3% of the patients developed resistance to major drugs in use Single viral load test is efficient for treatment failure definition

5 Patients active in peer support programs had good adherence Patient with good adherence had lower viral load Peer support improves adherence & treatment outcome * ** Adherence Peer Support * ** Viral load

6 HIV as a collection of sub-epidemics of many virus strains Observed increased diversity of HIV in the drug-target genes Identified HIV-1 subtype B, only common in Europe & the Americas Multiple strains complicate disease & treatment outcomes SUBTYPE/Strain % HIV diversity within in Envelope (vaccine target)Pol (drug target) A79 67 B 0 5 C014 D010 Recombinants215

7 Increased burden of infection among substance users. 66.2% injectors and 33.8% non-injectors HIV-1 prevalence; 87.5% among injectors. Hepatitis C prevalence; injectors (16.3%) & non-injectors (4.3%)

8 ①Implement point-of-care viral load testing to monitor failure ②Implement patient-focused adherence support programs Strengthen patient-physician and patient-patient relationships ③Regularize drug toxicity testing- D4T regimen phase-out per WHO ④Institutionalize drug resistance testing (reference testing centers) ⑤Capacity building- train and impart relevant skills on testing Policy decision-points:

9 6). Public health approach to alleviate behavioral risks Substance replacement therapy; treatment-as-a-prevention Pre-exposure prophylaxis; Test-and-treat’; self-reporting support 7). Ministry of Health to partner with research groups to Support research activities that will enhance informed policy decisions Actively monitor disease epidemiology and genetics Policy decision-points-cont…

10 Summary HIV treatment access has improved- Monitoring needs scaling Patient Participation in adherence programs useful Drug/substance abuse compromising gains Policy decisions to intersect with Research evidence Other outcomes: Graduate & undergraduate trainings, publications, Conferences

11 Acknowledgement Centre for Research in Therapeutic Sciences (CREATES) Consortium for National Health Research (CNHR) for funding


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