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  • Slide 1
  • Simplification, cost-reduction strategies and examples from the field Teri Roberts Diagnostics Advisor Medecins Sans Frontieres, Access Campaign 7th International AIDS Conference 2 July 2013
  • Slide 2
  • Virological monitoring detects treatment failure earlier than clinico-immunological monitoring
  • Slide 3
  • How viral load testing fits into the package of care to ensure people stay undetectable Early treatment Routine viral load Adherence support Community- based & self- managed therapy Drop routine CD4 monitoring for virally suppressed ART treated PLWHA and rather use routine VL monitoring to trigger the need for CD4 testing (is CD4 over 200 cells/ul?)
  • Slide 4
  • Viremic patients can re-suppress following an adherence intervention
  • Slide 5
  • The importance of preserving first line, affordable, robust, one-pill-a-day regimens
  • Slide 6
  • Slide 7
  • Implementation is done in support of, and in collaboration with, the Ministries of Health and reference laboratories SAMBA CAVIDI BIOMERIEUX BIOCENTRIC
  • Slide 8
  • Slide 9
  • G. Patten et al. Poster TUPDD0106 (Oral abstract session: The point of point of care (Tuesday)) Youth and adolescents have been identified as a particularly vulnerable group, at greater risk of loss from both pre-ART and ART care. MSF supported clinic in Khayelitsha, Cape Town, South Africa: implemented POC CD4-testing at a clinic dedicated to youth aged 12 to 25 years. POC CD4 testing significantly improved assessment for ART eligibility, ensuring that most youth were made aware of their treatment needs on the day of HIV diagnosis. Does point-of-care (POC) CD4 testing reduce losses from care between HIV diagnosis, assessment for ART eligibility and ART initiation among HIV-positive youth in Khayelitsha, South Africa?
  • Slide 10
  • Group A (Before)Group B (After) HIV Testing Blood sample drawn for CD4 counting WHO Staging* ART preparation counselling sessions ART Initiation CD4 Result ART eligibility assessed Visit 1 Visit 2 Visit 3 Visit 4 Visit 5 Visit 6 HIV Testing Blood sample drawn for CD4 counting WHO Staging ART preparation counselling session ART Initiation CD4 Result ART eligibility assessed Visit 1 Visit 2 Visit 3 Visit 4 Visit 5 44% 50% 34 days 28 days P=0.6
  • Slide 11
  • Slide 12
  • Point-of-care versus laboratory-based tests for viral load testing Regional-level laboratory tests will use dried blood spot samples that can use finger or heel prick blood
  • Slide 13
  • Diagnostic accuracy of DBS using the COBAS Ampliprep/COBAS TaqMan HIV-1 v2.0 (CAP/CTM) NMRL, Harare, Zimbabwe in collaboration with MSF Sekesai Mtapuri-Zinyowera (WEPE610 - Poster Exhibition on Wednesday) 118 finger prick DBS, venous blood DBS and plasma specimens from ART patients attending two rural OI clinics in Buhera and Tsholotsho districts and one urban OI clinic in Harare good sensitivity of DBS compared to HIV-1 RNA plasma but very low specificity, which translated in a higher rate of false positive results with DBS at lower VLs (
  • Pooling methods, in combination with the use of fingerprick DBS as a sample type for VL testing, can importantly reduce costs while maintaining accuracy Efficiency expressed as cost savings: Example of Thyolo District Population: 620,000 HIV prevalence: 14,5% # VL tests needed/year: 23,000 Price per VL test: $24 Total cost/year = 23,000 x $24 = $552,000 Efficiency at 1,000 cps/mL = 28,6% => $157,800 saved Efficiency at 5,000 cps/mL = 51,4% => $283,700 saved Sample 1 500 L 100 L Pool 500 L Viral load testing 100 L Sample 2 500 L Sample 3 500 L Sample 4 500 L Sample 5 500 L What to do with pooled results? 1. Pooled VL result no further testing 2. Pooled VL result > threshold => further testing MSF has previously validated the use of fingerprick DBS on the bioMerieux NucliSENS EasyQ HIV-1 platform, which is RNA-specific
  • Slide 15
  • Reports: www.msfaccess.org/reports 2012 IAS poster TUPDD0102 and Oral abstract session: The point of point of care (Tuesday) 2013