International Journal of Infectious Diseases (Feb 2025)

The impact of adherence counseling incorporating a point of care urine tenofovir assay on virologic suppression among individuals failing tenofovir-lamivudine-dolutegravir: A pre-post intervention study

  • Leonard Bikinesi,
  • Matthew A. Spinelli,
  • Ntombizodwa Nyoni,
  • Daniella Mouton,
  • Assegid Mengistu,
  • Jacques Kamangu,
  • Iyaloo Konstantinus,
  • Pearl Kalimugogo,
  • Gram Mutandi,
  • Fekir Negussie,
  • Guohong Wang,
  • Susie Welty,
  • Willi McFarland,
  • R. Suzanne Beard,
  • Jessica Haberer,
  • Suzanne McCluskey,
  • Monica Gandhi,
  • Steven Y. Hong

Journal volume & issue
Vol. 151
p. 107328

Abstract

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Objectives: To examine if point-of-care (POC) urine tenofovir testing-informed counseling could be used to improve virologic suppression (VS) among participants with virologic failure (VF) after ≥1 prior round of enhanced adherence counseling (EAC). Methods: Participants were enrolled from 42 clinics across Namibia. At each monthly medication pick-up, participants completed the POC urine test and received EAC informed by this testing (EAC+). If VS was not achieved after 3 months of EAC+, up to 3 additional rounds of EAC+ were provided, with resistance testing at month (M)9. Results: Of 310 potentially eligible participants across 42 clinics in Namibia, we enrolled 211 participants with VF (median age 33 years, 61% female); 195 reached M3 defined as receiving EAC+ and follow-up viral load testing; 169 achieved VS within M3 (87%, P < 0.001) and 97% by M9 (181/186) compared to 40% (22/55) prior to the intervention (P < 0.001). Resistance testing was performed in five remaining participants with VF at M9, of whom 1/5 (20%) developed dolutegravir resistance. Conclusion: The urine tenofovir assay when incorporated into adherence counseling has potential to be a cost-effective intervention among participants failing tenofovir-based regimens, increasing VS to 97% in those failing Tenofovir-Lamivudine-Dolutegravir. Encouraging results of this pre-post intervention will be rigorously tested in a randomized trial.

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