The feasibility of fingerstick blood collection for point-of-care HIV-1 viral load monitoring in rural Zambia

Catherine Gayle Sutcliffe; Kara M. Palamountain; Sylvia Maunga; Kelly Searle; Philip E. Thuma; William J. Moss; Mark J. Fisher

doi:10.15641/ghi.v1i2.585

Authors

Catherine Gayle Sutcliffe Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Kara M. Palamountain Kellogg School of Management, Northwestern University, Evanston, IL, USA
Sylvia Maunga Macha Research Trust, Choma, Zambia
Kelly Searle Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Philip E. Thuma Macha Research Trust, Choma, Zambia; and Bloomberg School of Public Health, Johns Hopkins University, MD, USA
William J. Moss Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Mark J. Fisher Center for Innovation in Global Health Technologies, Northwestern University

DOI:

https://doi.org/10.15641/ghi.v1i2.585

Abstract

Viral load monitoring for HIV treatment is recommended but not feasible in many settings. A point-of-care test using capillary blood would increase access but may require up to 200 μL of blood to achieve a lower limit of detection of 1000 copies/mL. This cross-sectional study evaluated the feasibility of collecting 200 μL of capillary blood as well as blood collection preferences among adults in rural Zambia. Adults seeking HIV counseling and testing at Macha Hospital were recruited in 2015. Capillary blood was collected in four 50 μL tubes. Blood collection was categorized as complete (200 μL collected), partial (all tubes filled but <200 μL obtained due to collection techniques), or incomplete (1-4 tubes attempted; <200 μL obtained due to insufficient blood flow). One fingerstick was required for 90% of the 201 participants. A median blood volume of 196 μL was collected. Complete, partial and incomplete collection was achieved in 34%, 59% and 6% of participants. The majority of participants (95%) preferred fingerstick over venous blood collection. A point-of-care viral load test requiring up to 200 μL of blood is feasible in a rural setting but would require training and supervision to ensure that sufficient blood was collected.