In the context of a community-randomized trial of antiretrovirals for HIV prevention and treatment among sex workers in Zimbabwe (the SAPPH-IRe trial), we will measure the proportion of women with HIV viral load (VL) above 1000 copies/mL (“VL>1000”) as our primary endpoint. We sought to characterize VL assay performance by comparing results from finger prick dried blood spots (DBS) collected in the field with plasma samples, to determine whether finger prick DBS is an acceptable sample for VL quantification in the setting.We collected whole blood from a finger prick onto filter paper and plasma samples using venipuncture from women in two communities. VL quantification was run on samples in parallel using NucliSENS EasyQ HIV-1 v2.0. Our tri...
World Health Organization recommends using dried blood spots (DBS) for HIV RNA viral load (VL) measu...
Quantification of HIV-1 RNA is essential for clinical management of HIV patients. The limited throug...
In settings where plasma preparation and sample centralization are not feasible or inconvenient, dri...
In the context of a community-randomized trial of antiretrovirals for HIV prevention and treatment a...
Background In the context of a community-randomized trial of antiretrovirals for HIV prevention and ...
BACKGROUND: The use of dried blood spots (DBS) for HIV-1 viral load quantification can greatly impr...
Background: Viral load (VL) quantification is an important tool in determining newly developed drug ...
Quantitative plasma viral load (VL) at 1000 copies /mL was recommended as the threshold to confirm a...
Dried blood spots (DBS) can be used in developing countries to alleviate the logistic constraints of...
Viral suppression is a key indicator of antiretroviral therapy (ART) response among HIV-infected pat...
The use of dried blood spot (DBS) specimens for HIV viral load (VL) monitoring is recommended to sup...
ideally requires periodic viral load measurements to ascertain adequate response to treatment. While...
There is a global need for HIV viral load point-of-care (PoC) assays to monitor patients receiving a...
Background. Monitoring of antiretroviral treatment (ART) with human immunodeficiency virus (HIV) vir...
World Health Organization recommends using dried blood spots (DBS) for HIV RNA viral load (VL) measu...
World Health Organization recommends using dried blood spots (DBS) for HIV RNA viral load (VL) measu...
Quantification of HIV-1 RNA is essential for clinical management of HIV patients. The limited throug...
In settings where plasma preparation and sample centralization are not feasible or inconvenient, dri...
In the context of a community-randomized trial of antiretrovirals for HIV prevention and treatment a...
Background In the context of a community-randomized trial of antiretrovirals for HIV prevention and ...
BACKGROUND: The use of dried blood spots (DBS) for HIV-1 viral load quantification can greatly impr...
Background: Viral load (VL) quantification is an important tool in determining newly developed drug ...
Quantitative plasma viral load (VL) at 1000 copies /mL was recommended as the threshold to confirm a...
Dried blood spots (DBS) can be used in developing countries to alleviate the logistic constraints of...
Viral suppression is a key indicator of antiretroviral therapy (ART) response among HIV-infected pat...
The use of dried blood spot (DBS) specimens for HIV viral load (VL) monitoring is recommended to sup...
ideally requires periodic viral load measurements to ascertain adequate response to treatment. While...
There is a global need for HIV viral load point-of-care (PoC) assays to monitor patients receiving a...
Background. Monitoring of antiretroviral treatment (ART) with human immunodeficiency virus (HIV) vir...
World Health Organization recommends using dried blood spots (DBS) for HIV RNA viral load (VL) measu...
World Health Organization recommends using dried blood spots (DBS) for HIV RNA viral load (VL) measu...
Quantification of HIV-1 RNA is essential for clinical management of HIV patients. The limited throug...
In settings where plasma preparation and sample centralization are not feasible or inconvenient, dri...