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. Author manuscript; available in PMC: 2015 Aug 1.
Published in final edited form as: Bioanalysis. 2014 Oct;6(20):2721–2732. doi: 10.4155/bio.14.139

Table 3.

Specificity: percentage difference ranges in antiretroviral analytes measured when hemolysis is present %PD = ([hemolyzed value − control value]/control value) ×100.

Analyte N (values reported) PD <±5 n(%) PD ± 5–10 n(%) PD >±10 n(%) CPL
ATV 5 5 (100%) 0 (-) 0 (-) -
DRV 7 4 (57%) 3 (43%) 0 (-) -
EFV 9 6 (67%) 2 (22%) 1 (11%) 8
FTC 4 2 (50%) 1 (25%) 1 (25%) 9
LPV 8 5 (63%) 2 (25%) 1 (12%) 6
NVP 5 1 (20%) 1 (20%) 3 (60%) 2, 6, 7
RGV 5 3 (60%) 2 (40%) 0 (-) -
RTV 8 5 (63%) 3 (37%) 0 (-) -
TFV 5 4 (80%) 0 (0%) 1 (20%) 7
Total 56 35 (62%) 14 (25%) 7 (13%) -

%PD = ([hemolyzed value − control value]/control value) ×100.

N = Total number of reported results; n = Number in subset of results within the PD range.

ARV: Antiretroviral; ATV: Atazanavir; CPL: Clinical pharmacology laboratory; DRV: Darunavir; EFV: Efaviren; FTC: Emtricitabine; LPV: Lopinavir; NVP: Nevirapine; RGV: Raltegravir; RPD: Relative percentage difference; RTV: Ritonavir; TFV: Tenofovir.