Research Article

Performance and Logistical Challenges of Alternative HIV-1 Virological Monitoring Options in a Clinical Setting of Harare, Zimbabwe

Table 2

Performance of the plasma VFA, DBS VFA, and p24 to identify virological failure using VLref as the reference assay.
(a) All patients ( ).

Number testedCorrectly classifiedMisclassifiedUndercalledOvercalledSensitivitySpecificity

VFA plasma (CO = 5,000 cp/mL) 300280 (93.3%)20 (6.6%)5/2015/2094.5%92.7%
VFA plasma (CO = 1,000 cp/mL) 300279 (93.0%)21 (7%)21/210/2180.1%100%
VFA DBS (CO = 5,000 cp/mL)299262 (87.6%)37 (12.3%)35/372/3761.9%99.0
p24 (CO = 5,000 cp/mL)301222 (73.5%)79 (26.2%)42/7937/7954.3%82.3%
p24 (CO = 1,000 cp/mL)301216 (71.7%)85 (28.2%)52/8533/8549.0%83.0%

(b) Treated patients ( ).

Number tested Correctly classifiedMisclassifiedUndercalledOvercalledSensitivitySpecificity

VFA plasma (CO = 5,000 cp/mL) 200194 (97.0%)6 (3.0%)3/63/672.7%98.0%
VFA plasma (CO = 1,000 cp/mL) 200191 (95.5%)9 (4.5%)9/90/935.7%100%
VFA DBS (CO = 5,000 cp/mL)199189 (95.0%)10 (5.0%)10/100/109.0%100%
p24 (CO = 5,000 cp/mL)201166 (82.5%)35 (17.5%)5/3530/3554.7%84.2%
p24 (CO = 1,000 cp/mL)201163 (81.0%)48 (19.0%)8/3830/3842.8%83.9%