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. 2019 Aug 23;22(8):e25368. doi: 10.1002/jia2.25368

Table 1.

Participant characteristics

Participant characteristic Group‐1: Early continued ART (n = 7) Group‐2: Suppressed viraemia and continued ART (n = 8) Group‐3: Suppressed viraemia and interrupted (n = 23)
Treatment regimen ABC, 3TC, LPV/ra AZT, 3TC, LPV/r AZT, 3TC, LPV/r
CHER Study arms NA ART‐Def (n = 6)
ART‐96W (n = 2)b
ART‐40W (n = 15)
ART‐96W (n = 6)
Part B ART‐40W (n = 2)c
Age ART first initiated (days); median (IQR) 5 (1.5 to 6.5) 156.5 (110.3 to 256.8) 55 (50.5 to 64.5)
Pre‐treatment log 10 HIV‐1 RNA load; median (IQR) 3.1 (2.7 to 3.3) 5.6 (5.3 to 5.9) 5.3 (4.0 to 5.8)
Baseline ART HIV‐1 DNA copies/million cells; median (IQR) 158 (40 to 398) 1107 (468 to 2999) 832 (363 to 1371)
CD4% nadird; median (IQR) 40 (38.7 to 54.5) 16.9 (14.0 to 19.1) 21.8 (15.9 to 25.2)
Absolute CD4 count nadir cells/microlitred; median (IQR) 1955 (1193 to 2064) 505 (440.5 to 759.5) 871 (577.5 to 1081.5)
Time interrupted (days); median (IQR) 214 (141 to 284)
Age at last sample (years); median (IQR) 1.0 (0.6 to 1.0) 8.8 (1.3 to 9.7) 9.2 (7.8 to 10.6)
CD4% (IQR) at last sample 34 (28.5 to 37.5) 34 (31 to 42) 37 (35 to 39)
Absolute CD4 (IQR) (per microlitre) at last sample 1920 (1440 to 2618) 1032 (814 to 1199) 1088 (847 to 1294)

ART, antiretroviral therapy; CHER, Children with HIV early antiretroviral therapy trial; IQR, interquartile range.

aOriginal regimen was AZT, 3TC, NVP, with NVP replaced by LPV/r at 42 weeks of age and AZT replaced by ABC at 3 months of age; bgroup‐2 included 2 ART‐96W participants who were not interrupted as both had signs suggestive of HIV encephalopathy; cpart B of CHER had screening CD4 <25%; dbefore continued phase of treatment.