Table 4.
Characteristics a | Univariable analysis b | Multivariable analysis b | ||
---|---|---|---|---|
Crude HR (95% CI) | p | Adjusted HR (95% CI) | p | |
LLV experience | <0.001 | <0.001 | ||
Sustained virologic suppression | Reference | Reference | ||
Ever experienced LLV | 2.86 (1.90 to 4.28) | 3.01 (1.97 to 4.60) | ||
Age | 0.046 | 0.03 | ||
<12 years | Reference | Reference | ||
12 to 14.9 years | 1.59 (1.04 to 2.48) | 1.69 (1.08 to 2.66) | ||
≥15 years | 2.02 (0.97 to 4.22) | 2.20 (1.02 to 4.76) | ||
Sex | 0.15 | |||
Male | Reference | |||
Female | 1.30 (0.90 to 1.92) | |||
Country of residence | 0.003 | 0.07 | ||
Thailand | 2.41 (0.59 to 8.87) | 1.92 (0.46 to 8.07) | ||
Malaysia | 8.04 (1.76 to 36.73) | 4.47 (0.94 to 21.3) | ||
Cambodia | Reference | Reference | ||
WHO clinical stage at cART initiation | 0.76 | |||
Stage 1 to 2 | Reference | |||
Stage 3 | 1.18 (0.72 to 1.94) | |||
Stage 4 | 0.90 (0.56 to 1.43) | |||
No event documented | 0.90 (0.50 to 1.60) | |||
CD4 T‐cell percentage | 0.001 | 0.002 | ||
<25% | 1.84 (1.25 to 2.71) | 1.90 (1.27 to 2.85) | ||
≥25% | Reference | Reference | ||
Unknown | 3.50 (1.48 to 8.26) | 2.82 (1.14 to 7.01) | ||
Current cART regimen | 0.03 | 0.10 | ||
NNRTI‐based | Reference | Reference | ||
PI/r‐based | 2.84 (1.24 to 6.52) | 2.26 (0.94 to 5.44) | ||
Period of cART initiation | 0.09 | 0.28 | ||
<2005 | Reference | Reference | ||
2005 to 2007 | 0.94 (0.58 to 1.53) | 1.13 (0.66 to 1.94) | ||
2008 to 2011 | 1.81 (1.08 to 3.04) | 1.71 (0.97 to 3.03) | ||
2012 to 2016 | 0.79 (0.24 to 2.60) | 0.83 (0.24 to 2.81) |
cART, combination antiretroviral therapy; CI, confidence interval; HR, hazard ratio; LLV, low‐level viraemia; NNRTI, non‐nucleoside reverse transcriptase inhibitor; PI/r, protease inhibitor‐boosted with ritonavir; WHO, World Health Organization.
Characteristics were evaluated at baseline, unless otherwise specified
The analyses were performed using Cox proportional hazards models.