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. 2018 Jul 24;41(12):1343–1353. doi: 10.1007/s40264-018-0698-3

Table 2.

Demographic and clinical characteristics of patients initiating second-line antiretroviral therapy from 1 April 2004 to 10 January 2016

Variables Total [N = 7708]
Sex at second-line initiation
 Female 5010 (65.0)
 Male 2698 (35.0)
Age at second-line initiation, years
 Median (IQR) 37.4 (32.3–43.9)
 18–29 1220 (15.8)
 30–39 3489 (45.3)
 ≥ 40 2999 (38.9)
CD4 cell count at second-line initiation, cells/mm3
 Median (IQR) 212 (101–344)
 0–199 1436 (47.2)
 200–349 864 (28.4)
 ≥ 350 742 (24.4)
Viral load at second-line initiation, copies/mL
 Median (IQR) 11,841 (2100–60,784)
 < 1000 941 (17.0)
 1000–9999 1686 (30.5)
 ≥ 10,000 2896 (52.4)
BMI at second-line initiation
 Underweight 440 (7.8)
 Normal 2681 (47.8)
 Overweight 1530 (27.3)
 Obese 959 (17.1)
WHO stage at second-line initiation
 I 2580 (62.8)
 II 582 (14.2)
 III/IV 944 (23.0)
Time on first-line ART before the switch, months
 Median (IQR) 25.5 (13.8–44.8)
 0–12 1564 (20.3)
 12–24 2086 (27.1)
 ≥ 24 4058 (52.7)
Regimen at second-line initiation
 3TC + ABC + LPVr 238 (3.1)
 AZT + 3TC + LPVr/ATVr 2686 (34.9)
 AZT + ddI + LPVr 1501 (19.5)
 TDF +  FTC/3TC + LPVr 3283 (42.6)
Year of second-line initiation
 2004–2009 1895 (24.6)
 2010–2012 3618 (46.9)
 2013–2016 2195 (28.5)
Non-ARV comedication at second-line initiation
 No 4752 (61.7)
 Yes 2956 (38.4)
*Time (days) to first AE in the first 24 months of second-line ART
 Median (IQR) 84 (28–237)
 0–90 1810 (52.8)
 91–180 547 (16.0)
 ≥ 181 1072 (31.3)
Time (days) to first AE in the first 24 months of second-line ART by initial second-line regimen [medium (IQR)]*
 ABC + 3TC + LPVr/ATVr 57 (5–155)
 AZT + 3TC + LPVr/ATVr 56 (26–181)
 AZT + ddI + LPVr 85 (28–224)
 TDF +  FTC/3TC + LPVr 134 (28–308)

Data are expressed as n (%) unless otherwise specified

IQR interquartile range, BMI body mass index, WHO World Health Organization, ART antiretroviral therapy, ARV antiretroviral, 3TC lamivudine, ABC abacavir, LPVr lopinavir/ritonavir, ATVr atazanavir/ritonavir, AZT zidovudine, ddI didanosine, TDF tenofovir, FTC emtricitabine, AE adverse event