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. 2013 Feb 13;8(2):e56088. doi: 10.1371/journal.pone.0056088

Table 1. Patients characteristics at study entry and crude rates of progression to death/loss to follow-up and virologic rebound by club participation.

Event rates (per 1000 person-years, 95% CI)
Death/loss to follow-up Virologic rebound*
N (%) In club** Not in club N (%)* In club** Not in club
All patients combined 2829 29.8 (17.9–49.5) 116.9 (105.2–129.8) 2517 31.8 (18.8–53.6) 90.4 (79.1–103.4)
Age in years at study entry
<25 284 (10.0) 30.8 (4.3–218.6) 192.8 (149.4–248.9) 228 (9.1) 68.0 (17.0–271.9) 151.4 (106.5–215.3)
25–34 1397(49.4) 18.8 (7.8–45.3) 120.6 (104.0–139.9) 1234 (49.0) 34.9 (17.5–69.9) 97.5 (80.9–117.4)
35–44 841 (29.7) 30.1 (12.9–74.4) 82.1 (65.3–103.3) 778 (30.9) 20.8 (6.7–64.6) 72.4 (55.4–94.5)
≥45 307 (10.9) 91.9 (34.5–244.9) 123.1 (90.6–167.2) 277 (11.0) 26.3 (3.7–186.5) 65.1 (41.0–103.4)
Median (IQR) 32.9 (28.5–39.0) 33.2 (28.7–39.3)
Gender
Male 831 (29.4) 41.5 (18.6–92.3) 123.1 (101.9–148.8) 749 (29.8) 7.8 (1.1–55.8) 75.2 (57.5–98.4)
Female 1997 (70.6) 25.1 (13.1–48.3) 114.3 (100.7–129.7) 1767 (70.2) 41.5 (24.1–71.5) 96.9 (83.1–113.2)
CD4 count (cells/µl) at ART start
<50 601 (21.2) 15.3 (3.8–61.0) 153.3 (124.6–188.4) 518 (20.6) 34.2 (12.8–91.3) 94.6 (69.9–128.1)
50–99 560 (19.8) 34.2 (12.8–91.2) 134.1 (107.3–167.7) 496 (19.7) 30.0 (9.6–93.0) 84.6 (61.6–116.3)
100–199 1276 (45.1) 37.8 (18.9–75.5) 100.8 (85.3–119.1) 1151 (45.4) 27.1 (11.3–65.1) 96.2 (79.5–116.4)
≥200 392 (13.4) 23.3 (3.3–165.7) 96.0 (71.1–129.2) 352 (14.0) 51.1 (12.8–204.5) 75.4 (52.0–109.2)
Median (IQR) 121 (60–176) 124 (62–177)
CD4 count (cells/µl) at study entry
<50 520 (18.4) 254.2 (216.5–298.4) 426 (16.9) 106.7 (79.7–142.9)
50–99 203 (7.2) 101.3 (68.9–148.7) 166 (6.6) 64.5 (37.4–110.9)
100–199 675 (23.9) 52.4 (7.4–372.0) 71.3 (55.3–91.7) 582 (23.1) 235.1 (75.8–728.8) 78.3 (59.8–102.5)
≥200 1431 (50.6) 29.6 (17.5–49.9) 87.3 (72.6–105.0) 1343 (53.4) 26.3 (14.5–47.5) 96.6 (79.7–117.2)
Median (IQR) 202 (97–386) 215 (110–404)
Duration on ART in months at study entry
<24 510 (18.1) 136.3 (109.9–168.9) 464 (18.4) 47.9 (32.6–70.3)
25–48 1084 (38.3) 76.7 (19.2–306.9) 132.9 (114.3–154.5) 961 (38.2) 90.6 (73.9–111.1)
>48 1235 (43.6) 27.3 (15.9–47.1) 87.2 (71.2–106.5) 1092 (43.4) 33.7 (19.9–56.9) 119.2 (97.5–145.7)
Median (IQR) 43.1 (28.0–61.1) 42.8 (27.7–60.9)
Virologic suppression at study entry
Yes 2501 (88.4) 28.6 (16.9–48.3) 110.6 (98.6–124.2)
No 327 (11.6) 74.9 (10.5–531.5) 160.0 (124.1–205.9)
WHO clinical stage at study entry
I/II 781 (27.6) 32.2 (10.4–100.3) 81.6 (64.7–102.8) 716 (28.5) 36.9 (11.9–114.4) 79.5 (61.6–102.7)
III/IV 2045 (72.4) 29.3 (16.6–51.5) 131.9 (117.2–148.4) 1789 (71.5) 30.6 (16.9–55.3) 95.6 (81.7–112.0)
*

Restricted to patients who had virologic suppression at study entry, n = 2517.

**

Patients who went on to enrol in a club contributed analysis time to the “not in club” group until they were enrolled in the club. There is no single point in time where characteristics of patients who enrol in clubs and other patients can be formally compared due to the progressive nature of club enrolment. Instead predictors of club participation are presented in Table 2. Table 1 shows event rates since study entry to the outcome endpoint or censoring.

ART: Antiretroviral therapy; WHO: World Health Organization; CI: Confidence interval; IQR (inter-quartile range).