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. Author manuscript; available in PMC: 2015 Aug 28.
Published in final edited form as: J Acquir Immune Defic Syndr. 2013 Apr 15;62(5):e146–e152. doi: 10.1097/QAI.0b013e3182840d4e

TABLE 1.

Characteristic of Patients Initiating ART by Clinic Model

Vertical, n = 6190 Integrated, n = 5585 P Total, N = 11,775
Female, n (%) 3542 (57) 3226 (58) 0.60 6768 (57)
Age (yrs), n (%)
    ≤15 to <25 752 (12) 721 (13) 0.19 1473 (12)
    ≤25 to <35 2412 (39) 2234 (40) 4646 (40)
    ≤35 to <45 1880 (30) 1652 (30) 3532 (30)
    ≤45 1133 (18) 960 (17) 2093 (18)
Education (yrs), mean (SD) 6 (4) 5 (3) <0.01 6 (3)
CD4 count (cells/μL), n (%)
    <100 1769 (30) 1648 (31) <0.01 3417 (31)
    ≤100 to <200 2351 (40) 1937 (36) 4288 (38)
    ≤200 to <300 1126 (19) 1053 (20) 2179 (19)
    ≤300 622 (11) 664 (12) 1286 (11)
WHO clinical stage, n (%)
    I/II 1568 (27) 1130 (24) <0.01 2698 (26)
    III 3684 (64) 3121 (66) 6805 (65)
    IV 492 (9) 488 (10) 980 (9)
Initial ART regimen, n (%)
    D4T + 3TC + NVP 5651 (91) 4647 (84) <0.01 10,298 (88)
    D4T + 3TC + EFV 462 (7) 766 (14) 1228 (10)
    AZT + 3TC + NVP 70 (1) 104 (2) 174 (1)
Follow-up time (person-years) 5171 3945 9117

AZT, azidothymidine; 3TC, Lamivudine; D4T, stavudine; EFV, efavirenz; NVP, nevirapine.