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. 2015 May 19;10(5):e0126647. doi: 10.1371/journal.pone.0126647

Table 1. Characteristics of pregnant women and ARTs for perinatal HIV prevention according to study.

Variable PHPT-1 PHPT-2 PHPT-2 OPEN Label PHPT-2 PK PHPT-5 Total
Number of women with at least 1 VL sample 1,398 1,784 128 26 423 3,759
Characteristics of pregnant women
Gestational age at enrollment (weeks)
Median 28.0 31.0 38.4 33.9 29.0 29.6
Interquartile range 27.7 to 28.2 30.1 to 33.1 36.5 to 40.0 31.3 to 37.3 28.0 to 30.0 28.0 to 31.6
CD4 at enrollment (cell count/ mm3)
Median 360 376 368 454 458 385
Interquartile range 240 to 500 247 to 528 243 to 542 270 to 582 368 to 576 260 to 526
Gestational age at delivery (weeks)
Median 39.0 38.6 38.6 39.4 38.7 38.7
Interquartile range 38.0 to 40.0 37.9 to 39.6 37.0 to 40.0 38.1 to 40.6 37.8 to 39.7 37.9 to 39.7
Type of delivery
1) emergency C/section 141 (10%) 265 (15%) 21 (16%) 7 (27%) 0 (0%) 434 (11%)
2) planned C/section 111 (8%) 105 (6%) 9 (7%) 3 (11%) 59 (14%) 287 (8%)
3) vaginal delivery 1,146 (82%) 1,414 (79%) 98 (77%) 16 (62%) 364 (86%) 3,038 (81%)
Maternal treatment
ZDV during pregnancy 1,387 (>99%) 1,784 (100%) 73 (57%) 23 (88%) 423 (100%) 3,690 (98%)
ZDV duration (days)
Median 57 67 0 52 71 65
Interquartile range 30 to 79 52 to 77 0 to 11.5 30 to 61 60 to 78 39 to 77
LPV during pregnancy - - - - 145 (4%) 145 (4%)
LPV duration (days)
Median - - - - 69 69
Interquartile range - - - - 55 to 77 55 to 77
NVP at onset of labor - 1407 (79%) 110 (86%) 26 (100%) 133 (31%) 1,676 (45%)
ZDV loading dose at onset of labor 1,336 (96%) 1,777 (>99%) 119 (93%) 26 (100%) 410 (97%) 3,668 (98%)
Infant treatment
ZDV prophylaxis 1,381 (99%) 1,779 (>99%) 127 (99%) 26 (100%) 420 (99%) 3,733 (99%)
ZDV duration (days)
Median 41 11 44 7 7 11
Interquartile range 3 to 42 10 to 14 41 to 48 6 to 7 7 to 7 7 to 41
Postnatal NVP (infants) - 729 (41%) 134 (97%) 26 (100%) 275 (65%) 1,154 (31%)
Perinatal NVPa - 1,424 (80%) 126 (98%) 26 (100%) 276 b (65%) 1,852 (49%)

a sdNVP either in the woman at onset of labor, in the infant or in both

b only in women who did not receive LPV/r