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. Author manuscript; available in PMC: 2012 Aug 28.
Published in final edited form as: Antivir Ther. 2010;15(1):41–49. doi: 10.3851/IMP1489

Table 1. Characteristics of women receiving HAART at conception and the available measurements on these women during pregnancy.

Women (n=127)

n (%)
Type of HAART regimen
 Pi-containing 78 (61)
 NNRTI-containing 49 (39)
Race by IDU status
 Black non-IDU 37 (32)
 White non-IDU 47 (41)
 White IDU 31 (27)
 Other 12
Age at delivery (years)
 Median (IQR) 33 (30-37)
 18-25 10 (8)
 26-34 63 (53)
 ≥35 46 (39)
 Unknown 8
Time period of delivery
 1998-1999 21 (16)
 2000-2001 49 (38)
 2002-2003 49 (38)
 2004-2006 8 (6)
Duration of HAART at time of conception
 Median months (IQR) 10 (5, 20)
 ≥ 15 months 42 (33)
 6-15 months 41 (32)
 < 6 months 44 (35)

Measurements (n=371)

n (%)

Median baseline VL* (log10 copies/ml) (IQR) 3.22 (2.61-3.92)
No. of undetectable measurements
 Total 79/363 (22)
 First trimester 1/74 (1)
 Second trimester 23/140 (16)
 Third trimester 36/100 (35)
 Delivery 21/50 (42)
  Median VL at delivery (log10 copies/ml) (IQR) 2.45 (1.45-2.99)
  Median VL at delivery among detectable 2.89 (2.57-3.48)
HIV RNA assay
 Roche 270 (73)
 Other 107 (27)
Median baseline* CD4 count (cells/mm3) (IQR) 380 (288-517)

- unless other stated

*

at first pregnancy measurement

Abbreviations: IQR, interquartile range; VL, VL; PI, protease inhibitor; NNRTI, non-nucleoside reverse transcriptase inhibitor