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Session 122 Poster Abstracts
Adverse Events in Pregnancy
Session Day and Time: Monday, 1:30 - 3:30 pm
Poster Hall


712    
Pregnancy Outcomes after Combined ART or Short-course AZT with Single-dose Nevirapine in Thai Women with High and Low CD4 Cell Counts
Nittaya Phanuphak*1, T Apornpong1, S Teeratakulpisarn1, S Limpongsanurak2, W Luesomboon3, A Tangsathapornpong4, C Vitavasiri5, N Singhakowinta6, E Abrams7, P Phanuphak1, and MTCT-Plus Initiative, Bangkok, Thailand
1Thai Red Cross AIDS Res Ctr, Bangkok; 2King Chulalongkorn Memorial Hosp, Bangkok, Thailand; 3Queen Sawangwattana Memorial Hosp, Chonburi, Thailand; 4Thammasat Univ Hosp, Pathumthani, Thailand; 5Police Gen Hosp, Bangkok, Thailand; 6Queen Sirikit hosp, Chonburi, Thailand; and 7Columbia Univ, Mailman Sch of Publ Hlth, New York, NY, US

Background:  The objectives of treatment for HIV-infected pregnant women are to maximize women’s health, minimize mother-to-child transmission (MTCT)of HIV while preserving future treatment options for women. In the developed world, both protease inhibitor-based and nevirapine (NVP)-based regimens are used, while the latter are more likely to be prescribed in the developing world. However, data are conflicting, whether the use of these regimens is associated with adverse pregnancy outcomes.

Methods:  Before April 2004, the Thai Red Cross AIDS Research Centre prevention of MTCT regimen was zidovudine (AZT) with single-dose (sd) NVP. After April 2004, all HIV-infected pregnant women received AZT/lamivudine (3TC)/NVP regardless of baseline CD4+ count. Pregnant women with baseline CD4+ 200 or >200 cells/mm3 started the regimen as early as 14 or 28 weeks, respectively. Data on pregnancy outcomes were retrieved from chart review from January 2003 to September 2005.

Results:  There were 352 pregnancy outcomes for 352 women. Mean duration on ART was 6.5 weeks in AZT + sdNVP group and 10.9 weeks in AZT/3TC/NVP group. Due to limited data in women on AZT + sdNVP with low CD4+ counts, we could only compare the effect of ART regimens among women with high CD4+ counts and could not detect any difference in pregnancy outcomes between AZT + sdNVP and AZT/3TC/NVP groups. Among AZT/3TC/NVP group, CD4 200 (RR = 2.1, 95%CI 1.1 to 3.9) and body mass index <24.5 (RR = 1.3, 95%CI 1.1 to 1.7) were risk factors for low birth weight. None of these remained significant by multivariate analysis. Neither duration on ART, ART discontinuation/switch, parity, nor age was associated with adverse pregnancy outcomes.

 

Pregnancy outcomes (%)

AZT + sdNVP

AZT/3TC/NVP

 

 

 

RR (95%CI)**

CD4 200
n = 2

CD4 >200
n = 63

Total
n = 65

CD4 200
n = 94

CD4 >200
n = 178

 

Total n = 272

 

 

 

RR (95%CI)*

Low birth
  weight
  <2500 g

Preterm birth
 (<37 weeks)

Stillbirth

Neonatal
  death

0

 

0

 

0

0

8.5

 

14.3

 

1.6

0

8.2

 

13.8

 

1.5

0

20.5

 

18.1

 

3.2

0

9.8

 

12.4

 

2.2

1.1

13.5

 

14.3

 

2.6

0.7

2.1 (1.1-3.9)

 

0.9 (0.8-1.0)

 

1.0 (0.9-1.0)

1.0 (1.0-1.0)

0.9 (0.3-2.3)

 

1.0 (0.9-1.1)

 

1.0 (1.0-1.0)

1.0 (1.0-1.0)

Transmission  
  rate

0

7.0

6.8

3.6

1.5

2.5

0.595

0.226

* AZT/3TC/NVP group, CD4<200 vs >200 ** CD4>200 only, AZT + SD-NVP vs AZT/3TC/NVP

 

Conclusions:  At least among women with high CD4 cell counts, NVP-based ART used in HIV-infected pregnant women was not associated with increased incidence of adverse pregnancy outcomes as compared with AZT + sdNVP and should be considered as a possible option for prevention of MTCT in the developing world.