Factors associated with time to achieve an undetectable HIV RNA viral load after start of antiretroviral treatment in HIV-1-infected pregnant women

被引:0
|
作者
van Snippenburg, W. [1 ]
Nellen, F. J. B. [2 ]
Smit, C. [3 ]
Wensing, A. M. J. [4 ]
Godfried, M. H. [2 ]
Mudrikova, T. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Internal Med & Infect Dis, Utrecht, Netherlands
[2] Acad Med Ctr, Dept Internal Med & Infect Dis, Amsterdam, Netherlands
[3] Stichting HIV Monitoring, Amsterdam, Netherlands
[4] Univ Med Ctr Utrecht, Dept Med Microbiol, Virol, Utrecht, Netherlands
关键词
pregnancy; HIV; suppression; undetectable; INFECTED WOMEN; RISK-FACTORS; THERAPY; DELIVERY; PREECLAMPSIA; SUPPRESSION; TOXICITY; OUTCOMES; COHORT;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To identify factors associated with the time to viral suppression in women starting antiretroviral treatment (ART) during pregnancy. Knowledge on duration of viral load (VL) decline could help deciding the timing of treatment initiation. Methods: Highly active antiretroviral treatment (HAART)-naive pregnant women over 18 years of age who started treatment during pregnancy were included. The time to viral suppression was calculated and compared between subgroups. Results: A total of 227 pregnancies matched our inclusion criteria. In 84.6% of these an undetectable VL was reached at the time of delivery. The median time to undetectable VL after initiation of treatment was 60 days (12-168 days). Only baseline VL <10,000 copies/mL showed an independent association with time to viral suppression in multivariate Cox regression analysis, with a mean time to reach a VL <50 HIV-1 copies/mL of 49 days (95% CI 44-53). No difference in time to undetectable VL was found between protease inhibitor and non-nucleoside reverse transcriptase inhibitor-based regimens. Integrase inhibitors were not part of any treatment regimen. Conclusion: Our results suggest that in patients with baseline HIV RNA <10,000 copies/mL ART initiation might be postponed up to the twentieth week of pregnancy, thus minimising the risk of possible drug-related teratogenicity and toxicity.
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页码:34 / 39
页数:6
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