CD4+ cell count and risk for antiretroviral drug resistance among women using peripartum nevirapine for perinatal HIV prevention
Article first published online: 24 DEC 2010
© 2010 The Authors Journal compilation © RCOG 2010 BJOG An International Journal of Obstetrics and Gynaecology
BJOG: An International Journal of Obstetrics & Gynaecology
Volume 118, Issue 4, pages 495–499, March 2011
How to Cite
Dorton, B., Mulindwa, J., Li, M., Chintu, N., Chibwesha, C., Mbewe, F., Frenkel, L., Stringer, J. and Chi, B. (2011), CD4+ cell count and risk for antiretroviral drug resistance among women using peripartum nevirapine for perinatal HIV prevention. BJOG: An International Journal of Obstetrics & Gynaecology, 118: 495–499. doi: 10.1111/j.1471-0528.2010.02835.x
- Issue published online: 10 FEB 2011
- Article first published online: 24 DEC 2010
- Accepted 14 November 2010. Published Online 24 December 2010.
- Antiretroviral therapy;
- CD4+ cell count;
- non-nucleoside reverse transcriptase inhibitor;
- prevention of mother-to-child transmission;
Please cite this paper as: Dorton B, Mulindwa J, Li M, Chintu N, Chibwesha C, Mbewe F, Frenkel L, Stringer J, Chi B. CD4+ cell count and risk for antiretroviral drug resistance among women using peripartum nevirapine for perinatal HIV prevention. BJOG 2011;118:495–499.
Objective To determine the association between the antenatal CD4+ cell count and the development of viral drug resistance following the use of peripartum nevirapine (NVP) for perinatal HIV prevention.
Design Secondary analysis of data from a previously conducted randomised controlled trial.
Setting Lusaka, Zambia.
Population HIV-positive pregnant women.
Methods We analysed the data from a clinical trial of single-dose tenofovir/emtricitabine (TDF/FTC) to reduce viral drug resistance associated with peripartum NVP. The trial population was categorised according to antenatal CD4+ cell count (200–350, 351–500 and >500 cells/μl).
Main outcome measures The relative risk for acquiring drug resistance, determined by consensus sequencing and oligonucleotide ligation assay (OLA), was estimated using multivariable logistic regression.
Results Of the 397 study participants, 119 (30%) had a CD4+ count of 200–350 cells/μl, 135 (34%) had a CD4+ count of 351–500 cells/μl and 143 (36%) had a CD4+ count of >500 cells/μl. Among women receiving no intervention, the risk for drug resistance appeared to increase as the CD4+ cell count decreased. Participants with CD4+ cell counts of 200–350 cells/μl randomised to the study arm had the lowest risk, suggesting a higher efficacy of the intervention within this stratum. These results were consistent at 2 and 6 weeks, regardless of how drug resistance was measured.
Conclusions Women with CD4+ cell counts of 200–350 cells/μl may be at increased risk for viral drug resistance following the use of peripartum NVP. Given the high prevalence of NVP resistance and the clear benefits of treatment, antiretroviral therapy should be initiated among pregnant women with CD4+ cell counts of ≤350 cells/μl.