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Peripartum nevirapine exposure and subsequent clinical outcomes among HIV‐infected women receiving antiretroviral therapy for at least 12 months
Author(s) -
Chintu Namwinga,
Giganti Mark J.,
Putta Nande B.,
Sinkala Moses,
Sadoki Ebedy,
Stringer Elizabeth M.,
Stringer Jeffrey S. A.,
Chi Benjamin H.
Publication year - 2010
Publication title -
tropical medicine and international health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.056
H-Index - 114
eISSN - 1365-3156
pISSN - 1360-2276
DOI - 10.1111/j.1365-3156.2010.02540.x
Subject(s) - nevirapine , medicine , hazard ratio , regimen , confidence interval , reverse transcriptase inhibitor , proportional hazards model , antiretroviral therapy , viral load , obstetrics , human immunodeficiency virus (hiv) , immunology
Summary Objective Prior exposure to intrapartum/neonatal nevirapine (NVP) is associated with compromised virologic treatment outcomes once non‐nucleoside reverse transcriptase inhibitor (NNRTI)–based antiretroviral therapy (ART) is initiated. We examined the longer‐term clinical outcomes in a programmatic setting. Methods We compared post‐12 month mortality and clinical treatment failure (defined by WHO clinical and immunologic criteria) among women with and without prior NVP exposure in Lusaka, Zambia. Results Between April 2004 and July 2006, 6740 women initiated an NNRTI‐containing regimen. At 12 months, 5172 (78%) remained active and were included in this analysis. Of these, 596 (12%) reported prior NVP exposure, whose time from exposure to ART initiation was: <6 months for 11%, 6–12 months for 13%, >12 months for 37%, unknown for 39%. Overall, women with prior NVP exposure trended towards increased survival (adjusted hazard ratio [AHR]: 0.53; 95% confidence interval [CI]: 0.27–1.06, P = 0.07) and towards increased hazard of clinical treatment failure (AHR: 1.18; 95% CI: 0.95–1.47, P = 0.14), particularly those with exposure for <6 months (AHR: 1.52; 95% CI: 0.94–2.45, P = 0.09). Conclusions Prior NVP exposure appeared to increase risk for clinical treatment failure after 12 months of follow‐up, but this finding did not reach statistical significance. With growing evidence linking recent NVP exposure to virologic failure, optimized monitoring algorithms should be considered for women with starting NNRTI‐based ART. The association between prior NVP exposure and improved survival has not been previously shown and may be a result of residual confounding around health‐seeking behaviours.