Abstract
Background Because of its good efficacy and tolerance, the association of tenofovir and emtricitabine (Truvada®) is recommended for treatment of naive HIV patients by local, European and North American HIV guidelines. Despite reduced bone mineral density during preclinical studies in animals at supraclinical dosages, there is no contra-indication for young women who could become pregnant. As a consequence more and more pregnant women under Truvada® are seen in OBGYN units. Since 2004, 125 pregnant women under tenofovir are registered in the French perinatal cohort. Therefore the question arises: continue tenofovir or not?
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