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              suppression to persist for weeks after stopping ART.  We   were performed by G.A., J.L. and K.B. G.A, C.R. and S.L.
              believe this could be because of low pre-ART viral loads in   co-wrote the article.
              our population (because of  women with  less advanced
              disease starting ART in pregnancy).
                                                                    Funding information
              Our study had several limitations. Firstly, our results are based   This project was funded by the National Institute of Child
              on a small number of observations making generalisability   Health and Human Development, and the National Institute
              challenging. Secondly, we did not report on minor drug   of Allergy and Infectious Diseases, NIH grant: R01HD061265.
              resistance variants and, finally, more than half (63%) of women
              tested at a median time of 5 weeks from EFV cessation were   Data availability statement
              still virally suppressed, which may suggest that we might
              have tested for resistance strain development early. Thirdly,   Data and associated documentation from this study will be
              we could not determine why the 7-day tail was inconsistently   made  available  for  external  use  only  under  a  data-sharing
              applied at the time of ART cessation and could therefore have   agreement that provides for (1) a commitment to using the
              missed evaluating possible confounders related to this factor.  data only for research purposes and not to identify any
              Conclusion                                            individual participant; (2) a commitment to securing the
                                                                    data  using appropriate computer technology; and (3) a
              Although guidelines no longer recommend discontinuation   commitment to destroying or returning the data after
              of ART after pregnancy, our study has general applicability   analyses are completed.
              for those requiring permanent or temporary treatment
              discontinuation when receiving an EFV-based regimen,   Disclaimer
              informing the risk of mutation emergence in the setting of
              abrupt three-drug discontinuation versus discontinuing with   The views and opinions expressed in this article are those of
              a TDF/FTC tail. Furthermore, despite the shift to the use of   the authors and do not necessarily reflect the official policy or
              newer drugs such as dolutegravir for which there is less   position of any affiliated agency of the authors.
              concern about the emergence of resistance than with NNRTIs,
              our data are relevant to millions of individuals still on   References
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