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10.1007/s40262-014-0185-7 http://scihub22266oqcxt.onion/10.1007/s40262-014-0185-7 C4214885!4214885!25223699     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25223699&cmd=llinks): Failed to open stream: HTTP request failed! 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Protecting the Fetus Against HIV Infection: A Systematic Review of Placental Transfer of Antiretrovirals |pdf=|usr=}}{{25223699}} gab.com Text Protecting the Fetus Against HIV Infection: A Systematic Review of Placental Transfer of Antiretrovirals JO: Clin Pharmacokinet http://www.kidney.de/pget.php?&tw=1&pmid=25223699 #FOAvip Background: Maternal-fetal transfer of antiretroviral drugs contributes to prevention of vertical transmission of HIV. Objective: This systematic review discusses published studies containing data pertaining to the pharmacokinetics of placental transfer in humans, including paired cord and maternal plasma samples collected at the time of delivery as well as ex vivo placental perfusion models. Methods: Articles pertaining to placental transfer of antiretrovirals were identified from PubMed, from references of included articles, and from U.S. Department of Health and Human Services Panel on Treatment of HIV-infected Pregnant Women and Prevention of Perinatal Transmission guidelines. Articles from non-human animal models or that had no original maternal-fetal transfer data were excluded. PRISMA guidelines were followed. Results: A total of 103 published studies were identified. Data across studies appeared relatively consistent for the nucleoside reverse transcriptase inhibitors (NRTIs) and the non-nucleotide reverse transcriptase inhibitors (NNRTIs), with cord to maternal ratios approaching 1 for many of these agents. The protease inhibitors atazanavir and lopinavir exhibited consistent maternal-to-fetal transfer across studies, although the transfer may be influenced by variations in drug-binding proteins. The protease inhibitors indinavir, nelfinavir, and saquinavir exhibited unreliable placental transport, with cord blood concentrations that were frequently undetectable. Limited data, primarily from case reports, indicate that darunavir and raltegravir provide detectable placental transfer. Conclusion: These findings appear consistent with current guidelines of using two NRTIs plus an NNRTI, atazanavir/ritonavir, or lopinavir/ritonavir to maximize placental transfer as well as to optimally suppress maternal viral load. Darunavir/ritonavir and raltegravir may reasonably serve as second-line agents. Twit Text FOAVip Protecting the Fetus Against HIV Infection: A Systematic Review of Placental Transfer of Antiretrovirals ????Clin Pharmacokinet http://www.kidney.de/pget.php?&tw=1&pmid=25223699 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25223699 #FOAvip English Wikipedia <ref>{{Cite pmid|25223699}}</ref> Protecting the Fetus Against HIV Infection: A Systematic Review of Placental Transfer of Antiretrovirals #MMPMID25223699 McCormack SA; Best BM Clin Pharmacokinet 2014[Nov]; 53 (11): 989-1004 PMID25223699show ga Background: Maternal-fetal transfer of antiretroviral drugs contributes to prevention of vertical transmission of HIV. Objective: This systematic review discusses published studies containing data pertaining to the pharmacokinetics of placental transfer in humans, including paired cord and maternal plasma samples collected at the time of delivery as well as ex vivo placental perfusion models. Methods: Articles pertaining to placental transfer of antiretrovirals were identified from PubMed, from references of included articles, and from U.S. Department of Health and Human Services Panel on Treatment of HIV-infected Pregnant Women and Prevention of Perinatal Transmission guidelines. Articles from non-human animal models or that had no original maternal-fetal transfer data were excluded. PRISMA guidelines were followed. Results: A total of 103 published studies were identified. Data across studies appeared relatively consistent for the nucleoside reverse transcriptase inhibitors (NRTIs) and the non-nucleotide reverse transcriptase inhibitors (NNRTIs), with cord to maternal ratios approaching 1 for many of these agents. The protease inhibitors atazanavir and lopinavir exhibited consistent maternal-to-fetal transfer across studies, although the transfer may be influenced by variations in drug-binding proteins. The protease inhibitors indinavir, nelfinavir, and saquinavir exhibited unreliable placental transport, with cord blood concentrations that were frequently undetectable. Limited data, primarily from case reports, indicate that darunavir and raltegravir provide detectable placental transfer. Conclusion: These findings appear consistent with current guidelines of using two NRTIs plus an NNRTI, atazanavir/ritonavir, or lopinavir/ritonavir to maximize placental transfer as well as to optimally suppress maternal viral load. Darunavir/ritonavir and raltegravir may reasonably serve as second-line agents. äProtecting the Fetus Against HIV Infection: A Systematic Review of Pla(epmc).pdf DeepDyve Pubget Overpricing