{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,15]],"date-time":"2026-05-15T00:42:41Z","timestamp":1778805761915,"version":"3.51.4"},"reference-count":38,"publisher":"Wiley","issue":"S1","license":[{"start":{"date-parts":[[2012,10,29]],"date-time":"2012-10-29T00:00:00Z","timestamp":1351468800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Addiction"],"published-print":{"date-parts":[[2012,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Aim<\/jats:title><jats:p>To determine pre\u2010 and post\u2010dosing effects of prenatal methadone compared to buprenorphine on fetal wellbeing.<\/jats:p><\/jats:sec><jats:sec><jats:title>Design<\/jats:title><jats:p>A secondary analysis of data derived from the <jats:styled-content style=\"fixed-case\">M<\/jats:styled-content>aternal <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>pioid <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>reatment: <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>uman <jats:styled-content style=\"fixed-case\">E<\/jats:styled-content>xperimental <jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>esearch (<jats:styled-content style=\"fixed-case\">MOTHER<\/jats:styled-content>) study, a double\u2010blind, double\u2010dummy, randomized clinical trial.<\/jats:p><\/jats:sec><jats:sec><jats:title>Setting<\/jats:title><jats:p>Six <jats:styled-content style=\"fixed-case\">U<\/jats:styled-content>nited <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>tates sites and one <jats:styled-content style=\"fixed-case\">E<\/jats:styled-content>uropean site that provided comprehensive opioid\u2010dependence treatment to pregnant women.<\/jats:p><\/jats:sec><jats:sec><jats:title>Participants<\/jats:title><jats:p>Eighty\u2010one of the 131 opioid\u2010dependent pregnant women completing the <jats:styled-content style=\"fixed-case\">MOTHER<\/jats:styled-content> clinical trial, assessed between 31 and 33 weeks of gestation.<\/jats:p><\/jats:sec><jats:sec><jats:title>Measurements<\/jats:title><jats:p>Two fetal assessments were conducted, once before and once after study medication dosing. Measures included mean fetal heart rate (<jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content>), number of <jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content> accelerations, <jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content> reactivity in the fetal non\u2010stress test (<jats:styled-content style=\"fixed-case\">NST<\/jats:styled-content>) and biophysical profile (<jats:styled-content style=\"fixed-case\">BPP<\/jats:styled-content>) score.<\/jats:p><\/jats:sec><jats:sec><jats:title>Findings<\/jats:title><jats:p>Significant group differences were found for number of <jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content> accelerations, non\u2010reactive <jats:styled-content style=\"fixed-case\">NST<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">BPP<\/jats:styled-content> scores (all <jats:italic><jats:styled-content style=\"fixed-case\">P<\/jats:styled-content><\/jats:italic>s\u2009&lt;\u20090.05). There were no significant group differences before time of dosing. Significant decreases (all <jats:italic><jats:styled-content style=\"fixed-case\">P<\/jats:styled-content><\/jats:italic>s\u2009&lt;\u20090.05) occurred from pre\u2010 to post\u2010dose assessment for mean <jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">FHR<\/jats:styled-content> accelerations, reactive <jats:styled-content style=\"fixed-case\">NST<\/jats:styled-content> and fetal movement. The decrease in accelerations and reactive <jats:styled-content style=\"fixed-case\">NST<\/jats:styled-content> were significant only for fetuses in the methadone group, and this resulted in a significantly lower likelihood of a reactive <jats:styled-content style=\"fixed-case\">NST<\/jats:styled-content> compared to fetuses in the buprenorphine group.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Buprenorphine compared with methadone appears to result in less suppression of mean fetal heart rate, fetal heart rate reactivity and the biophysical profile score after medication dosing and these findings provide support for the relative safety of buprenorphine when fetal indices are considered as part of the complete risk\u2013benefit 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