Noormohammadi Arezo, Forinash Alicia, Yancey Abigail, Crannage Erica, Campbell Kristin, Shyken Jaye
VA Outpatient Clinic, Corpus Christi, TX, USA
St Louis College of Pharmacy, St Louis, MO, USA.
Ann Pharmacother. 2016 Aug;50(8):666-72. doi: 10.1177/1060028016648367. Epub 2016 May 19.
To evaluate maternal and neonatal safety outcomes for methadone and buprenorphine in the obstetric population.
A literature search of PubMed (1966 to March 2016) and EMBASE (1973 to March 2016) was completed using the search terms buprenorphine, methadone, pregnancy, opioid, and neonatal abstinence syndrome Priority was given to randomized controlled trials and trials directly comparing buprenorphine and methadone during pregnancy. The bibliographies were reviewed for other relevant articles.
All human studies published in English, that compared methadone and buprenorphine use in pregnancy were evaluated. Because of the limited number of obstetric studies, only 5 critical studies were found.
Buprenorphine significantly improved or had similar outcomes to methadone for development of neonatal abstinence syndrome (NAS), percentage of infants requiring treatment for NAS (20%-47% vs 45.5%-57%, respectively), total amount of morphine used to treat NAS (0.472-3.4 vs 1.862-10.4 mg, respectively), duration of NAS (4.1-5.6 vs 5.3-9.9 days, respectively), peak NAS (3.9-11 vs 4.9-12.8 score, respectively), infant hospital stay (6.8-10.6 vs 8.1-17.5 days, respectively), and gestational age at delivery (38.8-39.7 vs 37.9-38.8 weeks, respectively). No difference was found with other neonatal or maternal outcomes.
Both methadone and buprenorphine are effective agents, with improved safety compared with continued nonmedical opioid use during pregnancy. There is evidence to suggest that buprenorphine should be considered as an equivalent option to methadone for use in pregnancy; however, larger studies are still needed to fully evaluate buprenorphine safety and advantages over methadone in the obstetric population.
评估美沙酮和丁丙诺啡应用于产科人群时孕产妇及新生儿的安全结局。
使用检索词“丁丙诺啡”“美沙酮”“妊娠”“阿片类药物”和“新生儿戒断综合征”,完成了对PubMed(1966年至2016年3月)和EMBASE(1973年至2016年3月)的文献检索。优先选择随机对照试验以及直接比较孕期丁丙诺啡和美沙酮的试验。对参考文献进行了审查以查找其他相关文章。
对所有以英文发表的、比较孕期使用美沙酮和丁丙诺啡的人体研究进行了评估。由于产科研究数量有限,仅发现5项关键研究。
在新生儿戒断综合征(NAS)的发生、需要接受NAS治疗的婴儿百分比(分别为20% - 47%和45.5% - 57%)、用于治疗NAS的吗啡总量(分别为0.472 - 3.4毫克和1.862 - 10.4毫克)、NAS持续时间(分别为4.1 - 5.6天和5.3 - 9.9天)、NAS峰值(分别为3.9 - 11分和4.9 - 12.8分)、婴儿住院时间(分别为6.8 - 10.6天和8.1 - 17.5天)以及分娩时的孕周(分别为38.8 - 39.7周和37.9 - 38.8周)方面,丁丙诺啡显著改善或与美沙酮有相似结局。在其他新生儿或孕产妇结局方面未发现差异。
美沙酮和丁丙诺啡均为有效药物,与孕期持续非医疗使用阿片类药物相比安全性有所提高。有证据表明,丁丙诺啡在孕期可被视为美沙酮的等效选择;然而,仍需要更大规模的研究来全面评估丁丙诺啡在产科人群中的安全性及其相对于美沙酮的优势。