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接受丁丙诺啡治疗阿片类物质使用障碍的孕妇早产的危险因素。

Risk factors for preterm birth among gravid individuals receiving buprenorphine for opioid use disorder.

作者信息

Abdelwahab Mahmoud, Petrich Michelle, Wang Heather, Walker Erin, Cleary Erin M, Rood Kara M

机构信息

Department of Obstetrics and Gynecology, The Ohio State University College of Medicine, Columbus, OH (Drs Abdelwahab, Petrich, Walker, Cleary, and Rood).

Department of Obstetrics and Gynecology, The Ohio State University College of Medicine, Columbus, OH (Drs Abdelwahab, Petrich, Walker, Cleary, and Rood).

出版信息

Am J Obstet Gynecol MFM. 2022 May;4(3):100582. doi: 10.1016/j.ajogmf.2022.100582. Epub 2022 Feb 2.

Abstract

BACKGROUND

Opioid use disorder (OUD) has dramatically increased over the last few decades, with 11.5 million American misusing opioids in 2016. Untreated OUD in pregnancy is associated with unique adverse obstetric and perinatal outcomes including insufficient prenatal care, preterm birth (PTB), fetal growth restriction, fetal demise, and placental abruption . The mainstay treatment for OUD management in pregnancy is medication for opioid use disorder (MOUD) including methadone or buprenorphine. The association of PTB and opioid use in pregnancy has been described for over 50 years, and efforts to significantly eliminate this risk are challenged by the many confounding risks described above. When comparing rates of PTB in individuals with OUD on methadone vs buprenorphine. Buprenorphine has been associated with overall lower PTB than Methadone by almost 50 %.

OBJECTIVE

Pregnancies complicated by opioid use disorder are at an increased risk for preterm birth, defined as delivery <37 weeks' gestation. Limited literature is available on the prevalence and risk factors for preterm birth in pregnancies complicated by opioid use disorder maintained on buprenorphine. Therefore, we sought to determine the rate of preterm birth and risk factors for preterm birth in this population.

STUDY DESIGN

We performed a retrospective cohort study of pregnant individuals with singleton gestations receiving buprenorphine for opioid use disorder, who delivered at a tertiary academic medical center between July 1, 2013 and June 30, 2018. Individuals who had at least 3 visits to our colocated clinic were included in the analysis. Patients were divided into 2 groups: the preterm group for patients who delivered at <37 weeks of gestation and the term group for those who delivered at ≥37 weeks of gestation. We defined "supplements to buprenorphine" to include any illicit drugs found on antepartum urine toxicology. Variables evaluated as potential risk factors for preterm birth included medical and infectious comorbidities and illicit polysubstance use.

RESULTS

The overall preterm birth rate in this cohort was 22.7% (115/507). There was a nonsignificant trend toward decrease in overall preterm birth and provider-initiated preterm birth rate over the study period. No differences were found between the groups in spontaneous preterm birth rate at <34 weeks of gestation. There were no differences between the groups in the use of tobacco or alcohol, number of prenatal visits, or gestational age when prenatal care started. Individuals with preterm birth in the index pregnancy were more likely to have a history of preterm birth than individuals with term delivery (73% vs 16%; P<.01). No medical or infectious comorbidity or any specific supplement increased the risk of preterm birth. Among individuals using 0, 1, 2, or 3 or more illicit supplements in addition to confirmed buprenorphine for opioid use disorder, the preterm birth rate was 27.4% (reference), 18.0% (P=.09), 18.1% (P=.44), and 15.8% (P=.77), respectively.

CONCLUSION

The preterm birth rate among individuals using buprenorphine for opioid use disorder (22.7%) is higher than the national average but lower than the reported preterm birth rate in individuals using methadone for the treatment of opioid use disorder. No medical or infectious comorbidity or use of additional illicit substances increased the risk of preterm birth.

摘要

背景

在过去几十年中,阿片类药物使用障碍(OUD)显著增加,2016年有1150万美国人滥用阿片类药物。孕期未经治疗的OUD与独特的不良产科和围产期结局相关,包括产前护理不足、早产(PTB)、胎儿生长受限、胎儿死亡和胎盘早剥。孕期OUD管理的主要治疗方法是阿片类药物使用障碍药物治疗(MOUD),包括美沙酮或丁丙诺啡。PTB与孕期阿片类药物使用的关联已被描述了50多年,而显著消除这种风险的努力受到上述许多混杂风险的挑战。在比较使用美沙酮与丁丙诺啡的OUD患者的PTB发生率时,丁丙诺啡与总体PTB发生率比美沙酮低近50%相关。

目的

合并阿片类药物使用障碍的妊娠早产风险增加,早产定义为妊娠<37周分娩。关于维持丁丙诺啡治疗的合并阿片类药物使用障碍的妊娠早产患病率和危险因素的文献有限。因此,我们试图确定该人群的早产率和早产危险因素。

研究设计

我们对2013年7月1日至2018年6月30日在一家三级学术医疗中心分娩且因阿片类药物使用障碍接受丁丙诺啡治疗且单胎妊娠的孕妇进行了一项回顾性队列研究。分析纳入了至少到我们同地诊所就诊3次的个体。患者分为两组:妊娠<37周分娩的患者为早产组,妊娠≥37周分娩的患者为足月组。我们将“丁丙诺啡补充剂”定义为产前尿液毒理学检测发现的任何非法药物。评估为早产潜在危险因素的变量包括医疗和感染合并症以及非法多物质使用。

结果

该队列的总体早产率为22.7%(115/507)。在研究期间,总体早产率和医疗人员发起的早产率有下降趋势,但无统计学意义。妊娠<34周时,两组间自然早产率无差异。两组在烟草或酒精使用、产前检查次数或开始产前护理时的孕周方面无差异。与足月分娩的个体相比,本次妊娠早产的个体更有可能有早产史(73%对16%;P<.01)。没有医疗或感染合并症或任何特定补充剂会增加早产风险。在除确诊因阿片类药物使用障碍使用丁丙诺啡外还使用0、1、2或3种或更多非法补充剂的个体中,早产率分别为27.4%(参考值)、18.0%(P=.09)、18.1%(P=.44)和15.8%(P=.77)。

结论

因阿片类药物使用障碍使用丁丙诺啡的个体的早产率(22.7%)高于全国平均水平,但低于报告的使用美沙酮治疗阿片类药物使用障碍的个体的早产率。没有医疗或感染合并症或使用额外非法物质会增加早产风险。

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