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在子宫内暴露于丁丙诺啡联合纳洛酮与丁丙诺啡单独使用的比较安全性。

Comparative Safety of In Utero Exposure to Buprenorphine Combined With Naloxone vs Buprenorphine Alone.

机构信息

Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.

出版信息

JAMA. 2024 Sep 10;332(10):805-816. doi: 10.1001/jama.2024.11501.

Abstract

IMPORTANCE

Buprenorphine combined with naloxone is commonly used to treat opioid use disorders outside of pregnancy. In pregnancy, buprenorphine alone is generally recommended because of limited perinatal safety data on the combination product.

OBJECTIVE

To compare perinatal outcomes following prenatal exposure to buprenorphine with naloxone vs buprenorphine alone.

DESIGN, SETTINGS, AND PARTICIPANTS: Population-based cohort study using health care utilization data from Medicaid-insured beneficiaries in the US from 2000 to 2018. The cohort was restricted to pregnant individuals linked to their liveborn infants, with maternal Medicaid enrollment from 3 months before pregnancy to 1 month after delivery and infant enrollment for the first 3 months after birth, unless they died sooner.

EXPOSURE

Use of buprenorphine with naloxone vs buprenorphine alone during the first trimester based on outpatient dispensings.

MAIN OUTCOMES AND MEASURES

Outcomes included major congenital malformations, low birth weight, neonatal abstinence syndrome, neonatal intensive care unit admission, preterm birth, respiratory symptoms, small for gestational age, cesarean delivery, and maternal morbidity. Confounder-adjusted risk ratios were calculated using propensity score overlap weights.

RESULTS

This study identified 3369 pregnant individuals exposed to buprenorphine with naloxone during the first trimester (mean [SD] age, 28.8 [4.6] years) and 5326 exposed to buprenorphine alone or who switched from the combination to buprenorphine alone by the end of the first trimester (mean [SD] age, 28.3 [4.5] years). When comparing buprenorphine combined with naloxone with buprenorphine alone, a lower risk for neonatal abstinence syndrome (absolute risk, 37.4% vs 55.8%; weighted relative risk, 0.77 [95% CI, 0.70-0.84]) and a modestly lower risk for neonatal intensive care unit admission (absolute risk, 30.6% vs 34.9%; weighted relative risk, 0.91 [95% CI, 0.85-0.98]) and small for gestational age (absolute risk, 10.0% vs 12.4%; weighted relative risk, 0.86 [95% CI, 0.75-0.98]) was observed. For maternal morbidity, the comparative rates were 2.6% vs 2.9%, respectively, and the weighted relative risk was 0.90 (95% CI, 0.68-1.19). No differences were observed with respect to major congenital malformations overall, low birth weight, preterm birth, respiratory symptoms, or cesarean delivery. Results were consistent across sensitivity analyses.

CONCLUSIONS AND RELEVANCE

There were similar and, in some instances, more favorable neonatal and maternal outcomes for pregnancies exposed to buprenorphine combined with naloxone compared with buprenorphine alone. For the outcomes assessed, compared with buprenorphine alone, buprenorphine with naloxone during pregnancy appears to be a safe treatment option. This supports the view that both formulations are reasonable options for the treatment of opioid use disorder in pregnancy, affirming flexibility in collaborative treatment decision-making.

摘要

重要性

布比卡因联合纳洛酮常用于治疗妊娠期以外的阿片类药物使用障碍。由于联合产品的围产期安全性数据有限,因此一般建议在怀孕期间单独使用布比卡因。

目的

比较产前暴露于布比卡因联合纳洛酮与单独使用布比卡因的围产期结局。

设计、地点和参与者:这是一项基于美国医疗补助保险受益人的医疗保健利用数据的基于人群的队列研究。该队列仅限于与活产婴儿相关联的孕妇,孕妇的医疗补助保险从怀孕前 3 个月到分娩后 1 个月纳入,除非她们更早死亡。

暴露

根据门诊配药,在孕早期使用布比卡因联合纳洛酮与布比卡因单独使用。

主要结果和措施

结局包括主要先天性畸形、低出生体重、新生儿戒断综合征、新生儿重症监护病房入院、早产、呼吸症状、小于胎龄儿、剖宫产和产妇发病率。使用倾向评分重叠权重计算混杂调整后的风险比。

结果

本研究确定了 3369 名在孕早期暴露于布比卡因联合纳洛酮的孕妇(平均[SD]年龄为 28.8[4.6]岁)和 5326 名暴露于布比卡因单独或在孕早期结束前从联合用药转为单独使用布比卡因的孕妇(平均[SD]年龄为 28.3[4.5]岁)。与单独使用布比卡因相比,布比卡因联合纳洛酮的新生儿戒断综合征风险较低(绝对风险,37.4%比 55.8%;加权相对风险,0.77[95%CI,0.70-0.84]),新生儿重症监护病房入院风险略低(绝对风险,30.6%比 34.9%;加权相对风险,0.91[95%CI,0.85-0.98])和小于胎龄儿风险较低(绝对风险,10.0%比 12.4%;加权相对风险,0.86[95%CI,0.75-0.98])。在产妇发病率方面,相应的比率分别为 2.6%和 2.9%,加权相对风险为 0.90(95%CI,0.68-1.19)。总体而言,先天性畸形、低出生体重、早产、呼吸症状或剖宫产的发生率无差异。敏感性分析结果一致。

结论和相关性

与单独使用布比卡因相比,暴露于布比卡因联合纳洛酮的妊娠具有相似的、在某些情况下更有利的新生儿和产妇结局。在评估的结局方面,与单独使用布比卡因相比,布比卡因联合纳洛酮在怀孕期间似乎是一种安全的治疗选择。这支持了两种制剂均为妊娠期阿片类药物使用障碍合理治疗选择的观点,肯定了在协作治疗决策中具有灵活性。

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