产后阿片类药物使用障碍患者接受阿片类药物处方用于产后急性疼痛治疗与丁丙诺啡停用之间的关系

Taylor N. Hallet, David T. Zhu, Hannah Shadowen, Lillia Thumma, Madison M. Marcus, Amy Salisbury, Caitlin E. Martin
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引用次数: 0

摘要

丁丙诺啡是治疗妊娠期患者阿片类药物使用障碍(OUD)的一种安全有效的药物,应在整个妊娠期、分娩期和至少一年的产后期间持续使用。然而,分娩时往往需要使用阿片类药物进行急性疼痛治疗,如剖腹产后。对于接受丁丙诺啡治疗的患者来说,提供处方阿片类药物可能会对 OUD 的治疗效果产生负面影响;但是,如果不对急性疼痛进行最佳管理,也可能会阻碍 OUD 的治疗效果。我们需要证据来厘清阿片类药物处方的提供和产后疼痛管理方法对 OUD 治疗轨迹的影响,最终为针对接受丁丙诺啡治疗的孕妇和产后患者的独特需求量身定制的临床指南提供依据。因此,本研究朝着这一目标迈出了第一步,对分娩时服用丁丙诺啡治疗 OUD 的孕妇队列(n = 142)进行了二次分析,以确定在分娩出院时获得阿片类药物处方是否与产后 12 个月内停用丁丙诺啡的时间有关。在样本中,26%(n = 37)在分娩出院时获得了阿片类药物处方。与未被处方阿片类药物的患者(中位数为 39 周;经 Mann-Whitney U 检验,P < 0.001)相比,被处方阿片类药物的患者在分娩后停用丁丙诺啡的周数更短(中位数为 11 周)。然而,Cox 回归模型显示,分娩后获得阿片类药物处方并不会显著增加丁丙诺啡停药的危险比。换句话说,与接受阿片类药物处方治疗的患者相比,分娩出院时未接受阿片类药物处方治疗的 OUD 患者在分娩后继续服用丁丙诺啡的时间中位数更长;然而,在考虑到其他临床变量的情况下,这一结果并未达到统计学意义。研究结果表明,有必要开展进一步研究,为产后 OUD 治疗患者提供基于证据的产后疼痛治疗方法。
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Association of Receipt of Opioid Prescription for Acute Post-Delivery Pain Management with Buprenorphine Discontinuation among Postpartum People with Opioid Use Disorder
Buprenorphine is a safe and effective medication to treat opioid use disorder (OUD) in pregnant patients and is intended to be continued throughout pregnancy, delivery, and at least the one-year postpartum period. However, delivery often involves the need for acute pain management with opioid medications, such as after a cesarean section. For patients receiving buprenorphine, the provision of prescription opioids may negatively impact OUD treatment outcomes; however, not optimally managing acute pain may also impede OUD treatment benefit. Evidence is needed to disentangle the impacts of opioid prescription provision and methods of pain management in the immediate postpartum period on OUD treatment trajectories, ultimately to inform clinical guidelines tailored to the unique needs of pregnant and postpartum people receiving buprenorphine. Accordingly, this study took an initial step towards this goal to conduct a secondary analysis of a retrospective cohort of pregnant patients taking buprenorphine for OUD at the time of delivery (n = 142) to determine whether receipt of an opioid prescription at birth hospitalization discharge was associated with the time of buprenorphine discontinuation within the 12 months following delivery. Among the sample, 26% (n = 37) were prescribed an opioid at the time of birth hospitalization discharge. The number of weeks post-delivery until buprenorphine discontinuation occurred was shorter amongst patients who were prescribed an opioid (median 11 weeks) compared to patients who were not prescribed an opioid (median 39 weeks; p < 0.001 by Mann–Whitney U test). However, a Cox regression model reported that receipt of an opioid prescription following delivery did not significantly increase the hazard ratio for buprenorphine discontinuation. In other words, OUD patients not prescribed an opioid at birth hospitalization discharge continued their buprenorphine for a longer median duration after delivery compared to their counterparts who received prescription opioids; yet, this finding did not reach statistical significance when taking into account additional clinical variables. The findings indicate how further research is warranted to inform evidence-based post-delivery pain practices for postpartum OUD treatment patients.
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