Jarlenski Marian, LoCiganic Wei-Hsuan, Chen Qingwen, Pudasainy Sabnum, Donohue Julie M, Cole Evan S, Krans Elizabeth E
Department of Health Policy and Management, University of Pittsburgh School of Public Health, Pittsburgh, PA; Division of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Division of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Am J Obstet Gynecol. 2025 Jul;233(1):59.e1-59.e15. doi: 10.1016/j.ajog.2024.12.001. Epub 2024 Dec 6.
Opioid use disorder contributes to maternal morbidity and mortality in the United States. Little is known about how the patterns of buprenorphine dose and duration throughout pregnancy may affect neonatal and postpartum outcomes.
To determine the associations between trajectories of buprenorphine utilization and dose during pregnancy on maternal and neonatal health outcomes.
Retrospective cohort study among 2925 pregnant persons with opioid use disorder, followed from the estimated start date of pregnancy through 90 days after delivery. We used administrative healthcare data from Medicaid-enrolled individuals to assess buprenorphine dose and use and maternal (postpartum buprenorphine continuation and overdose) and neonatal (low birthweight, neonatal abstinence syndrome (NAS)) outcomes. Group-based trajectory modelling was used to identify trajectories of buprenorphine dose and use during pregnancy. Weighted multivariable logistic regression assessed the association between buprenorphine trajectories and outcomes.
We identified 8 trajectories of buprenorphine utilization and dose during pregnancy. Regression analyses found that high doses of buprenorphine and a longer duration of buprenorphine use during pregnancy was associated with higher odds of postpartum buprenorphine continuation and reduced rates of overdose. Higher doses and longer duration of buprenorphine treatment were not associated with an increase in NAS or term low birth weight, relative to moderate or low doses or shorter treatment duration.
A longer duration and higher dose of buprenorphine treatment during pregnancy were associated with improved odds of postpartum buprenorphine continuation and were not associated with adverse neonatal outcomes.
在美国,阿片类药物使用障碍会导致孕产妇发病和死亡。关于整个孕期丁丙诺啡剂量和使用时长的模式如何影响新生儿及产后结局,目前知之甚少。
确定孕期丁丙诺啡使用轨迹和剂量与孕产妇及新生儿健康结局之间的关联。
对2925名患有阿片类药物使用障碍的孕妇进行回顾性队列研究,从预计的怀孕开始日期随访至产后90天。我们使用来自医疗补助参保者的行政医疗数据,以评估丁丙诺啡的剂量、使用情况以及孕产妇(产后丁丙诺啡继续使用和过量用药)和新生儿(低出生体重、新生儿戒断综合征(NAS))结局。基于群组的轨迹模型用于确定孕期丁丙诺啡的剂量和使用轨迹。加权多变量逻辑回归分析评估丁丙诺啡轨迹与结局之间的关联。
我们确定了孕期丁丙诺啡使用和剂量的8种轨迹。回归分析发现,孕期高剂量丁丙诺啡及较长的使用时长与产后继续使用丁丙诺啡的较高几率及较低的过量用药率相关。与中等或低剂量或较短治疗时长相比,较高剂量和较长疗程的丁丙诺啡治疗与NAS增加或足月低出生体重无关。
孕期较长疗程和较高剂量的丁丙诺啡治疗与产后继续使用丁丙诺啡的较高几率相关,且与不良新生儿结局无关。