Tolia V N, Murthy K, Bennett M M, Miller E S, Benjamin D K, Smith P B, Clark R H
Division of Neonatology, Department of Pediatrics, Baylor University Medical Center and Pediatrix Medical Group, Dallas, TX, USA.
Division of Neonatology, Department of Pediatrics, Feinberg School of Medicine, Northwestern University, and the Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
J Perinatol. 2018 Jan;38(1):75-79. doi: 10.1038/jp.2017.157. Epub 2017 Oct 19.
Antenatal exposure to methadone or buprenorphine often causes neonatal abstinence syndrome (NAS) in newborns. However, comparative effects on affected infants' hospital courses are inconclusive. We sought to estimate the relationship of antenatal exposure with methadone or buprenorphine and infants' length of stay among hospitalized infants with NAS.
This was a retrospective cohort study of hospitalized infants with NAS with either maternal exposure. Eligible infants were singleton infants born ⩾36 weeks' gestation and diagnosed with NAS<7 days of age between 2011 and 2014 in the Pediatrix Clinical Data Warehouse. Infant with congenital anomalies and those of multiple gestation were excluded.
Of 3364 eligible infants, 2202 (65%) were exposed to methadone and 1162 (34%) to buprenorphine. Infants exposed to buprenorphine had a lower rate of pharmacologic treatment for NAS (88 vs 91%, P<0.001). Median length of hospital stay was shorter among infants exposed to buprenorphine (21 days (inter-quartile range; 13-31) vs methadone (24 days (15-38), P<0.0001)). On multivariable Cox proportional hazard analyses, buprenorphine was associated with a shorter length of stay (hazard ratio (HR)=1.47 (95% confidence interval (CI): 1.32-1.62, P<0.001) after controlling for maternal age, parity, race or ethnicity, prenatal care, smoking status, use of antidepressants, use of benzodiazepines, and infant gestational age, small for gestational age status, cesarean delivery, sex, out born status, type of pharmacotherapy, breast milk use, year and center. We observed similar results in model using infants matched 1:1 with propensity scores for antenatal medication exposure (HR 1.39 for buprenorphine, CI 1.32-1.62, P<0.001).
Among infants born ⩾36 weeks' gestation with NAS, antenatal buprenorphine exposure was associated with a decreased length of stay relative to antenatal methadone exposure.
产前接触美沙酮或丁丙诺啡常导致新生儿出现新生儿戒断综合征(NAS)。然而,对于受影响婴儿住院病程的比较性影响尚无定论。我们试图评估产前接触美沙酮或丁丙诺啡与NAS住院婴儿住院时长之间的关系。
这是一项针对患有NAS且母亲有相应接触史的住院婴儿的回顾性队列研究。符合条件的婴儿为妊娠≥36周的单胎婴儿,于2011年至2014年期间在Pediatrix临床数据仓库中被诊断为NAS且年龄<7天。患有先天性异常和多胎妊娠的婴儿被排除。
在3364名符合条件的婴儿中,2202名(65%)接触过美沙酮,1162名(34%)接触过丁丙诺啡。接触丁丙诺啡的婴儿接受NAS药物治疗的比例较低(88%对91%,P<0.001)。接触丁丙诺啡的婴儿住院中位时长较短(21天(四分位间距:13 - 31天),而接触美沙酮的婴儿为24天(15 - 38天),P<0.0001)。在多变量Cox比例风险分析中,在控制了母亲年龄、产次、种族或民族、产前护理、吸烟状况、抗抑郁药使用情况、苯二氮䓬类药物使用情况以及婴儿胎龄、小于胎龄状况、剖宫产、性别、出生状况、药物治疗类型、母乳喂养情况、年份和中心等因素后,丁丙诺啡与较短的住院时长相关(风险比(HR)=1.47(95%置信区间(CI):1.32 - 1.62,P<0.001))。在使用根据产前药物接触倾向评分进行1:1匹配的婴儿的模型中,我们观察到了类似结果(丁丙诺啡的HR为1.39,CI为1.32 - 1.62,P<0.001)。
在妊娠≥36周且患有NAS的婴儿中,与产前接触美沙酮相比,产前接触丁丙诺啡与住院时长缩短相关。