接触大麻的早产儿的新生儿和儿童发病风险。

Sarah K Dotters-Katz, Marcela C Smid, Tracy A Manuck, Torri D Metz
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引用次数: 0

摘要

背景:有关胎儿期暴露于大麻(MJ)的婴儿(尤其是早产儿)的新生儿和神经发育结果的数据有限。我们假设,与未接触过大麻的婴儿相比,接触过大麻的早产儿的新生儿期和儿童期发育结果会更差:我们对产前硫酸镁预防脑瘫的多中心随机对照试验进行了二次分析。结果:1867 名婴儿符合纳入标准;1867 名婴儿的出生日期为出生时:1867名婴儿符合纳入标准;135名(7.2%)婴儿接触过硫酸镁。与未接触过 MJ 的婴儿相比,接触过 MJ 的婴儿在新生儿期(20% 对 26%,P = 0.14)或儿童期(26% 对 21%,P = 0.21)的结果没有差异。在调整模型中,暴露于 MJ 与新生儿不良结局(aOR 0.83 95% CI 0.47,1.44)或儿童早期结局(aOR 1.47, 95% CI 0.97,2.23)无关:结论
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Risk of neonatal and childhood morbidity among preterm infants exposed to marijuana.

Background: Limited data exist regarding the neonatal and neurodevelopmental outcomes of infants exposed to marijuana (MJ) in-utero, particularly among preterm infants. We hypothesized that MJ-exposed preterm infants would have worse neonatal and childhood developmental outcomes compared to MJ-unexposed infants.

Methods: Secondary analysis of multicenter randomized-controlled trial of antenatal magnesium sulfate for the prevention of cerebral palsy was conducted. Singleton nonanomalous infants delivered <35 weeks exposed to MJ in-utero were compared to MJ-unexposed. Primary neonatal outcome was death, grade 3/4 intraventricular hemorrhage, periventricular leukomalacia, bronchopulmonary dysplasia, and/or stage II/III necrotizing enterocolitis before discharge. Primary childhood outcome was death, moderate/severe cerebral palsy, or/and Bayley II Scales <70 at age 2. Backward-stepwise regression used to estimate odds of primary outcomes.

Results: 1867 infants met inclusion criteria; 135(7.2%) were MJ-exposed. There were no differences in neonatal (20% vs. 26%, p = 0.14) or childhood (26% vs. 21%, p = 0.21) outcomes in MJ-exposed infants compared to MJ-unexposed infants. In adjusted models, MJ-exposure was not associated with adverse neonatal outcomes (aOR 0.83 95% CI 0.47,1.44) or early childhood outcomes (aOR 1.47, 95% CI 0.97,2.23).

Conclusions: Among infants born <35 weeks of gestation, MJ-exposure was not associated with adverse neonatal or childhood outcomes. Long-term follow-up studies are needed to assess later childhood neurodevelopmental outcomes following MJ-exposure.

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