Abstract
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 prevention of cerebral palsy was conducted. Singleton non-anomalous 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. Backwards-stepwise regression used to estimate odds of primary outcomes.
RESULTS:
1,867 infants met inclusion criteria; 135(7.2%) were MJ-exposed. There were no differences in neonatal (20%vs26%, p = 0.14) or childhood (26%vs21%, 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.
KEYWORDS:
developmental outcomes; marijuana; neonatal morbidity; prematurity
- PMID: 27921445
- DOI: 10.1080/14767058.2016.1269165
- [PubMed – as supplied by publisher]
-
LinkOut – more resources