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General movements and magnetic resonance imaging in the prediction of neuromotor outcome in children born extremely preterm

机译:全身运动和磁共振成像预测极早产儿神经运动预后

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Background: Extremely preterm (EPT) birth is a major risk factor for brain injury and neurodevelopmental impairment. Reliable tools for early prediction of outcome are warranted. Aim: To investigate the predictive value of general movements (GMs) at "fidgety age" for neurological outcome at age 30. months in EPT infants, both in comparison and in combination with structural magnetic resonance imaging (MRI) at term equivalent age (TEA). Study design: Fifty-three infants born <. 27. weeks of gestation were included prospectively. MRI was performed at TEA and images were evaluated for white and grey matter abnormalities. GMs were assessed at age 3. months corrected ("fidgety age"). Outcome measures: Neuromotor outcome was assessed at age 30. months corrected. Children were classified as having a normal neurological status, unspecific signs, or cerebral palsy (CP). Results: Abnormal GMs were a common finding, seen in 32% (17/53) of infants. Of these, six infants (11%) had definitely abnormal GMs. Four infants (8%) had a diagnosis of CP at follow up. Definitely abnormal GMs were significantly associated to CP at 30. months (Fisher's Exact test p. =. 0.03, sensitivity 50%, specificity 92%). Moderate-severe white matter abnormalities on MRI were more strongly associated with CP (Fisher's Exact test p. <. 0.001, sensitivity 100%, specificity 98%) than GMs. Combining GMs with MRI-findings at TEA increased the predictive specificity to 100% (Fisher's Exact test, p. =. 0.005), whereas sensitivity remained unchanged. Conclusions: The presence of definitely abnormal GMs was predictive of CP: prediction was significantly enhanced when the GMs assessment was combined with findings from MRI obtained at TEA.
机译:背景:极早(EPT)出生是脑损伤和神经发育障碍的主要危险因素。需要可靠的工具来早期预测结果。目的:通过比较和结合足月等效年龄(TEA)并结合结构磁共振成像(MRI),研究EPT婴儿在“烦躁年龄”进行一般运动(GM)对30个月大的神经系统结局的预测价值)。研究设计:五十三岁婴儿<。前瞻性地包括妊娠27周。在TEA进行MRI,并评估图像中的白色和灰色物质异常。在3岁时评估了GM,并纠正了三个月(“烦躁的年龄”)。结果测量:在30.个月大时评估神经运动预后。儿童被分类为具有正常的神经系统状态,非特异性体征或脑瘫(CP)。结果:异常的GM是常见的发现,在32%(17/53)的婴儿中可见。在这些婴儿中,有六个婴儿(11%)确实患有异常的GM。随访时有四名婴儿(8%)被诊断为CP。在30个月时,肯定异常的GM与CP显着相关(Fisher精确检验p。= 0.03,敏感性50%,特异性92%)。 MRI上的中度至重度白质异常与CP的相关性更高(Fisher's Exact test p。<0.001,敏感性100%,特异性98%),而与GMs相关。在TEA上将GM与MRI发现结合使用可使预测特异性提高到100%(Fisher's Exact检验,p = 0.005),而敏感性保持不变。结论:肯定异常的GMs的存在可预测CP:将GMs评估与从TEA获得的MRI结果相结合,可显着增强预测。

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