Department of Neonatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands; Division of Neonatology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Canada.
Department of Neonatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.
J Pediatr. 2020 Feb;217:79-85.e1. doi: 10.1016/j.jpeds.2019.09.081. Epub 2019 Nov 6.
To describe the sonographic characteristics of periventricular hemorrhagic infarction (PVHI) and their association with mortality and neurodevelopmental disability in very preterm infants born in 2008-2013.
Retrospective multicenter observational cohort study. Diagonal PVHI size was measured and severity score assessed. PVHI characteristics were scored and temporal trends were assessed. Neurodevelopmental outcome at 2 years of corrected age was assessed using either the Bayley Scales of Infant and Toddler Development, Third Edition or the Griffiths Mental Development Scales. Multigroup analyses were applied as appropriate.
We enrolled 160 infants with median gestational age of 26.6 weeks. PVHI was mostly unilateral (90%), associated with an ipsilateral grade III intraventricular hemorrhage (84%), and located in the parietal lobe (51%). Sixty-four (40%) infants with PVHI died in the neonatal period. Of the survivors assessed at 2 years of corrected age, 65% had normal cognitive and 69% had normal motor outcomes. The cerebral palsy rate was 42%. The composite outcome of death or severe neurodevelopmental disability was observed in 58%, with no trends over the study period (P = .6). Increasing PVHI severity score was associated with death (P < .001). Increasing PVHI size and severity score were negatively associated with gross motor scores (P = .01 and .03, respectively). Trigone involvement was associated with cerebral palsy (41% vs 14%; P = .004). Associated posthemorrhagic ventricular dilation (36%) was an independent risk factor for poorer cognitive and motor outcomes (P < .001 for both).
Increasing PVHI size and severity score were predictive of less optimal gross motor outcome and death in very preterm infants.
描述 2008-2013 年出生的极早产儿脑室内出血性梗死(PVHI)的超声特征及其与死亡率和神经发育障碍的关系。
回顾性多中心观察性队列研究。测量对角 PVHI 大小并评估严重程度评分。评分 PVHI 特征并评估时间趋势。使用贝利婴幼儿发育量表第三版或格里菲斯心理发育量表评估校正年龄 2 岁时的神经发育结局。适当应用多组分析。
我们纳入了 160 名中位胎龄为 26.6 周的婴儿。PVHI 主要为单侧(90%),伴同侧 III 级脑室内出血(84%),位于顶叶(51%)。64 名(40%)PVHI 婴儿在新生儿期死亡。在 2 岁校正年龄时接受评估的幸存者中,65%认知正常,69%运动正常。脑瘫发生率为 42%。死亡或严重神经发育障碍的复合结局发生率为 58%,研究期间无趋势(P=0.6)。PVHI 严重程度评分增加与死亡相关(P<0.001)。PVHI 大小和严重程度评分增加与粗大运动评分呈负相关(P=0.01 和 P=0.03)。三角区受累与脑瘫相关(41%比 14%;P=0.004)。并发出血后脑室扩张(36%)是认知和运动结局较差的独立危险因素(均 P<0.001)。
PVHI 大小和严重程度评分增加可预测极早产儿粗大运动结局较差和死亡。