Individualized Neuroprognostication in Neonates With Hypoxic-Ischemic Encephalopathy Treated With Hypothermia.

IF 2.3 Q3 CLINICAL NEUROLOGY Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200370
Andrea Van Steenis, Mehmet N Cizmeci, Floris Groenendaal, Marianne Thoresen, Frances M Cowan, Linda S de Vries, Sylke J Steggerda
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Abstract

Background and objectives: To determine whether post-rewarming brain MRI enables individualized domain-specific prediction of neurodevelopmental outcomes at 2 years of age in infants treated with hypothermia for hypoxic-ischemic brain injury.

Methods: We conducted a retrospective multicenter study of infants with moderate-to-severe hypoxic-ischemic encephalopathy (HIE) treated with hypothermia. Brain MRI abnormalities and the prediction of domain-specific 2-year neurodevelopmental outcomes were scored independently by 2 investigators after which consensus was reached for both imaging findings and outcome prediction. Neuroimaging patterns were categorized as normal, white matter (WM)/watershed-predominant, deep gray matter (DGM)-predominant, and near-total injury. Outcomes were predicted separately for mortality, cerebral palsy (CP) type and severity, cognitive delay, epilepsy, cerebral visual impairment (CVI), and feeding difficulties; these outcomes were predicted as highly unlikely, possible, probable, or highly likely.

Results: Of the 152 study infants, 27 (18%) died. The neurodevelopmental outcome at 2 years was available in all 125 survivors. CP was seen in 21 of 125 surviving infants (17%). No infants in the highly unlikely category developed CP while 90% in the highly likely category did. When CP was predicted as possible, 40% developed CP; all were mild and ambulatory. When CP was predicted as probable, 67% developed CP of whom 40% were severe and nonambulatory. Cognitive scores were available in 104 of 125 infants (83%). Cognitive delay was seen in 23 of 104 infants (22%) (15% mild and 7% severe). When cognitive delay was predicted as highly unlikely, 92% did not develop cognitive delay and the delay was mild in those who did. When cognitive delay was considered highly likely, this developed in 100%. When epilepsy, CVI, and feeding problems were predicted as highly unlikely, 98% did not develop epilepsy; for CVI and feeding problems, this was 100% and 97%, respectively. In 27 of 152 infants (18%), the investigators reached consensus that the overall injury was severe enough to consider redirection of care; 21 of 27 infants (78%) died. Of the survivors, 5 infants developed severe CP and 1 had a mild dyskinetic CP with swallowing problems and CVI.

Discussion: Individualized domain-specific categorical neuroprognostication mainly based on brain MRI is feasible, reliable, and highly accurate in infants with HIE.

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低温治疗缺氧缺血性脑病新生儿的个性化神经诊断。
背景和目的:确定回温后脑部核磁共振成像能否对因缺氧缺血性脑损伤而接受低体温治疗的婴儿2岁时的神经发育结局进行个体化领域特异性预测:我们对接受低体温治疗的中重度缺氧缺血性脑病(HIE)婴儿进行了一项回顾性多中心研究。脑部核磁共振成像异常和对特定领域两年神经发育结果的预测由两名研究人员独立评分,然后就成像结果和结果预测达成共识。神经影像学模式分为正常、白质(WM)/分水岭为主、深灰质(DGM)为主和接近完全损伤。对死亡率、脑瘫(CP)类型和严重程度、认知发育迟缓、癫痫、脑性视力障碍(CVI)和喂养困难分别进行了预测;这些结果被预测为极不可能、可能、可能或极有可能:结果:在研究的 152 名婴儿中,27 名(18%)死亡。所有 125 名存活者均有 2 岁时的神经发育结果。125名存活婴儿中有21名(17%)患有CP。极不可能发生 CP 的婴儿中没有人发生 CP,而极有可能发生 CP 的婴儿中有 90% 的人发生了 CP。在预测可能患上 CP 的情况下,40% 的婴儿患上了 CP;所有患儿的病情都很轻微,可以行走。当 CP 被预测为可能时,67% 的婴儿患上了 CP,其中 40% 的婴儿病情严重且无法行走。125 名婴儿中有 104 名(83%)可获得认知评分。104 例婴儿中有 23 例(22%)出现认知发育迟缓(15% 为轻度,7% 为重度)。当认知迟缓被预测为极不可能发生时,92% 的婴儿未出现认知迟缓,出现认知迟缓的婴儿认知迟缓程度较轻。当认知迟缓被认为极有可能发生时,100%的婴儿都出现了认知迟缓。当癫痫、CVI 和喂养问题被预测为极不可能发生时,98% 的婴儿没有发生癫痫;CVI 和喂养问题的发生率分别为 100% 和 97%。在 152 名婴儿中,有 27 名婴儿(占 18%)的整体损伤严重到需要考虑调整护理方向,调查人员对此达成了共识;27 名婴儿中有 21 名(占 78%)死亡。在幸存者中,5 名婴儿发展为重度脊髓灰质炎,1 名婴儿患有轻度运动障碍脊髓灰质炎,并伴有吞咽困难和 CVI:讨论:主要基于脑磁共振成像的个体化特定领域分类神经诊断对 HIE 婴儿是可行、可靠和高度准确的。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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