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本文引用的文献

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Retrospective study on neonatal seizures in a tertiary center of northern Italy after ILAE classification: Incidence, seizure type, EEG and etiology.意大利北部一家三级中心基于 ILAE 分类的新生儿惊厥回顾性研究:发生率、惊厥类型、脑电图和病因。
Epilepsy Behav. 2024 Oct;159:109971. doi: 10.1016/j.yebeh.2024.109971. Epub 2024 Aug 1.
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Neonatal Seizures.
Pediatr Rev. 2024 Jul 1;45(7):381-393. doi: 10.1542/pir.2023-006016.
3
Seizure semiology: ILAE glossary of terms and their significance.癫痫发作的临床表现:ILAE 术语及其意义词汇表。
Epileptic Disord. 2022 Jun 1;24(3):447-495. doi: 10.1684/epd.2022.1430.
4
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions.国际抗癫痫联盟儿童期起病的癫痫综合征分类和定义:ILAE 分类和定义工作组的立场文件。
Epilepsia. 2022 Jun;63(6):1398-1442. doi: 10.1111/epi.17241. Epub 2022 May 3.
5
Neonatal seizures: stepping outside the comfort zone.新生儿惊厥:走出舒适区
Clin Exp Pediatr. 2022 Nov;65(11):521-528. doi: 10.3345/cep.2022.00115. Epub 2022 Apr 4.
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Neonatal seizures: diagnostic updates based on new definition and classification.新生儿惊厥:基于新定义和分类的诊断进展
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7
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Neurotherapeutics. 2021 Jul;18(3):1564-1581. doi: 10.1007/s13311-021-01085-8. Epub 2021 Aug 12.
8
Seizures in the neonate: A review of etiologies and outcomes.新生儿惊厥:病因与结局的综述。
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9
Risk Factors for Mortality among Newborns with Neonatal Seizures.新生儿惊厥患者的死亡危险因素。
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10
Biochemical abnormalities in neonatal seizures.新生儿惊厥的生化异常
Indian J Pediatr. 2003 Mar;70(3):221-4. doi: 10.1007/BF02725588.

新生儿非代谢性癫痫发作分布与生化异常的关系

Neonatal Non-metabolic Seizure Distribution in Relation to Biochemical Abnormalities.

作者信息

Rajesh Reddy Kothakapu, Potpalle Dnyaneshwar, Mohammed Abdul Muqeeth, Dinesh Eshwar Mummareddi

机构信息

Paediatrics and Child Health, Mahavir Institute of Medical Sciences, Vikarabad, IND.

Biochemistry, Mahavir Institute of Medical Sciences, Vikarabad, IND.

出版信息

Cureus. 2025 Feb 26;17(2):e79723. doi: 10.7759/cureus.79723. eCollection 2025 Feb.

DOI:10.7759/cureus.79723
PMID:40161050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11954420/
Abstract

Introduction Neonatal seizures are a significant neurological manifestation in the early days of life. They can cause long-term developmental disabilities and increase mortality rates if not properly managed. They can also be a sign of underlying neurological disorders, metabolic disturbances, or hypoxic-ischemic injury. Among the numerous etiologies, birth asphyxia, neonatal meningitis, and biochemical abnormalities are widespread. Biochemical abnormalities occur either as an underlying cause or as an associated abnormality. So biochemical anomalies should be excluded in every case of neonatal seizure, despite the presence of other causes of neonatal seizures. Early recognition and treatment of these biochemical disturbances are essential for optimal management and satisfactory outcomes. We assessed the proportion of newborn seizures caused by different etiologies in the current study with due emphasis on biochemical causes. Methods A prospective observational study was conducted in a university-affiliated teaching hospital between November 2015 and April 2017 (17 months). The study recruited 100 neonates who had a history of seizures. A comprehensive history and examination have been recorded upon admission, along with appropriate investigations. The study was approved by the institutional ethics committee, and all participants provided their voluntary informed consent. Results Among 100 cases of neonatal seizures, biochemical abnormalities were identified in 75 cases, comprising 52 (69.3%) non-metabolic seizures and 23 (30.6%) pure metabolic convulsions. The predominant biochemical abnormalities in neonatal seizures are hypoglycemia in 34 of 75 cases (45.3%) and hypocalcemia in 17 of 75 cases (22.7%). The most frequent abnormality in non-metabolic seizure patients was low blood sugar in 23 (44.2%), followed by low calcium in 12 (23.1%), low phosphate in eight (15.4%), high sodium in six (11.5%), low sodium in two (3.8%), and low magnesium in one (1.9%). Out of the 23 subjects with hypoglycemia in non-metabolic seizures, 12 (52.1%) were associated with perinatal asphyxia, while 11 (47.9%) were linked to septicemia. The biochemical abnormalities identified in metabolic seizures were hypophosphatemia in four (17.4%), hypomagnesemia in three (13%), hypoglycemia in 11 of 23 patients (47.8%), and hypocalcemia in five (21.7%). Conclusion Improving outcomes and quality of life for newborns impacted by non-metabolic neonatal seizures requires a comprehensive approach to treatment. This includes the appropriate therapy, the results of the biochemical testing, and the clinical evaluation.

摘要

引言

新生儿惊厥是生命早期一种重要的神经学表现。如果处理不当,它们会导致长期发育障碍并增加死亡率。它们也可能是潜在神经疾病、代谢紊乱或缺氧缺血性损伤的迹象。在众多病因中,出生窒息、新生儿脑膜炎和生化异常较为常见。生化异常既可以是根本原因,也可以是相关异常。因此,在每一例新生儿惊厥病例中,无论是否存在其他新生儿惊厥病因,都应排除生化异常。早期识别和治疗这些生化紊乱对于优化管理和取得满意结果至关重要。在本研究中,我们评估了不同病因导致的新生儿惊厥比例,并特别强调了生化原因。

方法

2015年11月至2017年4月(17个月)期间,在一家大学附属医院进行了一项前瞻性观察研究。该研究招募了100名有惊厥病史的新生儿。入院时记录了全面的病史和检查情况,并进行了适当的调查。该研究得到了机构伦理委员会的批准,所有参与者均提供了自愿知情同意书。

结果

在100例新生儿惊厥病例中,75例发现有生化异常,其中52例(69.3%)为非代谢性惊厥,23例(30.6%)为单纯代谢性惊厥。新生儿惊厥中主要的生化异常是75例中的34例(45.3%)低血糖和75例中的17例(22.7%)低钙血症。非代谢性惊厥患者最常见的异常是23例(4'4.2%)低血糖,其次是12例(23.1%)低钙,8例(15.4%)低磷,6例(11.5%)高钠',2例(3.8%)低钠,1例(1.9%)低镁。在非代谢性惊厥的23例低血糖患者中,12例(52.1%)与围产期窒息有关,而11例(47.9%)与败血症有关。代谢性惊厥中发现的生化异常为4例(17.4%)低磷血症,3例(13%)低镁血症,23例患者中的11例(47.8%)低血糖,5例(21.7%)低钙血症。

结论

改善受非代谢性新生儿惊厥影响的新生儿的预后和生活质量需要综合治疗方法。这包括适当的治疗、生化检测结果和临床评估。