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Clinical and etiological profile of neonatal seizures: a tertiary care hospital based study

机译:新生儿惊厥的临床和病因学特征:基于三级医院的研究

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Background: The most vulnerable period of life to develop seizures is the neonatal period. These events very often signify serious damage or malfunction of the immature developing central nervous system. Neonatal seizures may arise as a result of diverse etiologies and can have varied presentations. Objective: Our study was aimed at finding the incidence, etiological factors, and time of onset, clinical types and various biochemical abnormalities in neonatal seizures. Methods: A hospital based prospective observational study was undertaken in a tertiary care paediatric hospital of Government Medical College Srinagar. A total of 100 consecutive neonates presenting with seizures from September 2013 to August 2014 were enrolled in the study. Detailed antenatal history and baseline characteristics of convulsing neonate were recorded at admission. Clinical details of each seizure episode reported by the mother and subsequently observed by the resident doctors on duty were recorded. Venous blood was collected as soon as possible and blood glucose, total serum calcium levels, Na+, K+, Mg and P-levels were done immediately after baby had seizures and before instituting any treatment. Data was described as mean ± SE and %age. SPSS 16.0 and MS Excel software were used for data analysis. Results: Cumulative frequency of 3.9% was recorded in neonatal seizures in our setup. Hypoxic ischemic encephalopathy was the commonest etiology of neonatal seizures. Intracranial haemorrhage followed by Hypoxic ischemic encephalopathy was the commonest seizure etiology in preterm neonates. Majority of Hypoxic ischemic encephalopathy patients presented with seizures in the first 72 hrs. of life. Focal clonic and subtle seizures were the commonest seizure types encountered. 17 neonates (31%) had primary metabolic seizures. Hypocalcaemia was the commonest biochemical abnormality in primary metabolic seizures and was present in 70% neonates in this group. Hypoglycaemia was the next commonest abnormality and was present in 41% neonates within this group. Conclusions: Hypoxic ischemic encephalopathy was the commonest etiology with focal clonic and subtle seizures being the commonest clinical types encountered. Hypocalcaemia was the most frequent biochemical abnormality found.
机译:背景:发生癫痫发作的最脆弱时期是新生儿时期。这些事件通常表示未成熟的中枢神经系统受到严重损害或故障。新生儿癫痫发作可能是由多种病因引起的,并且表现形式也可能不同。目的:我们的研究旨在发现新生儿癫痫发作的发生率,病因,发作时间,临床类型和各种生化异常。方法:在斯利那加政府医学院的三级儿科医院进行了一项基于医院的前瞻性观察研究。从2013年9月至2014年8月,共有100例连续发作的新生儿入选了该研究。入院时记录了惊厥新生儿的详细产前病史和基线特征。记录母亲报告的每次癫痫发作的临床细节,随后由值班的驻诊医生观察。婴儿癫痫发作后立即采取静脉血,并在进行任何治疗前立即进行血糖,总血清钙水平,Na +,K +,Mg和P-水平的测定。数据描述为平均值±SE和%age。使用SPSS 16.0和MS Excel软件进行数据分析。结果:在我们的设置中,新生儿癫痫发作的累积频率为3.9%。缺氧缺血性脑病是新生儿惊厥的最常见病因。颅内出血继发缺氧缺血性脑病是早产儿最常见的癫痫发作病因。多数缺氧缺血性脑病患者在最初的72小时内出现癫痫发作。生活。局灶性阵挛性发作和轻微发作是最常见的发作类型。 17例新生儿(31%)患有原发性代谢性惊厥。低钙血症是原发性代谢性癫痫发作中最常见的生化异常,该组中70%的新生儿中存在低钙血症。低血糖是第二常见的异常,该组中41%的新生儿中存在低血糖。结论:缺氧缺血性脑病是最常见的病因,局灶性阵挛性和轻度惊厥是最常见的临床类型。低钙血症是最常见的生化异常。

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