南非儿科重症监护室对创伤后癫痫发作的药物治疗。

N Yachad, K D Naidoo
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引用次数: 0

摘要

背景:创伤性脑损伤(TBI)是南非儿科重症监护病房(PICU)收治病人的常见原因。对这些患者的最佳护理包括预防和控制创伤后癫痫发作(PTS),以尽量减少继发性脑损伤:描述南非一家儿童重症监护病房收治的儿童的人口统计学特征,描述创伤后癫痫发作的特征,并描述该病房内对创伤后癫痫发作的预防和治疗管理:从2015年7月1日至2018年6月30日,在约翰内斯堡索韦托克里斯-哈尼-巴拉夸那思学术医院(CHBAH)的PICU进行了为期3年的回顾性病历审查:78名患者入住PICU,均为严重创伤性脑损伤患者。共有66份患者档案可供分析。入院年龄中位数为6岁(四分位数间距(IQR)为4 - 9),大部分创伤继发于机械性损伤(89%)。44名患者(79%)开始服用预防性抗癫痫药物(AED)。11名(25%)患者接受了预防性治疗,4名(33%)患者未接受预防性治疗,均出现了早期 PTS。3名患者(5%)出现了晚期 PTS,因此 PTS 的总发生率为 43%。最常见的癫痫发作类型是全身强直阵挛发作(82%)。被诊断出患有 PTS 的儿童比未患有 PTS 的儿童平均年龄小 2 岁,2 岁以下儿童的癫痫发作率增加(83% 对 38%)。所有患者均按照推荐剂量开始接受维持治疗。在维持治疗期间服用的总共 167 种抗癫痫药物中,只有 56% 在目标范围内。在最初的 78 名患者中,有 8 人死亡(10%)。PTS患儿在重症监护室和医院的中位住院时间分别延长了7天(IQR 5 - 12)和8天(IQR 8 - 24):结论:PTS 是儿童严重创伤性脑损伤的常见并发症。预防和维持治疗 PTS 的方法在药物选择、剂量、药物监测频率和处理亚治疗水平的方法方面存在很大差异。显然,需要进行更多高水平的研究,以便更好地为这些做法提供依据:据我们所知,这篇文章首次描述了儿科创伤后癫痫发作的发生率和管理方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pharmacological management of post-traumatic seizures in a South African paediatric intensive care unit.

Pharmacological management of post-traumatic seizures in a South African paediatric intensive care unit.

Pharmacological management of post-traumatic seizures in a South African paediatric intensive care unit.

Pharmacological management of post-traumatic seizures in a South African paediatric intensive care unit.

Background: Traumatic brain injury (TBI) is a common cause of paediatric intensive care unit (PICU) admissions in South Africa. Optimal care of these patients includes the prevention and control of post-traumatic seizures (PTS) in order to minimise secondary brain injury.

Objectives: To describe the demographics of children admitted to a South African PICU, to describe the characteristics of PTS, and to describe the prophylactic and therapeutic management of PTS within the unit.

Methods: A 3-year retrospective chart review was conducted at the PICU of the Chris Hani Baragwanath Academic Hospital (CHBAH) in Soweto, Johannesburg, from 1 July 2015 to 30 June 2018.

Results: Seventy-eight patients were admitted to the PICU, all with severe TBI. A total of 66 patient files were available for analysis. The median age of admission was 6 years (interquartile range (IQR) 4 - 9) with the majority of trauma secondary to mechanical injury (89%). Prophylactic anti-epileptic drugs (AEDs) were initiated in 44 (79%) patients. Early PTS occurred in 11 (25%) patients who received prophylaxis and 4 (33%) who did not. Three (5%) patients developed late PTS, resulting in an overall incidence of PTS of 43%. The most common seizure type was generalised tonic clonic (82%). Children diagnosed with PTS were a median of 2 years younger than those without PTS, with increased prevalence of seizures (83% v. 38%) in children below 2 years of age. Maintenance therapy was initiated in all patients consistent with recommended dosages. Of the total 167 anti-epileptic levels taken during maintenance, only 56% were within target range. Of the initial 78 patients, 8 died (10%). The median length of stay was 7 (IQR 5 - 12) and 8 (IQR 8 - 24) days longer in ICU and hospital respectively, in children with PTS.

Conclusion: PTS is a frequent complication of severe TBI in children. There was considerable variation in the approach to both prophylaxis and maintenance therapy of PTS in terms of choice of agent, dosage, frequency of drug monitoring and approach to subtherapeutic levels. It is clear that more high-level studies are required in order to better inform these practices.

Contributions of the study: To the best of our knowledge, this article represents the first description of incidence and management practices of paediatric post traumatic seizures.

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