新生儿脑病多器官评分系统:系统性审查
Noor Adeebah Mohamed Razif1, Aidan D'Arcy1, Sarah Waicus1
1Discipline of Pediatrics, Trinity College Dublin, The University of Dublin, Dublin, Ireland.
Frontiers in pediatrics
|October 17, 2024
概括
新生儿脑病变 (NE) 多器官功能障碍 (MOD) 评分系统显示出显著的异质性. 一个标准化的系统应该包括神经,,肝,呼吸,血液和心血管评估新生儿.
科学领域:
- 新生儿医学 新生儿医学
- 儿科神经学 儿科神经学
- 关键的护理关键的护理
背景情况:
- 新生儿脑病变 (NE) 是一种严重的疾病,导致新生儿多器官损伤.
- 治疗性低温 (TH) 是标准的治疗方法,但在NE中评估多器官功能障碍 (MOD) 的严重程度仍然具有挑战性.
- 目前对NE中MOD评估的方法缺乏标准化.
研究的目的:
- 确定目前用于评估新生儿脑病变 (NE) 中多器官功能障碍 (MOD) 的方法.
- 根据对现有文献的系统审查,确定NE中MOD的最佳评分系统.
主要方法:
- 按照PRISMA指南进行了系统审查.
- 在多个数据库 (PubMed,EMBASE,MEDLINE,Cochrane,Scopus,CINAHL) 进行了搜索,以研究东北地区的MOD评分系统.
- 从12项纳入研究中提取和分析了数据.
主要成果:
- 五项研究表明,NE严重程度和MOD之间存在正相关性.
- 在评分系统中,在资格标准,器官系统评估方法,随访持续时间和结果方面观察到显著的异质性.
- 神经系统,肝脏系统,心血管系统,呼吸系统,血液系统和脏系统通常都被包括在内,而胃肠系统则不太常见.
结论:
- 一个理想的NE多器官评分系统应该包括神经系统,脏系统,肝脏系统,呼吸系统,血液系统和心血管系统.
- 尽管异质,这些系统提供了标准化NE中MOD评分的候选人.
- 需要进一步验证和考虑治疗性低温的影响.
更多相关视频
05:52Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy
Published on: October 28, 2022
738
08:17Author Spotlight: Unveiling the Pathway Linking Obesity to Autoimmune Inflammation in Multiple Sclerosis
Published on: February 23, 2024
4.0K
相关概念视频
Encephalitis ll: Pathophysiology
30
Encephalitis is inflammation of the brain parenchyma caused by direct viral invasion or immune-mediated mechanisms triggered by infections or tumors. Both processes lead to neuronal injury, disrupted neurotransmission, and diverse neurological symptoms, often with overlapping clinical and pathological features.Autoimmune EncephalitisIn autoimmune encephalitis, antibodies target neuronal antigens on cell surfaces, synapses, or within neurons. A key example is anti-NMDAR encephalitis, which can...
30
Hepatic Encephalopathy
71
DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic...
71
