未接受低温治疗的轻度缺氧缺血性脑病婴儿的预后

Biomedicine Hub Pub Date : 2019-10-10 eCollection Date: 2019-09-01 DOI:10.1159/000502936
Jonathan Reiss, Mridu Sinha, Jeffrey Gold, Julie Bykowski, Shelley M Lawrence
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引用次数: 18

摘要

准确诊断和治疗轻度缺氧缺血性脑病(HIE)的婴儿是很重要的,因为大多数出生后出现HIE体征和症状的新生儿不符合中度或重度疾病的临床标准。然而,新出现的证据表明,患有轻度HIE (mHIE)的婴儿出现神经发育障碍(NDI)的风险增加。方法:本回顾性描述性研究调查了2012年1月1日至2015年12月31日期间在加州单一III级新生儿重症监护病房(NICU)出生的所有≥35周胎龄的新生儿。使用国际疾病分类代码作为代理来识别患有mHIE但未接受治疗性低温(TH)的新生儿。记录了短期和长期的神经发育结果,包括:(1)出生10天内的脑磁共振成像异常提示HIE,(2)伴有电图癫痫的脑电图异常,(3)神经系统出院检查,或(4)新生儿重症监护病房出院后的NDI。结果:在4年的研究期间,25名婴儿符合纳入标准。25名婴儿中有8名(32%)表现出神经功能障碍,定义为四类中至少一种异常。其余17名婴儿没有不良结果的记录证据。结论:我们的研究结果表明,患有mHIE的儿童有显著的神经损伤风险,可能从更积极的干预措施中受益。进一步的前瞻性研究应该完成,以确定在这一特定的患者群体的疗效TH。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Outcomes of Infants with Mild Hypoxic Ischemic Encephalopathy Who Did Not Receive Therapeutic Hypothermia.

Outcomes of Infants with Mild Hypoxic Ischemic Encephalopathy Who Did Not Receive Therapeutic Hypothermia.

Outcomes of Infants with Mild Hypoxic Ischemic Encephalopathy Who Did Not Receive Therapeutic Hypothermia.

Introduction: Accurately diagnosing and treating infants with mild forms of hypoxic ischemic encephalopathy (HIE) is important, as the majority of neonates with signs and symptoms of HIE after birth do not meet clinical criteria for moderate or severe disease. Emerging evidence, however, suggests that infants with mild HIE (mHIE) have an increased risk for neurodevelopmental impairment (NDI).

Methods: This retrospective descriptive study examined all inborn infants ≥35 week's gestational age at a single, level III neonatal intensive care unit (NICU) in California between January 1, 2012, and December 31, 2015. International Classification of Diseases codes were used as a proxy to identify neonates with mHIE but who did not receive therapeutic hypothermia (TH). Short- and long-term neurodevelopmental outcomes were documented, including abnormal (1) brain magnetic resonance imaging within 10 days of birth suggestive of HIE, (2) electroencephalogram with electrographic seizures, (3) neurologic discharge examination, or (4) NDI following NICU discharge.

Results: Over the 4-year study period, 25 infants met inclusion criteria. Eight of 25 (32%) infants demonstrated neurologic impairment, defined by an abnormality in at least one of the four categories. The remaining 17 infants were without documented evidence for adverse outcomes.

Conclusion: Our results indicate that children with mHIE are at significant risk for neurologic injury and may benefit from more aggressive interventions. Further prospective studies should be completed to determine the efficacy of TH in this specific patient population.

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