全身麻醉对脑发育的影响:从动物到临床研究的证据

Xinyue Liu, J. Jing, Guo-Qing Zhao
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引用次数: 12

摘要

随着全身麻醉与脊髓麻醉(GAS)研究的最新更新以及其他临床证据于2019年发表,人体研究提供了压倒性的混合证据,证明儿童早期麻醉暴露与儿童后期神经发育变化之间存在关联。动物临床前研究提供了强有力的证据,证明麻醉和镇静剂(ASAs)如何在发育中的大脑中引起神经毒性和长期认知功能缺陷。然而,临床前结果不能直接转化为临床实践。三个设计良好的基于人群的大型人体研究强烈表明,单次短暂的全身麻醉(GAs)暴露与儿童大脑的任何长期神经发育缺陷无关。多次接触可能导致儿童的处理速度和运动技能下降。然而,气体与儿童神经发育之间的关系仍然没有定论。为了提供更多结论性和信息性的数据,未来需要更多的临床研究、更大规模的观察、更长时间的气体暴露和随访的随机试验、更敏感的结果测量和严格的混杂对照。新的研究领域已经发展,有助于寻找解决方案的临床实践,如减轻神经毒性作用的asa。氙和右美托咪定已经作为神经保护和麻醉保留作用在临床中使用,但仍需要更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
General Anesthesia Affecting on Developing Brain: Evidence from Animal to Clinical Research
As the recent update of General Anaesthesia compared to Spinal anaesthesia (GAS) studies has been published in 2019, together with other clinical evidence, the human studies provided an overwhelming mixed evidence of an association between anaesthesia exposure in early childhood and later neurodevelopment changes in children. Pre-clinical studies in animals provided strong evidence on how anaesthetic and sedative agents (ASAs) causing neurotoxicity in developing brain and deficits in long-term cognitive functions. However pre-clinical results cannot translate to clinical practice directly. Three well designed large population-based human studies strongly indicated that a single brief exposure to general anesthesia (GAs) is not associated with any long-term neurodevelopment deficits in children’s brain. Multiple exposure might cause decrease in processing speed and motor skills of children. However, the association between GAs and neurodevelopment in children is still inconclusive. More clinical studies with larger scale observations, randomized trials with longer duration exposure of GAs and follow-ups, more sensitive outcome measurements, and strict confounder controls are needed in the future to provide more conclusive and informative data. New research area has been developed to contribute in finding solutions for clinical practice as attenuating the neurotoxic effect of ASAs. Xenon and Dexmedetomidine are already used in clinical setting as neuroprotection and anaesthetic sparing-effect, but more research is still needed.
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