From the School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.
Bristol Anaesthesia, Pain and Critical Care Sciences, Translational Health Sciences, Bristol Medical School, Bristol Royal Infirmary, Bristol, United Kingdom.
Anesth Analg. 2019 Apr;128(4):681-694. doi: 10.1213/ANE.0000000000004052.
Neurodegeneration has been reported in young animals after exposure to all commonly used general anesthetic agents. The brain may be particularly vulnerable to anesthetic toxicity during peak synaptogenesis (in gestation and infancy). Human studies of long-term neurodevelopmental outcome following general anesthesia in early childhood report contradictory findings. This review assesses the strengths and deficiencies in human research methodologies to inform future studies. We identified 76 studies, published between 1990 and 2017, of long-term neurodevelopmental outcome following early childhood or in utero general anesthesia exposure: 49 retrospective, 9 ambidirectional, 17 prospective cohort studies, and 1 randomized controlled trial. Forty-nine studies were explicitly concerned with anesthetic-induced neurotoxicity. Full texts were appraised for methodological challenges and possible solutions. Major challenges identified included delineating effects of anesthesia from surgery, defining the timing and duration of exposure, selection of a surgical cohort and intervention, addressing multiple confounding life course factors, detecting modest neurotoxic effects with small sample sizes (median, 131 children; interquartile range, 50-372), selection of sensitive neurodevelopmental outcomes at appropriate ages for different developmental domains, insufficient length of follow-up (median age, 6 years; interquartile range, 2-12 years), and sample attrition. We discuss potential solutions to these challenges. Further adequately powered, multicenter, prospective randomized controlled trials of anesthetic-induced neurotoxicity in children are required. However, we believe that the inherent methodological challenges of studying anesthetic-induced neurotoxicity necessitate the parallel use of well-designed observational cohort studies.
神经退行性变在接触所有常用全身麻醉剂的年轻动物中已有报道。在突触形成高峰期(妊娠期和婴儿期),大脑可能特别容易受到麻醉毒性的影响。在幼儿期全身麻醉后进行的长期神经发育结局的人类研究报告结果相互矛盾。本综述评估了人类研究方法的优缺点,为未来的研究提供信息。我们确定了 76 项研究,发表于 1990 年至 2017 年之间,研究内容为幼儿期或子宫内全身麻醉暴露后长期神经发育结局:49 项回顾性研究、9 项双向研究、17 项前瞻性队列研究和 1 项随机对照试验。49 项研究专门关注麻醉诱导的神经毒性。评估了全文的方法学挑战和可能的解决方案。确定的主要挑战包括从手术中区分麻醉的影响、定义暴露的时间和持续时间、选择手术队列和干预措施、解决多个混杂的生命过程因素、用小样本量检测轻微的神经毒性效应(中位数为 131 名儿童;四分位距为 50-372)、在不同发育领域选择适当年龄的敏感神经发育结局、随访时间不足(中位数年龄为 6 岁;四分位距为 2-12 岁)以及样本流失。我们讨论了这些挑战的潜在解决方案。需要进一步开展充分的、多中心的、前瞻性的随机对照试验,研究麻醉诱导的神经毒性。然而,我们认为研究麻醉诱导的神经毒性所固有的方法学挑战需要并行使用设计良好的观察性队列研究。