Green M S, Aman M M, Stevens L, Voralu K, Saththasivam P, Mychaskiw G, Katsetos C D
Department of Anesthesiology, Drexel University College of Medicine, Hahnemann University Hospital, Philadelphia, PA, USA -
Minerva Anestesiol. 2015 Dec;81(12):1329-37. Epub 2015 Sep 3.
Numerous animal models have demonstrated neuronal damage resulting from anesthetic exposure in the developing brain. Studies have shown a relationship between anesthetic exposure and brain hypoxia, neurodegeneration and apoptosis. The relevance of data derived from controlled experimental studies to human neuropathology is a subject of debate. This study compares histopathological findings in post-mortem brain tissue specimens from children with and without exposure to inhalational anesthetic agents.
Autopsy reports were reviewed. Patients were divided into exposure and non-exposure groups defined as any procedure involving inhalational anesthetic agents. A retrospective chart review was performed collecting pathological findings of the brain. The autopsy results examined the presence of twelve different histopathological parameters reflecting morphologic changes in thirteen regions of interest in the central nervous system.
Post-mortem neuropathological findings were analyzed. Thirteen different areas were focused upon and changes were categorized into twelve histopathological parameters. Gliosis, which was confirmed by immunohistochemical staining for glial fibrillary acidic protein, was more prevalent in the exposure group (N.=48) compared to the non-exposure group (N.=20) (P<0.05).
The role of anesthetic neurotoxicity is not well understood. Numerous animal models have demonstrated neuronal apoptotic changes linked to anesthetic exposure, there is no tangible evidence supporting this relationship in humans. Our analysis demonstrates histopathological brain changes in children with anesthetic exposure not seen in the non-exposed group. Analysis was based on histopathological parameters representative of salient morphological findings of injury, which were encountered in anatomically divergent regions. Gliosis was the only statistically significant finding in post-mortem brain samples of patients who had received anesthetics.
众多动物模型已证明发育中的大脑因接触麻醉剂会导致神经元损伤。研究表明麻醉剂接触与脑缺氧、神经退行性变和细胞凋亡之间存在关联。来自对照实验研究的数据与人类神经病理学的相关性是一个有争议的话题。本研究比较了接触和未接触吸入性麻醉剂的儿童尸检脑组织标本中的组织病理学发现。
回顾尸检报告。患者被分为接触组和非接触组,接触组定义为任何涉及吸入性麻醉剂的手术。进行回顾性病历审查以收集脑部的病理结果。尸检结果检查了反映中枢神经系统13个感兴趣区域形态变化的12种不同组织病理学参数的存在情况。
对尸检神经病理学发现进行了分析。重点关注13个不同区域,并将变化归类为12种组织病理学参数。通过胶质纤维酸性蛋白免疫组化染色证实的胶质增生在接触组(N = 48)中比非接触组(N = 20)更普遍(P < 0.05)。
麻醉剂神经毒性的作用尚未完全了解。众多动物模型已证明与麻醉剂接触相关的神经元凋亡变化,但在人类中没有确凿证据支持这种关系。我们的分析表明,接触麻醉剂的儿童脑组织出现了未接触组未见的组织病理学变化。分析基于代表损伤显著形态学发现的组织病理学参数,这些变化出现在解剖学上不同的区域。胶质增生是接受麻醉剂患者尸检脑样本中唯一具有统计学意义的发现。