Milbrandt Eric B, Angus Derek C
CRISMA Laboratory, Department of Critical Care Medicine, University of Pittsburgh School of Medicine, 641 Scaife Hall, 3550 Terrace St, Pittsburgh, PA 15261, USA.
Crit Care. 2006;10(6):238. doi: 10.1186/cc5078.
Cognitive dysfunction is common in critically ill patients, not only during the acute illness but also long after its resolution. A large number of pathophysiologic mechanisms are thought to underlie critical illness-associated cognitive dysfunction, including neuro-transmitter abnormalities and occult diffuse brain injury. Markers that could be used to evaluate the influence of specific mechanisms in individual patients include serum anticholinergic activity, certain brain proteins, and tissue sodium concentration determination via high-resolution three-dimensional magnetic resonance imaging. Although recent therapeutic advances in this area are exciting, they are still too immature to influence patient care. Additional research is needed if we are to understand better the relative contributions of specific mechanisms to the development of critical illness-associated cognitive dysfunction and to determine whether these mechanisms might be amenable to treatment or prevention.
认知功能障碍在重症患者中很常见,不仅在急性疾病期间如此,在疾病缓解后的很长时间内也是如此。大量病理生理机制被认为是重症相关认知功能障碍的基础,包括神经递质异常和隐匿性弥漫性脑损伤。可用于评估个体患者特定机制影响的标志物包括血清抗胆碱能活性、某些脑蛋白以及通过高分辨率三维磁共振成像测定组织钠浓度。尽管该领域最近的治疗进展令人兴奋,但它们仍不够成熟,无法影响患者护理。如果我们想更好地理解特定机制对重症相关认知功能障碍发生发展的相对贡献,并确定这些机制是否可能适合治疗或预防,就需要更多的研究。