Division of Neurocritical Care and Emergency Neurology, Department of Neurology, Yale School of Medicine, New Haven, CT, USA.
Critical Illness, Brain Dysfunction, Survivorship (CIBS) Center, Department of Pulmonary and Critical Care Medicine, Veteran's Affairs Tennessee Valley Geriatric Research Education and Clinical Center (GRECC), Vanderbilt University School of Medicine, Nashville, TN, USA.
Crit Care. 2019 Nov 12;23(1):352. doi: 10.1186/s13054-019-2626-z.
Acute respiratory distress syndrome (ARDS) survivors experience a high prevalence of cognitive impairment with concomitantly impaired functional status and quality of life, often persisting months after hospital discharge. In this review, we explore the pathophysiological mechanisms underlying cognitive impairment following ARDS, the interrelations between mechanisms and risk factors, and interventions that may mitigate the risk of cognitive impairment. Risk factors for cognitive decline following ARDS include pre-existing cognitive impairment, neurological injury, delirium, mechanical ventilation, prolonged exposure to sedating medications, sepsis, systemic inflammation, and environmental factors in the intensive care unit, which can co-occur synergistically in various combinations. Detection and characterization of pre-existing cognitive impairment imparts challenges in clinical management and longitudinal outcome study enrollment. Patients with brain injury who experience ARDS constitute a distinct population with a particular combination of risk factors and pathophysiological mechanisms: considerations raised by brain injury include neurogenic pulmonary edema, differences in sympathetic activation and cholinergic transmission, effects of positive end-expiratory pressure on cerebral microcirculation and intracranial pressure, and sensitivity to vasopressor use and volume status. The blood-brain barrier represents a physiological interface at which multiple mechanisms of cognitive impairment interact, as acute blood-brain barrier weakening from mechanical ventilation and systemic inflammation can compound existing chronic blood-brain barrier dysfunction from Alzheimer's-type pathophysiology, rendering the brain vulnerable to both amyloid-beta accumulation and cytokine-mediated hippocampal damage. Although some contributory elements, such as the presenting brain injury or pre-existing cognitive impairment, may be irreversible, interventions such as minimizing mechanical ventilation tidal volume, minimizing duration of exposure to sedating medications, maintaining hemodynamic stability, optimizing fluid balance, and implementing bundles to enhance patient care help dramatically to reduce duration of delirium and may help prevent acquisition of long-term cognitive impairment.
急性呼吸窘迫综合征(ARDS)幸存者常伴有认知功能障碍,同时存在功能状态和生活质量受损,这种情况往往在出院后数月仍持续存在。在这篇综述中,我们探讨了 ARDS 后认知障碍的病理生理机制、机制与危险因素之间的相互关系,以及可能减轻认知障碍风险的干预措施。ARDS 后认知能力下降的危险因素包括:存在认知障碍、脑损伤、谵妄、机械通气、镇静药物暴露时间延长、脓毒症、全身炎症反应和重症监护病房的环境因素,这些因素可以协同作用,以各种组合方式出现。ARDS 患者认知障碍的检测和特征赋予了临床管理和纵向结局研究入组的挑战。经历 ARDS 的脑损伤患者构成了一个具有特定危险因素和病理生理机制的特殊人群:脑损伤引起的考虑因素包括神经源性肺水肿、交感神经激活和胆碱能传递的差异、呼气末正压对脑微循环和颅内压的影响,以及对血管加压素使用和容量状态的敏感性。血脑屏障是认知障碍相互作用的生理界面,机械通气和全身炎症引起的急性血脑屏障减弱会加重由阿尔茨海默病样病理生理学引起的慢性血脑屏障功能障碍,使大脑容易受到淀粉样β蛋白积累和细胞因子介导的海马损伤的影响。虽然一些促成因素,如现有的脑损伤或存在的认知障碍,可能是不可逆的,但干预措施,如最小化机械通气潮气量、最小化镇静药物暴露时间、维持血流动力学稳定、优化液体平衡,并实施护理增强措施,有助于显著减少谵妄持续时间,并可能有助于预防长期认知障碍的发生。