认知障碍与社区获得性肺炎住院后的死亡率

Julio A. Ramirez, S. Furmanek, T. Chandler, W. Mattingly, Anupama Raghuram, Ashley M. Wilde, Smita S Ghare, Paula M. Chilton, Shirish S Barve
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摘要

在美国,社区获得性肺炎(CAP)每年影响约 150 万名患者,导致严重的急性和长期临床后果。人们日益认识到,CAP 是一种多系统疾病,可能会对神经、肺、心血管、肌肉骨骼、新陈代谢和肾脏等多个器官系统造成影响。本研究的主要目的是回顾有关 CAP 住院后长期认知障碍、痴呆和存活率下降的文献。此外,还探讨了肠道-肺-脑轴在这些结果的发病机制中的潜在作用。我们对现有文献进行了全面回顾,重点研究了 CAP 住院患者的认知障碍、痴呆和死亡率。通过对医学数据库进行系统检索,确定了相关研究,并提取了有关研究设计、人群特征、认知评估和结果的数据。综述还纳入了对肠道-肺-脑轴的机理认识,以假设其在 CAP 长期后遗症中的作用。综述发现多项研究表明,CAP 住院后认知功能障碍和痴呆症的风险增加。与对照组相比,因 CAP 住院的患者出现认知障碍的风险要高出 1.5 到 2.5 倍。这种认知能力的下降并不局限于老年患者,而是跨越了所有成年年龄组。此外,CAP 还与预期寿命的显著缩短有关。CAP住院后出院的患者在三年内的死亡率达到50%,而因其他原因住院的患者在七年内的死亡率为50%。需要入住重症监护室的 CAP 患者和免疫力低下的患者的存活率下降最为明显。CAP 与严重的长期认知障碍和生存率下降有关。所提出的肠道-肺-脑轴机制表明,与 CAP 相关的菌群失调会导致慢性全身性炎症和神经炎症,从而可能导致认知能力下降和死亡率升高。了解这一轴心的作用可为控制 CAP 的长期神经后果提供新的治疗策略。未来的研究应重点关注高危人群,以制定有针对性的干预措施,减轻这些严重后果。
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Cognitive Impairment and Mortality after Hospitalization for Community-Acquired Pneumonia
Community-acquired pneumonia (CAP) affects approximately 1.5 million patients annually in the United States, leading to significant acute and long-term clinical outcomes. CAP is increasingly recognized as a multisystemic disease with potential sequelae affecting various organ systems, including the neurologic, pulmonary, cardiovascular, musculoskeletal, metabolic, and renal systems. The primary objective of this study is to review literature on long-term cognitive impairment, dementia, and decreased survival following CAP hospitalization. Additionally, the potential role of the gut-lung-brain axis in the pathogenesis of these outcomes is explored. A comprehensive review of existing literature was conducted, focusing on studies that examined cognitive impairment, dementia, and mortality in patients hospitalized for CAP. Relevant studies were identified through a systematic search of medical databases, and data were extracted on study design, population characteristics, cognitive assessments, and outcomes. The review also incorporated mechanistic insights into the gut-lung-brain axis to hypothesize its role in the long-term sequelae of CAP. The review identified multiple studies demonstrating an increased risk of cognitive impairment and dementia following CAP hospitalization. Patients hospitalized for CAP had a 1.5 to 2.5 times higher risk of developing cognitive deficits compared to controls. This cognitive decline was not limited to elderly patients but spanned all adult age groups. Furthermore, CAP was associated with a significant reduction in life expectancy. Patients discharged after CAP hospitalization reached 50% mortality within three years, compared to seven years for those hospitalized for other reasons. The most pronounced decrease in survival was observed in CAP patients requiring ICU admission and immunocompromised patients. CAP is associated with significant long-term cognitive impairment and decreased survival. The proposed gut-lung-brain axis mechanism suggests that CAP-related dysbiosis leads to chronic systemic inflammation and neuroinflammation, potentially contributing to cognitive decline and increased mortality. Understanding the role of this axis may offer new therapeutic strategies for managing the long-term neurological consequences of CAP. Future research should focus on high-risk populations to develop targeted interventions aimed at mitigating these severe outcomes.
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