Delayed inflammatory pulmonary syndrome: A distinct clinical entity in the spectrum of inflammatory syndromes in COVID-19 infection?

Prithviraj Bose, Binila Chacko, Ashwin Oliver Arul, Leena Robinson Vimala, Balamugesh Thangakunam, George M Varghese, Mohan Jambugulam, Audrin Lenin, John Victor Peter
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Abstract

Background: During the second wave of the coronavirus disease 2019 (COVID-19) pandemic, a subset of critically ill patients developed delayed respiratory deterioration in the absence of new infection, fluid overload or extra-pulmonary organ dysfunction.

Aim: To describe the clinical and laboratory characteristics, outcomes, and management of these patients, and to contrast this entity with other post COVID-19 immune dysregulation related inflammatory disorders.

Methods: This was a retrospective observational study of adult patients admitted to the medical intensive care unit of a 2200-bed university affiliated teaching hospital, between May and August 2021, who fulfilled clearly defined inclusion and exclusion criteria. Outcome was assessed by a change in PaO2/FiO2 ratio and levels of inflammatory markers before and after immunomodulation, duration of mechanical ventilation after starting treatment, and survival to discharge.

Results: Five patients developed delayed respiratory deterioration in the absence of new infection, fluid overload or extra-pulmonary organ dysfunction at a median interquartile range (IQR) duration of 32 (23-35) d after the onset of symptoms. These patients had elevated inflammatory markers, required mechanical ventilation for 13 (IQR 10-23) d, and responded to glucocorticoids and/or intravenous immunoglobulin. One patient died (20%).

Conclusion: This delayed respiratory worsening with elevated inflammatory markers and clinical response to immunomodulation appears to contrast the well described Multisystem Inflammatory Syndrome - Adults by the paucity of extrapulmonary organ involvement. The diagnosis can be considered in patients presenting with delayed respiratory worsening, that is not attributable to cardiac dysfunction, fluid overload or ongoing infections, and associated with an increase in systemic inflammatory markers like C-reactive protein, inteleukin-6 and ferritin. A good response to immunomodulation can be expected. This delayed inflammatory pulmonary syndrome may represent a distinct clinical entity in the spectrum of inflammatory syndromes in COVID-19 infection.

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延迟性炎症性肺综合征:新冠肺炎感染炎症综合征谱系中的一个独特临床实体?
背景:在2019年第二波冠状病毒病(新冠肺炎)大流行期间,在没有新感染、液体过载或肺外器官功能障碍的情况下,一部分危重患者出现了延迟性呼吸恶化。目的:描述这些患者的临床和实验室特征、结果和管理,并将其与其他新冠肺炎后免疫失调相关炎症性疾病进行对比。方法:这是一项对2021年5月至8月期间入住一家拥有2200张床位的大学附属教学医院重症监护室的成年患者的回顾性观察性研究,这些患者符合明确的纳入和排除标准。通过免疫调节前后PaO2/FiO2比率和炎症标志物水平的变化、开始治疗后机械通气的持续时间以及出院存活率来评估结果。结果:5名患者在症状出现后32(23-35)天的中位四分位间距(IQR)持续时间内,在没有新感染、液体超负荷或肺外器官功能障碍的情况下出现延迟性呼吸恶化。这些患者的炎症标志物升高,需要机械通气13天(IQR 10-23),并对糖皮质激素和/或静脉注射免疫球蛋白有反应。一名患者死亡(20%)。结论:这种炎症标志物升高的延迟性呼吸道恶化和对免疫调节的临床反应似乎与描述良好的成人多系统炎症综合征形成了对比,因为肺外器官很少受累。该诊断可用于出现延迟性呼吸恶化的患者,这不是由于心脏功能障碍、液体过载或持续感染,而是与C反应蛋白、白细胞介素-6和铁蛋白等全身炎症标志物增加有关。可以预期对免疫调节有良好的反应。这种迟发性炎症性肺综合征可能是新冠肺炎感染炎症综合征谱系中的一个独特的临床实体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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