Bose Prithviraj, Chacko Binila, Arul Ashwin Oliver, Robinson Vimala Leena, Thangakunam Balamugesh, Varghese George M, Jambugulam Mohan, Lenin Audrin, Peter John Victor
Department of Medical Intensive Care, Christian Medical College, Vellore 632004, Tamil Nadu, India.
Department of Radiodiagnosis, Christian Medical College, Vellore 632004, Tamil Nadu, India.
World J Crit Care Med. 2023 Sep 9;12(4):226-235. doi: 10.5492/wjccm.v12.i4.226.
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.
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.
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 PaO/FiO ratio and levels of inflammatory markers before and after immunomodulation, duration of mechanical ventilation after starting treatment, and survival to discharge.
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%).
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.
在2019冠状病毒病(COVID-19)大流行的第二波期间,一部分重症患者在没有新感染、液体超负荷或肺外器官功能障碍的情况下出现了延迟性呼吸恶化。
描述这些患者的临床和实验室特征、结局及治疗方法,并将这一实体与其他与COVID-19后免疫失调相关的炎症性疾病进行对比。
这是一项对2021年5月至8月期间入住一家拥有2200张床位的大学附属医院医学重症监护病房的成年患者进行的回顾性观察研究,这些患者符合明确界定的纳入和排除标准。通过免疫调节前后的动脉血氧分压/吸入氧分数值(PaO/FiO)比值变化、炎症标志物水平、开始治疗后机械通气的持续时间以及出院生存率来评估结局。
5例患者在症状出现后的中位四分位间距(IQR)为32(23 - 35)天,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了延迟性呼吸恶化。这些患者炎症标志物升高,需要机械通气13(IQR 10 - 23)天,并对糖皮质激素和/或静脉注射免疫球蛋白有反应。1例患者死亡(20%)。
这种伴有炎症标志物升高和对免疫调节有临床反应的延迟性呼吸恶化,似乎与描述详尽的成人多系统炎症综合征形成对比,因其肺外器官受累较少。对于出现延迟性呼吸恶化且不能归因于心脏功能障碍、液体超负荷或持续感染,并伴有C反应蛋白、白细胞介素-6和铁蛋白等全身炎症标志物升高的患者,可以考虑作出这一诊断。有望对免疫调节产生良好反应。这种延迟性炎症性肺综合征可能代表了COVID-19感染炎症综合征谱中的一种独特临床实体。