COVID-19结局的预后及发生后综合征的风险预测

M. G. Atazhakhova, G. Chudilova, I. Nesterova
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摘要

目前,需要新的实验室诊断标志物来预测COVID-19后的并发症,并提高对COVID-19患者后综合征的诊断。尽管呼吸系统的变化是COVID-19最常见的表现,但肺外表现随后出现广泛的持续症状和/或延迟并发症,可能导致不同严重程度的多器官病变:从无症状到致命形式。出现后冠状病毒综合征的一些症状可能持续3周,或延长至6个月或更长时间。该研究的目的是研究由我们开发的早期综合诊断指数的信息性,该指数能够预测COVID-19的结局,以及早期后covid综合征的潜在发展。对60例(38 ~ 82岁)诊断为COVID-19中度严重程度(CT-2.3)的患者在住院治疗期间进行外周血检测;术后早期30例(38 ~ 62岁),早期34例(38 ~ 65岁)。对照组由100名性别和年龄相匹配的健康志愿者组成。IDP是一种综合诊断指数,作为一种标志物,包括中性粒细胞与淋巴细胞的相对数量之比,以及c反应蛋白(CRP)水平,计算公式如下:IDP =(中性粒细胞CRP %) /淋巴细胞%。我们发现,在住院治疗期间,一旦出现急性临床表现,研究1组的IDP比对照组增加了12.5倍。应当指出的是,根据《临时准则》,所有患者均按照官方标准出院。在研究组2中,在covid后早期,IDP仍比对照组高3.4倍。胸部CT资料显示,患者有纤维成分、肺炎组织期及肺组织实变灶征象。在第3组患者(早期后冠状病毒综合征)中,IDP比对照组增加了3倍,并伴有慢性疲劳综合征和认知障碍的记录迹象。IDP可作为临床预后的标志,并可作为COVID-19后早期并发症发展的预测指标,以及COVID-19后早期综合征的发展。
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Prognosis of COVID-19 outcomes and risk prediction for the development of post-COVID syndrome
At the present time, the new laboratory diagnostic markers are required which may predict complications over the post-COVID period, as well as improve diagnostics of post-COVID syndrome in the patients who underwent COVID-19. Despite the fact that changes in respiratory system are the most common manifestations of COVID-19, extrapulmonary manifestations followed by the wide range of persistent symptoms and/or delayed complications may lead to multiple organ lesions of varying severity: from symptomless to fatal forms. A number of symptoms in the developed post-COVID syndrome may persist for 3 weeks, or to be prolonged up to 6 months and later. The purpose of the study was to investigate the informativity of an early integrative diagnostic index developed by us, enabling prediction of the COVID-19 outcome, and potential development of early post-COVID syndrome. Peripheral blood samples were examined in 60 patients (38-82 years old) diagnosed with COVID-19 of moderate severity (CT-2.3) during their inpatient treatment; 30 patients (38-62 years old) in the early post-COVID period and 34 patients (38-65 years old) with early post-COVID syndrome. The comparison group consisted of 100 healthy sex- and age-matched volunteers. The IDP, an integrative diagnostic index, was calculated as a marker including the ratio of the relative neutrophil-to-lymphocyte numbers, as well as the levels of C-reactive protein (CRP), by the following formule: IDP = (% neutrophilic granulocytes CRP) / % lymphocytes. We have found that, during the inpatient treatment, upon acute clinical manifestations, IDP in study group 1 was increased 12.5 times against the comparison group. It should be noted that all patients were discharged from the hospital in compliance with official criteria, according to Temporary Guidelines. In the study group 2, during early postcovid period, IDP remained 3.4-fold elevated against the comparison group. According to the chest CT data, the patients had signs of a fibrous component, organizing stage of pneumonia and consolidation foci in the lung tissue. Among the group 3 patients (early post-COVID syndrome), IDP was increased three-fold against the comparison group, accompanied by the documented signs of chronic fatigue syndrome and cognitive impairment. The IDP can be used as a marker for the prognosis of clinical outcome and a predictor of the evolving complications during the early post-COVID period and upon development of early post-COVID syndrome in the patients who have undergone COVID-19.
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