灌注缺陷可能是严重 COVID-19 疾病造成肺和肾损伤的原因:一项多中心国际队列研究的启示。

Alice Nova, Bairbre McNicholas, Aurora Magliocca, Matthew Laffey, Vanessa Zambelli, Ilaria Mariani, Minahel Atif, Matteo Giacomini, Giovanni Vitale, Roberto Rona, Giuseppe Foti, John Laffey, Emanuele Rezoagli
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引用次数: 0

摘要

背景:主要由内皮和凝血活化引起的肺灌注缺陷是导致 COVID-19 呼吸衰竭的关键因素。COVID-19 患者还可能因肾脏灌注不足而发生急性肾损伤(AKI)。我们旨在探索 AKI 相关因素以及标准化分钟通气量(MV)--肺泡死腔的代表--对 COVID-19 机械通气患者 AKI 发生和持续的独立预测:这是一项多中心观察性队列研究。我们招募了 157 名需要机械通气并入住重症监护室(ICU)的 COVID-19 患者。我们收集了临床信息、通气和实验室数据。根据 2012 年 KDIGO 指南对 AKI 进行了定义,并根据 48 小时内血清肌酐标准的持续性将其分为一过性和持续性:在 157 名接受机械通气的 COVID-19 患者中,47% 出现了 AKI:10% 为一过性 AKI,37% 为持续性 AKI。缺氧程度与 AKI 严重程度的差异无关。在 AKI 严重程度不断增加的各组中,尽管 paCO2 水平相似,但我们观察到肺活量和标准化肺活量(肺泡死腔的可靠代表)增加。在对其他临床和实验室协变量进行调整后,标准化肺活量仍然是 AKI 发生和持续的独立预测因子。持续性 AKI 患者的 D-二聚体水平较高:结论:在 COVID-19 呼吸衰竭的重症患者中,虚脱通气量的增加与持续性 AKI 的更高风险独立相关。这些假设性发现可能表明,在我们的人群中,灌注失调可能与通气量减少和急性肾损伤的病理生理学有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perfusion deficits may underlie lung and kidney injury in severe COVID-19 disease: insights from a multicenter international cohort study.

Background: Lung perfusion defects, mainly due to endothelial and coagulation activation, are a key contributor to COVID-19 respiratory failure. COVID-19 patients may also develop acute kidney injury (AKI) because of renal perfusion deficit. We aimed to explore AKI-associated factors and the independent prediction of standardized minute ventilation (MV)-a proxy of alveolar dead space-on AKI onset and persistence in COVID-19 mechanically ventilated patients.

Methods: This is a multicenter observational cohort study. We enrolled 157 COVID-19 patients requiring mechanical ventilation and intensive care unit (ICU) admission. We collected clinical information, ventilation, and laboratory data. AKI was defined by the 2012 KDIGO guidelines and classified as transient or persistent according to serum creatinine criteria persistence within 48 h. Ordered univariate and multivariate logistic regression analyses were employed to identify variables associated with AKI onset and persistence.

Results: Among 157 COVID-19 patients on mechanical ventilation, 47% developed AKI: 10% had transient AKI, and 37% had persistent AKI. The degree of hypoxia was not associated with differences in AKI severity. Across increasing severity of AKI groups, despite similar levels of paCO2, we observed an increased MV and standardized MV, a robust proxy of alveolar dead space. After adjusting for other clinical and laboratory covariates, standardized MV remained an independent predictor of AKI development and persistence. D-dimer levels were higher in patients with persistent AKI.

Conclusions: In critically ill COVID-19 patients with respiratory failure, increased wasted ventilation is independently associated with a greater risk of persistent AKI. These hypothesis-generating findings may suggest that perfusion derangements may link the pathophysiology of both wasted ventilation and acute kidney injury in our population.

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