Rates of AKI in ICU Patients Admitted Under Suspicion for COVID-19 Do Not Differ by SARS-CoV2 Status or SARS-CoV-2 Genomic Load

F. Farias, L. Zelnick, M. Thau, T. West, W. Liles, C. Mikacenic, E. Morrell, M. Wurfel, P. Bhatraju
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Abstract

Rationale: Since the onset of coronavirus disease 2019 (COVID-19), the disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), studies have suggested a high incidence of acute kidney injury (AKI) among patients with COVID-19. However, these studies lack contemporaneously enrolled critically ill patients to understand whether high rates of AKI are unique to COVID-19. It is also unknown whether the risk of AKI is related to SARS-CoV-2 genomic load. Methods: We prospectively enrolled a cohort of patients admitted to the ICU with suspicion of COVID-19 (persons under investigation) from April to September 2020. Of these patients, 78 (46%) tested positive for SARS-CoV-2 (COVID-19) and 91 (54%) tested negative (non-COVID-19). AKI was defined as an increase ≥ 0.3 mg/dL in 48 hours or ≥ 50% increase in serum creatinine (sCr) measured during hospitalization compared to a 'baseline' sCr measured at study enrollment. New dialysis was defined as initiation of dialysis during hospitalization. SARS-CoV-2 qRT-PCR was performed across four different platforms with comparable cycle threshold (Ct) values. Ct values were a semiquantitative measure of genomic load with an inverse relationship of Ct to genomic load. We used relative risk regression to determine if there was an increased risk of AKI in COVID-19 compared to non-COVID-19 and whether SARS-CoV-2 genomic load was associated with AKI. Analyses were adjusted for age, sex, body mass index, and APACHE III scores. Results: Rates of AKI and new dialysis were similar in COVID-19 compared to non-COVID-19 (AKI: n=23 (29%) vs n=24 (26%) and Dialysis: n=8 (10%) vs n=6 (6%). Unadjusted and adjusted analyses demonstrated a non-significant difference in risk of AKI (adjusted RR = 1.04 (95% CI: 0.65-1.66) or new dialysis (adjusted RR = 1.55 (95% CI 0.58-4.12) in COVID-19 compared to non-COVID-19. We had Ct values available prior to ICU admission in 47 patients. In unadjusted and adjusted analyses, a 10-unit decrement in Ct values was not associated with AKI (adjusted RR = 0.40 (95% CI: 0.14-1.14) or new dialysis (adjusted RR = 0.96 (95% CI: 0.23-2.69) (Figure 1). Conclusions: Our study demonstrates that rates of AKI and new dialysis in ICU patients with COVID-19 are similar to rates in non-COVID-19 ICU patients. Moreover, the lack of association between Ct values and AKI in COVID-19, suggests that immune and host response to SARS-CoV-2 may contribute more to risk of AKI in ICU patients rather than the pathogen itself.
疑似COVID-19的ICU患者AKI发生率不因SARS-CoV2状态或SARS-CoV-2基因组负荷而异
理由:自COVID-19(由严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)引起的疾病)发病以来,研究表明COVID-19患者的急性肾损伤(AKI)发生率很高。然而,这些研究缺乏同时招募的危重患者,以了解高AKI发生率是否仅为COVID-19所独有。AKI的风险是否与SARS-CoV-2基因组负荷有关也尚不清楚。方法:前瞻性纳入2020年4月至9月ICU疑似COVID-19患者(正在调查者)队列。在这些患者中,78人(46%)的SARS-CoV-2 (COVID-19)检测呈阳性,91人(54%)检测呈阴性(非COVID-19)。AKI被定义为48小时内升高≥0.3 mg/dL或住院期间测定的血清肌酐(sCr)与研究入组时测定的“基线”sCr相比升高≥50%。新透析定义为住院期间开始透析。在四个不同的平台上进行SARS-CoV-2 qRT-PCR,具有可比较的周期阈值(Ct)值。Ct值是基因组负荷的半定量测量,Ct与基因组负荷呈反比关系。我们使用相对风险回归来确定与非COVID-19患者相比,COVID-19患者发生AKI的风险是否增加,以及SARS-CoV-2基因组负荷是否与AKI相关。分析根据年龄、性别、体重指数和APACHE III评分进行调整。结果:与非COVID-19患者相比,COVID-19患者AKI和新透析的发生率相似(AKI: n=23 (29%) vs n=24(26%),透析:n=8 (10%) vs n=6(6%)。未经调整和调整分析显示,与非COVID-19相比,COVID-19患者的AKI风险(调整RR = 1.04 (95% CI: 0.65-1.66)或新透析(调整RR = 1.55 (95% CI: 0.58-4.12)无显著差异。我们有47例患者在ICU入院前的Ct值。在未调整和调整的分析中,10个单位的Ct值下降与AKI(调整RR = 0.40 (95% CI: 0.14-1.14)或新透析(调整RR = 0.96 (95% CI: 0.23-2.69)无关(图1)。结论:我们的研究表明,COVID-19 ICU患者的AKI和新透析率与非COVID-19 ICU患者相似。此外,Ct值与COVID-19患者AKI之间缺乏相关性,表明免疫和宿主对SARS-CoV-2的反应可能比病原体本身更有助于ICU患者AKI的风险。
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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