尿碱化对COVID-19危重患者肾功能的影响:一项概念验证随机临床试验

IF 2.8 Q2 CRITICAL CARE MEDICINE
Nuttha Lumlertgul, John A Kellum, Jonah Powell-Tuck, Moncy Mathew, Sunita Sardiwal, Marlies Ostermann
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引用次数: 0

摘要

背景:急性肾损伤(AKI)是COVID-19的常见并发症。虽然确切的机制尚不清楚,但假设病毒直接感染肾小管上皮细胞。鉴于冠状病毒进入宿主细胞的ph依赖性,尿液碱化被认为是一种潜在的预防策略。方法:这是一项在COVID-19危重患者中进行的概念验证前瞻性随机临床试验。患者随机分为尿碱化组和常规组。干预组在随机分组后10天内静脉注射8.4%碳酸氢钠,使尿液pH值≥7.5。主要结局是达到目标尿ph的患者比例。次要结局包括尿组织金属蛋白酶抑制剂-2 (TIMP-2)和胰岛素样生长因子结合蛋白7 (IGFBP7)的变化、AKI发展、肾脏替代治疗和不良反应。结果:由于招募缓慢和COVID-19大流行结束,试验提前终止。16例患者入组(中位年龄48岁,75%为男性)。干预组达到尿pH目标的患者多于对照组(75% vs 37.5%, P = 0.315)。两组在10 d内尿pH值存在差异(相互作用P = 0.097)。然而,干预没有显著影响尿[TIMP-2]x[IGFBP7]浓度(相互作用P = 0.813)或临床结果,包括AKI的发生(风险比0.6(95%可信区间0.21,1.70),P = 0.619)。干预组出现高钠血症和代谢性碱中毒较多。值得注意的是,尿[TIMP-2]x[IGFBP7]浓度升高和AKI患者的ICU和60天死亡率更高。结论:虽然尿碱化是可行的,可以增加尿pH值,但我们无法证明重症COVID-19患者AKI发生率或尿[TIMP-2]x[IGFBP7]浓度的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The effects of urine alkalinization on kidney function in critically ill patients with COVID-19: a proof-of-concept randomized clinical trial.

The effects of urine alkalinization on kidney function in critically ill patients with COVID-19: a proof-of-concept randomized clinical trial.

The effects of urine alkalinization on kidney function in critically ill patients with COVID-19: a proof-of-concept randomized clinical trial.

The effects of urine alkalinization on kidney function in critically ill patients with COVID-19: a proof-of-concept randomized clinical trial.

Background: Acute kidney injury (AKI) is a common complication of COVID-19. While the exact mechanisms remain unclear, direct viral infection of renal tubular epithelial cells is hypothesized. Given the pH-dependent entry of coronaviruses into host cells, urine alkalinization was proposed as a potential preventive strategy.

Methods: This was a proof-of-concept prospective, randomized clinical trial in critically ill patients with COVID-19. Patients were randomized to urine alkalinization versus usual care. The intervention group received intravenous 8.4% sodium bicarbonate to achieve a urine pH ≥ 7.5 up to 10 days after randomization. The primary outcome was the proportion of patients achieving target urine pH. Secondary outcomes included changes in urine tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulin-like growth factor-binding protein 7 (IGFBP7), AKI development, renal replacement therapy, and adverse effects.

Results: The trial was terminated early due to slow recruitment and the end of the COVID-19 pandemic. Sixteen patients were enrolled (median age 48 years old, 75% male). More patients in the intervention group achieved target urine pH than in the control group (75% vs 37.5%, P = 0.315). There was a separation of urine pH between both groups throughout 10 days (P = 0.097 for interaction). However, the intervention did not significantly impact urine [TIMP-2]x[IGFBP7] concentrations (P = 0.813 for interaction) or clinical outcomes, including AKI occurrence (risk ratio 0.6 (95% confidence interval 0.21, 1.70), P = 0.619). More patients in the intervention group experienced hypernatremia and metabolic alkalosis. Notably, patients with elevated urine [TIMP-2]x[IGFBP7] concentrations and AKI had higher ICU and 60-day mortality.

Conclusions: While urine alkalinization is feasible and can increase urine pH, we could not demonstrate differences in AKI rates or changes in urine [TIMP-2]x[IGFBP7] concentrations in critically ill COVID-19 patients.

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来源期刊
Intensive Care Medicine Experimental
Intensive Care Medicine Experimental CRITICAL CARE MEDICINE-
CiteScore
5.10
自引率
2.90%
发文量
48
审稿时长
13 weeks
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