Pijpe Anouk, Papendorp Stephan G, van der Heijden Joost W, Vermin Ben, Ertugrul Iris, Ritt Michael W J, Stessel Björn, Callebaut Ina, Beishuizen Albertus, Vlig Marcel, Jimmink Joost, Huijgen Henk J, van Zuijlen Paul P M, Middelkoop Esther, de Jong Evelien
Department of Intensive Care, Red Cross Hospital, Vondellaan 13, 1942 LE Beverwijk, The Netherlands.
Department of Plastic, Reconstructive and Hand Surgery, Amsterdam UMC Location Vrije Universiteit, Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.
Biomedicines. 2024 Mar 25;12(4):723. doi: 10.3390/biomedicines12040723.
Efforts to identify therapies to treat hospitalised patients with COVID-19 are being continued. Alkaline phosphatase (AP) dephosphorylates pro-inflammatory adenosine triphosphate (ATP) into anti-inflammatory adenosine.
In a randomised controlled trial, we investigated the safety and efficacy of AP in patients with SARS-CoV-2 infection admitted to the ICU. AP or a placebo was administered for four days following admission to the ICU. The primary outcome was the duration of mechanical ventilation. Mortality in 28 days, acute kidney injury, need for reintubation, safety, and inflammatory markers relevant to the described high cytokine release associated with SARS-CoV-2 infection were the secondary outcomes.
Between December 2020 and March 2022, 97 patients (of the intended 132) were included, of which 51 were randomised to AP. The trial was terminated prematurely based on meeting the threshold for futility. Compared to the placebo, AP did not affect the duration of mechanical ventilation (9.0 days vs. 9.3 days, = 1.0). No safety issues were observed. After 28 days, mortality was 9 (18%) in the AP group versus 6 (13%) in the placebo group ( = 0.531). Additionally, no statistically significant differences between the AP and the placebo were observed for the other secondary outcomes.
Alkaline phosphatase (AP) therapy in COVID-19 ICU patients showed no significant benefits in this trial.
确定治疗新冠肺炎住院患者的疗法的工作仍在继续。碱性磷酸酶(AP)可将促炎三磷酸腺苷(ATP)去磷酸化为抗炎腺苷。
在一项随机对照试验中,我们调查了AP对入住重症监护病房(ICU)的新型冠状病毒2(SARS-CoV-2)感染患者的安全性和疗效。入住ICU后,给予AP或安慰剂治疗四天。主要结局是机械通气时间。次要结局包括28天死亡率、急性肾损伤、再次插管需求、安全性以及与所述SARS-CoV-2感染相关的高细胞因子释放相关的炎症标志物。
在2020年12月至2022年3月期间,纳入了97例(计划纳入132例)患者,其中51例被随机分配至AP组。该试验因达到无效阈值而提前终止。与安慰剂相比,AP不影响机械通气时间(9.0天对9.3天,P = 1.0)。未观察到安全问题。28天后,AP组死亡率为9例(18%),安慰剂组为6例(13%)(P = 0.531)。此外,在其他次要结局方面,AP与安慰剂之间未观察到统计学显著差异。
在本试验中,新冠肺炎ICU患者的碱性磷酸酶(AP)治疗未显示出显著益处。