Kotani Yuki, Lezzi Martina, Murru Carlotta Pia, Khanna Ashish K, Zarbock Alexander, Bellomo Rinaldo, Landoni Giovanni
Department of Intensive Care Medicine, Kameda Medical Center, Kamogawa, Japan.
Department of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy.
J Cardiothorac Vasc Anesth. 2025 Mar;39(3):653-665. doi: 10.1053/j.jvca.2024.12.022. Epub 2024 Dec 18.
To summarize evidence regarding intravenous angiotensin II administration in critical illness and provide an updated understanding of its effects on various organ dysfunction and renin-angiotensin system (RAS) biomarkers.
A systematic review.
A search of PubMed, Embase, and the Cochrane Library from inception to May 3, 2024. Randomized controlled trials (RCTs), nonrandomized trials, quasi-randomized trials, observational studies, case reports, and case series were included. Comparative studies (RCTs and observational studies with comparator) were used for the main analysis.
Critically ill adults and children.
Intravenous angiotensin II administration.
Fifty-nine studies with a total of 2,918 participants (5 RCTs, 15 observational studies, and 39 case reports or case series) were analyzed. Septic shock and cardiac surgery were the most common clinical conditions (14 studies for each). In 14 comparative studies (5 RCTs and 9 observational studies), mortality was not different from that in controls, except in 1 observational study. Several studies reported decreased renal replacement therapy use, improved oxygenation and blood pressure response, and decreased rate of myocardial injury with angiotensin II therapy. There was no increase in thrombotic events or adverse events. Angiotensin II therapy reduced renin and angiotensin I levels without affecting other RAS biomarkers.
Intravenous angiotensin II has been reported in almost 3000 critically ill patients with diverse types of shock. Despite unclear mortality impacts, angiotensin II seems to confer beneficial effects on several organ systems and RAS derangements, without increasing adverse events.
总结关于在危重病中静脉输注血管紧张素II的证据,并更新对其对各种器官功能障碍和肾素-血管紧张素系统(RAS)生物标志物影响的认识。
系统评价。
检索从开始到2024年5月3日的PubMed、Embase和Cochrane图书馆。纳入随机对照试验(RCT)、非随机试验、半随机试验、观察性研究、病例报告和病例系列。主要分析采用比较性研究(RCT和有对照的观察性研究)。
危重病成人和儿童。
静脉输注血管紧张素II。
分析了59项研究,共2918名参与者(5项RCT、15项观察性研究以及39项病例报告或病例系列)。感染性休克和心脏手术是最常见的临床情况(各14项研究)。在14项比较性研究(5项RCT和9项观察性研究)中,除1项观察性研究外,死亡率与对照组无差异。几项研究报告称,血管紧张素II治疗可减少肾脏替代治疗的使用、改善氧合和血压反应,并降低心肌损伤发生率。血栓形成事件或不良事件没有增加。血管紧张素II治疗可降低肾素和血管紧张素I水平,而不影响其他RAS生物标志物。
近3000名患有不同类型休克的危重病患者接受了静脉血管紧张素II治疗。尽管对死亡率的影响尚不清楚,但血管紧张素II似乎对多个器官系统和RAS紊乱具有有益作用,且不会增加不良事件。