The Efficacy and Safety of Angiotensin II for Treatment of Vasoplegia in Critically Ill Patients: A Systematic Review
- PMID: 39800604
- DOI: 10.1053/j.jvca.2024.12.022
The Efficacy and Safety of Angiotensin II for Treatment of Vasoplegia in Critically Ill Patients: A Systematic Review
Abstract
Objectives: 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.
Design: A systematic review.
Setting: 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.
Participants: Critically ill adults and children.
Interventions: Intravenous angiotensin II administration.
Measurements and main results: 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.
Conclusions: 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.
Keywords: angiotensin II; renin-angiotensin system; septic shock; systematic review; vasoconstrictor agents; vasoplegia.
Copyright © 2024 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest Y.K. reports receipt of consulting fees from Viatris. A.K.K. reports receipt of consulting fees from Medtronic, Edwards Life Sciences, Philips Research North America, Hillrom, GE Healthcare, Potrero Medical, Viatris, Trevena Pharma, Fifth Eye, Pharmazz, Retia Medical, and Caretaker Medical and a Wake Forest Clinical and Translational Science Institute grant on renin dysfunction in septic shock. A.Z. reports consulting fees from Astute-Biomerieux, Baxter, Bayer, Novartis, Guard Therapeutics, AM Pharma, Paion, and Fresenius; research funding from Astute-Biomerieux, Fresenius, and Baxter; and speaking fees from Astute-Biomerieux, Fresenius, Baxter, and Paion. R.B. reports grants and consultancy fees from La Jolla Pharmaceuticals, Paion AG, and Viatris. G.L. reports speaking fees from Medis, Paion, and Viatris and consulting fees from Paion and Viatris. All other authors report no conflicts of interest.
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