Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33381
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dc.contributor.authorCoulson, Tim G-
dc.contributor.authorMiles, Lachlan F-
dc.contributor.authorZarbock, Alex-
dc.contributor.authorBurrell, Louise M-
dc.contributor.authorPatel, Sheila K-
dc.contributor.authorvon Groote, Thilo-
dc.contributor.authorPilcher, David-
dc.contributor.authorWeinberg, Laurence-
dc.contributor.authorLandoni, Giovanni-
dc.contributor.authorBellomo, Rinaldo-
dc.date2023-
dc.date.accessioned2023-07-26T06:36:56Z-
dc.date.available2023-07-26T06:36:56Z-
dc.date.issued2023-10-
dc.identifier.citationBritish Journal of Anaesthesia 2023-10; 131(4)en_US
dc.identifier.issn1471-6771-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33381-
dc.description.abstractThe role of the renin-angiotensin-aldosterone axis in vasoplegia after cardiac surgery remains unclear. We tested the hypothesis that, compared with norepinephrine, infusion of angiotensin II titrated to achieve similar mean arterial pressure (MAP) would suppress plasma renin concentration (PRC) while maintaining aldosterone levels. In a double-blind, randomised controlled trial, subjects received either an infusion of angiotensin II or norepinephrine to maintain MAP 70-80 mm Hg from induction of anaesthesia. We compared PRC, aldosterone, dipeptidyl peptidase-3, and angiotensin-converting enzyme 2 activity between treatment groups, before surgery, on ICU admission, and 24 h after surgery. In 60 patients (11.7% female; mean age 68 yr [11 yr]), norepinephrine increased median PRC at ICU admission (median difference [MD] 46 [inter-quartile range, IQR, 3-88] μU ml-1; P<0.001) but angiotensin II did not (MD -3 [IQR -62 to 35] μU ml-1; P=0.36). Aldosterone levels increased with both. The aldosterone:PRC ratio did not change with norepinephrine (MD -0.01 [IQR -0.14 to 0.03] μU ml-1 per ng dl-1, P=0.76) but increased with angiotensin II (MD 0.05 [IQR 0.004-0.26] μU ml-1 per ng dl-1, P<0.001). The upper quartile of PRC before surgery was associated with higher vasopressor requirements when norepinephrine was used to maintain MAP, but not angiotensin II. Dipeptidyl peptidase-3 levels and angiotensin-converting enzyme 2 activities were similar at all time points. Angiotensin II suppressed renin release while maintaining aldosterone levels compared with norepinephrine. Higher plasma renin concentration before surgery was associated with greater vasopressor requirement for norepinephrine, but not angiotensin II. Australian and New Zealand Clinical Trials Registry-ACTRN12621000195853 23/02/2021.en_US
dc.language.isoeng-
dc.subjectaldosteroneen_US
dc.subjectangiotensin IIen_US
dc.subjectcardiac surgeryen_US
dc.subjectnoradrenalineen_US
dc.subjectreninen_US
dc.subjectvasoplegiaen_US
dc.subjectvasopressoren_US
dc.titleRenin-angiotensin-aldosterone system dynamics after targeted blood pressure control using angiotensin II or norepinephrine in cardiac surgery: mechanistic randomised controlled trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBritish Journal of Anaesthesiaen_US
dc.identifier.affiliationDepartment of Anaesthesiology and Perioperative Medicine, Alfred Health and Monash University, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Critical Care, University of Melbourne, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationDepartment of Anaesthesiology, Intensive Care and Pain Medicine, University Hospital Münster, Munster, Germany.en_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationDepartment of Anaesthesiology, Intensive Care and Pain Medicine, University Hospital Münster, Munster, Germany.en_US
dc.identifier.affiliationDepartment of Intensive Care, Alfred Hospital, Melbourne, VIC, Australia; Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Critical Care, University of Melbourne, Melbourne, VIC, Australia; Department of Anaesthesia and Pain Medicine, Austin Health, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Anaesthesia, IRCCS San Raffaele Scientific Institute, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy.en_US
dc.identifier.affiliationDepartment of Critical Care, University of Melbourne, Melbourne, VIC, Australia; Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia; Department of Intensive Care, Royal Melbourne Hospital, Melbourne, VIC, Australia; Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia; Data Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationAnaesthesiaen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.doi10.1016/j.bja.2023.06.056en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37481435-
local.name.researcherBellomo, Rinaldo-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptAnaesthesia-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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