Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34943
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dc.contributor.authorCosta-Pinto, Rahul-
dc.contributor.authorNeto, Ary Serpa-
dc.contributor.authorMatthewman, Madeline Coxwell-
dc.contributor.authorOsrin, Dean-
dc.contributor.authorLiskaser, Grace-
dc.contributor.authorLi, Jasun-
dc.contributor.authorYoung, Marcus-
dc.contributor.authorJones, Daryl A-
dc.contributor.authorUdy, Andrew-
dc.contributor.authorWarrillow, Stephen J-
dc.contributor.authorBellomo, Rinaldo-
dc.date.accessioned2024-01-30T23:22:46Z-
dc.date.available2024-01-30T23:22:46Z-
dc.date.issued2024-04-
dc.identifier.citationJournal of Critical Care 2024-04; 80en_US
dc.identifier.issn1557-8615-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34943-
dc.description.abstractNoradrenaline and metaraminol are commonly used vasopressors in critically ill patients. However, little is known of their dose equivalence. We conducted a single centre retrospective cohort study of all ICU patients who transitioned from metaraminol to noradrenaline infusions between August 26, 2016 and December 31, 2020. Patients receiving additional vasoactive drug infusion were excluded. Dose equivalence was calculated based on the last hour metaraminol dose (in μg/min) and the first hour noradrenaline dose (in μg/min) with the closest matched mean arterial pressure (MAP). Sensitivity analyses were performed on patients with acute kidney injury (AKI), sepsis and mechanical ventilation. We studied 195 patients. The median conversion ratio of metaraminol to noradrenaline was 12.5:1 (IQR 7.5-20.0) for the overall cohort. However, the coefficient of variation was 77% and standard deviation was 11.8. Conversion ratios were unaffected by sepsis or mechanical ventilation but increased (14:1) with AKI. One in five patients had a MAP decrease of >10 mmHg during the transition period from metaraminol to noradrenaline. Post-transition noradrenaline dose (p < 0.001) and AKI (p = 0.045) were independently associated with metaraminol dose. The proportion of variation in noradrenaline dose predicted from metaraminol dose was low (R2 = 0.545). The median dose equivalence for metaraminol and noradrenaline in this study was 12.5:1. However, there was significant variance in dose equivalence, only half the proportion of variation in noradrenaline infusion dose was predicted by metaraminol dose, and conversion-associated hypotension was common.en_US
dc.language.isoeng-
dc.subjectAcute kidney injuryen_US
dc.subjectDose equivalenceen_US
dc.subjectMetaraminolen_US
dc.subjectNoradrenalineen_US
dc.subjectSepsisen_US
dc.subjectVasodilatory shocken_US
dc.titleDose equivalence for metaraminol and noradrenaline - A retrospective analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Critical Careen_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen_US
dc.identifier.affiliationDepartment of Critical Care, Department of Medicine, the University of Melbourne, Parkville, Victoria, Australia; Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia; Department of Intensive Care, The Alfred Hospital, 55 Commercial Road, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia; Data Analytics Research and Evaluation Centre, The University of Melbourne and Austin Hospital, Melbourne, Australia; Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.1016/j.jcrc.2023.154430en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38245376-
dc.description.volume80-
dc.description.startpage154430-
dc.subject.meshtermssecondarySepsis/complications-
dc.subject.meshtermssecondaryAcute Kidney Injury/complications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.dept3D Medical Printing Laboratory-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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