A comparison of epinephrine and norepinephrine in critically ill patients
Abstract
Objective To determine whether there was a difference between epinephrine and norepinephrine in achieving a mean arterial pressure (MAP) goal in intensive care (ICU) patients.Design Prospective, double-blind, randomised-controlled trial.Setting Four Australian university-affiliated multidisciplinary ICUs.Patients and participants Patients who required vasopressors for any cause at randomisation. Patients with septic shock and acute circulatory failure were analysed separately.Interventions Blinded infusions of epinephrine or norepinephrine to achieve a MAP >or=70 mmHg for the duration of ICU admission.Measurements Primary outcome was achievement of MAP goal >24 h without vasopressors. Secondary outcomes were 28 and 90-day mortality. Two hundred and eighty patients were randomised to receive either epinephrine or norepinephrine. Median time to achieve the MAP goal was 35.1 h (interquartile range (IQR) 13.8-70.4 h) with epinephrine compared to 40.0 h (IQR 14.5-120 h) with norepinephrine (relative risk (RR) 0.88; 95% confidence interval (CI) 0.69-1.12; P = 0.26). There was no difference in the time to achieve MAP goals in the subgroups of patients with severe sepsis (n = 158; RR 0.81; 95% CI 0.59-1.12; P = 0.18) or those with acute circulatory failure (n = 192; RR 0.89; 95% CI 0.62-1.27; P = 0.49) between epinephrine and norepinephrine. Epinephrine was associated with the development of significant but transient metabolic effects that prompted the withdrawal of 18/139 (12.9%) patients from the study by attending clinicians. There was no difference in 28 and 90-day mortality.Conclusions Despite the development of potential drug-related effects with epinephrine, there was no difference in the achievement of a MAP goal between epinephrine and norepinephrine in a heterogenous population of ICU patients.
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A randomized blinded study comparing epinephrine with norepinephrine in shock found no difference in 90-day mortality and vasopressor-free days.
“A randomised blinded study comparing epinephrine with norepinephrine in patients with shock showed no difference in 90-day mortality (HR 0.88; 95% CI 0.63–1.25) and vasopressor-free days [351].”
From Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021 (2021) · cites this paper as [351]
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- Authors
- Myburgh, J. A., Higgins, A., Jovanovska, A., Lipman, J., Ramakrishnan, N., Santamaria, J., & the CAT Study investigators
- Affiliations
- St George Hospital (AU)
- Monash University (AU)
- The University of Queensland (AU)
- Royal North Shore Hospital (AU)
- St Vincent's Hospital Melbourne (AU)
- Corresponding author
- Myburgh, John A.
- Venue
- Intensive Care Medicine
- Published
- 2008-07-25
- Volume
- 34
- Issue
- 12
- Pages
- 2226-2234
- ISSN
- 0342-4642 (ISSN-L)
- 1432-1238
- OpenAlex
- W2066473574
- Cited by
- 368
- References
- 27
- Citations by year
- 2026: 10 · 2025: 34 · 2024: 24 · 2023: 23 · 2022: 26 · 2021: 30 · 2020: 19 · 2019: 33 · 2018: 18 · 2017: 20 · 2016: 24 · 2015: 19 · 2014: 25 · 2013: 14 · 2012: 9
- FWCI
- 9.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Intensive Care Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
- Health Sciences › Medicine › Surgery › Hemodynamic Monitoring and Therapy
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Failure Treatment and Management
- Keywords
- epinephrine, norepinephrine, vasopressors, septic shock, acute circulatory failure, critically ill patients, 28-day mortality, 90-day mortality, adverse drug reactions, metabolic effects, vasopressor withdrawal, ICU length of stay
- MeSH terms
- Aged, Blood Pressure, Double-Blind Method, Epinephrine, Female, Humans, Hypotension, Intensive Care Units, Male, Middle Aged, Norepinephrine, Shock, Septic, Vasoconstrictor Agents, Critical Illness, Kaplan-Meier Estimate
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