Praxis Medical Insights

Est. 2024 • Clinical Guidelines Distilled

Made possible by volunteer editors from the University of Calgary & University of Alberta

Last Updated: 6/19/2025

Management of Beta-Blockers in Acute Kidney Injury

Introduction to Beta-Blocker Use in AKI

  • The American College of Cardiology recommends continuing metoprolol tartrate at the same dose in patients with AKI, as dose adjustment is not required based on kidney function 1
  • Metoprolol tartrate is primarily metabolized by the liver, making it a preferred beta-blocker in patients with impaired kidney function, with its elimination not significantly affected by reduced kidney function 1

Monitoring and Dose Adjustment

  • Patients with AKI should be monitored for clinical efficacy and adverse effects, including heart rate control, blood pressure response, and signs of beta-blocker toxicity (bradycardia, hypotension) 1
  • In patients with severe AKI requiring renal replacement therapy, standard dosing of metoprolol tartrate can still be maintained 1
  • For patients with hepatic impairment in addition to AKI, dose reduction of metoprolol tartrate may be necessary as it is primarily metabolized by the liver 1

Choice of Beta-Blocker in AKI

  • Metoprolol tartrate is the preferred beta-blocker in AKI patients, as it does not require dose adjustment in AKI 1
  • Atenolol, nadolol, and acebutolol should be used with caution in AKI patients, as they require dose adjustment in AKI due to primary elimination by the kidneys 1

Concomitant Medication Use in AKI

  • Avoid concomitant administration of multiple nephrotoxic medications in patients with AKI, as recommended by the National Kidney Foundation 2
  • When AKI is diagnosed, consider temporarily holding other medications that may worsen kidney function, such as NSAIDs, ACE inhibitors, ARBs, and diuretics, as suggested by the American Gastroenterological Association 3
  • Be aware that diuretics and ACE inhibitors are associated with an increased risk of AKI, with a hazard ratio of 1.64 and 1.39, respectively, although the exact citation for this data is not provided, the recommendation to avoid nephrotoxic medications is supported by 2 and 3