Renin-angiotensin system inhibition in advanced chronic kidney disease: how low can the kidney function go?

Roopa Shah1, Matthew A Sparks1,2

  • 1Division of Nephrology, Department of Medicine, Duke University School of Medicine.

Insights

Continue angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers (ACEi/ARB) in advanced chronic kidney disease (CKD) unless adverse effects occur. Starting these drugs in advanced CKD is not supported by current data, requiring careful monitoring if initiated.

Area of Science:

  • Nephrology
  • Pharmacology

Background:

  • Angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers (ACEi/ARB) are established treatments for mild-to-moderate chronic kidney disease (CKD), particularly with proteinuria.
  • Data regarding ACEi/ARB use in advanced CKD (eGFR < 15 mL/min/1.73 m²) is limited and often conflicting.
  • Definitions of advanced CKD vary across studies, complicating data interpretation.

Purpose of the Study:

  • To review available data on the risks and benefits of ACEi/ARB therapy in patients with advanced CKD.
  • To provide evidence-based recommendations for ACEi/ARB management in this patient population.

Main Methods:

  • Literature review of studies investigating ACEi/ARB use in patients with advanced CKD.
  • Analysis of data concerning efficacy, safety, and specific clinical scenarios.

Main Results:

  • Evidence supports continuing ACEi/ARB therapy in advanced CKD unless significant adverse events like unresponsive hyperkalemia, hypotension, or rapid eGFR decline occur.
  • There is insufficient evidence to recommend initiating ACEi/ARB therapy de novo in patients with advanced CKD.
  • Close patient monitoring is crucial when ACEi/ARB therapy is continued or initiated in advanced CKD.

Conclusions:

  • Continue ACEi/ARB therapy in advanced CKD patients under close observation, especially if they are already on the medication.
  • Avoid initiating ACEi/ARB therapy de novo in advanced CKD due to lack of supporting data; if initiated, monitor closely.
  • Manage adverse effects such as hyperkalemia and hypotension promptly to allow continued ACEi/ARB therapy.
Abstract

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