What are the preferred antihypertensive agents for patients with End-Stage Renal Disease (ESRD) on dialysis?

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Preferred Antihypertensive Agents for ESRD Patients on Dialysis

ACE inhibitors or ARBs should be used as first-line antihypertensive agents in most ESRD patients on dialysis, followed by calcium channel blockers and beta-blockers as needed for adequate blood pressure control. 1

Initial Management Approach

  • Achievement of dry weight through ultrafiltration and dietary sodium restriction is the cornerstone of blood pressure management in dialysis patients 1
  • Target predialysis blood pressure should be 140/90 mmHg (measured in sitting position) 1
  • Lifestyle modifications including salt restriction should be continuously emphasized 1

First-Line Medication Selection

  • ACE inhibitors or ARBs are recommended as first-line agents for most dialysis patients 1
    • These agents reduce left ventricular hypertrophy in hemodialysis patients 1
    • ACE inhibitors have been associated with decreased mortality in observational studies of ESRD patients 1
    • ARBs may be more potent than ACE inhibitors for LVH reduction 1

Special Considerations for Medication Selection

  • For patients with previous myocardial infarction or established coronary artery disease, beta-blockers should be preferred 1
    • Beta-blockers are associated with decreased mortality in CKD patients 1
  • Calcium channel blockers (CCBs) should be considered as part of the regimen when additional agents are needed 1
    • Observational studies suggest CCBs are associated with decreased total and cardiovascular mortality in dialysis patients 1
  • For patients with residual kidney function (RKF), ACE inhibitors or ARBs are particularly beneficial 1
    • These agents slow the decline in residual kidney function in peritoneal dialysis patients 1

Pharmacokinetic Considerations

  • Consider the dialyzability of medications when selecting agents 1:
    • Hemodialysis reduces blood levels of some ACE inhibitors (enalapril, ramipril) but not others (benazepril, fosinopril) 1
    • Levels of clonidine, carvedilol, labetalol, CCBs, and ARBs do not change significantly during dialysis 1
    • For patients prone to intradialytic hypotension, medications removed by dialysis may be preferred 2
    • For patients with intradialytic hypertension, non-dialyzable medications are preferred 2

Management of Resistant Hypertension

  • Resistant hypertension is defined as BP >140/90 mmHg despite achieving dry weight and using three appropriate antihypertensive agents 1
  • If BP remains uncontrolled with three agents, evaluate for secondary causes of resistant hypertension 1
  • For severe resistant hypertension, consider adding minoxidil as a potent vasodilator 1, 3
  • If hypertension remains uncontrolled after a trial with minoxidil, consider switching to peritoneal dialysis 1
  • If peritoneal dialysis proves ineffective, surgical or embolic nephrectomy may be considered 1

Common Pitfalls and Caveats

  • Avoid using ACE inhibitors in patients treated with polyacrylonitrile dialysis membranes due to risk of anaphylactoid reactions 1
  • Monitor for hyperkalemia when using ACE inhibitors or ARBs, especially with non-selective beta-blockers 3
  • Be cautious with aggressive BP lowering in elderly patients with isolated systolic hypertension 1
  • Low predialysis systolic BP (<110 mmHg) and diastolic BP (<70 mmHg) are associated with increased mortality 4
  • Paradoxical rise in blood pressure can occur during dialysis due to removal of certain antihypertensive drugs or excessive volume depletion 1

Medication Dosing Strategy

  • For medications with predominant renal excretion (like lisinopril and atenolol), thrice-weekly supervised administration after hemodialysis can enhance BP control 3
  • Most dialysis patients will require a combination of several antihypertensive drugs for adequate BP control 2, 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Hemodialysis-associated hypertension: pathophysiology and therapy.

American journal of kidney diseases : the official journal of the National Kidney Foundation, 2002

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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