What are the recommended SLED (Slow Low-Efficiency Dialysis) settings for a patient with Heart Failure with Reduced Ejection Fraction (HFrEF) undergoing hemodialysis?

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Last updated: January 13, 2026View editorial policy

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SLED Settings for HFrEF Patients

For HFrEF patients requiring renal replacement therapy, peritoneal dialysis or more frequent/longer duration hemodialysis sessions are preferred over conventional hemodialysis due to slower ultrafiltration rates that minimize intradialytic hypotension and allow better volume control, which is critical for maintaining guideline-directed medical therapy (GDMT). 1

Dialysis Modality Selection

Preferred Approaches for HFrEF

  • Peritoneal dialysis should be strongly considered as first-line renal replacement therapy in HFrEF patients because it provides continuous, gentle ultrafiltration that avoids the hemodynamic stress of intermittent hemodialysis 1
  • SLED (Slow Low-Efficiency Dialysis) or extended hemodialysis sessions are superior to conventional hemodialysis when peritoneal dialysis is not feasible, as slower ultrafiltration rates (typically 100-200 mL/hour vs 500-1000 mL/hour in conventional HD) reduce cardiovascular stress 1
  • The slower fluid removal with SLED/extended sessions allows better preservation of cardiac output and blood pressure, which is essential for tolerating life-saving HFrEF medications 1

Critical Rationale

  • Approximately 20% of dialysis patients have HFrEF, and this population faces exceptionally high mortality rates that are compounded by intolerance to GDMT due to hemodynamic instability from aggressive ultrafiltration 1
  • Conventional hemodialysis causes rapid volume shifts that trigger intradialytic hypotension, forcing clinicians to inappropriately discontinue or down-titrate GDMT medications that provide 73% mortality reduction over 2 years 2, 1

Specific SLED Parameters for HFrEF

Session Duration and Frequency

  • SLED sessions should run 6-12 hours per session, 5-7 days per week to achieve adequate clearance while maintaining hemodynamic stability 1
  • Longer, more frequent sessions are better tolerated than shorter, less frequent sessions in HFrEF patients 1

Ultrafiltration Rate

  • Target ultrafiltration rate should not exceed 10-13 mL/kg/hour (approximately 100-200 mL/hour for most patients) to minimize intradialytic hypotension 1
  • This slower rate allows the vascular refilling rate to match fluid removal, preventing hypovolemia and hypotension 1

Dialysate Composition Modifications

Temperature

  • Use cooled dialysate (35-36°C instead of standard 37°C) as this reduces intradialytic hypotension by promoting peripheral vasoconstriction and maintaining blood pressure 1
  • Dialysate cooling has demonstrated benefits specifically in hemodynamically unstable patients 1

Calcium Concentration

  • Consider higher dialysate calcium concentration (3.0-3.5 mEq/L) as this improves cardiac contractility and vascular tone, reducing hypotensive episodes 1
  • Higher calcium dialysate has shown benefits in maintaining blood pressure during dialysis 1

Vascular Access Considerations

Protecting Future Options

  • Strongly consider leadless pacemakers and subcutaneous ICDs rather than transvenous devices in HFrEF patients who may require dialysis, as transvenous leads can compromise future hemodialysis access options 1
  • This is particularly important because many HFrEF patients will eventually require ICD or CRT-D devices for primary prevention (LVEF ≤35% despite optimal therapy) 3, 2

Medication Management During SLED

Maintaining GDMT During Dialysis

The single most important principle: Never discontinue or down-titrate GDMT for asymptomatic hypotension or modest changes in renal function during dialysis optimization. 3

SGLT2 Inhibitors (First Priority)

  • Continue SGLT2 inhibitors (dapagliflozin or empagliflozin) even on dialysis as they provide mortality and hospitalization benefits independent of their glucose-lowering or diuretic effects 2, 4
  • Dapagliflozin can be used with eGFR ≥20 mL/min/1.73 m², empagliflozin with eGFR ≥30 mL/min/1.73 m² 2, 4
  • These agents have minimal blood pressure effects (only -1.50 mmHg in patients with baseline SBP 95-110 mmHg) 2

Beta-Blockers (Second Priority)

  • Continue evidence-based beta-blockers (carvedilol, metoprolol succinate, or bisoprolol) throughout dialysis as they reduce mortality by at least 20% and sudden cardiac death 3, 2
  • Only bisoprolol may accumulate in renal impairment, but patients should still be titrated to target dose (10 mg daily) or maximally tolerated dose 4
  • If carvedilol causes excessive hypotension during SLED, switch to metoprolol succinate or bisoprolol rather than discontinuing beta-blockade 3

Renin-Angiotensin System Inhibition (Third Priority)

  • Sacubitril/valsartan (ARNI) is NOT recommended with eGFR <30 mL/min/1.73 m², so most dialysis patients cannot use this agent 4
  • ACE inhibitors or ARBs should be continued in dialysis patients despite limited trial data, as they are commonly used and generally well-tolerated 1, 4
  • Monitor closely for hyperkalemia and worsening hemodynamics, but do not discontinue for modest changes alone 4, 5

Mineralocorticoid Receptor Antagonists (Fourth Priority)

  • MRAs (spironolactone or eplerenone) require eGFR ≥30 mL/min/1.73 m², so most dialysis patients cannot use these agents 3, 4
  • If eGFR is borderline (25-30 mL/min/1.73 m²), start with very low doses (spironolactone 6.25-12.5 mg daily or every other day) with intensive potassium monitoring 4

Diuretic Management

  • Reduce or discontinue loop diuretics once on dialysis as volume control is achieved through ultrafiltration 3
  • This diuretic reduction often improves blood pressure tolerance and allows better GDMT optimization 3

Common Pitfalls to Avoid

Critical Errors in HFrEF Dialysis Management

  • Never discontinue GDMT medications solely due to low blood pressure readings if the patient has adequate perfusion (warm extremities, normal mentation, adequate urine output if not anuric) 3
  • Never use conventional 3-4 hour hemodialysis sessions in HFrEF patients as rapid ultrafiltration causes intradialytic hypotension that forces inappropriate GDMT discontinuation 1
  • Never attribute hypotension to GDMT without first evaluating for other causes including excessive ultrafiltration, dialysate temperature, infection, or non-HF medications like alpha-blockers 3, 2

Monitoring Requirements

  • Check blood pressure, heart rate, and volume status before and after each SLED session to guide ultrafiltration goals and medication adjustments 1
  • Monitor potassium and renal function weekly initially, then monthly when stable on GDMT during dialysis 4, 5
  • Accept modest increases in creatinine (up to 30% above baseline) if the patient is clinically stable, as this does not indicate harm and should not prompt GDMT discontinuation 5

Evidence Limitations and Clinical Judgment

Knowledge Gaps

  • High-quality randomized trial data for GDMT in dialysis patients is essentially non-existent because dialysis patients were systematically excluded from major HFrEF trials 1, 5
  • No trials have specifically evaluated SLED vs conventional hemodialysis in HFrEF, so recommendations are based on physiologic principles and observational data 1
  • ICD and CRT-D devices have not shown consistent benefit in the limited dialysis studies, unlike in non-dialysis HFrEF populations, though this may reflect the competing risk of non-arrhythmic death 1

Real-World Application

  • Despite limited evidence, beta-blockers and ACE inhibitors/ARBs are commonly used in dialysis patients with HFrEF and appear reasonably well-tolerated in clinical practice 1
  • The benefits of GDMT in non-dialysis CKD patients (eGFR 30-60 mL/min/1.73 m²) are well-established, with most drug classes safe and effective up to CKD stage 3B 5
  • SGLT2 inhibitors show safety and efficacy even in CKD stage 4 (eGFR 15-30 mL/min/1.73 m²), making them the most evidence-based GDMT option for advanced kidney disease 5

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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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