What to do if a dialyzer (artificial kidney) clots twice during the same hemodialysis treatment?

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Last updated: December 29, 2025View editorial policy

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Management of Dialyzer Clotting Twice During Same Hemodialysis Treatment

When a dialyzer clots twice during the same hemodialysis session, terminate the treatment and investigate the underlying cause of inadequate anticoagulation rather than attempting a third dialyzer, as recurrent clotting indicates systemic anticoagulation failure that compromises dialysis adequacy and patient safety. 1

Immediate Actions During the Session

First Priority: Assess Adequacy Impact

  • Recognize that dialyzer clotting reduces effective dialyzer surface area and compromises the delivered dose of hemodialysis below prescribed levels. 1
  • Document the exact treatment time lost during each dialyzer replacement, as interruptions for dialyzer replacement secondary to clotting reduce actual dialysis time and effective treatment delivery. 1
  • Calculate whether the patient can still achieve minimum adequate Kt/V of 1.2 (or URR ≥65%) given the time lost and reduced clearance from partial clotting before complete occlusion. 1

Second Priority: Decision to Continue or Terminate

  • If two dialyzers have clotted during the same session, strongly consider terminating the treatment rather than attempting a third dialyzer, as this pattern indicates inadequate systemic anticoagulation that is unlikely to be corrected mid-session. 1
  • The rationale is that repeated clotting events suggest either insufficient heparin dosing, heparin resistance, or a hypercoagulable state that requires systematic evaluation rather than repeated attempts. 2, 3
  • Document all interruptions meticulously, as failure to account for treatment interruptions due to dialyzer replacement is a common cause of inadequate delivered dialysis dose. 1

Root Cause Investigation (Post-Session)

Anticoagulation Assessment

  • Review the heparin protocol used: verify the initial bolus dose (typically 5,000 units IV for full-dose anticoagulation) and maintenance infusion rate (typically 1,000-2,000 units/hour). 4
  • For extracorporeal dialysis specifically, a dose of 25-30 units/kg followed by an infusion rate of 1,500-2,000 units/hour is suggested if manufacturer recommendations are unavailable. 4
  • Consider whether the patient has risk factors for heparin resistance, including active infection, recent surgery, or inflammatory states. 2

Technical and Equipment Factors

  • Check blood flow rate adequacy from the vascular access, as inadequate blood flow is a primary cause of compromised clearance and increased clotting risk. 1
  • Verify blood pump calibration, as errors result in actual blood flow rates that are less than assumed and reported, promoting stasis and clotting. 1
  • Review extracorporeal pressures during the session, particularly pre-pump arterial pressure for values ≤-200 mmHg, which indicate access flow problems. 1
  • Assess for access recirculation using slow flow/stop pump sampling technique if hydraulic compression testing suggests problems. 1

Patient-Specific Factors

  • Evaluate for hypercoagulable states: recent thrombotic events, malignancy, antiphospholipid syndrome, or heparin-induced thrombocytopenia. 2, 5
  • Recognize that hemodialysis patients are inherently pro-thrombotic, with baseline activation of platelets and the clotting cascade even before dialysis begins. 5
  • Review medications: aspirin or coumarin use for fistula thrombosis prevention may paradoxically contribute to clotting through platelet activation. 2

Prevention Strategies for Future Sessions

Anticoagulation Modification

  • For patients with recurrent clotting, increase heparin dosing: consider a higher initial bolus (up to 10,000 units) and increased maintenance infusion (up to 2,000 units/hour for standard patients). 4
  • Alternative strategies for high-risk clotting patients include regional heparin anticoagulation or minimal heparinization protocols. 2
  • For patients actively bleeding or at extreme bleeding risk, consider heparin-free hemodialysis, peritoneal dialysis, or regional anticoagulation with citrate. 2

Dialyzer and Circuit Optimization

  • Ensure mandatory preprocessing of all new dialyzers before first patient use to remove manufacturing residuals that can promote clotting. 6
  • Measure total cell volume (TCV) before first use to establish baseline dialyzer function and account for variability among dialyzers. 1, 6
  • During reprocessing, check TCV after each use; dialyzers with TCV <80% of original measured value should not be reused, as fiber loss from clotting reduces clearance. 1

Blood Flow and Access Management

  • Optimize blood flow rates to the maximum tolerated by the vascular access (typically 350-450 mL/min for adequate clearance). 1
  • Address any access dysfunction promptly, as inadequate access flow is a primary driver of both inadequate dialysis and circuit clotting. 1

Common Pitfalls to Avoid

  • Do not assume that absence of visible red clots at session end means adequate anticoagulation occurred, as subclinical fiber clotting can reduce clearance without obvious macroscopic thrombus. 1, 7
  • Avoid relying solely on pre-/post-dialyzer pressure difference (ΔP) monitoring to detect clotting, as urea clearance may not change significantly until minutes before complete circuit occlusion. 7
  • Do not continue attempting multiple dialyzer replacements in the same session without addressing the underlying anticoagulation failure, as this wastes resources and delays definitive treatment. 1
  • Recognize that continuous monitoring of ΔP during intermittent hemodialysis does not significantly help unmask inefficient sessions, unlike in continuous renal replacement therapy. 7

Documentation Requirements

  • Record exact times of dialysis initiation, each interruption for dialyzer replacement, and treatment termination to calculate true effective treatment time. 1
  • Document visual inspection of each clotted dialyzer to characterize the extent and pattern of clotting. 1
  • Calculate and report the delivered Kt/V or URR for the session, accounting for reduced treatment time and compromised clearance. 1

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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