What are the steps to manage graft failure?

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Last updated: December 2, 2025View editorial policy

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Management of Kidney Allograft Failure

Managing kidney allograft failure requires a systematic approach centered on early identification, coordinated multidisciplinary care, strategic immunosuppression adjustment, and timely preparation for kidney replacement therapy or retransplantation. 1

Initial Assessment and Communication

When eGFR declines to ≤20 ml/min per 1.73 m² or rapid irreversible decline occurs at any eGFR level, immediately initiate communication with the dialysis team and begin transition planning. 1 This threshold represents the critical window for intervention and preparation, regardless of whether the patient is a retransplant candidate.

Begin modality counseling immediately at this stage, including discussion of different dialysis options, retransplantation possibilities (preemptive if living donor available), and conservative/palliative care when appropriate. 1

Multidisciplinary Care Coordination

Establish care through either:

  • Referral to a general nephrology multidisciplinary clinic (MDC) with expertise in imminent dialysis needs, OR
  • Enhanced transplant clinic with providers capable of managing transition to next treatment modality 1

The MDC team must include nephrologists, social workers, dieticians, healthcare navigators, and emotional support staff. 1 Access to clinical psychology is strongly recommended given the psychological vulnerability during this period. 1

Critical pitfall to avoid: Do not blame patients for graft failure even if medication nonadherence contributed—maintain a supportive approach throughout. 1

Immunosuppression Management Strategy

For Retransplant Candidates with Residual Function (Not Yet on Dialysis)

Maintain immunosuppression to preserve residual kidney function and urine output. 1

  • Continue calcineurin inhibitor (CNI) at low therapeutic range to minimize new donor-specific antibody (DSA) development 1
  • Monitor CNI trough levels closely and adjust for side effects 1
  • Consider reducing antimetabolite by 50% to decrease complications while maintaining CNI 1
  • Maintain low-dose corticosteroids 1

For Patients on Dialysis After Graft Failure

Implement a staged immunosuppression taper over 12 months based on retransplant candidacy: 1

At dialysis initiation:

  • Reduce antimetabolite by 50%
  • Maintain CNI ± low-dose prednisone 1

At 3 months post-dialysis:

  • Stop antimetabolite completely
  • Maintain low-dose CNI ± low-dose prednisone 1

At 6 months post-dialysis:

  • Reduce CNI by 50%
  • Continue low-dose prednisone 1

At 9-12 months post-dialysis:

  • Consider additional CNI reduction or cessation of all immunosuppression if no graft intolerance syndrome and no significant increase in calculated panel reactive antibody (CPRA) 1

Critical consideration: Corticosteroids should be the last medication tapered due to adrenal dependency—taper slowly over the first 6 months after graft failure to avoid hypocortisolism. 1

For Non-Retransplant Candidates

Taper immunosuppression more aggressively, particularly in patients with severe complications, infections, or malignancies. 1 Once graft function ceases on dialysis, maintain only corticosteroids initially and taper as the last medication. 1

Dialysis Access Planning

Place arteriovenous (AV) access when eGFR approaches 20 ml/min per 1.73 m² if no living donor is available for preemptive retransplantation. 1

  • Patients should protect existing AV fistulas after transplantation, as prior access often fails over time 1
  • No evidence supports routine access maintenance procedures (angioplasty, stenting) with nephrotoxic dye exposure in transplant recipients 1
  • For retransplant candidates with established surgical dates for living-donor transplant, short-term dialysis via tunneled catheter is acceptable 1

Timing of dialysis initiation should be based on clinical factors and symptoms rather than eGFR alone. 1

Retransplantation Planning

Encourage identification of potential living donors immediately to maximize preemptive retransplantation opportunities. 1 However, listing for retransplantation should never be conditional on having potential living donors. 1

  • Establish baseline panel reactive antibody (PRA) value when eGFR approaches 20 ml/min 1
  • Monitor CPRA every 3-6 months while wait-listed 1
  • Optimize wait-list management strategies to decrease time to transplantation 1

Allograft Nephrectomy Indications

Perform allograft nephrectomy only for specific clinical indications: 1

  • Graft intolerance syndrome (hematuria, abdominal pain, fever, failure to thrive, or source of infection) unresponsive to immunosuppression 1
  • Renal vein or renal artery thrombosis with graft infarction and risk of rupture 1
  • Severe acute rejection unresponsive to bolus corticosteroids with pain and hemorrhage 1
  • Severe anemia and chronic inflammation refractory to medical management 1

Important caveat: Evidence regarding nephrectomy's effect on HLA sensitization is conflicting—weigh risks and benefits carefully. 1

Chronic Kidney Disease Management

Manage CKD complications according to severity for non-transplant patients: 1

  • Blood pressure control
  • Anemia management
  • Proteinuria treatment
  • Secondary hyperparathyroidism management
  • Routine malignancy surveillance 1

Communication and Patient Education

Confirm the accepting dialysis unit understands the transition plan and verify patient comprehension. 1 Develop better educational tools including videos, webinars, and brochures with peer support incorporated. 1

Allow adequate time for patients to accept and prepare for transition away from functioning-transplant health state. 1 Educate clinicians about conservative/palliative care options that assist through transition periods, not simply at end of life. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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