Plasmapheresis as rescue therapy in accelerated acute humoral rejection

✍ Scribed by Kottarathil A. Abraham; Catherine Brown; Peter J. Conlon; John Donohoe; David P. Hickey; Derek O'Neill; Mary T. Keogan; Anthony M. Dorman; Joseph Walshe

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 104 KB
• Volume: 18
• Category: Article
• ISSN: 0733-2459
• DOI: 10.1002/jca.10062

✦ Synopsis

Abstract

Accelerated acute humoral rejection (AHR) continues to occur in renal transplantation despite improved crossmatching, with potentially devastating consequences. Between 1 June 1998 and 31 December 2000, 440 renal transplants were performed in our center. AHR was diagnosed by the demonstration of typical pathological features on renal histology and positive direct immunofluorescence or detection of anti‐HLA antibodies in serum. AHR developed in 20 (4.5%) of our renal transplant recipients, nine male and eleven female at an average of 16.3 days post transplantation. All of these patients had a negative current cytotoxic crossmatch prior to transplantation. The median serum creatinine at diagnosis was 5.96 mg/dL, and 83% of these individuals developed oliguric renal failure requiring dialysis after having initially attained good graft function (median of best serum creatinine before AHR was 2.64 mg/dL). The 18 recipients who had not infarcted their grafts at the time of diagnosis of AHR received plasmapheresis in conjunction with intensification of their immunosuppressive regimen. This regimen was successful in reversing AHR in 78% of those treated with apheresis. In the 14 responders, graft survival at 6 months was 100% and at 12 months was 91%. Median serum creatinine at 6 and 12 months was 1.26 and 1.33 mg/dL, respectively. Patients received an average of 8.1 plasma exchanges. However, responders received a significantly higher frequency of plasmapheresis (P = .0053), despite undergoing a similar number of exchanges overall. Plasmapheresis appears to be an effective modality for reversing AHR and maintaining graft function. J. Clin. Apheresis 18:103–110, 2003. © 2003 Wiley‐Liss, Inc.