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NDT Advance Access published online on July 26, 2005

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfi018
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© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org
Received April 26, 2005
Accepted June 21, 2005


Case Report

Successful reintroduction of a different erythropoiesis-stimulating agent after pure red cell aplasia: relapse after successful therapy with prednisone

Jason Andrade 1, Paul A. Taylor 2, Janet M. Love 3, and Adeera Levin 2*

1 Department of Medicine, University of British Columbia, St Paul's Hospital, Vancouver BC, Canada
2 Department of Medicine, University of British Columbia, St Paul's Hospital, Vancouver BC, Canada; Division of Nephrology, University of British Columbia, St Paul's Hospital, Vancouver BC, Canada
3 Kidney Function Clinic, Vancouver BC, Canada

* To whom correspondence should be addressed.
Adeera Levin, E-mail: alevin{at}providencehealth.bc.ca



  Abstract

We report a 3-year case history that describes a 78-year-old woman with recurrent transfusion-dependent pure red cell aplasia (PRCA) secondary to recombinant epoetin use that was responsive to immunosuppressant therapy. The patient had kidney disease of unknown aetiology (estimated glomerular filtration rate of 13 ml/min/1.73 m2) and was not on dialysis. After 16 months of therapy with subcutaneous Eprex, she developed anti-erythropoietin antibody-confirmed PRCA and was started on high dose prednisone (50 mg per day). Within 5 months, the patient's serum was clear of antibodies and, under the cover of low dose prednisone (5-7.5 mg per day), therapy with a different erythropoiesis-stimulating compound (Aranesp) was initiated due to persistent fatigue and anaemia. At 3 months of therapy, the serum anti-erythropoietin antibodies remained negative and, due to the patient's requests, and after discussion, prednisone therapy was discontinued. Unfortunately, 3 months after cessation of prednisone, a recurrence of PRCA was confirmed by the development of profound anaemia and reappearance of anti-erythropoietin antibodies in the patient's serum. High dose prednisone (50 mg per day) was reinstituted, whereupon, 2 months later, antibodies were again confirmed to be negative. This case report demonstrates the responsiveness of PRCA to simple immunosuppressive therapy, and the ability to introduce different erythropoiesis-stimulating agents in the presence of such therapy. It appears that there may be problems associated with discontinuation of immunosuppressive therapy in the presence of sustained erythropoiesis-stimulating agent therapy in those in whom the condition has occurred previously.

Keywords: darbepoetin; erythropoietin; pure red cell aplasia; steroids.
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