Publication: Rechallenge with intravenous recombinant human erythropoietin can be successful following the treatment of anti-recombinant erythropoietin associated pure red cell aplasia
| dc.contributor.author | Kearkiat Praditpornsilpa | en_US |
| dc.contributor.author | Khajohn Tiranathanakul | en_US |
| dc.contributor.author | Saengsuree Jootar | en_US |
| dc.contributor.author | Kriang Tungsanga | en_US |
| dc.contributor.author | Somchai Eiam-Ong | en_US |
| dc.contributor.other | Chulalongkorn University | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-11-09T02:54:29Z | |
| dc.date.available | 2018-11-09T02:54:29Z | |
| dc.date.issued | 2014-01-01 | en_US |
| dc.description.abstract | Anti recombinant human erythropoietin (r-HuEpo) associated pure red cell aplasia (PRCA) is an immunologic adverse effect of using subcutaneous r-HuEpo. Immunosuppressive agents have been suggested as treatment of this serious complication. After the reversal of anti-r-HuEpo antibody, the patients continue to have renal anemia and require long-term blood transfusion, albeit less frequently than when the antibody is positive. It is controversial whether re-challenging the patients with r-HuEpo is appropriate because re-challenging may cause the reappearance of the antibody. To balance the risk of antir-HuEpo antibody reappearance and longterm blood transfusion complications, we re-challenged r-HuEpo in five anti-r-HuEpo associated PRCA cases after a successful reversal of antibody using prednisolone in combination with cyclophosphamide. The rechallenge was performed intravenously since there were no reports of anti-r-HuEpo associated PRCA cases using this administration route. The duration after the reversal of antibody was 2.4 months before the re-challenge. Two patients were immediately re-challenged as soon as the antibodies reversed. After rechallenge with intravenous r-HuEpo, all patients responded to r-HuEpo: target level of Hb was maintained, blood transfusion was not required, and anti-r-HuEpo was consistently negative. All patients were followed for at least 6 months after re-challenge. Our data suggest that re-challenge with intravenous r-HuEpo can successfully treat anti-r-HuEpo associated PRCA. © 2014 Dustri-Verlag Dr. K. Feistle. | en_US |
| dc.identifier.citation | Clinical Nephrology. Vol.81, No.5 (2014), 355-358 | en_US |
| dc.identifier.doi | 10.5414/CN107690 | en_US |
| dc.identifier.issn | 03010430 | en_US |
| dc.identifier.other | 2-s2.0-84899657734 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/34643 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84899657734&origin=inward | en_US |
| dc.subject | Medicine | en_US |
| dc.title | Rechallenge with intravenous recombinant human erythropoietin can be successful following the treatment of anti-recombinant erythropoietin associated pure red cell aplasia | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84899657734&origin=inward | en_US |
