Posttransplant Erythrocytosis in Renal Transplant Recipients at Jeddah Kidney Center, Kingdom of Saudi Arabia
| dc.contributor.author | Basri, Nawal | |
| dc.contributor.author | Gendo, M. Z. | |
| dc.contributor.author | Haider, R. | |
| dc.contributor.author | Abdullah, K. A. K. | |
| dc.contributor.author | Hassan, A. | |
| dc.contributor.author | Shaheen, F. A. M. | |
| dc.date.accessioned | 2025-10-08T11:29:16Z | |
| dc.date.issued | 2007-06 | |
| dc.description.abstract | Objectives: Posttransplant erythrocytosis is a well-known complication of renal transplant. It is a persistently elevated hematocrit level equal to or greater than 51%, or a hemoglobin level equal to or greater than 16 g/L, or both, in the absence of other causes. Materials and Methods: We retrospectively reviewed this complication in patients who had received a renal transplant at our center between January 1991 and December 2005. Results: Of 1655 renal transplant recipients, 159 patients (9.6%; 154 men, 5 women; mean age, 42 ± 9 years) developed posttransplant erythrocytosis. The mean follow-up was 96 ± 4 months. Posttransplant erythrocytosis appeared at an average of 8.2 ± 5 months after transplant (range, 3-40 months) and lasted an average of 10.3 ± 3 months (range, 7-35 months). In all 159 patients, the immunosuppressive medication regimen included prednisolone; in 144, cyclosporine was used, and in 108 patients, azathioprine was used, while in another group of patients, the latter 2 were changed to mycophenolate mofetil (n=38) and tacrolimus (n=13). Twenty-four patients (15%) were treated with phlebotomies, while 29 patients (18.2%) were given angiotensin-converting enzyme inhibitors. One hundred six patients were left untreated including 92 patients (57.9%) who received prophylactic anti-platelet medications. Remission of posttransplant erythrocytosis was seen in all treated and untreated patients. No thromboembolic complications occurred. Only 9 patients (5.7%) developed chronic allograft nephropathy during follow-up. Conclusions: Our findings suggest that posttransplant erythrocytosis is a benign condition affecting males more than females, usually manifesting in the first year after transplant. Remission of posttransplant erythrocytosis can be seen in all patients; however, some patients may require treatment with phlebotomy or angiotensin-converting enzyme inhibitors. Posttransplant erythrocytosis has no adverse effects on renal graft function. | |
| dc.identifier.citation | Experimental and Clinical Transplantation, Cilt 5, Sayı 1, 2007, ss. 607-609 | en |
| dc.identifier.eissn | 2146-8427 | en |
| dc.identifier.issn | 1304-0855 | |
| dc.identifier.issue | 1 | en |
| dc.identifier.uri | https://hdl.handle.net/11727/13752 | |
| dc.identifier.volume | 5 | en |
| dc.language.iso | en_US | |
| dc.publisher | Başkent Üniversitesi | |
| dc.source | Experimental and Clinical Transplantation | en |
| dc.subject | Polycthemia | |
| dc.subject | Kidney transplant | |
| dc.subject | Phlebotomy | |
| dc.subject | Angiotensin-converting enzyme (ACE) inhibitors | |
| dc.subject | Erythropoiesis | |
| dc.title | Posttransplant Erythrocytosis in Renal Transplant Recipients at Jeddah Kidney Center, Kingdom of Saudi Arabia | |
| dc.type | Article |