Basiliximab (Simulect) in Acute Tubular Necrosis High-Risk Kidney Transplantation
| Autor: | A. Alonso Hernández, S. Cillero Rego, C Fernández Rivera, J. Oliver Garcı́a, F. Valdés Cañedo, P. Villaverde Verdejo |
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| Rok vydání: | 2005 |
| Předmět: |
Male
medicine.medical_specialty Basiliximab Recombinant Fusion Proteins Urinary system medicine.medical_treatment Urology Drug Administration Schedule Postoperative Complications medicine Humans Adverse effect Acute tubular necrosis Dialysis Kidney transplantation Transplantation business.industry Histocompatibility Testing Antibodies Monoclonal Kidney Tubular Necrosis Acute Middle Aged medicine.disease Kidney Transplantation Tacrolimus Surgery Regression Analysis Drug Therapy Combination Female business Immunosuppressive Agents medicine.drug |
| Zdroj: | Transplantation Proceedings. 37:3733-3735 |
| ISSN: | 0041-1345 |
| DOI: | 10.1016/j.transproceed.2005.09.179 |
| Popis: | Background Basiliximab (Simulect) therapy reduces acute rejection episodes in renal transplantation. Posttransplant acute tubular necrosis (ATN) is a predisposing factor for acute rejection and reduced graft survival. Anti-lymphocyte antibodies have been used to delay the use of calcineurin antagonists in patients receiving cadaveric renal transplants and to prevent acute rejection episodes. The aim of our study was to learn about the effects of Simulect on ATN in high-risk cadaveric renal transplantation recipients. Materials and methods We studied 93 patients including, 45 who received Simulect (20 mg before transplantation and 20 mg at day 4 posttransplant and 48 patients who did not receive Simulect. All patients received mycophenolate mofetil, steroids, and cyclosporine (46%) or tacrolimus (54%). We defined ATN as the need for dialysis during the first week after transplantation. Risk factors for ATN were: cold ischemia time, donor and recipient age, donor cause of death as stroke, HLA matching, and panel-reactive antibodies. Results Among 54 patients who experienced ATN, 44% were in the Simulect group and 71% in the other group ( P = .01). In the regression analysis, Simulect was shown to be a protective factor: 0.19 (0.05 to 0.62). Presence of de novo diabetes was more frequent in the group that did not receive Simulect (16 [33%] vs 6 [13%]; P = .02). Acute rejection episodes were similar in both groups: 2.5% in the Simulect group versus 4% in the other group ( P = .34). CMV infections occurred in 15 patients (33%) from the Simulect group and in 20 patients (42%) in the other group. Seven patients died in the Simulect group, and five patients died in the other group. In general, Simulect was well tolerated and the degree of complications was similar in both groups. Conclusion Simulect reduced the incidence of ATN among patients receiving a high-risk renal graft. It was well tolerated and no adverse effects were observed. The use of Simulect should be considered for patients receiving renal grafts at high risk for ATN. |
| Databáze: | OpenAIRE |
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