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  4. Induction Immunosuppression With Basiliximab in Heart Transplantation
 
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Induction Immunosuppression With Basiliximab in Heart Transplantation

Journal
Transplantation Proceedings
Journal Volume
40
Journal Issue
8
Pages
2623-2625
Date Issued
2008
Author(s)
NAI-KUAN CHOU  
SHOEI-SHEN WANG  
YIH-SHARNG CHEN  
HSI-YU YU  
NAI-HSIN CHI  
CHIH-HSIEN WANG  
Ko W.J.
Tsao C.I.
Sun C.D.
DOI
10.1016/j.transproceed.2008.07.113
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-53149128006&doi=10.1016%2fj.transproceed.2008.07.113&partnerID=40&md5=8bf5b5b9193267a5645aa11897e3e74f
https://scholars.lib.ntu.edu.tw/handle/123456789/560336
Abstract
After clinical heart transplantation (HT), it is crucial to use appropriate immunosuppressive agents to prevent rejection. The use of basiliximab or rabbit anti-thymocyte globulin (RATG) for induction therapy has significantly reduced the incidence of acute rejection episodes after kidney transplantation. In this study we sought to examine the effects of basiliximab after HT. From June 2006 to July 2007, we performed 43 HT including patients 18-65 years old undergoing primary HT who were included in this study of basiliximab induction (20 mg intravenous [iv] on days 0 and 4). Cyclosporine and everolimus were given with basiliximab induction. All others received RATG induction (1.5-2.5 mg/kg iv infusion on days 0, 1, and 2) followed by cyclosporine or tacrolimus combined with mycophenolate mofetil. All patients underwent the same operative procedure, steroid-tapering protocol, and postoperative care with protocol endomyocardial biopsy. Basiliximab was well-tolerated and easy to use. There was only 1 operative mortality; the patient died of sepsis due to Enterobacter cloacae. All others survived the operation and are alive and in good health with a 2-year survival rate of 92.86%. No severe adverse events were noted during the first postoperative month. No acute rejection ? grade 2R or rejection associated with hemodynamic compromise was noted during the whole course. Basiliximab as induction immunosuppressant was simple, safe, and effective after HT. ? 2008 Elsevier Inc. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
basiliximab; cyclosporin; everolimus; methylprednisolone; mycophenolic acid 2 morpholinoethyl ester; prednisolone; steroid; tacrolimus; thymocyte antibody; adult; aged; article; clinical article; controlled study; drug effect; drug efficacy; drug safety; drug tolerability; Enterobacter cloacae; female; graft failure; graft rejection; heart muscle biopsy; heart transplantation; hemodynamics; human; immunosuppressive treatment; male; postoperative care; postoperative infection; priority journal; sepsis; surgical mortality; surgical technique; survival rate; Adolescent; Adult; Aged; Animals; Antibodies, Monoclonal; Antilymphocyte Serum; Cardiomyopathy, Dilated; Enterobacter cloacae; Enterobacteriaceae Infections; Female; Graft Rejection; Heart Transplantation; Humans; Immunosuppressive Agents; Male; Middle Aged; Myocardial Ischemia; Postoperative Complications; Rabbits; Recombinant Fusion Proteins; Retrospective Studies; Sepsis
Type
journal article

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