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  4. Can cyclosporine blood level be reduced to half after heart transplantation?
 
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Can cyclosporine blood level be reduced to half after heart transplantation?

Journal
Transplantation Proceedings
Journal Volume
42
Journal Issue
3
Pages
930-933
Date Issued
2010
Author(s)
SHOEI-SHEN WANG  
NAI-KUAN CHOU  
NAI-HSIN CHI  
SHU-CHIEN HUANG  
I-HUI WU  
CHIH-HSIEN WANG  
HSI-YU YU  
YIH-SHARNG CHEN  
Tsao C.-I.
Ko W.-J.
CHIA-TUNG SHUN  
DOI
10.1016/j.transproceed.2010.03.014
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-77955506095&doi=10.1016%2fj.transproceed.2010.03.014&partnerID=40&md5=13d140e6dc2d043590c8f460c4b6e425
https://scholars.lib.ntu.edu.tw/handle/123456789/560050
Abstract
Background Cyclosporine (CsA) is widely used after heart transplantation. The purpose of this prospective randomized study was to evaluate the safety and efficacy of reduction of CsA blood level to one-half of the traditional blood concentration under a regimen of everolimus (EVL), CsA, and steroid. Materials and Methods This prospective, 6 month, randomized, open-label study included adult (aged 18 to 65 years) recipients of a primary heart transplant with serum creatinine ?2.8 mg/dL. Among 52 patients who underwent heart transplantation from December 2004 to March 2006 we excluded those who were hepatitis B or C carriers, who were recipients of organs from donors >60 years old, had cold ischemia time >6 hours, or had plasma renin activity ?25%. All patients received CsA (C2 blood level 1000-1400 ng/mL), EVL (C0 target 3-8 ng/mL), and corticosteroids to day 60, before random entry into one of 2 groups: SE (C2 blood level from days 60-149 = 800-1200 ng/mL, and days 150-180 C2 = 600-1000 ng/mL), or RE group with CsA reduced by one-half after 3 months (days 90-149 C2 = 400-600 ng/mL, and from days 150-180 C2 = 300-500 ng/mL). Results The 25 recipients eligible for this study included 13 patients in the SE and 12 in the RE group. There was no operative mortality in either group. No death or graft loss was noted within 6-months in either group. Mean serum creatinine at month 6 tended to be lower in the RE cohort (1.23 ± 0.44 mg/dL versus 1.55 ± 0.85 mg/dL; P =.093). Biopsy-proven acute rejection ? grade 3A was observed in only 1 patient (7.7%), who was in the SE group. There were no acute rejection episodes associated with hemodynamic compromise. The incidences of adverse events in each group were similar. Conclusions Concentration-controlled EVL (C0 target 3-8 ng/mL) in combination with reduced CsA exposure of one-half the usual concentration achieved good efficacy and safety over 6 months. The renal function at 6 months among the RE group showed a trend toward improvement, suggesting a benefit of halving the target CsA blood level after heart transplantation. ? 2010 Elsevier Inc.
SDGs

[SDGs]SDG3

Other Subjects
creatinine; cyclosporin; drug derivative; everolimus; immunosuppressive agent; rapamycin; adolescent; adult; aged; article; blood; classification; clinical trial; controlled clinical trial; controlled study; donor; dose response; female; heart disease; heart transplantation; human; immunology; kidney function test; male; middle aged; patient selection; physiology; randomized controlled trial; statistics; Adolescent; Adult; Aged; Creatinine; Cyclosporine; Dose-Response Relationship, Drug; Female; Heart Diseases; Heart Transplantation; Humans; Immunosuppressive Agents; Kidney Function Tests; Male; Middle Aged; Patient Selection; Sirolimus; Tissue Donors; Young Adult
Type
conference paper

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