Two years postconversion from a prograf-based regimen to a once-daily tacrolimus extended-release formulation in stable kidney transplant recipients

Tacrolimus extended-release (XL) is a once-daily formulation recently developed to reduce the frequency of dosing for patients currently using the twice-a-day formulation of tacrolimus (TAC). As reported previously, 67 kidney transplant recipients were safely converted (1:1 mg basis, total daily dos...

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Veröffentlicht in:Transplantation 2007-06, Vol.83 (12), p.1648-1651
Hauptverfasser: ALLOWAY, Rita, STEINBERG, Steven, WISEMANDLE, Kathleen, FITZSIMMONS, William, FIRST, M. Roy, KHALIL, Kassem, GOURISHANKAR, Sita, MILLER, Joshua, NORMAN, Douglas, HARIHARAN, Sundaram, PIRSCH, John, MATAS, Arthur, ZAITZMAN, Jeffrey
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container_end_page 1651
container_issue 12
container_start_page 1648
container_title Transplantation
container_volume 83
creator ALLOWAY, Rita
STEINBERG, Steven
WISEMANDLE, Kathleen
FITZSIMMONS, William
FIRST, M. Roy
KHALIL, Kassem
GOURISHANKAR, Sita
MILLER, Joshua
NORMAN, Douglas
HARIHARAN, Sundaram
PIRSCH, John
MATAS, Arthur
ZAITZMAN, Jeffrey
description Tacrolimus extended-release (XL) is a once-daily formulation recently developed to reduce the frequency of dosing for patients currently using the twice-a-day formulation of tacrolimus (TAC). As reported previously, 67 kidney transplant recipients were safely converted (1:1 mg basis, total daily dose) from TAC twice-a-day to XL once-daily in the morning and were maintained on an am dosing regimen of XL using the same therapeutic monitoring and patient care techniques currently employed with TAC. The 2-year postconversion patient (100%) and graft (98.5%) survival, incidence of biopsy-confirmed acute rejection (6.0%), incidence of multiple rejections (1.5%), and safety profile (posttransplant diabetes, hyperlipidemia, hypertension, infections, renal dysfunction, hepatic dysfunction, and malignancies) were consistent with or more favorable than those previously reported for TAC twice-a-day.
doi_str_mv 10.1097/01.tp.0000264056.20105.b4
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The 2-year postconversion patient (100%) and graft (98.5%) survival, incidence of biopsy-confirmed acute rejection (6.0%), incidence of multiple rejections (1.5%), and safety profile (posttransplant diabetes, hyperlipidemia, hypertension, infections, renal dysfunction, hepatic dysfunction, and malignancies) were consistent with or more favorable than those previously reported for TAC twice-a-day.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/01.tp.0000264056.20105.b4</identifier><identifier>PMID: 17589351</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Delayed-Action Preparations ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Fundamental and applied biological sciences. 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source MEDLINE; Journals@Ovid Complete
subjects Antibacterial agents
Antibiotics. Antiinfectious agents. Antiparasitic agents
Biological and medical sciences
Delayed-Action Preparations
Dose-Response Relationship, Drug
Drug Administration Schedule
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunosuppressive Agents - administration & dosage
Immunosuppressive Agents - pharmacokinetics
Immunosuppressive Agents - therapeutic use
Kidney Transplantation - immunology
Medical sciences
Pharmacology. Drug treatments
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Tacrolimus - administration & dosage
Tacrolimus - pharmacokinetics
Tacrolimus - therapeutic use
Tissue, organ and graft immunology
title Two years postconversion from a prograf-based regimen to a once-daily tacrolimus extended-release formulation in stable kidney transplant recipients
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