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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Authors: | Alloway Rita Steinberg Steven Khalil Kassem Gourishankar Sita Miller Joshua Norman Douglas Hariharan Sundaram Pirsch John Matas Arthur Zaltzman Jeffrey Wisemandle Kathleen Fitzsimmons William First M Roy |
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Affiliation: | Department of Medicine, University of Cincinnati, College of Medicine, Cincinnati, OH, and California Institute of Renal Research, Sharp Memorial Hospital, San Diego, CA, USA. |
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Abstract: | 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. |
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