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Assessment of tacrolimus intrapatient variability in stable adherent transplant recipients: Establishing baseline values.
Leino, Abbie D; King, Eileen C; Jiang, Wenlei; Vinks, Alexander A; Klawitter, Jost; Christians, Uwe; Woodle, E Steve; Alloway, Rita R; Rohan, Jennifer M.
Afiliación
  • Leino AD; Division of Transplantation, Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • King EC; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Jiang W; Division of Biostatistics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Vinks AA; Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research, U.S. Food & Drug Administration, Silver Spring, Maryland.
  • Klawitter J; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Christians U; Division of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Woodle ES; iC42 Clinical Research and Development, University of Colorado, Aurora, Colorado.
  • Alloway RR; iC42 Clinical Research and Development, University of Colorado, Aurora, Colorado.
  • Rohan JM; Division of Transplantation, Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Am J Transplant ; 19(5): 1410-1420, 2019 05.
Article en En | MEDLINE | ID: mdl-30506623
ABSTRACT
The purpose of this study was to determine the intrapatient (within the same patient) variability of tacrolimus in adherent patients. Daily tacrolimus trough levels were obtained at home using dried blood spot technology in kidney and liver transplant recipients. Patients were randomized to receive 3 formulations of tacrolimus, each for two 1-week periods. Adherence was monitored by patient diary, pill counts, and use of the Medication Event Monitoring System (MEMS). Variability was quantified as the coefficient of variation (CV). Comparison of CV between groups was by independent t test or one-way ANOVA as appropriate. The population was found to be adherent with a rate of 99.9% with a mean interval between the evening and morning dose of tacrolimus of 11.86 hours. The median CV for the entire population was 15.2% (range 4.8%-110%). There were no differences in CV by allograft type or tacrolimus formulation. The multivariate analysis did not identify any demographic characteristics associated with a CV > 30%. In a highly adherent population, tacrolimus did not display high intrapatient variability. Given the association between IPV and poor allograft outcomes, future studies are needed to quantitate the influence of adherence and establish target IPV goals.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Posoperatorias / Trasplante de Riñón / Trasplante de Hígado / Tacrolimus / Receptores de Trasplantes / Rechazo de Injerto / Supervivencia de Injerto Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Posoperatorias / Trasplante de Riñón / Trasplante de Hígado / Tacrolimus / Receptores de Trasplantes / Rechazo de Injerto / Supervivencia de Injerto Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2019 Tipo del documento: Article