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Limited sampling strategy for cyclosporine (Neoral ® ) area under the curve monitoring in pediatric kidney transplant recipients
Author(s) -
Strong Dawn K.,
Lai Amanda,
Primmett Dennis,
White Colin T.,
Lirenman David S.,
Carter James E.,
Morrison Hurley R.,
Virji Mumtaz,
Ensom Mary H.H.
Publication year - 2005
Publication title -
pediatric transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 69
eISSN - 1399-3046
pISSN - 1397-3142
DOI - 10.1111/j.1399-3046.2005.00339.x
Subject(s) - medicine , trough level , area under the curve , urology , therapeutic drug monitoring , pharmacokinetics , transplantation , blood sampling , ciclosporin , kidney transplantation , trough concentration , renal transplant , morning , renal function , tacrolimus
Cyclosporine (CSA; Neoral ® ) is one of the most common immunosuppressants used in pediatric renal transplantation. Research in adult renal transplant recipients has shown that 2‐h post‐dose concentration ( C 2 ) monitoring and limited sampling strategies (LSSs) are better at predicting drug exposure and outcome than trough concentrations ( C 0 ). While C 0 monitoring is the usual practice in pediatric renal transplant patients, area under the curve (AUC) monitoring has been shown to be superior in terms of predictive ability and outcomes. However, AUC monitoring is impractical and inconvenient in a clinic setting because it involves many blood samples. An LSS provides a reliable alternative. The purpose of this study was to prospectively define an LSS (AUC 0−12 ) for CSA monitoring and to test its predictive performance. As well, an LSS (AUC 0−4 ) for CSA was developed and its predictive performance tested. Blood samples for CSA concentrations were collected in 29 stable pediatric renal transplant patients prior to ( t = 0) and at 0.5, 1, 2, 4, 6, and 8 h following a steady‐state morning CSA dose. AUC was calculated by the trapezoidal method; LSSs for AUC 0−12 and AUC 0−4 were determined using multiple regression analysis in 14 patients; and the LSSs’ predictive performance was tested in 15 additional patients. Both LSSs require two blood samples. For the LSS (AUC 0−12 ), blood samples are required immediately before the dose and 2 h post‐dose: AUC 0−12 = 12.45 C 0 + 2.17 C 2 + 723.16 (r 2 = 0.909). For the LSS (AUC 0−4 ), blood samples are required at one and 2 h post‐dose, AUC 0−4 = 1.17 C 1 + 1.85 C 2 − 41.00 (r 2 = 0.971). The LSSs demonstrated low bias and high precision for both AUC 0−12 and AUC 0−4 . Our two‐concentration LSSs are accurate and precise predictors that are more clinically useful for our patient population than other LSSs that have been developed for pediatric renal transplant patients. Our study template provides a guide for other centers to develop accurate and precise LSSs specific to their own patient population.