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一种用于估计肾移植中他克莫司八小时曲线下面积的有限采样策略。

A limited sampling strategy for the estimation of eight-hour neoral areas under the curve in renal transplantation.

作者信息

Meier-Kriesche H U, Kaplan B, Brannan P, Kahan B D, Portman R J

机构信息

Division of Pediatric Nephrology and Hypertension Renal Disease and Hypertension, and Immunology and Organ Transplantation, The University of Texas Medical School at Houston, 77030, USA.

出版信息

Ther Drug Monit. 1998 Aug;20(4):401-7. doi: 10.1097/00007691-199808000-00009.

Abstract

Neoral, the microemulsion formulation of cyclosporine (CsA), demonstrates more consistent bioavailability than the corn oil formulation Sandimmune. Because of Neoral's rapid peak and metabolism, 8-hour dosing has to be used in many pediatric and some adult patients to maintain adequate CsA peak-to-trough ratios. Although the area under the curve (AUC) is considered the best estimate of total drug exposure, it requires repeated blood sampling. Abbreviated AUC profiles yielding excellent estimates of Neoral AUC with twice daily dosing have been described, but no such abbreviated strategy exists for 8-hour dosing. One hundred fifty-two pharmacokinetic profiles in 23 patients were used to derive and prospectively test a limited two-sample strategy to predict Neoral AUCs in pediatric and adult patients on 8-hour dosing regimens of Neoral. The formula was derived from 69 full 8-hour CsA pharmacokinetic profiles in nine children who underwent renal transplantation. Stepwise forward linear and multiple-curve regression techniques assessed the relative importance of single and combination concentration time points to predict AUC. The abbreviated profiles were validated by comparing the mean prediction error for each regression equation. The abbreviated profile calculated by second (C2)- and fourth (C4)-hour levels (AUC = 129 + 1.84 x C2 + 4.39 x C4) correlated well with the full AUC (r2 = 0.96; p < 0001). Mean prediction error was -0.4% +/- 5.48%, and no values fell outside the clinically acceptable 15% prediction error limit. Prospectively applying the formula to 83 AUCs of 14 adults who underwent renal transplantation and were taking Neoral three times a day demonstrated an excellent fit (r2 = 0.93; p < 0.001), with 94% of predicted values falling inside the +/-15% limit. The authors describe the development of a clinically acceptable, limited sampling strategy to predict 8-hour Neoral AUCs in children and adults who underwent renal transplantation.

摘要

新山地明,即环孢素(CsA)的微乳剂配方,与玉米油配方的山地明相比,其生物利用度更稳定。由于新山地明的血药浓度峰值出现快且代谢迅速,许多儿科患者和部分成年患者必须采用每8小时给药一次的方案,以维持CsA的谷峰比值在适当水平。虽然曲线下面积(AUC)被认为是药物总暴露量的最佳评估指标,但它需要多次采血。已有研究描述了通过每日两次给药得出的简化AUC曲线,可对新山地明的AUC进行良好评估,但对于每8小时给药一次的方案,尚无此类简化策略。本研究利用23例患者的152份药代动力学曲线,推导并前瞻性地测试了一种有限的两点取样策略,以预测接受新山地明每8小时给药方案的儿科和成年患者的AUC。该公式源自9例接受肾移植儿童的69份完整的8小时CsA药代动力学曲线。逐步向前线性回归和多曲线回归技术评估了单一浓度时间点和组合浓度时间点对预测AUC的相对重要性,并通过比较每个回归方程的平均预测误差对简化曲线进行验证。通过第二个小时(C2)和第四个小时(C4)的血药浓度水平计算出的简化曲线(AUC = 129 + 1.84 × C2 + 4.39 × C4)与完整的AUC具有良好的相关性(r2 = 0.96;p < 0.001)。平均预测误差为 -0.4% ± 5.48%,且所有数值均未超出临床可接受的15%预测误差范围。前瞻性地将该公式应用于14例接受肾移植且每日服用新山地明三次的成年患者的83份AUC,结果显示拟合良好(r2 = 0.93;p < 0.001),94%的预测值落在±15%的范围内。作者描述了一种临床可接受的有限取样策略的开发过程,该策略可用于预测接受肾移植的儿童和成年患者的8小时新山地明AUC。

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