Burckart G J, Ptachcinski R J, Venkataramanan R, Iwatsuki S, Esquivel C, Van Thiel D H, Starzl T E
Transplant Proc. 1986 Dec;18(6 Suppl 5):188-93.
Trough blood or plasma concentration measurements of CsA must be carefully interpreted in OLT patients in relation to hepatic function, sample timing, assay specificity, and concurrent drug therapy. The RIA:HPLC ratio of blood or plasma measurements will vary with the patient's liver function, the time of blood sampling in reference to the time of drug administration, the absolute CsA concentration, and concurrent use of drugs that may alter the metabolism of CsA. The RIA assay should be used in conjunction with HPLC for trough blood or plasma measurement during the first postoperative weeks, during periods of changing hepatic function, and during changing drug regimens. In the future, the specific measurement of active or toxic metabolites of CsA should improve trough CsA concentration monitoring in OLT patients.
对于肝移植患者,必须结合肝功能、采样时间、检测特异性和联合药物治疗情况,仔细解读环孢素A(CsA)的谷血药浓度或谷血浆浓度测量结果。血药浓度或血浆浓度测量的放射免疫分析(RIA)与高效液相色谱法(HPLC)的比值会因患者肝功能、相对于给药时间的采血时间、CsA绝对浓度以及可能改变CsA代谢的联合用药情况而有所不同。在术后最初几周、肝功能变化期间以及药物治疗方案改变期间,应将RIA检测与HPLC结合用于谷血药浓度或谷血浆浓度测量。未来,CsA活性或毒性代谢物的特异性检测应能改善肝移植患者的谷CsA浓度监测。