Leson C L, Bryson S M, Giesbrecht E E, Saunders E F
Department of Pharmacy, Hospital for Sick Children, Toronto, Ontario, Canada.
DICP. 1989 Apr;23(4):300-3. doi: 10.1177/106002808902300405.
Blood concentrations are commonly used to guide dosing requirements of cyclosporine, due to large variations in pharmacokinetics both between and within individuals. Bone marrow transplant patients at The Hospital for Sick Children are prescribed intravenous cyclosporine as part of the posttransplant immunosuppression protocol. Sampling for blood concentration measurement is generally done via a single-lumen central venous line (CVL). Cyclosporine concentrations sampled by this route were compared with concentrations in peripheral capillary samples taken concurrently. Results from the CVL blood were substantially higher despite appropriate flushing of the CVL between the end of the infusion and the time of sample collection. This discrepancy disappeared once the patient was converted to oral cyclosporine. We conclude that the sampling error is due to drug adsorbed to the silicone CVL catheters during intravenous administration and displaced during blood sample collection.
由于个体间和个体内药代动力学存在很大差异,血药浓度常用于指导环孢素的给药剂量。病童医院的骨髓移植患者被开了静脉注射环孢素,作为移植后免疫抑制方案的一部分。血药浓度测量的采样通常通过单腔中心静脉导管(CVL)进行。将通过该途径采集的环孢素浓度与同时采集的外周毛细血管样本中的浓度进行比较。尽管在输注结束至样本采集时间之间对CVL进行了适当冲洗,但CVL血样的结果仍显著更高。一旦患者改用口服环孢素,这种差异就消失了。我们得出结论,采样误差是由于静脉给药期间药物吸附在硅胶CVL导管上,并在采集血样时被置换出来所致。