Hill H, Mackie A, Coda B, Schaffer R, Jacobson R, Benedetti C
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Eur J Clin Pharmacol. 1992;43(1):67-75. doi: 10.1007/BF02280757.
Bone marrow transplant patients having severe, prolonged oral mucositis pain (expected to last for one to three weeks) used a computer-controlled infusion system to self-administer morphine for pain control. Individual patient pharmacokinetic information, derived from a pretreatment bolus morphine dose, was used in a new bolus-elimination transfer algorithm to produce rapid adjustments of steady plasma morphine concentrations when the patient requested more or less drug. We evaluated the performance characteristics (bias and precision) of this pharmacokinetically based patient-controlled analgesic infusion system (PKPCA) in a group of 15 cancer patients over six to 14 days. Although we found a three- to fivefold pharmacokinetic variability in the tailoring morphine dose data, the PKPCA system was free of systematic bias (insignificant overall prediction error) during the patient-controlled infusions in this study population. The absolute prediction error was 19.9% for the group on the first study day and 25.6% over the entire study period (aggregate results; 6-14 days of continuous use). Two-thirds of the patients exhibited no bias throughout the study period, and individual bias in the others was symmetrically distributed (three patients with underpredictions and two overpredicted). Magnitude of prediction error during the patient-controlled morphine infusions was not related to the magnitude of pharmacokinetic deviation of individual subjects from group parameters. Our results indicate that this PKPCA system provides accurate control of plasma morphine concentration when used by patients to self-administer opioid for prolonged pain relief continuously over 1 to 2 weeks.(ABSTRACT TRUNCATED AT 250 WORDS)
患有严重、持续性口腔黏膜炎疼痛(预计持续一至三周)的骨髓移植患者使用计算机控制的输注系统自行注射吗啡以控制疼痛。根据预处理时的单次注射吗啡剂量得出的个体患者药代动力学信息,被用于一种新的单次注射 - 消除转移算法中,以便在患者要求增加或减少药物时快速调整血浆吗啡稳态浓度。我们在一组15名癌症患者中,对该基于药代动力学的患者自控镇痛输注系统(PKPCA)进行了六至十四天的性能特征(偏差和精密度)评估。尽管我们发现定制吗啡剂量数据存在三至五倍的药代动力学变异性,但在本研究人群的患者自控输注过程中,PKPCA系统没有系统性偏差(总体预测误差不显著)。在研究的第一天,该组的绝对预测误差为19.9%,在整个研究期间(汇总结果;连续使用6 - 14天)为25.6%。三分之二的患者在整个研究期间没有偏差,其他患者的个体偏差呈对称分布(三名患者预测不足,两名患者预测过度)。患者自控注射吗啡期间的预测误差大小与个体受试者与组参数的药代动力学偏差大小无关。我们的结果表明,当患者连续一至两周自行注射阿片类药物以长期缓解疼痛时,这种PKPCA系统能够准确控制血浆吗啡浓度。(摘要截选至250字)