White J R, Rockwood T, Wilson D, Bettesworth L, Icenogle T
College of Pharmacy, Washington State University, Spokane.
Clin Ther. 1994 Jul-Aug;16(4):673-9.
The objective of this trial was to determine if oral pentoxifylline (PTX) reduced cyclosporine (CSA)-induced renal dysfunction in cardiac transplant patients in the 8 months following transplantation. The study was a prospective, open-label, crossover trial evaluating the renal effects of PTX in nine postcardiac transplant patients. Patients received PTX 2 weeks posttransplant and continued therapy for 4 months. Patients were evaluated for an additional 4 months thereafter. During the trial, various renal function tests were performed and CSA concentrations were measured at set intervals. Baseline measurements were compared with all subsequent measurements. In addition, "on-PTX" data were compared with "off-PTX" data. Significant alterations in results of renal function tests were not seen during the trial when compared with baseline values. Although no significant changes in renal function were observed during the study, no patient developed CSA-induced acute renal failure during the 4 months posttransplant. This finding suggests that PTX may offer a nephroprotective effect against CSA-induced toxicity.
本试验的目的是确定口服己酮可可碱(PTX)是否能在心脏移植患者移植后的8个月内减轻环孢素(CSA)所致的肾功能障碍。该研究是一项前瞻性、开放标签、交叉试验,评估PTX对9例心脏移植术后患者肾功能的影响。患者在移植后2周开始接受PTX治疗,并持续治疗4个月。此后,对患者进行了另外4个月的评估。在试验期间,进行了各种肾功能测试,并在设定的时间间隔测量CSA浓度。将基线测量值与所有后续测量值进行比较。此外,还将“服用PTX期间”的数据与“未服用PTX期间”的数据进行了比较。与基线值相比,试验期间肾功能测试结果未出现显著变化。尽管在研究期间未观察到肾功能的显著变化,但在移植后的4个月内,没有患者发生CSA所致的急性肾衰竭。这一发现表明,PTX可能对CSA所致的毒性具有肾保护作用。