Bookstein J J, Bookstein F L
Division of Research, VA Hospital, La Jolla, California, USA.
J Vasc Interv Radiol. 2000 Nov-Dec;11(10):1353-62. doi: 10.1016/s1051-0443(07)61316-5.
To further improve methods for pulsed plasminogen-enriched thrombolysis and to compare results with the best obtainable with use of tissue plasminogen activator (tPA) alone.
Parameters of plasminogen-enriched pulse-spray thrombolysis were manipulated in groups of rabbits with inferior vena cava thrombosis, and weights of 1-hour residual thrombus were compared. Variables evaluated were (i) tPA pulse frequency, (ii) amount of plasminogen used for enrichment, (iii) tPA concentration and amount, (iv) pulsed versus infused tPA, and (v) admixture versus separation of plasminogen and tPA.
With use of 3 mg of tPA and approximately 0.9 mg plasminogen enrichment, efficacy varied directly with pulse frequency over a pulse range of every 15 minutes to every 30 seconds. With use of 30-second pulses of tPA at a concentration 0.125 mg/mL, efficacy also correlated directly with increasing plasminogen enrichment up to, but not beyond, approximately 1.8 mg per 1.24 g of clot. Optimized methodology yielded 89% lysis in 1 hour, as compared to 74% lysis previously reported with use of optimized low-concentration (0.01 mg/ mL) tPA alone. Plasminogen enrichment in conjunction with low concentrations of tPA, admixture of tPA and plasminogen, and fractionation of the plasminogen enrichment all proved to be nonproductive or counterproductive.
Optimized in vivo postthrombotic plasminogen enrichment significantly accelerated thrombolysis of experimental clots compared to use of optimized tPA alone.
进一步改进富含纤溶酶原的脉冲溶栓方法,并将结果与单独使用组织纤溶酶原激活剂(tPA)所能获得的最佳结果进行比较。
在患有下腔静脉血栓形成的兔群中操纵富含纤溶酶原的脉冲喷雾溶栓参数,并比较1小时残余血栓的重量。评估的变量包括:(i)tPA脉冲频率;(ii)用于富集的纤溶酶原量;(iii)tPA浓度和量;(iv)脉冲式与输注式tPA;(v)纤溶酶原与tPA的混合与分离。
使用3mg tPA和约0.9mg纤溶酶原富集时,在每15分钟至每30秒的脉冲范围内,疗效与脉冲频率直接相关。使用浓度为0.125mg/mL的tPA进行30秒脉冲时,疗效也与纤溶酶原富集的增加直接相关,直至但不超过每1.24g凝块约1.8mg。优化方法在1小时内产生了89%的溶解,相比之下,之前单独使用优化的低浓度(0.01mg/mL)tPA报道的溶解率为74%。纤溶酶原富集与低浓度tPA联合使用、tPA与纤溶酶原混合以及纤溶酶原富集的分级分离均被证明无成效或适得其反。
与单独使用优化的tPA相比,优化的体内血栓形成后纤溶酶原富集显著加速了实验性凝块的溶栓。