Hirano T, Komatsu M, Saeki T, Uenohara H, Takahashi A, Takayama K, Yoshimoto T
Department of Neurosurgery, Tohoku University Graduate School of Medicine, 1-1, Seiryou-machi, Aoba-ku, Sendai 980-8574, Japan.
Lasers Surg Med. 2001;29(4):360-8. doi: 10.1002/lsm.1129.
There are several problems inherent in the treatment of cerebral embolisms, such as the narrow therapeutic time window and the severe side effects of fibrinolytic drugs. There is thus need of a new method of removing a cerebral thrombus more rapidly using smaller amounts of fibrinolytics.
STUDY DESIGN/MATERIALS AND METHODS: The liquid-jet generator was made by insertion of an optical fiber (diameter: 0.6 mm) into a balloon catheter (6 Fr). A pulsed holmium (Ho) YAG laser (pulse duration time = 350 micros) was used as a laser source. The maximum penetration depth of a liquid jet generated with this device into a gelatin artificial thrombus was measured at various stand-off distances (L; distance between the optical fiber end and the catheter exit). Based on the result, a stand-off distance of 13 mm was chosen to investigate the enhancement of urokinase (UK) efficacy by only a single operation of the liquid-jet device in artificial thrombi made of human blood.
Maximum penetration depth increased in proportion to L and reached a maximum value (9 mm) when L was around 13 mm. Fibrinolysis rates (%) after incubation with a small amount of UK for 10 and 30 minutes were predominantly raised by a single use of the laser-induced liquid jet (5.4 +/- 2.4 vs. 22.6 +/- 6.1 and 7.3 +/- 3.8 vs. 38.3 +/- 5.6, respectively (mean +/- SD, P < 0.001)).
A laser-induced liquid jet effectively promoted fibrinolysis in vitro with use of only a small amount of fibrinolytics.
脑栓塞治疗存在一些固有问题,如治疗时间窗狭窄以及纤溶药物的严重副作用。因此,需要一种新方法,能够使用更少量的纤溶药物更快地清除脑内血栓。
研究设计/材料与方法:通过将一根光纤(直径:0.6毫米)插入球囊导管(6F)制成液体喷射发生器。使用脉冲钬(Ho)YAG激光(脉冲持续时间 = 350微秒)作为激光源。在不同的间隔距离(L;光纤末端与导管出口之间的距离)下,测量该装置产生的液体射流进入明胶人工血栓的最大穿透深度。基于该结果,选择13毫米的间隔距离,以研究在由人血制成的人工血栓中,仅通过液体喷射装置的单次操作对尿激酶(UK)疗效的增强作用。
最大穿透深度与L成正比增加,当L约为13毫米时达到最大值(9毫米)。在与少量UK孵育10分钟和30分钟后的纤维蛋白溶解率(%),通过单次使用激光诱导液体射流显著提高(分别为5.4±2.4对22.6±6.1以及7.3±3.8对38.3±5.6,均值±标准差,P<0.001)。
激光诱导液体射流仅使用少量纤溶药物就能在体外有效促进纤维蛋白溶解。