Theiss W, Hofer E, Kriessmann A, Lutilsky L, Sauer E, Wirtzfeld A
Med Klin. 1980 Aug 1;75(16):580-6.
Prolonged infusion of streptokinase at the customary dose of 100 000 u/h results in undesired plasminogen depletion in many patients. This can be avoided by adaptation of the streptokinase maintenance dose to the presumed rate of plasminogen synthesis of each individual patient. The practicability of this approach was tested in 52 patients who had streptokinase therapy of 3 to 9 days duration for deep vein thrombosis. Twice daily measurements of thrombin time and fibrinogen concentration were performed for immediate clinical surveyance and dosage adjustments. These led to a change from the original 100 000 u/h in most patients: in 65% the dose was reduced and in 10% it was increased. By this measure excessive plasminogen depletion was avoided in 88% of the patients. In them the final maintenance dose ranged from 40 000 to 150 000 u/h. Side effects were similar to those reported for the standard dosage scheme, and clinical results were good with a phlebographic success rate of 91% in recent and 65% in subacute or chronic deep vein thrombosis.
以100000单位/小时的常规剂量长时间输注链激酶,会导致许多患者出现不希望的纤溶酶原耗竭。通过根据每个患者推测的纤溶酶原合成速率调整链激酶维持剂量,可以避免这种情况。在52例接受链激酶治疗3至9天以治疗深静脉血栓形成的患者中测试了这种方法的实用性。每天两次测量凝血酶时间和纤维蛋白原浓度,以便进行即时临床监测和剂量调整。这导致大多数患者的初始剂量从100000单位/小时发生变化:65%的患者剂量降低,10%的患者剂量增加。通过这种措施,88%的患者避免了过度的纤溶酶原耗竭。在这些患者中,最终维持剂量范围为40000至150000单位/小时。副作用与标准剂量方案报告的相似,临床结果良好,近期深静脉血栓形成的静脉造影成功率为91%,亚急性或慢性深静脉血栓形成为65%。