Timmis G C, Mammen E F, Ramos R G, Gordon S, Gangadharan V, Hauser A M, Westveer D C, Stewart J R
Arch Intern Med. 1986 Apr;146(4):667-72.
To determine whether or not the timing of heparin infusion affects either bleeding or reocclusion following intracoronary streptokinase for acute myocardial infarction, heparin was infused immediately after streptokinase in 89 patients and was delayed for 12 hours in the subsequent 93. Bleeding occurred in 22 immediate-heparin patients and was major in five (one fatal); there were 14 hemorrhages in the delayed-heparin group, all minor. At discharge, reocclusions were observed in 18% (12/68) of immediate-heparin patients, and 11% (3/27) of the latter. Bioassayed fibrinogen levels displayed sustained depression regardless of bleeding for 20 hours after streptokinase; however, defibrinogenation measured by immunoassay was much less striking. This suggests that high levels of fibrinogen degradation products spuriously affect the bioassay of fibrinogen. We conclude that bleeding is related to the anticoagulant effects of fibrinogen degradation products interacting with heparin, and may be largely independent of hypofibrinogenemia. Delaying heparin for 12 hours may decrease the risk of bleeding while little affecting the risk of reocclusion.
为了确定肝素输注时间是否会影响急性心肌梗死患者冠状动脉内注射链激酶后的出血或再闭塞情况,对89例患者在注射链激酶后立即输注肝素,并对随后的93例患者延迟12小时输注肝素。立即输注肝素的患者中有22例发生出血,其中5例为大出血(1例死亡);延迟输注肝素组有14例出血,均为小出血。出院时,立即输注肝素的患者中有18%(12/68)出现再闭塞,延迟输注肝素的患者中有11%(3/27)出现再闭塞。生物测定的纤维蛋白原水平在链激酶注射后20小时内持续下降,与出血无关;然而,通过免疫测定法测得的纤维蛋白原减少情况则不那么明显。这表明高水平的纤维蛋白原降解产物会虚假地影响纤维蛋白原的生物测定。我们得出结论,出血与纤维蛋白原降解产物与肝素相互作用的抗凝作用有关,并且可能在很大程度上独立于纤维蛋白原血症。将肝素延迟12小时输注可能会降低出血风险,同时对再闭塞风险影响不大。