Hassan WM, Flaker GC, Feutz C, Petroski GF, Smith D
Division of Cardiology, Department of Medicine and the Department of Pathology, University of Missouri Hospital and Clinics, Columbia, MO.
J Thromb Thrombolysis. 1995;2(3):245-249. doi: 10.1007/BF01062717.
The optimal heparin dosing schedule to achieve rapid and therapeutic anticoagulation has not been established. The objective of this study is to determine whether an intravenous heparin dosing nomogram based on body weight achieves adequate anticoagulation more rapidly than a standard-care nomogram. Sixty-four patients requiring intravenous heparin treatment for acute coronary syndromes, but who did not receive thrombolytic therapy, were randomized to a standard-care nomogram in which heparin was given as a 5000 unit IV bolus followed by 1000 U/hr, or a weight-adjusted nomogram in which heparin was given as an 80 U/kg IV bolus and 18 U/kg/hr. Activated partial thromboplastin time (APTT) values were checked at 6, 12, 18, 24, and 48 hours and adjusted either by 100-200 U/hr (standard-care nomogram) or by 2-4 U/kg/hr (weight-based nomogram). Activated partial thromboplastin times were measured using a widely generalizable laboratory method. The primary goal was to achieve and maintain the APTT between 60 and 90 seconds. The median APTT values were higher in the weight-adjusted group compared with the standard-care group at 6, 12, 18, 24, and 48 hours: 150 versus 83 (p = 0.001), 100 versus 79 (p = 0.09), 66 versus 61 (p = 0.005), 63 versus 56 (p = 0.09), and 64 versus 56 (p = 0.11). At 18 hours only 11% of patients in the weight-adjusted group had an APTT <61 compared with 26% in the standard-care nomogram (p = 0.007). No major bleeding complications were noted in either group. A weight-adjusted heparin nomogram offers improved anticoagulation in the first 24 hours after heparin initiation compared with a standard-care nomogram in patients with acute coronary artery syndromes.
尚未确定实现快速和治疗性抗凝的最佳肝素给药方案。本研究的目的是确定基于体重的静脉注射肝素给药方案是否比标准护理方案能更快地实现充分抗凝。64例因急性冠状动脉综合征需要静脉注射肝素治疗但未接受溶栓治疗的患者被随机分为标准护理方案组(给予5000单位静脉推注肝素,随后以1000 U/小时持续输注)和体重调整方案组(给予80 U/千克静脉推注肝素和18 U/千克/小时持续输注)。在6、12、18、24和48小时检查活化部分凝血活酶时间(APTT)值,并根据标准护理方案以100 - 200 U/小时或根据体重方案以2 - 4 U/千克/小时进行调整。使用广泛适用的实验室方法测量活化部分凝血活酶时间。主要目标是使APTT达到并维持在60至90秒之间。在6、12、18、24和48小时,体重调整组的APTT中位数高于标准护理组:分别为150对83(p = 0.001)、100对79(p = 0.09)、66对61(p = 0.005)、63对56(p = 0.09)和64对56(p = 0.11)。仅在18小时时,体重调整组中只有11%的患者APTT <61,而标准护理方案组为26%(p = 0.007)。两组均未观察到重大出血并发症。与急性冠状动脉综合征患者的标准护理方案相比,体重调整的肝素给药方案在开始使用肝素后的头24小时内可改善抗凝效果。