首页> 外文期刊>Journal of clinical monitoring and computing >Activated clotting time systems vary in precision and bias and are not interchangeable when following heparin management protocols during cardiopulmonary bypass.
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Activated clotting time systems vary in precision and bias and are not interchangeable when following heparin management protocols during cardiopulmonary bypass.

机译:激活的凝血时间系统的精度和偏差各不相同,在体外循环过程中遵循肝素管理方案时不能互换。

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OBJECTIVE: Our aim was to test the hypothesis that new activated clotting time (ACT) technology, with modifications to instruments and reagents designed to detect earlier clot formation, would be associated with more precise but lower results. A secondary objective was to evaluate the potential impact of any change in ACT measurement on heparin requirements during cardiopulmonary bypass (CPB). METHODS: We compared the precision of two newer ACT systems: Actalyke, Helena Laboratories, Beaumont, TX and Hemochron Response, International Technidyne Corporation, Edison, NJ and assessed their bias with reference to a standard ACT system (Hemochron 801, International Technidyne Corporation, Edison, NJ). Bland-Altman analysis was applied to 81 duplicate samples from 22 patients undergoing CPB or percutaneous coronary interventions (PCI), covering the full clinical range of ACT values. We also estimated the change in heparin dose required to use the Actalyke rather than the Hemochron 801 results, to achieve ourtarget ACT for CPB (480 seconds), and used a mixed model to test for significance. RESULTS: The precision of the Actalyke was superior to the Hemochron Response (mean difference of duplicates +/- 0.1% versus +/- 4.2%). There was no significant bias (p = 0.93) between the results from the standard analyzers (Hemochron 801 and Response), but the results from the modified system (Actalyke) were on average 18% lower than the Hemochron 801 (p < 0.0001). Estimated heparin requirements established that fifty percent of CPB patients would have required additional heparin (5000 to 17500 units), an average increase of 1060 units per patient (p = 0.05), if the Actalyke values were used to guide anticoagulation during CPB. CONCLUSIONS: Our results support the hypothesis that the modified technology (Actalyke) is associated with more precise but lower ACT results. We estimated these lower values would lead to increased heparin dosing during CPB. The impact of this increase on bleeding after cardiac surgery with CPB is controversial and requires further study.
机译:目的:我们的目的是检验以下假设:新的活化凝血时间(ACT)技术,通过对旨在检测较早血凝块形成的仪器和试剂进行修改,可以带来更精确但较低的结果。第二个目标是评估在体外循环(CPB)期间ACT测量的任何变化对肝素需求的潜在影响。方法:我们比较了两种较新的ACT系统的精度:Actalyke,Helena Laboratories,Beaumont,TX和Hemochron Response,International Technidyne Corporation(新泽西州爱迪生),并参照标准ACT系统(Hemochron 801,International Technidyne Corporation,新泽西州爱迪生)。将Bland-Altman分析应用于22位接受CPB或经皮冠状动脉介入治疗(PCI)的患者的81个重复样本,涵盖了ACT值的整个临床范围。我们还估算了使用Actalyke而不是Hemochron 801结果达到CPB的目标ACT(480秒)所需的肝素剂量变化,并使用混合模型测试了显着性。结果:Actalyke的精度优于Hemochron Response(重复项的均值差异+/- 0.1%与+/- 4.2%)。标准分析仪(Hemochron 801和Response)的结果之间没有显着偏差(p = 0.93),但改良系统(Actalyke)的结果平均比Hemochron 801低18%(p <0.0001)。估计的肝素需求量确定,如果使用Actalyke值指导CPB期间的抗凝,则50%的CPB患者将需要额外的肝素(5000至17500单位),每位患者平均增加1060单位(p = 0.05)。结论:我们的结果支持这样的假设,即改良技术(Actalyke)与更精确但较低的ACT结果相关。我们估计这些较低的值将导致CPB期间肝素剂量增加。这种增加对CPB心脏手术后出血的影响尚有争议,需要进一步研究。

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