沈瑞环, 王旭, 鲁中原, 姜亚洲. 先天性心脏病患儿手术aPTT监测肝素的两种抗凝状况的比较[J]. 心脏杂志, 2021, 33(5): 487-490, 494. DOI: 10.12125/j.chj.202012081
    引用本文: 沈瑞环, 王旭, 鲁中原, 姜亚洲. 先天性心脏病患儿手术aPTT监测肝素的两种抗凝状况的比较[J]. 心脏杂志, 2021, 33(5): 487-490, 494. DOI: 10.12125/j.chj.202012081
    Rui-huan SHEN, Xu WANG, Zhong-yuan LU, Ya-zhou JIANG. Activated partial thromboplastin time-based monitoring of unfractionated heparin: clinical value after cavo-pulmonary connections undergoing cardiopulmonary bypass[J]. Chinese Heart Journal, 2021, 33(5): 487-490, 494. DOI: 10.12125/j.chj.202012081
    Citation: Rui-huan SHEN, Xu WANG, Zhong-yuan LU, Ya-zhou JIANG. Activated partial thromboplastin time-based monitoring of unfractionated heparin: clinical value after cavo-pulmonary connections undergoing cardiopulmonary bypass[J]. Chinese Heart Journal, 2021, 33(5): 487-490, 494. DOI: 10.12125/j.chj.202012081

    先天性心脏病患儿手术aPTT监测肝素的两种抗凝状况的比较

    Activated partial thromboplastin time-based monitoring of unfractionated heparin: clinical value after cavo-pulmonary connections undergoing cardiopulmonary bypass

    • 摘要:
        目的  比较先天性心脏病患儿手术的活化部分凝血活酶时间(activated partial thromboplastin time, aPTT)监测肝素的两种抗凝状况。
        方法  入选(2018年6月~2019年12月)在阜外医院接受体外循环下双向格林手术全腔静脉与肺动脉连接术的(6月~6岁)患儿50例。所有普通肝素剂量调整都基于aPTT指导的肝素监测方案进行。根据能否在48 h内达到治疗性抗凝并且之后始终维持aPTT于治疗范围内,将入选患儿分为达标组(n = 27)与未达标组(n = 23)。采用单因素分析比较两组间的围术期临床资料。
        结果  与未达标组比较,达标组的患儿在启用肝素24 h与48 h时的aPTT均较长(P<0.01);且在肝素启用48 h达标组患儿的抗凝血酶III水平较高(P<0.01),术后24 h与48 h内的胸管引流量较少(P<0.05);48 h内的新鲜冰冻血浆总输注量较少(P<0.05)。机械通气时间与ICU住院时间较短(P<0.01)。但两组患儿间的肝素维持剂量差异无统计学意义。
        结论  达到基于aPTT指导的肝素监测方案标准可以改善患儿在腔静脉-肺动脉连接术后的出血情况;缩短机械通气时间;减少ICU住院时间。

       

      Abstract:
        AIM  To evaluate the clinical value of heparin monitoring protocol based on activated partial thromboplastin time (aPTT) in children after cavo-pulmonary connections undergoing cardiopulmonary bypass.
        METHODS  Children aged from 6 months to 6 years old who underwent bidirectional Glenn procedure or total cavo-pulmonary connection in our hospital from June 2018 to December 2019 were prospectively selected. All dose adjustments of unfractionated heparin were based on the heparin monitoring protocol guided by aPTT. According to whether the therapeutic anticoagulation could be achieved within 48 hours and the aPTT could always be maintained within the target range, the selected children were categorized into two groups: up-to-standard group and non-up-to-standard group. Univariate analysis was used to compare the perioperative clinical data between the two groups.
        RESULTS  A total of 50 children were selected and all were included in the final statistical analysis, including 27 cases (54%) in the up-to-standard group and 23 cases (46%) in the non-up-to-standard group. The aPTT of the non-standard group was shorter than that in the standard group at 24 hours and 48 hours after the administration of heparin. When heparin had administrated for 48 hours, the level of antithrombin III was lower in the up-to-standard group (P<0.05). The chest tube output in the up-to-standard group was less than that in the non-up-to-standard group within 24 hours (P <0.01) and 48 hours after surgery (P = 0.014). Moreover, the total amount of fresh frozen plasma transfusion within 48 hours in the up-to-standard group was less than that in the non-up-to-standard group (P <0.01). However, there was no statistically significant difference in the heparin maintenance dose between the two groups. In addition, the duration of mechanical ventilation and the ICU stay time in the up-to-standard group were shorter than those in the non-up-to-standard group.
        CONCLUSION  The protocol of activated partial thromboplastin time-based unfractionated heparin monitoring proposed in this study may improve the clinical outcomes in children after cavo-pulmonary connections undergoing cardiopulmonary bypass.

       

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