凝血因子活性水平的变化导致活化部分凝血活素时间和肝素监测抗xa活性之间的差异:一项回顾性观察研究。

IF 3.8 2区 医学 Q1 CRITICAL CARE MEDICINE
Tomoyo Saito, Mineji Hayakawa, Osamu Kumano, Yoshinori Honma, Mone Murashita, Jun Kato, Syouki Fukui, Masaki Takahashi, Yuki Takahashi, Takumi Tsuchida, Asumi Mizugaki, Shuhei Takauji, Mariko Hayamizu, Tomonao Yoshida, Kenichi Katabami, Takeshi Wada, Kunihiko Maekawa
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引用次数: 0

摘要

背景:未分离肝素(UFH)主要监测使用活化部分凝血活素时间(APTT)。然而,最近引入的抗活化因子X (anti-Xa)活性测试提供了抗凝剂对Xa抑制的直接评估。本研究旨在探讨危重患者在UFH监测期间APTT和抗xa活性之间的差异,并探讨其潜在原因。方法:对99例持续静脉注射UFH的危重患者血液标本271对化验结果进行分析。理论APTT值计算使用拟合曲线方程从尖刺样品测量抗xa活性。根据测量的APTT/理论APTT比率将样本分为三组:较低组(120%)。结果:APTT与抗xa活性的总体一致性为45%,差异率为55%。低剂量组经常出现明显的肝素过量,而低剂量组和高剂量组凝血因子活性分别高于和低于和谐组。特别是,较低的组表现出比较高和和谐组更高的因子VIII活性水平。结论:APTT和抗xa活性之间的差异经常被观察到,受凝血因子活性水平变化的影响。下、上两组分别分为伪肝素耐药型和凝血障碍型。在危重患者中准确监测肝素至关重要,特别是在假肝素耐药的情况下,APTT值可能错误地指示肝素剂量不足,尽管抗xa活性足够。了解这些差异对于管理危重患者的肝素治疗非常重要。试验注册:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variation in coagulation factor activity levels cause discrepancies between activated partial thromboplastin time and anti-Xa activity for heparin monitoring: a retrospective observational study.

Background: Unfractionated heparin (UFH) is primarily monitored using activated partial thromboplastin time (APTT). However, the recent introduction of anti-activated factor X (anti-Xa) activity testing has provided a direct evaluation of Xa inhibition by anticoagulants. This study aimed to investigate discrepancies between APTT and anti-Xa activity during UFH monitoring in critically ill patients and explore their underlying causes.

Methods: This study analyzed 271 pairs of laboratory test results from blood samples of 99 critically ill patients receiving continuous intravenous UFH. Theoretical APTT values were calculated using fitted curve equations from spiked sample measurements with anti-Xa activity. Samples were categorized into three groups based on the measurement of the APTT/theoretical APTT ratio: the lower group (< 80%), the concordant group (80-120%), and the upper group (> 120%).

Results: The overall concordance rate between APTT and anti-Xa activity was 45%, with a 55% discrepancy rate. The lower group frequently showed apparent heparin overdoses, while coagulation factor activities in the lower and upper groups were higher and lower, respectively, than those in the concordant group. Particularly, the lower group exhibited higher factor VIII activity levels than the upper and concordant groups.

Conclusions: Discrepancies between APTT and anti-Xa activity were frequently observed, influenced by changes in coagulation factors activity levels. The lower and upper groups were classified as pseudo-heparin-resistant and coagulopathy types, respectively. Accurate monitoring of heparin in critically ill patients is crucial, especially in cases of pseudo-heparin resistance, where APTT values may wrongly indicate inadequate heparin dosing despite sufficient anti-Xa activity. Understanding these discrepancies is important for managing heparin therapy in critically ill patients.

Trial registration: Not applicable.

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来源期刊
Journal of Intensive Care
Journal of Intensive Care Medicine-Critical Care and Intensive Care Medicine
CiteScore
11.90
自引率
1.40%
发文量
51
审稿时长
15 weeks
期刊介绍: "Journal of Intensive Care" is an open access journal dedicated to the comprehensive coverage of intensive care medicine, providing a platform for the latest research and clinical insights in this critical field. The journal covers a wide range of topics, including intensive and critical care, trauma and surgical intensive care, pediatric intensive care, acute and emergency medicine, perioperative medicine, resuscitation, infection control, and organ dysfunction. Recognizing the importance of cultural diversity in healthcare practices, "Journal of Intensive Care" also encourages submissions that explore and discuss the cultural aspects of intensive care, aiming to promote a more inclusive and culturally sensitive approach to patient care. By fostering a global exchange of knowledge and expertise, the journal contributes to the continuous improvement of intensive care practices worldwide.
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