VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.
VA Center for Health Equity Research and Promotion, Pittsburgh, PA, USA.
Ann Pharmacother. 2021 May;55(5):575-583. doi: 10.1177/1060028020961503. Epub 2020 Sep 23.
Accurate monitoring of intravenous unfractionated heparin (UFH) is essential to mitigate the risk of adverse drug events associated with dosing errors. Although recent data support anti-factor Xa (anti-Xa) monitoring preferentially over activated partial thromboplastin time (aPTT) to improve time to therapeutic anticoagulation, the utility of incorporating anti-Xa monitoring with a calculation-free weight-based UFH nomogram has not been formally evaluated.
The primary objective of this study was to evaluate the time to therapeutic anticoagulation of a calculation-free weight-based UFH nomogram integrated with anti-Xa monitoring versus a historical control of aPTT monitoring utilizing manual dose calculations.
This was a retrospective analysis of patients with anti-Xa monitoring and a novel calculation-free weight-based UFH nomogram compared with a historical control with aPTT monitoring and manual calculations.
A total of 103 patients in the aPTT cohort and 100 patients in the anti-Xa cohort were analyzed. The anti-Xa cohort achieved goal therapeutic target 3.8 hours sooner than the aPTT cohort ( = 0.03). Patients with anti-Xa monitoring required 1 fewer adjustment per 2.5 patient-days of UFH with the venous thromboembolism nomogram ( = 0.02). Patients in the aPTT cohort required more infusion interruptions because of supratherapeutic values ( = 0.007) and boluses because of subtherapeutic values ( = 0.044). There were no differences in rates of thromboembolism, major bleeding, or clinically relevant nonmajor bleeding between the cohorts.
This study demonstrated that anti-Xa UFH monitoring integrated with a calculation-free nomogram results in faster time to therapeutic anticoagulation and fewer dose adjustments compared with aPTT monitoring with manual calculations.
准确监测静脉普通肝素(UFH)对于降低因剂量错误导致的不良药物事件风险至关重要。尽管最近的数据支持抗因子 Xa(anti-Xa)监测优于激活部分凝血活酶时间(aPTT),以改善达到治疗抗凝所需的时间,但尚未正式评估将 anti-Xa 监测与无计算基于体重的 UFH 剂量方案相结合的效用。
本研究的主要目的是评估无计算基于体重的 UFH 剂量方案与 anti-Xa 监测相结合与使用手动剂量计算的 aPTT 监测的历史对照相比,达到治疗性抗凝的时间。
这是一项回顾性分析,比较了具有 anti-Xa 监测和新型无计算基于体重的 UFH 剂量方案的患者与具有 aPTT 监测和手动计算的历史对照。
aPTT 组共 103 例患者,anti-Xa 组 100 例患者。anti-Xa 组达到目标治疗目标的时间比 aPTT 组早 3.8 小时(=0.03)。使用静脉血栓栓塞症剂量方案,每 2.5 天患者中,anti-Xa 监测组需要调整的次数减少 1 次(=0.02)。由于 aPTT 监测值过高,需要中断输液的患者更多(=0.007),由于 aPTT 监测值过低,需要给予推注的患者更多(=0.044)。两组之间血栓栓塞、大出血或有临床意义的非大出血的发生率无差异。
本研究表明,与手动计算的 aPTT 监测相比,将 anti-Xa UFH 监测与无计算方案相结合可更快达到治疗性抗凝,且剂量调整次数更少。