Lysogorski Michaela C, Hassan Amany K, Lampkin Stacie J, Geisler Richard
School of Pharmacy, D'Youville College, Buffalo, NY, USA.
Mercy Hospital of Buffalo, Buffalo, NY, USA.
Int J Clin Pharm. 2017 Aug;39(4):844-850. doi: 10.1007/s11096-017-0482-y. Epub 2017 May 15.
Background Intravenous unfractionated heparin (IV UFH) has a narrow therapeutic index and poses a high risk of bleeding. Objective To determine the impact of pharmacy monitoring and intervention on adherence to and appropriate implementation of IV UFH protocol. Setting A 438 bed hospital specializing in cardiac services. Methods This is a retrospective chart review study. Pre-pharmacy intervention data were collected from November 2013 to January 2014 and compared to post-pharmacy intervention data obtained between August 2014 and October 2014. Patients were included if they received IV UFH for at least 24 hours. The first three daytime laboratory draws were collected for each patient and analyzed using generalized estimating equations to quantify the association between pharmacy monitoring and adherence to the institution's protocol. Main outcome measures Designation of appropriate protocol, accurate selection of initial infusion rate, timing of anti-Xa levels within 60 min of anticipated due time, change of infusion rate within 120 min of laboratory result, and appropriate adjustment of infusion rates. Results A total of 195 data points were included. The initial selection of infusion rate and subsequent adjustments were more appropriate in the post-intervention period with an odds ratio of 8.36 (95% CI 2.41-29.01, p value = 0.0008), and 4.66 (95% CI 1.41-15.43, p value = 0.0118), respectively. Conclusion The results of this study indicate that pharmacy monitoring of IV UFH therapy has improved adherence to an institution's protocol and is associated with more accurate selection of initial infusion rates and adjustment of infusions based upon laboratory results.
静脉注射普通肝素(IV UFH)治疗指数狭窄,出血风险高。目的:确定药学监测与干预对IV UFH方案依从性和正确实施的影响。地点:一家拥有438张床位的心脏专科医院。方法:这是一项回顾性病历审查研究。收集2013年11月至2014年1月药学干预前的数据,并与2014年8月至2014年10月获得的药学干预后数据进行比较。接受IV UFH治疗至少24小时的患者纳入研究。收集每位患者白天的前三次实验室检查结果,并使用广义估计方程进行分析,以量化药学监测与机构方案依从性之间的关联。主要观察指标:正确方案的指定、初始输注速率的准确选择、在预期时间的60分钟内抗Xa水平的测定时间、实验室结果后120分钟内输注速率的变化以及输注速率的适当调整。结果:共纳入195个数据点。干预后时期初始输注速率的选择和随后的调整更合适,优势比分别为8.36(95%CI 2.41-29.01,p值=0.0008)和4.66(95%CI 1.41-15.43,p值=0.0118)。结论:本研究结果表明,药学对IV UFH治疗的监测提高了机构方案的依从性,并与更准确地选择初始输注速率以及根据实验室结果调整输注有关。