Clinical pharmacist-led anticoagulation stewardship program: improve physician adherence to evidence-based guidelines and reduce anticoagulant-related medication errors

IF 3.4 Q2 PHARMACOLOGY & PHARMACY
Heba M. El-Bosily, Khaled R. Abd El Meguid, Nagwa A. Sabri, Marwa Adel Ahmed
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引用次数: 0

Abstract

Background

Due to their high risk of medication errors (MEs) and the potentially devastating thrombotic and bleeding events, anticoagulants are a class of high-risk medications that require regular monitoring by healthcare professionals. The pharmacist is in the ideal position to provide patient care during anticoagulation therapy which is still prone to inappropriate prescribing. The pharmacist is capable of anticoagulation therapy monitoring, provision of drug information, dosing protocol preparation, drug interaction screening, and educating patients. It has been demonstrated that specialized anticoagulation management programs enhance clinical safety and quality of anticoagulant therapy. This study aimed to evaluate the effect of implementing a pharmacist-led anticoagulation stewardship program in reducing anticoagulant-related MEs. We conducted a prospective pre-and post-intervention study in a tertiary hospital on 233 patients with 4132 anticoagulant doses to assess the impact of this program implementation.

Results

This study found that MEs were significantly reduced after implementing the anticoagulation stewardship program. Specifically, the “Medication without indication” and the “Incorrect dose (low dose)” types of MEs were remarkably decreased from 14.4% pre- to 3.3% post-, and from 47.6% pre- to 28.7% post-implementation, respectively. Interestingly, the “Wrong route” disappeared in the post-implementation phase of the study. The proportion of wrong doses/total doses decreased from 0.474 ± 0.044 to 0.432 ± 0.04 (p = 0.003), while category F decreased from 8.3% to 4.7% (p = 0.001). Physician adherence to evidence-based guidelines (EBG) improved as full adherence increased from 38.8 to 60.2% (p = 0.001) and non-adherence decreased from 26.7 to 3.4% (p = 0.001). These statistically significant findings further suggest valuable clinical benefits since implementing this pharmacist-led program could improve patient outcomes by reducing ME and increasing physician adherence to EBG guidelines.

Conclusions

Although the study was limited by the hospital clinical pharmacist team's working hours, as they work 12 h/day rather than 24, and hence, the program was only observed during this time, the study concluded that the anticoagulation stewardship program encouraged the safe use of anticoagulants, lessened MEs and their severity, and improved physician adherence to EBG. Future studies should assess the effect of such programs on other clinical outcomes beyond MEs and determine their impact on healthcare costs.

Clinical Trial registration: Clinicaltrials.gov: NCT03812848. Date: January 1, 2018.

临床药师领导的抗凝管理计划:提高医生对循证指南的依从性,减少抗凝相关药物错误
背景:抗凝药物由于其药物错误(MEs)的高风险和潜在的破坏性血栓形成和出血事件,是一类高风险药物,需要医疗保健专业人员定期监测。在抗凝治疗期间,药剂师处于提供患者护理的理想位置,但仍容易出现处方不当的情况。药剂师有能力监测抗凝治疗,提供药物信息,制定给药方案,筛选药物相互作用,并教育患者。已经证明,专门的抗凝管理程序可以提高抗凝治疗的临床安全性和质量。本研究旨在评估实施药剂师主导的抗凝管理计划在减少抗凝相关MEs方面的效果。我们在一家三级医院对233名使用4132剂抗凝剂的患者进行了前瞻性干预前和干预后研究,以评估该计划实施的影响。结果本研究发现,实施抗凝管理计划后,MEs显著降低。其中,“无指征用药”和“剂量不正确(低剂量)”类型的MEs分别从实施前的14.4%和实施后的47.6%显著下降到3.3%和实施后的28.7%。有趣的是,“错误路线”在研究的实施后阶段消失了。错误剂量占总剂量的比例从0.474±0.044降至0.432±0.04 (p = 0.003), F类从8.3%降至4.7% (p = 0.001)。医生对循证指南(EBG)的依从性得到改善,完全依从性从38.8%增加到60.2% (p = 0.001),不依从性从26.7%下降到3.4% (p = 0.001)。这些具有统计学意义的研究结果进一步表明了有价值的临床益处,因为实施药剂师主导的项目可以通过减少ME和提高医生对EBG指南的依从性来改善患者的预后。结论:虽然该研究受限于医院临床药师团队的工作时间,因为他们每天工作12小时而不是24小时,因此,该计划仅在这段时间内观察,但研究得出结论,抗凝管理计划鼓励抗凝剂的安全使用,减少MEs及其严重程度,并提高医生对EBG的依从性。未来的研究应该评估这些项目对MEs以外的其他临床结果的影响,并确定它们对医疗成本的影响。临床试验注册:Clinicaltrials.gov: NCT03812848。日期:2018年1月1日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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