发展合作药房实践协议,以提高效率和管理处方在肾移植诊所

Rachel Chelewski, K. Johnson, A. Zuckerman, Joshua DeClercq, Leena Choi, Megan E. Peter, A. Langone
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引用次数: 0

摘要

背景:移植后患者需要复杂的药物治疗方案,以确保移植器官的存活和患者的整体健康。这些方案在移植后经常调整、开始或停止。药剂师(PharmD)的专业知识可以用来优化移植后药物的使用。目的:本研究描述了一个肾移植诊所的药学博士和医生之间的合作药学实践协议(CPPA)的创建和相应的结果。方法:在田纳西州(TN)药剂师协会和田纳西州医学协会最终通过立法批准田纳西州注册药房的CPPA(2014年7月1日生效)后,范德比尔特肾移植诊所和综合卫生系统药房(IHSP)制定了CPPA,该CPPA得到了范德比尔特大学医学中心(VUMC)制药、诊断和治疗委员会和VUMC医学委员会的批准。为了评估CPPA的结果,我们评估了免疫抑制剂(IS)处方的授权人类型(护士、医生或药学博士;以IS处方的百分比衡量)和三个7个月间隔的IS处方量:1)PharmD诊所整合之前(11/1/14-5/31/15),2)没有CPPA的PharmD整合(12/1/15-6/30/16),以及3)PharmD整合和CPPA(4/1/17-10/31/17)。在每个时间间隔内至少有一个IS处方的成年患者被纳入研究。收集了因CPPA而引起的安全问题和人员需求的频率。最后,我们评估了IHSP的处方总量。结果:在CPPA的药学处方管理下,医生和护士对IS处方的补药工作量分别从42.7%和57.3%降低到8.7%和5.9%。IHSP的处方总量从整合药学博士之前的13,523张增加到与CPPA整合后的45,320张。在七次季度评估中,没有任何一次报告存在安全问题,IHSP的团队从2015年的8人增加到2018年的23人。结论:实施CPPA后,药师开具了更多的IS和非IS处方,减轻了医师和护士的负担,促进了药学人员的增长。合作实践协议中的药剂师特别适合密切监测患者移植后的药物治疗方案,确保治疗的安全性和有效性。
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Development of a collaborative pharmacy practice agreement to improve efficiency and management of prescribing in a renal transplant clinic
Abstract Background: Post-transplant patients require complex medication regimens to ensure the survival of the transplanted organ and patient overall well-being. These regimens are frequently adjusted, initiated, or discontinued after transplantation. Pharmacist (PharmD) expertise can be utilized to optimize post-transplant medication use. Aims: This study describes the creation and corresponding outcomes of a Collaborative Pharmacy Practice Agreements (CPPA) between PharmDs and physicians within a renal transplant clinic. Methods: After the Tennessee (TN) Pharmacist Association and TN Medical Association finalized legislation approving CPPAs for licensed PharmDs in TN (effective July 1, 2014), the Vanderbilt Renal Transplant Clinic and integrated health system pharmacy (IHSP) developed a CPPA, which was approved by the Vanderbilt University Medical Center (VUMC) Pharmaceutical, Diagnostics, and Therapeutics Committee and VUMC Medical Board. To evaluate the outcomes of the CPPA, we assessed the type of authorizer for immunosuppressant (IS) prescriptions (nurse, physician, or PharmD; measured as % of IS prescriptions) and the volume of IS prescriptions across three 7-month intervals: 1) before PharmD clinic integration (11/1/14–5/31/15), 2) with PharmD integration without a CPPA (12/1/15–6/30/16), and 3) with PharmD integration and a CPPA (4/1/17–10/31/17). Adult patients with at least one IS prescription generated in each time interval were included. Frequency of safety concerns and staffing requirements resulting from the CPPA were collected. Finally, we assessed the total volume of prescriptions filled by the IHSP. Results: Following PharmD prescription management under a CPPA, physician and nurse refill workload for IS prescriptions reduced from 42.7% and 57.3% to 8.7% and 5.9%, respectively. Overall prescription generation to the IHSP increased from 13,523 prior to PharmD integration to 45,320 after integration with a CPPA. No safety concerns were reported in any of seven quarterly reviews, and the IHSP has grown from a team of eight in 2015 to 23 team members in 2018. Conclusions: After implementing a CPPA, more IS and non-IS prescriptions were generated by pharmacists, which reduced physician and nurse burden and allowed pharmacy staff growth. Pharmacists in collaborative practice agreements are uniquely suited to closely monitor patients’ post-transplant medication regimens, ensuring safety and effectiveness of therapy.
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Journal of Drug Assessment
Journal of Drug Assessment PHARMACOLOGY & PHARMACY-
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