Pharmacists prescribing COVID-19 therapeutics (nirmatrelvir/ritonavir) in a community pharmacy: An observational time and motion study

Yelim Joung, Richard H. Dang, Michelle Hormozian, Allison Chacon, Wendy Mack
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Abstract

Background

Nirmatrelvir/ritonavir (NMV/r) (Paxlovid) was the first oral therapeutic agent available for outpatient treatment of mild-to-moderate coronavirus disease 2019, reducing morbidity and mortality. As part of the emergency use authorization (EUA), pharmacists were granted the authority to prescribe NMV/r subject to the conditions and eligibility criteria of the EUA. Owing to the additional steps required for pharmacists to prescribe NMV/r, widespread adoption of pharmacist-led NMV/r services may have been hindered.

Objective

This study aimed to assess the feasibility of a pharmacist-led NMV/r prescribing service by quantifying the procedural time spent to prescribe NMV/r and to identify obstacles to service integration.

Methods

A direct observational time-motion study of a pilot program was conducted at a community pharmacy in an academic medical center in Southern California from December 1, 2022, to March 31, 2023. Each encounter was tracked from the initial patient request to the prescription of NMV/r, and the time spent to complete each step was recorded. Data were collected using the Research Electronic Data Capture tool.

Results

Twenty-two patients were observed, 8 of whom were eligible for NMV/r. The median time from patient outreach to prescription generation was 22 minutes (interquartile range [IQR] = 15, 84) and 5 minutes (IQR = 3, 11) for referral to a physician for ineligible patients. Patient screening to comply with the EUA criteria took 10 minutes (IQR = 7, 10) for eligible patients and 4 minutes (IQR = 2, 6) for ineligible patients. Barriers such as multitasking and the mode of initial patient outreach affected or delayed service provision.

Conclusion

This study suggests that the NMV/r prescribing service adds a manageable amount of time to pharmacist workflow at this site, comparable with other clinical services in pharmacy settings. Feasibility may vary depending on the pharmacy setting and patient volume.
药剂师在社区药房处方COVID-19治疗药物(尼马特韦/利托那韦):一项观察时间和运动研究
nirmatrelvir /ritonavir (NMV/r) (Paxlovid)是第一个可用于轻中度冠状病毒病2019门诊治疗的口服治疗剂,可降低发病率和死亡率。作为紧急使用授权(EUA)的一部分,药剂师有权根据EUA的条件和资格标准规定NMV/r。由于药剂师在开NMV/r处方时需要采取额外步骤,因此可能阻碍了药剂师主导的NMV/r服务的广泛采用。目的通过量化NMV/r处方的程序时间,评估药师主导的NMV/r处方服务的可行性,并识别服务整合的障碍。方法于2022年12月1日至2023年3月31日在南加州某学术医疗中心的社区药房对试点项目进行直接观察时动研究。从最初的患者请求到NMV/r的处方,每次就诊都被跟踪,并记录完成每个步骤所花费的时间。使用研究电子数据采集工具收集数据。结果共观察22例患者,其中8例符合NMV/r标准。从患者外展到开出处方的中位时间为22分钟(四分位数间距[IQR] = 15,84),不符合条件的患者转诊到医生的中位时间为5分钟(IQR = 3,11)。符合EUA标准的患者筛查需要10分钟(IQR = 7,10),不符合EUA标准的患者筛查需要4分钟(IQR = 2,6)。多任务处理和最初患者外展模式等障碍影响或延迟了服务提供。结论NMV/r处方服务与其他临床服务相比,为该站点的药剂师工作流程增加了可管理的时间。可行性可能因药房设置和患者数量而异。
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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