Evaluation of pharmacist-prescribed nirmatrelvir/ritonavir for patients with COVID-19.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Jason Srey, Samantha Divan, Andrew J Sowles, Michelle Rasmussen, Ralph A Yates, Adriane N Irwin
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引用次数: 0

Abstract

Purpose: Authorization of nirmatrelvir/ritonavir expanded outpatient treatment options for those with coronavirus disease 2019 (COVID-19), but prescribing of the medication is complex. The objective of this study was to evaluate the appropriateness of nirmatrelvir/ritonavir prescribing through a pharmacist-driven service as compared to usual care.

Methods: This was a retrospective cohort study. Patients prescribed nirmatrelvir/ritonavir by a pharmacist between May 1 and December 31, 2022, were temporally matched to those who received nirmatrelvir/ritonavir through usual care. The primary outcome was the percentage of patients appropriately prescribed nirmatrelvir/ritonavir by meeting criteria related to authorization-specific requirements, assessment of hepatic and renal function, and management of drug interactions. Descriptive and inferential statistics were performed.

Results: There were 106 patients in each cohort (N = 212). Patients were mainly female (n = 135, 63.7%) and 65 years of age or older (n = 117, 55.2%). All study-defined criteria for appropriate nirmatrelvir/ritonavir prescribing were met in 88.7% of patients (n = 94) who received care through the pharmacist-driven service, as compared to 41.5% of patients (n = 44) managed through usual care (P < 0.0001). In both groups nirmatrelvir/ritonavir was consistently prescribed within 5 days of symptom onset (P > 0.999) and to patients with a qualifying comorbid condition (P = 0.498). However, hepatic (P = 0.030) and renal (P = 0.024) laboratory values were more likely to be current when the prescription arose from a pharmacist as opposed to the usual care process. Drug interactions also were more likely to be identified and mitigated by pharmacists (P < 0.0001).

Conclusion: Nirmatrelvir/ritonavir was appropriately prescribed by pharmacists in most cases, demonstrating that pharmacists can support safe and effective use of nirmatrelvir/ritonavir for patients with complex comorbidities and medication regimens.

医师处方尼马替韦/利托那韦治疗COVID-19患者的评价
免责声明:为了加快文章的发表,AJHP在接受稿件后将尽快在网上发布。被接受的稿件已经过同行评审和编辑,但在技术格式化和作者校对之前会在网上发布。这些手稿不是记录的最终版本,稍后将被最终文章(按照AJHP风格格式化并由作者校对)所取代。目的:尼马特利韦/利托那韦的授权扩大了2019冠状病毒病(COVID-19)患者的门诊治疗选择,但药物处方复杂。本研究的目的是通过药剂师驱动的服务评估尼马特利韦/利托那韦处方的适宜性,与常规护理相比。方法:回顾性队列研究。在2022年5月1日至12月31日期间,由药剂师处方尼马特利韦/利托那韦的患者暂时与通过常规护理接受尼马特利韦/利托那韦的患者相匹配。主要结局是通过符合相关授权特定要求、肝肾功能评估和药物相互作用管理标准,适当处方尼马特利韦/利托那韦的患者百分比。进行描述性和推断性统计。结果:每组患者106例(N = 212)。患者以女性为主(n = 135, 63.7%),以65岁及以上患者为主(n = 117, 55.2%)。通过药剂师驱动的服务接受治疗的患者中,88.7% (n = 94)的患者(n = 44)达到了适当的尼马特利韦/利托那韦处方的所有研究定义的标准,而通过常规治疗的患者中,这一比例为41.5% (P < 0.0001)。在两组中,尼马特韦/利托那韦均在症状出现后5天内和符合合并症条件的患者中使用(P = 0.498)。然而,当处方来自药剂师而不是通常的护理过程时,肝脏(P = 0.030)和肾脏(P = 0.024)的实验室值更有可能是最新的。药物相互作用也更有可能被药剂师识别和减轻(P < 0.0001)。结论:在大多数情况下,药剂师合理开具尼马特利韦/利托那韦处方,表明药剂师可以支持复杂合并症和用药方案的患者安全有效地使用尼马特利韦/利托那韦。
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
CiteScore
2.90
自引率
18.50%
发文量
341
审稿时长
3-8 weeks
期刊介绍: The American Journal of Health-System Pharmacy (AJHP) is the official publication of the American Society of Health-System Pharmacists (ASHP). It publishes peer-reviewed scientific papers on contemporary drug therapy and pharmacy practice innovations in hospitals and health systems. With a circulation of more than 43,000, AJHP is the most widely recognized and respected clinical pharmacy journal in the world.
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