Design and evaluation of an electronic prospective medication order review system for medication orders in the inpatient setting

Author:

Ojha Pooja1,Anderson Benjamin J1,Draper Evan W1,Flaker Susan M1,Siska Mark H1,Mara Kristin C2,Kennedy Brian D1,Schreier Diana J1

Affiliation:

1. Department of Pharmacy Services, Mayo Clinic , Rochester, MN 55905, United States

2. Department of Quantitative Health Sciences, Mayo Clinic , Rochester, MN 55905, United States

Abstract

Abstract Objectives Since the 1970s, a plethora of tools have been introduced to support the medication use process. However, automation initiatives to assist pharmacists in prospectively reviewing medication orders are lacking. The review of many medications may be protocolized and implemented in an algorithmic fashion utilizing discrete data from the electronic health record (EHR). This research serves as a proof of concept to evaluate the capability and effectiveness of an electronic prospective medication order review (EPMOR) system compared to pharmacists’ review. Materials and methods A subset of the most frequently verified medication orders were identified for inclusion. A team of clinical pharmacist experts developed best-practice EPMOR criteria. The established criteria were incorporated into conditional logic built within the EHR. Verification outcomes from the pharmacist (human) and EPMOR (automation) were compared. Results Overall, 13 404 medication orders were included. Of those orders, 13 133 passed pharmacist review, 7388 of which passed EPMOR. A total of 271 medication orders failed pharmacist review due to order modification or discontinuation, 105 of which passed EPMOR. Of the 105 orders, 19 were duplicate orders correctly caught by both EPMOR and pharmacists, but the opposite duplicate order was rejected, 51 orders failed due to scheduling changes. Discussion This simulation was capable of effectively discriminating and triaging orders. Protocolization and automation of the prospective medication order review process in the EHR appear possible using clinically driven algorithms. Conclusion Further research is necessary to refine such algorithms to maximize value, improve efficiency, and minimize safety risks in preparation for the implementation of fully automated systems.

Funder

Mayo Midwest Pharmacy Research Committee

Publisher

Oxford University Press (OUP)

Reference12 articles.

1. ASHP guidelines: minimum standard for pharmacies in hospitals;American Society of Health-System Pharmacists;Am J Health Syst Pharm,2013

2. The impact of drug order complexity on prospective medication order review and verification time;Dakwa;J Am Med Inform Assoc,2020

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