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Screening for Medication Errors and Adverse Events Using Outlier Detection Screening Algorithms in an Inpatient Setting

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Abstract

Objectives

To evaluate the potential of a novel system using outlier detection screening algorithms and to identify medication related risks in an inpatient setting.

Methods

In the first phase of the study, we evaluated the transferability of models refined at another medical center using a different electronic medical record system (EMR) on 3 years of historical data (2017–2019), extracted from the local EMR system. Following the retrospective analysis, the system’s models were fine-tuned to the specific local practice patterns. In the second, prospective phase of the study, the system was fully integrated in the local EMR and after a short run-in period was activated live. All alerts generated by the system, in both phases, were analyzed by a clinical team of physicians and pharmacists for accuracy and clinical relevance.

Results

In the retrospective phase of the study, 226,804 medical orders were analyzed, generating a total of 2731 alerts (1.2% of medical orders). Of the alerts analyzed, 69% were clinically relevant alerts and 31% were false alerts. In the prospective phase of the study, 399 alerts were generated by the system (1.6% of medical orders). The vast majority of the alerts (72%) were considered clinically relevant, and 41% of the alerts caused a change in prescriber behavior (i.e. cancel/modify the medical order).

Conclusion

In an inpatient setting of a 600 bed computerized decision support system (CDSS) -naïve medical center, the system generated accurate and clinically valid alerts with low alert burden enabling physicians to improve daily medical practice.

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All data is included in this manuscript.

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Acknowledgements

Not applicable.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for profit sectors.

Author information

Authors and Affiliations

Authors

Contributions

• All authors made substantial contributions to all of the following:

(1) The conception and design of the study: Milena Tocut, Galit Mor, Gisele Zandman-Goddard, Gideon Y. Stein.

(2) Acquisition of data, or analysis and interpretation of data: Milena Tocut, Mayan Moalem, Israel Feinberg.

(3) Drafting the article or revising it critically for important intellectual content: Galit Mor Naor, Milena Tocut, Anat Engel, Gisele Zandman-Goddard, Gideon Y. Stein.

(4) Final approval of the version to be submitted: approved by all authors.

Corresponding author

Correspondence to Milena Tocut.

Ethics declarations

Ethical Approval and Consent to participate

according to the Declaration of Helsinki Wolfson medical center Nr. 0049-20-WOMC, this article was retrospective therefore no patient consent was needed.

Human and Animal Ethics

Not applicable.

Consent for publication

All authors approve this manuscript for publication.

Conflict of Interest

GYS reports personal fees from MedAware Ltd. during the conduct of the study.

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Appendix 1 - Causes of False Alerts Produced by the System, in Phase #1

Appendix 1 - Causes of False Alerts Produced by the System, in Phase #1

  1. 1.

    Model transferability issues: MedAware’s system is based on artificial intelligence algorithms that use medical records data from the patient to create a model for each drug (using data such as patient’s age, sex, drug indications and contraindications, etc.). When the system detects an irregularity between the treatment prescribed to the patient and his clinical profile, it creates an alert. These models are fine-tuned per each medical institution, using historical data which represents local practices. In the retrospective phase we evaluated the system’s performance prior to fine-tuning of the models.

  2. 2.

    Mapping issues: MedAware’s system maps the hospital’s drug catalog. The medication mapping is done semi-automatically. If an error was made in the mapping of a medication, a false alert will be created by the system.

  3. 3.

    Data issues: any error in the transfer of data or its decipherment by MedAware software. In order to build a clinical profile of a patient, the system receives data from the local EMR including diagnoses, instructions, demographic details, blood tests, vital signs (blood pressure, pulse). In some cases, the data is not transmitted in full due to a glitch. In other cases, the data is transmitted properly, but is not received properly by the system. There are several places from where data is extracted from the local EMR. At times, this data will be extracted only from one source and not from all the sources available

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Naor, G.M., Tocut, M., Moalem, M. et al. Screening for Medication Errors and Adverse Events Using Outlier Detection Screening Algorithms in an Inpatient Setting. J Med Syst 46, 88 (2022). https://doi.org/10.1007/s10916-022-01864-6

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  • DOI: https://doi.org/10.1007/s10916-022-01864-6

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