Evidence map›Paper›PMID 35193547›Full record

ArticleBMC medical informatics and decision making2022

Overall performance of a drug-drug interaction clinical decision support system: quantitative evaluation and end-user survey.

Greet Van De Sijpe, Charlotte Quintens, Karolien Walgraeve, Eva Van Laer, Jens Penny, Greet De Vlieger, Rik Schrijvers, Paul De Munter, Veerle Foulon, Minne Casteels and 2 more

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Greet Van De SijpePharmacy Department, University Hospitals Leuven, Leuven, Belgium. greet.vandesijpe@uzleuven.be.ORCID 0000-0003-1475-6178
Charlotte QuintensPharmacy Department, University Hospitals Leuven, Leuven, Belgium.
Karolien WalgraevePharmacy Department, University Hospitals Leuven, Leuven, Belgium.
Eva Van LaerPharmacy Department, University Hospitals Leuven, Leuven, Belgium.
Jens PennyDepartment of Information Technology, University Hospitals Leuven, Leuven, Belgium.
Greet De VliegerDepartment of Intensive Care Medicine, University Hospitals Leuven, Leuven, Belgium.ORCID 0000-0002-6579-6965
Rik SchrijversDepartment of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Paul De MunterDepartment of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Veerle FoulonClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Minne CasteelsClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Lorenz Van der LindenPharmacy Department, University Hospitals Leuven, Leuven, Belgium.
Isabel SprietPharmacy Department, University Hospitals Leuven, Leuven, Belgium.ORCID 0000-0001-6342-0676

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical decision support systems are implemented in many hospitals to prevent medication errors and associated harm. They are however associated with a high burden of false positive alerts and alert fatigue. The aim of this study was to evaluate a drug-drug interaction (DDI) clinical decision support system in terms of its performance, uptake and user satisfaction and to identify barriers and opportunities for improvement.

methodsA quantitative evaluation and end-user survey were performed in a large teaching hospital. First, very severe DDI alerts generated between 2019 and 2021 were evaluated retrospectively. Data collection comprised alert burden, override rates, the number of alert overrides reviewed by pharmacists and the resulting pharmacist recommendations as well as their acceptance rate. Second, an e-survey was carried out among prescribers to assess satisfaction, usefulness and relevance of DDI alerts as well as reasons for overriding.

resultsA total of 38,409 very severe DDI alerts were generated, of which 88.2% were overridden by the prescriber. In 3.2% of reviewed overrides, a recommendation by the pharmacist was provided, of which 79.2% was accepted. False positive alerts were caused by a too broad screening interval and lack of incorporation of patient-specific characteristics, such as QTc values. Co-prescribing of a non-vitamin K oral anticoagulant and a low molecular weight heparin accounted for 49.8% of alerts, of which 92.2% were overridden. In 88 (1.1%) of these overridden alerts, concurrent therapy was still present. Despite the high override rate, the e-survey revealed that the DDI clinical decision support system was found useful by prescribers.

conclusionsIdentified barriers were the lack of DDI-specific screening intervals and inclusion of patient-specific characteristics, both leading to a high number of false positive alerts and risk for alert fatigue. Despite these barriers, the added value of the DDI clinical decision support system was recognized by prescribers. Hence, integration of DDI-specific screening intervals and patient-specific characteristics is warranted to improve the performance of the DDI software.

Indexed as

Decision Support Systems, ClinicalMedical Order Entry SystemsDrug InteractionsHumansMedication ErrorsRetrospective StudiesAlert fatigueClinical decision support systemsDrug–drug interactionDrug interactions

Identifiers

PMID35193547
PMCPMC8864797

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.