Evidence map›Paper›PMID 32268389›Full record

ArticleApplied clinical informatics2020

Design and Usability of an Electronic Health Record-Integrated, Point-of-Care, Clinical Decision Support Tool for Modeling and Simulation of Antihemophilic Factors.

Susan M Abdel-Rahman, Harpreet Gill, Shannon L Carpenter, Pathe Gueye, Brian Wicklund, Matt Breitkreutz, Arindam Ghosh, Avinash Kollu

Open access · bronzeAbstract read
In one paragraph

Article in Applied clinical informatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Susan M Abdel-RahmanDivision of Clinical Pharmacology, Toxicology, and Therapeutic Innovation, Children's Mercy, Kansas City, Missouri, United States.
Harpreet GillDepartment of Research Informatics, Children's Research Institute, Children's Mercy, Kansas City, Missouri, United States.
Shannon L CarpenterDepartment of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, United States.
Pathe GueyeDepartment of Research Informatics, Children's Research Institute, Children's Mercy, Kansas City, Missouri, United States.
Brian WicklundDepartment of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, United States.
Matt BreitkreutzDepartment of Research Informatics, Children's Research Institute, Children's Mercy, Kansas City, Missouri, United States.
Arindam GhoshDepartment of Research Informatics, Children's Research Institute, Children's Mercy, Kansas City, Missouri, United States.
Avinash KolluDepartment of Research Informatics, Children's Research Institute, Children's Mercy, Kansas City, Missouri, United States.
Mercy Research · USUniversity of Missouri–Kansas City · USChildren's Mercy Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the consequences of inadequate dosing ranging from increased bleeding risk to excessive drug costs and undesirable administration regimens, the antihemophilic factors are uniquely suited to dose individualization. However, existing options for individualization are limited and exist outside the flow of care. We developed clinical decision support (CDS) software that is integrated with our electronic health record (EHR) and designed to streamline the process for our hematology providers.

objectivesThe aim of this study is to develop and examine the usability of a CDS tool for antihemophilic factor dose individualization.

methodsOur development strategy was based on the features associated with successful CDS tools and driven by a formal requirements analysis. The back-end code was based on algorithms developed for manual individualization and unit tested with 23,000 simulated patient profiles created from the range of patient-derived pharmacokinetic parameter estimates defined in children and adults. A 296-item heuristic checklist was used to guide design of the front-end user interface. Content experts and end-users were recruited to participate in traditional usability testing under an institutional review board approved protocol.

resultsCDS software was developed to systematically walk the point-of-care clinician through dose individualization after seamlessly importing the requisite patient data from the EHR. Classical and population pharmacokinetic approaches were incorporated with clearly displayed estimates of reliability and uncertainty. Users can perform simulations for prophylaxis and acute bleeds by providing two of four therapeutic targets. Testers were highly satisfied with our CDS and quickly became proficient with the tool.

conclusionWith early and broad stakeholder engagement, we developed a CDS tool for hematology provider that affords seamless transition from patient assessment, to pharmacokinetic modeling and simulation, and subsequent dose selection.

Indexed as

Decision Support Systems, ClinicalElectronic Health RecordsPoint-of-Care SystemsAdultHemophilia AHumans

Identifiers

PMID32268389
PMCPMC7141904
OpenAlexW3014950226

What OpenQuestion holds

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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.