Hi Russ,
Dan mentioned to me earlier that this thread was intended for these discussions, so I copied over our thread from the "notes" chain here for easier retrieval in the archive. So far, CMH is implementing Discovere and has been using PowerTrials to track an adverse-event study for the past couple of years. Discovere is slated to be fully live by the end of the year, at which point they will most likely be adding several studies (with a focus on >1y longitudinal studies). The biggest EHR integration point for Discovere is that there is an Integrated Data Capture (IDC) function that allows study designers to map data elements in Cerner to data elements in Discovere for automatic population of values that are recorded in the Cerner chart, to reduce duplication and manual data entry. I think as we flesh these functionalities out further, we'll definitely find some common points of functionality to leverage for PCORI! Thanks, Nate Apathy Program Manager, Cerner Research -----Original Message----- From: Russ Waitman [mailto:[email protected]] Sent: Thursday, September 11, 2014 9:59 AM To: Apathy,Nate; Hickman, Hubert B; [email protected] Subject: RE: GPC Dev notes for 9/9/2014 Hi Nate, Very helpful. What portions of this are used at CMH today or over the next year or two? Really look forward to working with you on how much of this Cerner capability and corresponding Epic capability we can understand how to use across our network for our PCORI goals, Russ -----Original Message----- From: [email protected]<mailto:[email protected]> [mailto:[email protected]] On Behalf Of Apathy,Nate Sent: Thursday, September 11, 2014 8:54 AM To: Hickman, Hubert B; [email protected]<mailto:[email protected]> Subject: RE: GPC Dev notes for 9/9/2014 Hi all, In reviewing the notes I realized that I never responded to the first question for Cerner around integrating research into the clinical workflow. From a Cerner perspective, we have a few solutions that do this, including PowerTrials, Discovere, and our new OnCore interface that works with PowerTrials. PowerTrials is a solution for entering protocols and recruiting patients for a study, and includes an indicator in the banner bar of each patient's chart who is on a trial, to alert all clinicians that encounter that individual's chart. PT allows researchers to manage accrual, recruit patients for studies, and includes a "Clinical Research" tab in the primary chart that is dedicated to the available clinical trials at the institution as well as gives providers the ability to check what trials a patient might be eligible for. Eligibility screenings are built into the Cerner Millennium system via Discern Rules that can be designed to logically evaluate the inclusion/exclusion criteria for a study within a patient's chart, or across the entire patient population. The newest development with PowerTrials, since it is not a full CTMS within Millennium, is our OnCore interface, which we have established with our alpha client and are now prepared to implement more broadly. We've been working closely with Forte to establish that relationship, and one of our folks, Ryan Moog, is actually at Forte today discussing the next steps for improving that interface and making the implementation more repeatable across clients. Let me know if I need to update the notes and re-send the pdf. Thanks, Nate Apathy Program Manager, Cerner Research From: [email protected] [mailto:[email protected]] On Behalf Of Dan Connolly Sent: Monday, September 08, 2014 5:49 PM To: [email protected] Cc: John Steinmetz Subject: Embed research within healthcare systems In a KUMC GPC planning meeting today, we realized we'd like to identify leading sites for embedding research withing healthcare systems. Who has a well-trodden path to getting changes deployed in your EMR and clinical workflow? Care to give an example or two? What was the nature of the change, and about how long did it take to plan and execute? The deadlines are a ways out, but my (very limited) experience suggests that getting changed deployed in a production EMR should be planned well over 6 months in advance. Embed research within healthcare systems Jun-15 5.2 Randomize patients and/or sites for participation in clinical trials Lead sites: Mar-15 All sites: Aug-15 5.4 -- Dan CONFIDENTIALITY NOTICE This message and any included attachments are from Cerner Corporation and are intended only for the addressee. The information contained in this message is confidential and may constitute inside or non-public information under international, federal, or state securities laws. Unauthorized forwarding, printing, copying, distribution, or use of such information is strictly prohibited and may be unlawful. If you are not the addressee, please promptly delete this message and notify the sender of the delivery error by e-mail or you may call Cerner's corporate offices in Kansas City, Missouri, U.S.A at (+1) (816)221-1024.
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