About how the technical plans will affect clinicians

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Reference no: EM133353517

An integrated delivery network (IDN) serving a large urban and rural demographic area is using separate EHR systems in its inpatient and outpatient settings. Some of the specialty departments have also purchased their own systems for documentation. Unfortunately, this means that information collected in the inpatient setting is not available when patients are seen in the IDN's outpatient clinics (and vice versa). The clinicians need this information to be better informed about their patients and to provide optimal care. In addition, Meaningful Use requirements for problems, medications, and allergies, as well as new chronic disease care initiatives that the IDN is implementing for its patient population, are being hindered by the separate systems. The clinicians have been given accounts on both EHRs, but this is cumbersome for the users because they must be trained on multiple systems, they use valuable time logging into different systems and navigating for information, and there is a potential safety issue if the user selects different patients on the two EHRs. A coordinated decision support environment has also been difficult to implement because the two EHRs use different coding systems and do not share most of their information. This means, for example, that admission rules for congestive heart failure patients cannot be linked to the ambulatory medication list and recent vital signs measurements to run the IDN's standard care process models.

The IDN realizes that it will not be able to replace either EHR in the near future and that, even if it could, there will still be issues with integrating information from the specialty care systems. It decides on a strategic plan to create a CDR that is fed with high-value data from each of the clinical systems. The outpatient EHR's MPI already was being used as the master unique identifier for most of the IDN's systems, so it can be incorporated with the new CDR. A robust IE is implemented to supply data from the clinical systems to the CDR. To normalize the different terminologies used on their various systems, the IDN engages a terminology-services vendor to provide a central data dictionary for the CDR and map the concepts from the current systems to the central standard terminology. The IE uses the terminology services to normalize inbound data to the CDR from the other systems.

The second phase of the strategic plan is to build a CDS system on top of the CDR to develop and maintain enterprise patient-care rules. As rules are executed, their results will be both sent through the IE to the existing EHRs and stored in the CDR; storing the decision support results in the CDR provides a link to supporting data from all clinical systems, which can help with rule triage and maintenance. Another effort in this phase is to provide clinician views into the CDR. The IDN plans to build data services, possibly based on FHIR resources, that can be called by third-party EHRs to display longitudinal, enterprise-wide patient data from within the EHRs. Several simple web- and mobile-based viewing applications using the data services will also be developed and will be available in a stand-alone mode or as callable modules within the current EHRs. The IDN will use SMART to provide the user and patient context from the EHR to these viewing apps so that the clinicians will not have to log in twice and find the patient.

1. Describe the advantages and disadvantages of the situation in the case study.

2. You are the chief medical informatics officer for the organization. You are asked to comment about how the technical plans will affect clinicians. Based on the case study, how do you respond?

3. The organization receives a $3 million gift from an informatics benefactor. What would your technical priorities be to remedy the issues in the case study?

CDR, Clinical data repository; CDS, clinical decision support; EHR, electronic health record; IDN, integrated delivery network; IE, interface engine; SMART, Substitutable Medical Applications, Reusable Technologies.

Reference no: EM133353517

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