This page is part of the US Medication REMS (v2.0.0-ballot: STU2 Ballot) based on FHIR (HL7® FHIR® Standard) R4. This version is a pre-release. The current official version is 1.0.0. For a full list of available versions, see the Directory of published versions
This guide reflects initial efforts to establish guidance for using FHIR to automate data exchange and facilitate system interactions between providers and REMS Administrators. The REMS community intends to continue work toward system integration to improve the process for patients, providers and others involved in the treatment of patients with a REMS drugs.
Support for additional scenarios and stakeholders such as those described below may be covered in future versions of this guide.
A provider prescribes a medication that has a REMS for a patient and fills out the required patient enrollment forms. The patient receives a notification to attest that they have received any required education/documentation required by the REMS as well as the accuracy of the information contained on the forms.
The patient logs into their provider's patient portal and launches an application to fill out the required information and submits the results back to the REMS Administration system. This information may include required lab testing information such as pregnancy tests.
A provider prescribes a medication that has a REMS for a patient. The provider asks the patient what their preferred pharmacy is. Before sending the prescription to the pharmacy, the EMR queries the REMS Administration systems to determine if the pharmacy is enrolled in the REMS if required and can dispense the medication. The REMS Administration system sends back a notification stating if the pharmacy can dispense the medication. An alert is displayed in the user interface of the EMR if the pharmacy is incapable of dispensing the medication. Electronic prescription (ePrescribing) intermediaries may hold this list of enrolled pharmacies as well, thus allowing them to forward the medication to the correct pharmacy.
REMS drugs may be administered through the use of outpatient healthcare sites. The workflow involving these may be different to those explored in the IG. Future releases of this guide may explore the workflows involving outpatient healthcare sites providing a more complete approach to all REMS interactions.
Once the patient has started on the REMS drug, REMS activities may include monitoring programs and additional authorization steps, and many participants may be involved during this period. New scenarios related to ongoing care may be identified and addressed in future versions of this guide, potentially providing additional visibility of pertinent information or improved communication between stakeholders through use of FHIR.
As the CDS Hooks and SMART App Launch standards continue to evolve and respond to implementers' experience, new features such as additional CDS "hook" events or additional SMART App Launch options might become available. Future releases of this guide may utilize new features in those standards to support REMS workflows.
Further data and process integration between REMS stakeholders may be pursued in future versions of this guide, potentially including:
In addition to supporting additional workflow scenarios, work is needed to address technical challenges that cause setup and maintenance work for stakeholders and may hinder broad implementation of the FHIR approaches described here. One possibility is to use AI to analyze connections that fail and self-heal by automatically reconfiguring the interconnected system.
Easing Health System Configuration. Future versions of this guide may include approaches for reducing the burden on health systems to configure their Provider Systems to support REMS workflows. Future approaches may support:
Future versions of this guide may include further interactions between the Provider EHR system and Pharmacy systems beyond sending the Prescription. These could include: