This page is part of the US Medication REMS (v1.0.0: STU1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
REMS programs vary widely with respect to the steps and requirements they impose on the patient and providers, as described below. Because different drugs' programs impact patient care activities in different ways and at different steps, this guide doesn't attempt to describe a fixed set of use case scenarios that cover all variations. Instead, it defines basic patterns for interaction between a Provider System and REMS Administrator System that can be applied at multiple points in treating a patient with a REMS drug.
Before reading this section, it will be helpful to review Participant Roles and Needs for descriptions of the actors and systems referenced below, and REMS Steps and Terminology for an overview of how REMS steps might fit into a given patient's care.
REMS requirements for providers, patients and other participants vary considerably between drugs, based on the nature of the risk each drug presents and other aspects of its use. For example:
In addition, real world treatment situations for individual patients will differ due to other factors. For example:
As a result, the scenario descriptions in this section will include aspects that don't apply to all REMS programs or treatment situations. The guide's FHIR approaches are intended to be applied if they fit a particular drug's program and applicable workflow conditions.
This guide supports scenarios encountered in two different system contexts, where the provider is either:
The interaction options differ between these contexts, and each can be useful.
This guide recommends initiating exchanges with the REMS Administrator System from within the Provider System workflow wherever possible–to enable interactions to be triggered based on relevant treatment actions and to avoid the need for the provider to manually navigate to external applications, maintain separate login credentials, etc.
However, there are situations where starting therapy with a REMS drug may involve steps prior to the provider entering the Provider System's order flow or where it may otherwise not be possible to initiate exchange with the REMS Administrator System based on Provider System activities. In these cases, the interaction may be initiated from an external REMS Administrator App using standalone SMART app launch.
When seeing a patient, the prescriber decides to prescribe a drug, and is alerted by the Provider System that the drug has a REMS program. At an appropriate point in the workflow (e.g., when the prescriber starts creating the medication order, at the start of a related encounter, etc.), the Provider System connects with the REMS Administrator System and enables the prescriber to interact with it.
At the start of this interaction, the Provider System supplies patient, provider and medication information to the REMS Administrator.
Depending on the drug and other variables described in the previous section, the REMS Administrator System responds to the CDS Hooks request with information about the REMS program, a SMART app to gather needed information, alerts about steps the prescriber must take before ordering the drug, etc.
The Provider System then presents the returned information, gives the prescriber the option to open the REMS Administrator's SMART app (if one was returned) or to place the app into their work queue to launch later. When the provider launches the SMART app, it first retrieves information that it needs from the patient record in the Provider System–reducing manual data entry for the provider. The prescriber reviews the pre-filled data, makes adjustments as needed, and then completes any other app steps.
Note that in some situations, the REMS Administrator will have no information or requests to return. For example, the REMS Administrator may determine that there are no unmet REMS requirements to be addressed at the time of the interaction. In this case, the Provider System will receive an empty response and allow the prescriber's workflow to continue without interruption.
Use Case One Scenarios
Below are possible response scenarios (which are detailed further in this section of the IG). Note that at a given point in a patient's care, more than one of these might apply.
In this scenario, the REMS Administrator notifies the provider of the need and may…
If the patient's information indicate that treatment with the proposed drug is not appropriate, the REMS Administrator alerts the provider and optionally provides a URL link to additional related information.
The REMS Administrator alerts the provider to patient requirements that must be met before proceeding with treatment, such as education or enrollment. The Administrator may optionally include…
The REMS Administrator may request information required to meet REMS program requirements, such as a lab result or patient status information.
Along with notifying the provider of the need, the REMS Administrator may optionally:
The REMS Administrator may return information about the patient's participation in the REMS program to be saved to the patient's record in the Provider System.
systemAction
that saves a note containing the information in the form of a FHIR DocumentReference.If the REMS Administrator does not wish to present any information or requests to the prescriber, it may return an empty response. In this scenario, the Provider System will not interrupt the provider's workflow with REMS-related information.
The REMS Administrator may recognize the opportunity to share other information or request other actions beyond those described above.
This implementation guide does not constrain information or requests that a REMS Administrator may return in its CDS Hooks response. Other alerts, resources or information gathering steps may be implemented, as needed.
In this variation, the provider accesses an external REMS Administrator application from outside the Provider System workflow. In a process facilitated by the provider, the external application retrieves patient, provider and drug information from the Provider System using standalone SMART launch.
During that application's workflow: