This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. If the element is present, it must have either a @value, an @id, or extensions An absolute URI that is used to identify this plan definition when it is referenced in a specification, model, design or an instance; also called its canonical identifier. This SHOULD be globally unique and SHOULD be a literal address at which an authoritative instance of this plan definition is (or will be) published. This URL can be the target of a canonical reference. It SHALL remain the same when the plan definition is stored on different servers. A formal identifier that is used to identify this plan definition when it is represented in other formats, or referenced in a specification, model, design or an instance. The identifier that is used to identify this version of the plan definition when it is referenced in a specification, model, design or instance. This is an arbitrary value managed by the plan definition author and is not expected to be globally unique. For example, it might be a timestamp (e.g. yyyymmdd) if a managed version is not available. There is also no expectation that versions can be placed in a lexicographical sequence. To provide a version consistent with the Decision Support Service specification, use the format Major.Minor.Revision (e.g. 1.0.0). For more information on versioning knowledge assets, refer to the Decision Support Service specification. Note that a version is required for non-experimental active artifacts. Indicates the mechanism used to compare versions to determine which is more current. A natural language name identifying the plan definition. This name should be usable as an identifier for the module by machine processing applications such as code generation. A short, descriptive, user-friendly title for the plan definition. An explanatory or alternate title for the plan definition giving additional information about its content. A high-level category for the plan definition that distinguishes the kinds of systems that would be interested in the plan definition. The status of this plan definition. Enables tracking the life-cycle of the content. A Boolean value to indicate that this plan definition is authored for testing purposes (or education/evaluation/marketing) and no version of this resource will ever be intended for genuine usage. A code, group definition, or canonical reference that describes or identifies the intended subject of the plan definition. Canonical references are allowed to support the definition of protocols for drug and substance quality specifications, and is allowed to reference a MedicinalProductDefinition, SubstanceDefinition, AdministrableProductDefinition, ManufacturedItemDefinition, or PackagedProductDefinition resource. The date (and optionally time) when the plan definition was last significantly changed. The date must change when the business version changes and it must change if the status code changes. In addition, it should change when the substantive content of the plan definition changes. The name of the organization or individual responsible for the release and ongoing maintenance of the plan definition. Contact details to assist a user in finding and communicating with the publisher. A free text natural language description of the plan definition from a consumer's perspective. The content was developed with a focus and intent of supporting the contexts that are listed. These contexts may be general categories (gender, age, ...) or may be references to specific programs (insurance plans, studies, ...) and may be used to assist with indexing and searching for appropriate plan definition instances. A legal or geographic region in which the authority that maintains the resource is operating. In general, the jurisdiction is also found in the useContext. The useContext may reference additional jurisdictions because the defining jurisdiction does not necessarily limit the jurisdictions of use. Explanation of why this plan definition is needed and why it has been designed as it has. A detailed description of how the plan definition is used from a clinical perspective. A copyright statement relating to the plan definition and/or its contents. Copyright statements are notices of intellectual property ownership and can include restrictions on the use and publishing of the plan definition. A short string (<50 characters), suitable for inclusion in a page footer that identifies the copyright holder, effective period, and optionally whether rights are restricted. (e.g. 'All rights reserved', 'Some rights reserved'). The date on which the resource content was approved by the publisher. Approval happens once when the content is officially approved for usage. The date on which the resource content was last reviewed. Review happens periodically after approval but does not change the original approval date. The period during which the plan definition content was or is planned to be in active use. Descriptive topics related to the content of the plan definition. Topics provide a high-level categorization of the definition that can be useful for filtering and searching. An individiual or organization primarily involved in the creation and maintenance of the content. An individual or organization primarily responsible for internal coherence of the content. An individual or organization asserted by the publisher to be primarily responsible for review of some aspect of the content. An individual or organization asserted by the publisher to be responsible for officially endorsing the content for use in some setting. Related artifacts such as additional documentation, justification, or bibliographic references. A reference to a Library resource containing any formal logic used by the plan definition. A goal describes an expected outcome that activities within the plan are intended to achieve. For example, weight loss, restoring an activity of daily living, obtaining herd immunity via immunization, meeting a process improvement objective, meeting the acceptance criteria for a test as specified by a quality specification, etc. Actors represent the individuals or groups involved in the execution of the defined set of activities. An action or group of actions to be taken as part of the plan. For example, in clinical care, an action would be to prescribe a particular indicated medication, or perform a particular test as appropriate. In pharmaceutical quality, an action would be the test that needs to be performed on a drug product as defined in the quality specification or the steps that are planned in a manufacturing process of a drug product or a drug substance. If a CodeableConcept is present, it indicates the pre-condition for performing the service. For example "pain", "on flare-up", etc. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. Indicates a category the goal falls within. Human-readable and/or coded description of a specific desired objective of care, such as "control blood pressure" or "negotiate an obstacle course" or "dance with child at wedding". Identifies the expected level of importance associated with reaching/sustaining the defined goal. The event after which the goal should begin being pursued. Identifies problems, conditions, issues, or concerns the goal is intended to address. Didactic or other informational resources associated with the goal that provide further supporting information about the goal. Information resources can include inline text commentary and links to web resources. Indicates what should be done and within what timeframe. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. The parameter whose value is to be tracked, e.g. body weight, blood pressure, or hemoglobin A1c level. The target value of the measure to be achieved to signify fulfillment of the goal, e.g. 150 pounds or 7.0%, or in the case of pharmaceutical quality - NMT 0.6%, Clear solution, etc. Either the high or low or both values of the range can be specified. When a low value is missing, it indicates that the goal is achieved at any value at or below the high value. Similarly, if the high value is missing, it indicates that the goal is achieved at any value at or above the low value. Indicates the timeframe after the start of the goal in which the goal should be met. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. A descriptive label for the actor. A description of how the actor fits into the overall actions of the plan definition. The characteristics of the candidates that could serve as the actor. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. The type of participant in the action. The type of participant in the action. The type of participant in the action. The role the participant should play in performing the described action. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. An identifier that is unique within the PlanDefinition to allow linkage within the realized CarePlan and/or RequestOrchestration. A user-visible prefix for the action. For example a section or item numbering such as 1. or A. The textual description of the action displayed to a user. For example, when the action is a test to be performed, the title would be the title of the test such as Assay by HPLC. A brief description of the action used to provide a summary to display to the user. A text equivalent of the action to be performed. This provides a human-interpretable description of the action when the definition is consumed by a system that might not be capable of interpreting it dynamically. Indicates how quickly the action should be addressed with respect to other actions. A code that provides a meaning, grouping, or classification for the action or action group. For example, a section may have a LOINC code for the section of a documentation template. In pharmaceutical quality, an action (Test) such as pH could be classified as a physical property. A description of why this action is necessary or appropriate. Didactic or other informational resources associated with the action that can be provided to the CDS recipient. Information resources can include inline text commentary and links to web resources. Identifies goals that this action supports. The reference must be to a goal element defined within this plan definition. In pharmaceutical quality, a goal represents acceptance criteria (Goal) for a given action (Test), so the goalId would be the unique id of a defined goal element establishing the acceptance criteria for the action. A code, group definition, or canonical reference that describes the intended subject of the action and its children, if any. Canonical references are allowed to support the definition of protocols for drug and substance quality specifications, and is allowed to reference a MedicinalProductDefinition, SubstanceDefinition, AdministrableProductDefinition, ManufacturedItemDefinition, or PackagedProductDefinition resource. A description of when the action should be triggered. When multiple triggers are specified on an action, any triggering event invokes the action. An expression that describes applicability criteria or start/stop conditions for the action. Defines input data requirements for the action. Defines the outputs of the action, if any. A relationship to another action such as "before" or "30-60 minutes after start of". An optional value describing when the action should be performed. Identifies the facility where the action will occur; e.g. home, hospital, specific clinic, etc. Indicates who should participate in performing the action described. The type of action to perform (create, update, remove). All - meaning the applicability of each child action is evaluated independently; if a child action is applicable according to the applicability criteria, it is applied. Any - meaning that each child action is evaluated in order, and the first action that returns an applicability of true will be applied, and processing of the parent action will stop. If not specified, the default behavior of All is used. Defines the grouping behavior for the action and its children. Defines the selection behavior for the action and its children. Defines the required behavior for the action. Defines whether the action should usually be preselected. Defines whether the action can be selected multiple times. A reference to an ActivityDefinition that describes the action to be taken in detail, a Measure defining a measure to be evaluated, a MessageDefinition describing a message to be sent, a PlanDefinition that describes a series of actions to be taken, a Questionnaire that should be filled out, a SpecimenDefinition describing a specimen to be collected, an ObservationDefinition that specifies what observation should be captured, or an OperationDefinition that specifies what operation should be invoked. When the value is a uri, it is intended to be a reference to non-FHIR content that characterizes the action to be performed. This option is allowed to enable the PlanDefinition to be used to provide semi-structured representation, when the guidance is not computable, but there is still value in elaborating the overall structure with a PlanDefinition. The intended behavior when a definitionUri is realized as part of an apply is that it is copied to the resulting RequestOrchestration so that it is available to the consuming system. How that system interprets that uri is not specified. A reference to a StructureMap resource that defines a transform that can be executed to produce the intent resource using the ActivityDefinition instance as the input. Customizations that should be applied to the statically defined resource. For example, if the dosage of a medication must be computed based on the patient's weight, a customization would be used to specify an expression that calculated the weight, and the path on the resource that would contain the result. Sub actions that are contained within the action. The behavior of this action determines the functionality of the sub-actions. For example, a selection behavior of at-most-one indicates that of the sub-actions, at most one may be chosen as part of realizing the action definition. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. The kind of condition. An expression that returns true or false, indicating whether the condition is satisfied. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. A human-readable label for the data requirement used to label data flows in BPMN or similar diagrams. Also provides a human readable label when rendering the data requirement that conveys its purpose to human readers. Defines the data that is to be provided as input to the action. Points to an existing input or output element that provides data to this input. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. A human-readable label for the data requirement used to label data flows in BPMN or similar diagrams. Also provides a human readable label when rendering the data requirement that conveys its purpose to human readers. Defines the data that results as output from the action. Points to an existing input or output element that is results as output from the action. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. The element id of the target related action. The relationship of the start of this action to the related action. The relationship of the end of this action to the related action. A duration or range of durations to apply to the relationship. For example, 30-60 minutes before. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. A reference to the id element of the actor who will participate in this action. The type of participant in the action. The type of participant in the action. The type of participant in the action. The role the participant should play in performing the described action. Indicates how the actor will be involved in the action - author, reviewer, witness, etc. This resource allows for the definition of various types of plans as a sharable, consumable, and executable artifact. The resource is general enough to support the description of a broad range of clinical and non-clinical artifacts such as clinical decision support rules, order sets, protocols, and drug quality specifications. The path to the element to be customized. This is the path on the resource that will hold the result of the calculation defined by the expression. The specified path SHALL be a FHIRPath resolvable on the specified target type of the ActivityDefinition, and SHALL consist only of identifiers, constant indexers, and a restricted subset of functions. The path is allowed to contain qualifiers (.) to traverse sub-elements, as well as indexers ([x]) to traverse multiple-cardinality sub-elements (see the [Simple FHIRPath Profile](fhirpath.html#simple) for full details). An expression specifying the value of the customized element. Must Could Must Unless Documented If the element is present, it must have either a @value, an @id, or extensions Before Before Start Before End Concurrent Concurrent With Start Concurrent With End After After Start After End If the element is present, it must have either a @value, an @id, or extensions Visual Group Logical Group Sentence Group If the element is present, it must have either a @value, an @id, or extensions Any All All Or None Exactly One At Most One One Or More If the element is present, it must have either a @value, an @id, or extensions Single Multiple If the element is present, it must have either a @value, an @id, or extensions Yes No If the element is present, it must have either a @value, an @id, or extensions Applicability Start Stop If the element is present, it must have either a @value, an @id, or extensions All Any If the element is present, it must have either a @value, an @id, or extensions