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@medplum/fhirtypes

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Medplum FHIR Type Definitions

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/* * This is a generated file * Do not edit manually. */ import { Consent } from './Consent'; import { Extension } from './Extension'; import { Identifier } from './Identifier'; import { Meta } from './Meta'; import { Narrative } from './Narrative'; import { Patient } from './Patient'; import { Period } from './Period'; import { Reference } from './Reference'; import { ResearchStudy } from './ResearchStudy'; import { Resource } from './Resource'; /** * A physical entity which is the primary unit of operational and/or * administrative interest in a study. */ export interface ResearchSubject { /** * This is a ResearchSubject resource */ readonly resourceType: 'ResearchSubject'; /** * The logical id of the resource, as used in the URL for the resource. * Once assigned, this value never changes. */ id?: string; /** * The metadata about the resource. This is content that is maintained by * the infrastructure. Changes to the content might not always be * associated with version changes to the resource. */ meta?: Meta; /** * A reference to a set of rules that were followed when the resource was * constructed, and which must be understood when processing the content. * Often, this is a reference to an implementation guide that defines the * special rules along with other profiles etc. */ implicitRules?: string; /** * The base language in which the resource is written. */ language?: string; /** * A human-readable narrative that contains a summary of the resource and * can be used to represent the content of the resource to a human. The * narrative need not encode all the structured data, but is required to * contain sufficient detail to make it &quot;clinically safe&quot; for a human to * just read the narrative. Resource definitions may define what content * should be represented in the narrative to ensure clinical safety. */ text?: Narrative; /** * These resources do not have an independent existence apart from the * resource that contains them - they cannot be identified independently, * and nor can they have their own independent transaction scope. */ contained?: Resource[]; /** * May be used to represent additional information that is not part of * the basic definition of the resource. To make the use of extensions * safe and manageable, there is a strict set of governance applied to * the definition and use of extensions. Though any implementer can * define an extension, there is a set of requirements that SHALL be met * as part of the definition of the extension. */ extension?: Extension[]; /** * May be used to represent additional information that is not part of * the basic definition of the resource and that modifies the * understanding of the element that contains it and/or the understanding * of the containing element's descendants. Usually modifier elements * provide negation or qualification. To make the use of extensions safe * and manageable, there is a strict set of governance applied to the * definition and use of extensions. Though any implementer is allowed to * define an extension, there is a set of requirements that SHALL be met * as part of the definition of the extension. Applications processing a * resource are required to check for modifier extensions. * * Modifier extensions SHALL NOT change the meaning of any elements on * Resource or DomainResource (including cannot change the meaning of * modifierExtension itself). */ modifierExtension?: Extension[]; /** * Identifiers assigned to this research subject for a study. */ identifier?: Identifier[]; /** * The current state of the subject. */ status: 'candidate' | 'eligible' | 'follow-up' | 'ineligible' | 'not-registered' | 'off-study' | 'on-study' | 'on-study-intervention' | 'on-study-observation' | 'pending-on-study' | 'potential-candidate' | 'screening' | 'withdrawn'; /** * The dates the subject began and ended their participation in the * study. */ period?: Period; /** * Reference to the study the subject is participating in. */ study: Reference<ResearchStudy>; /** * The record of the person or animal who is involved in the study. */ individual: Reference<Patient>; /** * The name of the arm in the study the subject is expected to follow as * part of this study. */ assignedArm?: string; /** * The name of the arm in the study the subject actually followed as part * of this study. */ actualArm?: string; /** * A record of the patient's informed agreement to participate in the * study. */ consent?: Reference<Consent>; }