DSTU2 FHIR Release 3 (STU)

This page is part of the FHIR Specification (v1.0.2: DSTU (v3.0.2: STU 2). 3). The current version which supercedes this version is 5.0.0 . For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R4 R3 R2 R3 R2

QICore FHIR Infrastructure Work Group Maturity Level : N/A Ballot Status : Informative

This table lists profiles and extensions for the Basic resource. For background information, see Profiling Resources and Extensibility . Additional profiles and resources may be found in published Implementation Guide Guides , or in the Conformance resource registry .

No Profiles defined for this resource
QICore-AdverseEvent cqif-guidanceencounterClass An adverse event is an untoward occurrence during treatment that should be reported, encounterClass for example, to a clinical study sponsor or safety oversight organization. AEs include reportable serious medical errors such as those defined by National Quality Forum (see http://www.qualityforum.org/Topics/ SREs/List_of_SREs.aspx), and Patient Safety Healthcare Events as defined by AHRQ. Some AEs can involve conditions such as "recurring headaches" but others do not, such as accidental falls, surgical errors, sexual abuse of patient, and sudden death. An adverse event can also be an unsafe condition CQIF Guidance Extensions
cqif-guidanceencounterType encounterType for CQIF Guidance Extensions
cqif-guidanceinitiatingOrganization initiatingOrganization for CQIF Guidance Extensions
cqif-guidanceinitiatingPerson initiatingPerson for CQIF Guidance Extensions
cqif-guidancereceivingOrganization receivingOrganization for CQIF Guidance Extensions
cqif-guidancereceivingPerson receivingPerson for CQIF Guidance Extensions
cqif-guidancerecipientLanguage recipientLanguage for CQIF Guidance Extensions
cqif-guidancerecipientType recipientType for CQIF Guidance Extensions
cqif-guidancesystemUserLanguage systemUserLanguage for CQIF Guidance Extensions
cqif-guidancesystemUserTaskContext systemUserTaskContext for CQIF Guidance Extensions
cqif-guidancesystemUserType systemUserType for CQIF Guidance Extensions

Extensions that increases the probability of a patient safety event, and near-misses. An adverse event can be caused by exposure to some agent (e.g., a medication, immunization, food, or environmental agent). An adverse reaction can range from a mild reaction, such as a harmless rash reference this resource:

No Extensions refer to a severe and life-threatening condition. They can occur immediately or develop over time. For example, a patient may develop a rash after taking a particular medication. this resource
No Search Extensions defined for this resource