Connecting ResearchKit to the Health System Using i2b2 and FHIR, Read only SMART-FHIR façade for i2b2, Evaluation of SMART-on-FHIR I2b2 cell using PCORNET data model, SMART on FHIR Genomics: Facilitating standardized clinico-
نویسنده
چکیده
In addition to that, other available papers tackling the topic of applying FHIR to i2b2 CDW should be reviewed in the introduction/methodology in order to better assess this paper novelty (just to name a few: C3-PRO: Connecting ResearchKit to the Health System Using i2b2 and FHIR, Read only SMART-FHIR façade for i2b2, Evaluation of SMART-on-FHIR I2b2 cell using PCORNET data model, SMART on FHIR Genomics: Facilitating standardized clinicogenomic apps, etc.).
منابع مشابه
SMART-on-FHIR implemented over i2b2
We have developed an interface to serve patient data from Informatics for Integrating Biology and the Bedside (i2b2) repositories in the Fast Healthcare Interoperability Resources (FHIR) format, referred to as a SMART-on-FHIR cell. The cell serves FHIR resources on a per-patient basis, and supports the "substitutable" modular third-party applications (SMART) OAuth2 specification for authorizati...
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A renewed interest by consumer information technology giants in the healthcare domain is focused on transforming smartphones into personal health data storage devices. With the introduction of the open source ResearchKit, Apple provides a framework for researchers to inform and consent research subjects, and to readily collect personal health data and patient reported outcomes (PRO) from distri...
متن کاملA Fast Healthcare Interoperability Resources (FHIR) layer implemented over i2b2
BACKGROUND Standards and technical specifications have been developed to define how the information contained in Electronic Health Records (EHRs) should be structured, semantically described, and communicated. Current trends rely on differentiating the representation of data instances from the definition of clinical information models. The dual model approach, which combines a reference model (...
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BACKGROUND Supporting clinical decision support for personalized medicine will require linking genome and phenome variants to a patient's electronic health record (EHR), at times on a vast scale. Clinico-genomic data standards will be needed to unify how genomic variant data are accessed from different sequencing systems. METHODS A specification for the basis of a clinic-genomic standard, bui...
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Research networks for data sharing are growing into a large platform for pragmatic clinical trials to generate quality evidence for shared medical decision-making. Institutions partnering in the networks have made large investments in developing the infrastructure for sharing data. We investigate whether institutions partnering on Patient-Centered Outcomes Research Institute's (PCORI) network c...
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