Results 71 to 80 of about 1,234 (195)

OpenEHR modelling applied to Complementary Diagnostics Requests

open access: yesProcedia Computer Science, 2022
Complementary Diagnostic Requests (CDRs) are required for disease identification, monitoring, and prognosis. Diagnostic tests misuse, on the other hand, can lead to negative health outcomes as well as additional costs. Inappropriate diagnostic test requests are primarily the result of a lack of interoperability between Healthcare Information Systems ...
Daniela Oliveira 0003   +6 more
openaire   +2 more sources

Embedding Pharmacogenetics Into Clinical Practice to Improve Patient Outcomes

open access: yesAnnals of Human Genetics, Volume 89, Issue 5, Page 398-405, September 2025.
ABSTRACT Pharmacogenomics, the use of germline genomic data to guide prescription to improve effective and safer medication, holds promise as a clinical intervention. To date in most health systems, there has been limited uptake of pharmacogenomic testing confined to a few single drug–gene associations.
John Henry McDermott   +3 more
wiley   +1 more source

openEHR-spesifikaatioiden käyttö sähköisissä potilaskertomuksissa [PDF]

open access: yes, 2016
Tämä kirjoitus on tarkoitettu Helsingin Yliopiston Tietojenkäsittelytieteen laitokselle tehtäväksi Pro gradu- tutkielmaksi. Tavoitteena on selvittää, mitä käsitteitä sähköisestä potilastiedosta on käytetty sekä miten käsitteet eroavat toisistaan. Lisäksi
Pääkkö, Teemu
core  

Can openEHR archetypes empower multi-centre clinical research? [PDF]

open access: yes, 2005
The Electronic Health Record is of utmost importance to enable the provision of high-quality collaborative care; one prominent development is openEHR. On the other hand, a systematic approach to support the use of routine data for multi-centre clinical ...
T Schuler (9858443)   +3 more
core   +2 more sources

Application of openEHR archetypes to automate data quality rules for electronic health records: a case study

open access: yesBMC Medical Informatics and Decision Making, 2021
Background Ensuring data is of appropriate quality is essential for the secondary use of electronic health records (EHRs) in research and clinical decision support.
Qi Tian   +5 more
doaj   +1 more source

Pharmacogenomics in the UK National Health Service: Progress towards implementation

open access: yesBritish Journal of Clinical Pharmacology, Volume 91, Issue 8, Page 2241-2250, August 2025.
Over the past decade there has been considerable and growing enthusiasm about the promise of using genomics to inform healthcare. In particular, using genetic data to inform prescribing practice has emerged as a compelling policy priority for health systems around the world, not least in the NHS.
John H. McDermott   +3 more
wiley   +1 more source

Reflective openEHR-to-FHIR: Java class-based generator for transforming openEHR compositions to fast healthcase interoperability resources (FHIR) bundles

open access: yesHealth Informatics Journal
Background At our hospital’s university, the data integration center (DIC) has the primary task of importing data from various systems, including unstructured medical reports and structured laboratory data into the openEHR data repository.
Nektarios Ladas   +5 more
doaj   +1 more source

OpenEHR and General Data Protection Regulation: Evaluation of Principles and Requirements (Preprint) [PDF]

open access: yes, 2018
BACKGROUND Concerns about privacy and personal data protection resulted in reforms of the existing legislation in the European Union (EU).
Luís Filipe Antunes   +6 more
core   +1 more source

Developing a conformance methodology for clinically-defined medical record headings:a preliminary report. [PDF]

open access: yes, 2015
Background: The Professional Records Standards Body for health and social care (PRSB) was formed in 2013 to develop and assure professional standards for the content and structure of patient records across all care disciplines in the UK.
Wallhouse, Roger   +15 more
core   +1 more source

Design and Implementation of Clinical Databases with openEHR [PDF]

open access: yes, 2015
  Databases for Clinical Information Systems are difficult to design and implement, especially when the design should be compliant with a formal specification or standard.
Sérgio Miranda Freire (831519)   +3 more
core   +1 more source

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