Results 41 to 50 of about 6,070 (182)
BackgroundClinical trial registries increase transparency in medical research by making information and results of planned, ongoing, and completed studies publicly available.
Gulden, Christian +7 more
doaj +1 more source
ABSTRACT Aim Artificial intelligence (AI) has the potential to reshape the healthcare industry, particularly in disease detection, diagnosis and management, as well as in supporting clinical decision‐making to enhance patient care. However, realising the full potential of AI in healthcare depends on several interrelated factors, including data quality,
Shilpa Thakkar +3 more
wiley +1 more source
Background The Federal Ministry of Education and Research of Germany (BMBF) funds a network of university medicines (NUM) to support COVID-19 and pandemic research at national level.
Martin Bialke +15 more
doaj +1 more source
The exponential growth in the global population and significant advancements in healthcare broadened the scope of intervention for e-Healthcare through decentralized data access and information exchange, making complex clinical decisions.
R. Sreejith, S. Senthil
doaj +1 more source
Big Data in Cancer Genomics: Computational Foundations and Emerging Pathways for Precision Oncology
ABSTRACT This review aims to explore the computational foundations of big data in cancer genomics and examine emerging pathways that support precision oncology and personalized cancer care. A narrative review approach was adopted to synthesize evidence from PubMed, Scopus, Web of Science, and IEEE Xplore.
Nur Vanu +8 more
wiley +1 more source
Comparison and Analysis of ISO/IEEE 11073, IHE PCD-01, and HL7 FHIR Messages for Personal Health Devices [PDF]
ObjectivesIncreasing use of medical devices outside of healthcare facilities inevitably requires connectivity and interoperability between medical devices and healthcare information systems.
Sungkee Lee, Hyoungho Do
doaj +1 more source
ABSTRACT National Statistical Offices (NSOs) face an escalating “privacy‐utility” impasse, where the demand for high‐granularity data must compete with the near zero risk tolerance of legal frameworks like the General Data Protection Regulation (GDPR).
Hooreya Khunji +3 more
wiley +1 more source
Practical considerations for pathologists when selecting digital pathology systems: an ESDIP guide
Abstract The implementation of digital pathology (DP) has been reported across academic, public, and private laboratory settings, providing valuable insights into workflow transformation. However, comparatively little guidance exists on how DP systems should be evaluated prior to acquisition and deployment.
Diana Montezuma +9 more
wiley +1 more source
ABSTRACT Background Electronic patient‐reported outcome (ePRO) systems support symptom monitoring after chemotherapy; however, their integration into structured nurse‐led oncology workflows remains limited. In this study, we aimed to develop and evaluate the short‐term feasibility and usability of a nurse‐led ePRO system for home‐based postchemotherapy
Chiao‐Chi Kuan +6 more
wiley +1 more source
ABSTRACT Introduction Physical function (PF) is critical to quality of life and healthcare value, especially for older adults following hospitalization. Monitoring PF supports recovery, reduces adverse events, and improves care transitions. Despite the potential of electronic health records (EHRs) enabling systematic PF tracking, such data are rarely ...
Robin L. Marcus +6 more
wiley +1 more source

