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Clinical Research Informatics (3rd Ed., 3rd ed. 2023) Health Informatics Series

Langue : Anglais
Couverture de l’ouvrage Clinical Research Informatics

This extensively revised new edition comprehensively reviews the rise of clinical research informatics (CRI). It enables the reader to develop a thorough understanding of how CRI has developed and the evolving challenges facing the biomedical informatics professional in the modern clinical research environment. Emphasis is placed on the changing role of the consumer and the need to merge clinical care delivery and research as part of a changing paradigm in global healthcare delivery. 

Clinical Research Informatics presents a detailed review of using informatics in the continually evolving clinical research environment. It represents a valuable textbook reference for all students and practising healthcare informatics professional looking to learn and expand their understanding of this fast-moving and increasingly important discipline. 

Introduction.- Section I: Contexts of Clinical Research Informatics.- From Notations to Data: The Digital Transformation of Clinical Research.- The Clinical Research Environment.- Methodological Foundations of Clinical Research.- Informatics Approaches to Participant Recruitment.- The Evolving Role of Consumers.- Clinical Research in the Post-genomic Era.- Section II: Data Management and Systems in Clinical Research.- Clinical Research Information Systems.- Study Protocol Representation.- Data Quality in Clinical Research.- Patient-Reported Outcome Data.- Biobanking Challenges and Informatics Opportunities.- Laboratory Data.- Patient Registries.- Knowledge Representation and Discovery.- Section III: Knowledge Representation and Ontologies.- Non hypothesis-driven Research: Data Mining and Knowledge Discovery.- Natural Language Processing, Electronic Health Records, and Clinical Research.- The Future of Clinical Research, Health, and Clinical Research Informatics.- Data Governance.- Data Sharing: Electronic Health Records and Research Interoperability.- Standards Development and the Future of Research Data Sources, Interoperability, and Exchange.- Pharmacovigilance.- Clinical Trials Registries and Results Databases.- Future Directions in Clinical Research Informatics.

Dr. Richesson is a Professor of Informatics at the University of Michigan School of Medicine, Department of Learning Health Sciences. She works with a number of different clinical research networks and pragmatic clinical trials, and supports the development and use of data standards.

Dr. Andrews is an Associate Professor of Informatics in the School of Information at the University of South Florida. His scholarship focuses on a issues related to health information behaviors, particularly in the context of genetics, and terminologies in healthcare and research.

Ms. Fultz Hollis is an informatician at Oregon Health & Science University in Portland, Oregon USA. She is particularly interested in all aspects of sharing research data accurately and with care for the quality and respect for data use and ownership. She has been extremely active for the past 8 years in editing and evaluating biomedical informatics research for the International Medical Informatics Association (IMIA Yearbook) and for the AMIA Summit and AMIA Annual conferences.

Provides a rationale for merging clinical care delivery and research in global healthcare delivery

Reviews the intersection between clinical research, data standards, and information science

Contains numerous practical tools to reinforce key concepts

Date de parution :

Ouvrage de 528 p.

17.8x25.4 cm

Disponible chez l'éditeur (délai d'approvisionnement : 15 jours).

105,49 €

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