Clinical Research Informatics: Health Informatics
Editat de Rachel Richesson, James E. Andrewsen Limba Engleză Paperback – 27 aug 2013
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Specificații
ISBN-13: 9781447126607
ISBN-10: 1447126602
Pagini: 432
Dimensiuni: 155 x 235 x 23 mm
Greutate: 0.61 kg
Ediția:2012
Editura: SPRINGER LONDON
Colecția Springer
Seria Health Informatics
Locul publicării:London, United Kingdom
ISBN-10: 1447126602
Pagini: 432
Dimensiuni: 155 x 235 x 23 mm
Greutate: 0.61 kg
Ediția:2012
Editura: SPRINGER LONDON
Colecția Springer
Seria Health Informatics
Locul publicării:London, United Kingdom
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Public țintă
ResearchDescriere
This
book
provides
foundational
coverage
of
key
areas,
concepts,
constructs,
and
approaches
of
medical
informatics
as
it
applies
to
clinical
research
activities,
in
both
current
settings
and
in
light
of
emerging
policies.
The
field
of
clinical
research
is
fully
characterized
(in
terms
of
study
design
and
overarching
business
processes),
and
there
is
emphasis
on
information
management
aspects
and
informatics
implications
(including
needed
activities)
within
various
clinical
research
environments.
The purpose of the book is to provide an overview of clinical research (types), activities, and areas where informatics and IT could fit into various activities and business practices. This book introduces and applies informatics concepts only as they have particular relevance to clinical research settings.
The purpose of the book is to provide an overview of clinical research (types), activities, and areas where informatics and IT could fit into various activities and business practices. This book introduces and applies informatics concepts only as they have particular relevance to clinical research settings.
Cuprins
Section
I:
Contexts
of
Clinical
Research
Informatics.-
Introduction
to
Clinical
Research
Informatics.-
From
Notations
to
Data:
The
Digital
Transformation
of
Clinical
Research.-
Clinical
Research
Environment.
-
Statistical
and
Study
Design
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.-
Patient
Registries.-Section
III:
Knowledge
Representation
and
Discovery.-
Knowledge
Representation
and
Ontologies.-
Non-hypothesis
Driven
Research:
Data
Mining
and
Knowledge
Discovery.-
Natural
Language
Processing,
Electronic
Health
Records,
and
Clinical
Research.-Section
IV:
The
Future
of
Clinical
Research,
Health,
and
Clinical
Research
Informatics.-
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.-
Index.
Notă biografică
Rachel
Richesson,
MS,
PhD,
MPH,
FACMI,
a
noted
informaticist,
joined
the
Duke
University
School
of
Nuring
in
December
2011.
Dr.
Richesson
earned
her
BS
(Biology)
at
the
University
of
Massachusetts
in
1991,
and
holds
graduate
degrees
in
Community
Health
(MPH,
1995)
and
Health
Informatics
(MS,
2000
and
PhD,
2003)
from
the
University
of
Texas
Health
Sciences
Center
in
Houston.
Dr.
Richesson
spent
7
years
as
at
the
University
of
South
Florida
College
of
Medicine
directing
strategy
for
the
identification
and
implementation
of
data
standards
for
a
variety
of
multi-national
multi-site
clinical
research
and
epidemiological
studies
housed
within
the
USF
Department
of
Pediatrics,
including
the
NIH
Rare
Diseases
Clinical
Research
Network
(RDCRN)
and
The
Environmental
Determinants
of
Diabetes
in
the
Young
(TEDDY)
study.
Dr Andrews is the Director of the University of South Florida, School of Information, and an Associate Professor of Information Science. His research falls broadly within the interdisciplinary field of health informatics. He has specific interests in clinical research informatics, as well as health-related information behaviours, particularly in the context of cancer genetics. He works collaboratively with researchers from USF Health, within SI, and also across the US and internationally.
Dr Andrews is the Director of the University of South Florida, School of Information, and an Associate Professor of Information Science. His research falls broadly within the interdisciplinary field of health informatics. He has specific interests in clinical research informatics, as well as health-related information behaviours, particularly in the context of cancer genetics. He works collaboratively with researchers from USF Health, within SI, and also across the US and internationally.
Textul de pe ultima copertă
Clinical
research
informatics
(CRI)
is
the
application
of
informatics
principles
and
techniques
to
support
the
spectrum
of
activities
and
business
processes
that
instantiate clinical
research.
Informatics,
defined
generally
as
the
intersection
of
information
and
computer
science
with
a
health-related
discipline,
has
a
foundation
drawn
from
many
well-established,
theory-based
disciplines,
including
computer
science,
library
and
information
science,
cognitive
science,
psychology,
and
sociology.
The
newly
articulated
yet
fundamental
theorem
of
informatics
states
that
information
technology
should
be
used
to
enable
humans
to
function
and
perform
better
together
than
humans
alone,
and
so
informatics
is
a
source
for
supportive
technologies
and
tools
that
enhance
–
but
not
replace
–
unreservedly
human
processes.
Clinical Research Informaticscontributes to the ongoing dialogues among researchers and practitioners in CRI as they continue to rise to the challenges of a dynamic and evolving clinical research environment. The development of CRI as a sub-discipline of informatics, and as an independent/maturing professional practice area in its own right, drives a growing pool of scientific literature based on original CRI research, and high-impact tools and systems will be developed. CRI leaders and stakeholder groups will continue to support and create communities of discourse that will address much needed practice standards in CRI, improved safety and efficiencies in clinical research, data standards in clinical research, policy issues, educational standards and instructional resources.
The Editors and contributors to this book are among the most active and engaged in the CRI domain and provide an excellent primer for deeper explorations into this emerging discipline. Certain themes are highlighted, including the changing role of the consumer, movement toward transparency, growing needs for global coordination and cooperation on many levels, and the merging together of clinical care delivery and research as part of a changing paradigm in global healthcare delivery – all in the context of rapid innovations in technology and explosions of data sources, types, and volume. This book is therefore of considerable interest to all students of biomedical informatics, from the newcomer to the professional informatician.
Clinical Research Informaticscontributes to the ongoing dialogues among researchers and practitioners in CRI as they continue to rise to the challenges of a dynamic and evolving clinical research environment. The development of CRI as a sub-discipline of informatics, and as an independent/maturing professional practice area in its own right, drives a growing pool of scientific literature based on original CRI research, and high-impact tools and systems will be developed. CRI leaders and stakeholder groups will continue to support and create communities of discourse that will address much needed practice standards in CRI, improved safety and efficiencies in clinical research, data standards in clinical research, policy issues, educational standards and instructional resources.
The Editors and contributors to this book are among the most active and engaged in the CRI domain and provide an excellent primer for deeper explorations into this emerging discipline. Certain themes are highlighted, including the changing role of the consumer, movement toward transparency, growing needs for global coordination and cooperation on many levels, and the merging together of clinical care delivery and research as part of a changing paradigm in global healthcare delivery – all in the context of rapid innovations in technology and explosions of data sources, types, and volume. This book is therefore of considerable interest to all students of biomedical informatics, from the newcomer to the professional informatician.
Caracteristici
Detailed
focus on
clinical
research
informatics
without
being
diverted
into
areas
covering
actual
clinical
practice
Extensive coverage of the intersection between clinical research, data standards, and information science
Extensive coverage of the intersection between clinical research, data standards, and information science