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Clinical
& Medical informatics glossary & taxonomy
Evolving Terminology
for Emerging Technologies Comments? Questions?
Revisions? Mary Chitty MSLS
mchitty@healthtech.com
Last revised
January 09, 2020
Clinical Research News reports on innovative technologies
from clinical trials to medical informatics. Technology continues to
permeate all aspects of clinical trials and the patient experience, and
the tools to support these efforts are maturing rapidly. .. news, views,
and insights on the vast landscape of innovation between clinical trial
management Areas of regular coverage: include
Electronic data capture, Patient
recruitment technologies and practices, Clinical trial informatics
including ePRO (patient reported outcomes), clinical trial management
software, trial master files, and case report forms, Trial design,
Adaptive clinical trials, Contract and clinical research organizations,
Regulatory issues, Site Selection, Site Monitoring, Genomics in the
clinic, IT to support patient care and patient engagement, Telehealth and
telemedicine, Population health and data analytics, Personalized medicine
and care delivery, Clinical data mining, Point of Care clinical trials,
Healthcare informatics, Clinical trial monitoring and compliance
http://www.clinicalinformaticsnews.com/Editorial-Profile/
Related informatics glossaries include Algorithms
& data analysis,
Bioinformatics,
Cheminformatics
Drug
discovery informatics
Information
management & interpretation,
IT
infrastructure
Regulatory
Research
See also
Clinical trials Molecular
Medicine
Molecular Diagnostics Therapeutic areas Cancer
Cardiovascular
CNS & Neurology Immunology Infectious Diseases Inflammation
AI for Healthcare: Transforming
the Industry Landscape 2020 April 21-23 Boston MA Artificial
intelligence in the healthcare industry is predicted to save $150
billion annually for the US. As such, AI is being rapidly deployed in
many areas of the healthcare landscape. The Inaugural AI for
Healthcare track will primarily focus on the providers,
attracting CIOs, CTOs, VPs of IT and Informatics along with senior
physicians and clinicians from the leading US hospitals who will share
their experiences of using AI in clinical care and hospital operations.
http://www.bio-itworldexpo.com/ai-healthcare
Bayesian network:
Wikipedia http://en.wikipedia.org/wiki/Bayesian_network
Bayesian
networks: A quick intro, Karen Sachs, Biomedical
Computation Review, Summer 2005 http://www.biomedicalcomputationreview.org/1/1/9.pdf
A computational analysis approach, machine learning tool.
Bayesian statistics:
Bayesian statistics is an approach for learning from
evidence as it accumulates. In clinical trials, traditional (frequentist)
statistical methods may use information from previous studies only at the design
stage. Then, at the data analysis stage, the information from these studies is
considered as a complement to, but not part of, the formal analysis. In
contrast, the Bayesian approach uses Bayes’ Theorem to formally combine prior
information with current information on a quantity of interest. The Bayesian
idea is to consider the prior information and the trial results as part of a
continual data stream, in which inferences are being updated each time new data
become available.
Throughout
this document we will use the terms “prior distribution”, “prior
probabilities”, or simply “prior” to refer to the mathematical entity (the probability
distribution) that is used in these Bayesian calculations. The term
“prior information” refers to the set of all information that may be used to
construct the prior distribution. FDA, CBER, CDHR Guidance for the use of
Bayesian Statistics in Medical Device Clinical Trials Feb. 2010
http://www.fda.gov/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm071072.htm#1
biomathematics:
The application of mathematics to
problems in biology and medicine. An essential tool in fields such as population
genetics, cellular neurobiology, comparative genetics, biomedical imaging,
pharmacokinetics, and epidemiology. It plays an increasingly vital role in the
effort to understand diseases and disorders, and to improve therapies.
Collection Development Manual, National Library of Medicine, US 2004 http://www.nlm.nih.gov/tsd/acquisitions/cdm/subjects14.html Related
terms: bioinformatics, computational
biology
biomedical
informatics:
"the field
that is concerned with the optimal use of information, often aided by the use of
technology and people, to improve individual health, health care, public health,
and biomedical research"1. William Hersh 2010 , Biomedical
Informatics, Ohio State University http://medicine.osu.edu/bmi/Pages/index.aspx
http://en.wikipedia.org/wiki/Biomedical_informatics
Related terms: medical informatics
case
definition :
Optimal case definition is important in epidemiological research,
but can be problematic when no satisfactory gold standard is available. In
particular, difficulties arise where the pathology underlying a disorder is
unknown or cannot be reliably diagnosed. This problem can be overcome if
diagnoses are viewed not necessarily as labels for disease processes, but more
generally as a useful method for classifying people for the purpose of
preventing or managing illness. With this perspective, the value of a case
definition lies in its practical utility in distinguishing groups of people
whose illnesses share the same causes or determinants of outcome (including
response to treatment). A corollary is that the best-case definition for a
disorder may vary according to the purpose for which it is being applied. Assessing
case definitions in the absence of a diagnostic gold standard, D Coggon, C
Martyn, KT Palmer, B Evanoff, Intl J Epidemiol 34 (4): 949-952
CDISC
Clinical Data Interchange Standards Consortium:
An
open, multidisciplinary, non- profit organization committed to the development
of industry standards to support the electronic acquisition, exchange,
submission and archiving of clinical trials data and metadata for medical and
biopharmaceutical product development.
http://www.cdisc.org/
clinical
data repositories, shared:
Agency for
Healthcare Research & Quality http://healthit.ahrq.gov/portal/server.pt?open=514&objID=5554&mode=2&holderDisplayURL=http://prodportallb.ahrq.gov:7087/publis
clinical
forecasting: It is clear that late-stage clinical failures
account for a large proportion of the expenses. This can be as a result of both
the large out-of-pocket investments in Phase III clinical trials and because
unsuccessful trials tie up capital resources during their conduct, and
potentially also for the time spent during any attempted recovery following
regulatory rejection. So, there is an interest in strategies that could halt, as
early as possible, the development of drugs that eventually fail. Clinical
forecasting in drug development, Asher D. Schachter and Marco F. Ramoni,
Nature Reviews Drug Discovery 6, 107-108 (February 2007) |
doi:10.1038/nrd2246
http://www.nature.com/nrd/journal/v6/n2/full/nrd2246.html
Narrower term: Bayesian
clinical forecasting, Bayesian clinical trials
clinical informatics:
Integration of clinical workflow and business strategies of
any healthcare organization will spell success for the providers of the future.
Efficient exchange of data and information is essential for this merger, and
information technology is the tool with which to accomplish the consolidation.
Clinical Informatics is the practice evolving from this need in healthcare.
HIMSS Clinical informatics http://www.himss.org/ASP/topics_clinicalInformatics.asp
is the application of informatics and information technology to
deliver healthcare services. It is also referred to as applied clinical
informatics and operational informatics. AMIA considers informatics when used
for healthcare delivery to be essentially the same regardless of the health
professional group involved (whether dentist, pharmacist, physician, nurse, or
other health professional). Clinical Informatics is concerned with information
use in health care by clinicians. Clinical informatics includes a wide range of
topics ranging from clinical decision support to visual images (e.g.
radiological, pathological, dermatological, ophthalmological, etc); from
clinical documentation to provider order entry systems; and from system design
to system implementation and adoption issues. AMIA Clinical informatics
http://www.amia.org/applications-informatics/clinical-informatics
The application of informatics
approaches to the clinical- evaluation phase of drug development. These
approaches can include clinical- trial simulations to improve trial design and
patient selection, as well as electronic capturing and storing of clinical data
and protocols. The goal is to reduce expenses and time to market
Clinical Research
News
http://www.clinicalinformaticsnews.com/
Clinical Research & Translational Informatics
Transforming Biological Data to Clinical Development 2019 April 17-18
Boston MA
Advancing clinical trials and translational research requires transforming
biological insights and raw research data into clean, actionable data
using innovative techniques for its integration, visualization and
analysis. The Clinical Research & Translational Informatics track
explores new approaches to the integration, visualization, analysis, and
application of biological and clinical trial data, including machine
learning, artificial intelligence, big data analytics, and additional
technologies with case studies from across pharma and academia.
http://www.bio-itworldexpo.com/clinical-translational-informatics
clinomics: The application of
oncogenomic research. Daniel von Hoff, Univ. of Arizona "All hands on deck
at dawn" Nature Genetics 27 (4): 347-349, April 2001 cohort studies large
scale:
In
the past 20 years, birth cohort studies to assess the risks to developing
children from harmful chemicals in air, water and food have been undertaken in
many countries. These birth cohort studies usually started during pregnancy and
followed children through adolescence or beyond. Even the largest of these birth
cohort studies, however, were not big enough to study rare outcomes such as
childhood cancer or sudden infant death syndrome. To increase the sample size,
investigators working with these older cohort studies are now making an effort
to pool their data. Their efforts are hampered by the fact that the older
studies did not usually agree upon disease outcome definitions, time periods of
measurement, or methods for measuring biomarkers and chemical contaminants in
air, water and food. This makes pooling data extremely difficult. To avoid such problems in the next
generation of large-scale birth cohort studies, it is worthwhile for
investigators from various countries to invest time up front to agree on how to
assess disease outcomes, measure biomarkers, and measure environmental
exposures. Pooling of data, should that be desirable, with then be much more
straightforward. Coordination of new
large scale birth cohort studies, Children’s Environmental Health, WHO 2014 http://www.who.int/ceh/cohorts/en/
communications
standards:
It is clear that shared understanding of the
basic data elements within pharmacogenomics is a critical building block upon
which to build an information infrastructure. Methods for communicating these
data are therefore equally as important. The two main areas that require
progress are the definition of shared syntax (how information is
structured in a data file) and semantics (how the information should be
interpreted by others). Russ Altman "Challenges for Biomedical Informatics
and Pharmacogenomics, Stanford Medical Informatics, 2002 http://www.annualreviews.org/doi/abs/10.1146/annurev.pharmtox.42.082401.140850
Related terms: Information management
& interpretation controlled vocabularies, syntax, semantics
comparative data mining:
Algorithms
Useful for clinical trial meta-analyses
comparative
effectiveness research CER:
is
the conduct and synthesis of systematic research comparing different
interventions and strategies to prevent, diagnose, treat and monitor health
conditions. The purpose of this research is to inform patients, providers, and
decision-makers, responding to their expressed needs, about which interventions
are most effective for which patients under specific circumstances. To provide
this information, comparative effectiveness research must assess a comprehensive
array of health-related outcomes for diverse patient populations… [Internet.] Federal Coordinating Council for Comparative
Effectiveness Research [cited 28 July 2010].
Comparative Effectiveness Research, Health Services Research Information
Central, National Library of Medicine, NIH
http://www.nlm.nih.gov/hsrinfo/cer.html
complex: It has become common to use complicated and complex
interchangeably … The essence of ‘complicated’ is hard to figure out. ..Complex,
on the other hand is a term reserved for systems that display properties
that are not predictable from a complete description of their components,
and that are generally considered to be qualitatively different from the
sum of their parts. [Editorial, "Complicated is not complex" Nature Biotechnology
17: 511 June 1999] Would it be fair to say that Mendelian genetics
is linear, while genomics and polygenic diseases/traits are
nonlinear?
According to the Oxford English Dictionary one of the meanings of complicated
is complex, though it also means not easy to unravel or separate. Both complex
and complicated are contrasted with simple. Whatever the original senses of
these two words, the above distinction seems a useful one now. Related term:
complexity;
Narrower terms: biocomplexity, complex diseases, complex genomes; complex phenotypes, complex
traits
complex diseases:
Diseases characterized by risk to relatives
of an affected individual which is greater than the incidence of the disorder
in the population. [NHLBI]
The research
activities in the Department of Genetics and Complex Diseases and its pre
and postdoctoral training programs concentrate on the molecular, cellular,
and organismic adaptations and responses to nutrients, toxins, and
radiation stress and explore the genetic basis controlling the
heterogeneity of these interactions in experimental systems. The
integrated interdisciplinary opportunities also aim to apply this
knowledge to human populations to understand, prevent, and treat complex
human diseases. Dept of Genetics and Complex Diseases, Harvard School of
Public Health 2011 http://www.hsph.harvard.edu/departments/genetics-and-complex-diseases/
How are complex diseases
related to polygenic diseases? Related terms: SNPs
& genetic variations; Omes
& omics phenome, phenomics
computable phenotypes: A computable
phenotype is a clinical condition, characteristic, or set of clinical
features that can be determined solely from the data in EHRs and ancillary
data sources and does not require chart review or interpretation by a
clinician. These can also be referred to as EHR condition
definitions, EHR-based phenotype definitions, or simply phenotypes. We use
the term EHR broadly to reference data that are generated through
healthcare delivery and reimbursement practices; in practice, these
functions may be covered in multiple systems and can contain both practice
management data and data that are strictly limited to the clinical domain.
We use ancillary data sources to refer to sources such as disease
registries, claims data, or supplemental data collection that are related
to health care delivery but may not be directly integrated into the EHR
system. Electronic Health Records based phenotyping
http://rethinkingclinicaltrials.org/resources/ehr-phenotyping/
computational
pharmacology: Pharmacogenomics
computational
physiology: The International Union of Physiological
Sciences (IUPS) Physiome Project is an internationally collaborative open-
source project to provide a public domain framework for computational
physiology, including the development of modeling standards, computational tools
and web-accessible databases of models of structure and function at all spatial
scales [1,2,3]. It aims to develop an infrastructure for linking models of
biological structure and function across multiple levels of spatial organization
and multiple time scales. The levels of biological organisation, from genes to
the whole organism, includes gene regulatory networks, protein- protein and
protein- ligand interactions, protein pathways, integrative cell function,
tissue and whole heart structure- function relations. The whole heart models
include the spatial distribution of protein expression. Keynote: Peter J.
Hunter, Univ of Auckland, International Society of Computational Biology,
Detroit, MI, 2005 http://www.iscb.org/ismb2005/keynotes.html
computational
therapeutics:
An emerging biomedical field. It is concerned with the
development of techniques for using software to collect, manipulate and link
biological and medical data from diverse sources. It is also
concerned with the use of such information in simulation models to make
predictions or therapeutically relevant discoveries or advances. (Referred to by
some as in silico pharmacology) C. Anthony Hunt Lab, Biosystems at Univ.
of California, San Francisco, http://biosystems.ucsf.edu/
consumer
health informatics: is
the field devoted to informatics from multiple consumer or patient views.
These include patient-focused informatics, health literacy and consumer
education. The focus is on information structures and processes that
empower consumers to manage their own health--for example health
information literacy, consumer-friendly language, personal health records,
and Internet-based strategies and resources. The shift in this view of
informatics analyses consumers' needs for information; studies and
implements methods for making information accessible to consumers; and
models and integrates consumers' preferences into health information
systems. Consumer informatics stands at the crossroads of other
disciplines, such as nursing informatics, public health, health promotion,
health education, library science, and communication science. AMIA
Consumer Health Informatics http://www.amia.org/applications-informatics/consumer-health-informatics
digiceuticals: Digital Therapeutics is a different class
of product than Digiceuticals. Most people confuse the two. The difference
is similar to prescription medication versus nutritional supplements. Both
play their role, but the standards of efficacy, and thus pricing and
reimbursement are very different. Hundreds of millions of dollars have
been invested in digiceuticals: …But, the efficacy has not been evaluated
in prospective randomized clinical trials and found to be non-inferior to
the control group. Thus, while the app usage data might show correlation
with the end goal, it has not proven causation. Digiceuticals are
important, but like nutritional supplements, are a consumer-focused
business. Digital Therapeutics vs. Digiceuticals, Defining the software
mediated digital healthcare Landscape, Medium, 2016
https://medium.com/@Healthy.vc/digital-therapeutics-vs-digiceuticals-defining-the-software-mediated-healthcare-landscape-fd0eb9dbedec
digital
health:
Digital
health is not a new concept. Seth Frank, writing 13 years ago, penned
“Digital Health Care—The convergence of health care and the
Internet” in The
Journal of Ambulatory Care Management. Today, technology is
rapidly transforming healthcare. Eric Topol’s The
Creative Destruction of Medicine
enumerates how these digital
technologies, social networking, mobile connectivity and bandwidth,
increasing computing power and the data universe will converge with
wireless sensors, genomics, imaging, and health information systems to
creatively destroy medicine as we know it. He refers to this as digital
medicine, or the digitization of human beings.
At Rock Health, we support entrepreneurs working in the space Topol
describes—at the intersection of healthcare and technology; and not
solely in medicine, but across healthcare, including wellness and
administration. As part of our research, we track
companies and catalog venture funding in
the digital health space. Defining
digital health and choosing which companies to include is complex, so here
is some transparency as to how we catalog deals: What Digital Health is
[and Isn’t) Rock Health http://rockhealth.com/2013/04/what-digital-health-is-and-isnt/
The broad scope of digital health includes categories such as mobile
health (mHealth), health information technology (IT), wearable devices,
telehealth and telemedicine, and personalized medicine. FDA
Digital Health
https://www.fda.gov/medicaldevices/digitalhealth/
Digital
health is the convergence of the digital and genetics revolutions with
health and healthcare. As we are seeing and experiencing, digital health
is empowering us to better track, manage, and improve our own and our
family’s health. It’s also helping to reduce inefficiencies in
healthcare delivery, improve access, reduce costs, increase quality, and
make medicine more personalized and precise. …
The
essential elements of the digital health revolution include wireless
devices, hardware sensors and software sensing technologies,
microprocessors and integrated circuits, the Internet, social networking,
mobile and body area networks, health information technology, genomics,
and personal genetic information. The lexicon of Digital Health is
extensive and includes all or elements of mHealth (aka Mobile Health),
Wireless Health, Health 2.0, eHealth, Health IT, Big Data, Health Data,
Cloud Computing, e-Patients, Quantified Self and Self-tracking, Wearable
Computing, Gamification, Telehealth & Telemedicine, Precision and
Personalized Medicine, plus Connected Health. Story of Digital Health,
Paul Sonnier, 2014 http://storyofdigitalhealth.com/definition/
digital therapeutics:
The term digital
therapeutics began to circulate around 2013, in large part due to Sean
Duffy, CEO of Omada Health. He began using it at conferences and in
the company’s marketing materials to describe its online coaching
software to help pre-diabetics avoid getting sick by exercising more
and losing weight. About a
dozen startups now call themselves digital therapeutics providers, and
say they’re distinct from the rest of the digital health market of
activity monitors, smart scales, and sleep trackers.
But defining exactly what a
digital therapeutic actually is can be elusive…says Peter Hames …Hames
says digital therapies fall into two groups, which he calls
“medication augmentation” and “medication replacement.” …
Can “Digital Therapeutics” Be as Good as Drugs?,
Christina Farr,
April 7, 2017 MIT Technology
Review
https://www.technologyreview.com/s/604053/can-digital-therapeutics-be-as-good-as-drugs/
Related term: digiceuticals.
drug utilization:
The
utilization of drugs as reported in individual hospital studies, FDA studies,
marketing, or consumption, etc. This includes drug stockpiling, and patient drug
profiles. MeSH, 1973
drug utilization review:
Formal programs for assessing drug prescription against some standard. Drug
utilization review may consider clinical appropriateness, cost effectiveness,
and, in some cases, outcomes. Review is usually retrospective, but some analysis
may be done before drugs are dispensed (as in computer systems which advise
physicians when prescriptions are entered). Drug utilization review is mandated
for Medicaid programs beginning in 1993. MeSH, 1994 Related terms: ATC/DDD, EPhMRA,
PBIRG
eCommon
Technical Document: The Electronic
Common Technical Document (eCTD) is CDER/CBER’s standard format for electronic
regulatory submissions. The FDA would like to work closely with people who
plan to provide a submission using the eCTD specifications FDA, Common Technical
Document http://www.fda.gov/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/ucm153574.htm
Electronic Common Technical Document,
Wikipedia http://en.wikipedia.org/wiki/Electronic_Common_Technical_Document
EDC
electronic data capture: Wikipedia http://en.wikipedia.org/wiki/Electronic_Data_Capture
effectiveness research: See
comparative effectiveness research, see also under outcomes research
e-health:
(also written e-health)
is a relatively recent healthcare practice supported by electronic processes and
communication, dating back to at least 1999.[1] Usage
of the term varies. A study in 2005 found 51 unique definitions.[2] Some
argue that it is interchangeable with health
informatics with a
broad definition covering electronic/digital processes in health[3] while
others use it in the narrower sense of healthcare practice using the Internet.[4][5][6] It
can also include health applications and links on mobile phones, referred to as mHealth or
m-Health.[7] …
Several authors have noted the variable usage in the term, from being specific
to the use of the Internet in healthcare to being generally around any use of
computers in healthcare.[10] Various
authors have considered the evolution of the term and its usage and how this
maps to changes in health informatics and healthcare generally.[1][11][12] Oh et
al., in a 2005 systematic review of the term's usage, offered the definition
of eHealth as a set of technological themes in health today, more specifically
based on commerce, activities, stakeholders, outcomes, locations, or
perspectives.[2] One
thing that all sources seem to agree on is that e-Health initiatives do not
originate with the patient, though the patient may be a member of a patient
organization that seeks to do this, as in the e-Patient movement
. Wikipedia accessed 2018 march 15
https://en.wikipedia.org/wiki/EHealth
Electronic
Health Records EHRs:
Electronic
Health Records (EHRs) are safe and confidential records that your doctor, other
health care provider, medical office staff, or a hospital keeps on a computer
about your health care or treatments. If your providers use electronic health
records, they can join a network to securely share your records with each other.
EHRs can help lower the chances of medical errors, eliminate duplicate tests,
and may improve your overall quality of care.
EHRs can help your providers have the same up-to-date information about
your conditions, treatments, tests, and prescriptions. Electronic Health
Records, Medicare.gov http://www.medicare.gov/manage-your-health/electronic-health-records/electronic-health-records.html
The
healthcare environment will be profoundly changed by the convergence of
technology, and ready access to updated patient information. The program will
cover the use of combinatorial device technology to integrate healthcare
systems, and the novel connectivity of global electronic medical record efforts.
Clinical management of disease will be addressed through the use of handheld and
point-of-care devices. The value of real time patient information to the
clinical management team and the pharmaceutical researcher will be leveraged
while addressing the ethical and legal implications.
Electronic Medical Records EMR: The EMR or electronic
medical record refers to everything you’d find in a paper chart, such as
medical history, diagnoses, medications, immunization dates, allergies.
EHR vs, EMR: What’s the difference?
https://www.practicefusion.com/blog/ehr-vs-emr/#EHRvsEMR
electronic
prescribing:
Agency for Healthcare
Research & Quality,
http://healthit.ahrq.gov/portal/server.pt?open=514&objID=5554&mode=2&holderDisplayURL=http://prodportal
electronic records
Part 11 electronic signatures -- FDA:
https://www.fda.gov/regulatory-information/search-fda-guidance-documents/part-11-electronic-records-electronic-signatures-scope-and-application
Electronic standards for
the transfer of regulatory information,
Glossary of Abbreviations and Terms ICH m2, 2015
http://estri.ich.org/recommendations/M2_Glossary_v2%200%20_11%20June%202015.pdf
evidence based
medicine:
Wikipedia
https://en.wikipedia.org/wiki/Evidence-based_medicine BMJ
Evidence Based Medicine
http://ebm.bmj.com/
genomic epidemiology:
An emerging discipline involving population
studies and microarray/ expression studies. Related terms: environmental
factors, public health; molecular epidemiology, human genome epidemiology,
phenotypic prevention
health informatics: (also
called health care informatics, healthcare
informatics, medical informatics, nursing
informatics, clinical informatics, or biomedical
informatics) is informatics in health
care, essentially the management and use of patient healthcare
information. It is a multidisciplinary field[1] that
uses health
information technology (HIT) to improve health care via
any combination of higher quality, higher efficiency (spurring lower cost
and thus greater availability), and new opportunities. The disciplines
involved include information
science, computer
science, social
science, behavioral
science, management
science, and others. The NLM defines
health informatics as "the interdisciplinary study of the design,
development, adoption and application of IT-based innovations in
healthcare services delivery, management and planning".[2] It
deals with the resources, devices, and methods required to optimize the
acquisition, storage, retrieval, and use of information in health and
biomedicine. Health
informatics tools include computers, clinical
guidelines, formal medical terminologies, and information and
communication systems, amongst others.[3][4] It
is applied to the areas of nursing, clinical
medicine, dentistry, pharmacy, public
health, occupational
therapy, physical
therapy, biomedical
research, and alternative
medicine,[5][unreliable
medical source?]all of which are designed to improve
the overall of effectiveness of patient care delivery by ensuring that the
data generated is of a high quality.[6]
The international standards on the subject are covered by ICS
35.240.80[7] in
which ISO
27799:2008 is one of the core components.[8]
Wikipedia
accessed 2018 March
https://en.wikipedia.org/wiki/Health_informatics
"the
interdisciplinary study of the design, development, adoption and
application of IT-based innovations in healthcare services delivery,
management and planning." Procter, R. Dr. (Editor, Health Informatics
Journal, Edinburgh, United Kingdom). Definition of health informatics
[Internet]. Message to: Virginia Van Horne (Content Manager, HSR
Information Central, Bethesda, MD). 2009 Aug 16 [cited 2009 Sept 21].
National Library of Medicine http://www.nlm.nih.gov/hsrinfo/informatics.html
Related terms:
biomedical informatics, healthcare informatics, medical informatics
Wikipedia http://en.wikipedia.org/wiki/Health_informatics
In the fall of 2015, the TIGER
Committee began compiling interprofessional informatics
definitions. The purpose of creating this document was to
collaboratively define and document core health informatics terminology in
an effort to provide context to the global TIGER interprofessional,
interdisciplinary community for consideration when terms are referred to
on the TIGER’s
main landing page on HIMSS.org, in official documents, and
within the TIGER
Virtual Learning Environment (VLE). Our intention is for
this resource to serve as a helpful tool for those learning about
informatics and informatics competencies. The 3.0 version of this document
was published in June 2018.
https://www.himss.org/library/tiger-informatics-definitions?utm_source=commnews&utm_medium=email&utm_campaign=tiger
health IT tools:
Agency
for Healthcare Research & Quality, http://healthit.ahrq.gov/portal/server.pt?open=512&objID=919&parentname=CommunityPage&parentid=9&mode=2&in_h
health record:
Historically, the definition of a legal medical or health record seemed
straightforward. The contents of the paper chart formed the provider of care’s
legal business record. Patients had limited interest in or access to the
information contained in their record. With the advent of various electronic
media, the Internet, and the consumer’s enhanced role in compiling health
records, the definition of the legal health record became more complex. The need
remains to ensure information is accessible for its ultimate purposes regardless
of the technologies employed or users involved. The definition of the legal
health record (LHR) must therefore be reassessed in light of such new
technologies, users, and uses. Amatayakul, Margret et al. "Definition
of the Health Record for Legal Purposes (AHIMA Practice Brief)." Journal
of AHIMA 72, no.9 (2001): 88A-H. http://library.ahima.org/xpedio/groups/public/documents/ahima/bok1_009223.hcsp?dDocName=bok1_009223
Healthcare Informatics:
Despite the rapid advances in medical science, the healthcare
delivery system remains plagued with inefficiencies that hinder basic access to
quality care at a reasonable price. Soaring costs are placing severe strains on
an already overburdened system, and administrators are scrambling to organize an
ever-increasing stream of information from a variety of data sources. There is a
growing consensus that Information Technology (IT) provides the key to
cost-effective quality care for all. Our research applies core computer science
and mathematics to complex healthcare domain problems. We look to solve some of
healthcare’s greatest IT challenges with new technology and methods that often
translate to other industries. Our technologies and inventions focus on the
advancement of multi-modal analysis, complex information integration technology,
disease and event modeling and genomics. http://www.almaden.ibm.com/cs/disciplines/hc/
HL7:
Health Level Seven is one of several American
National Standards Institute (ANSI) -accredited Standards Developing
Organizations (SDOs) operating in the healthcare arena. … Health Level
Seven’s domain is clinical and administrative data. "Level
Seven" refers to the highest level of the International Organization
for Standardization (ISO) communications model for Open Systems
Interconnection (OSI) - the application level.
http://www.hl7.org/
human factors:
Human
factors/usability engineering focuses on the interactions between people and
devices. The critical element in these interactions is the device user interface
...
Human
factors/usability engineering is used to design the machine-human (device-user)
interface. The user interface includes all components with which users interact
while preparing the device for use (e.g., unpacking, set up, calibration), using
the device, or performing maintenance (e.g., cleaning, replacing a battery,
making repairs). FDA, CDHR Medical Devices General Human Factors
Information and Resources http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/HumanFactors/ucm124829.htm
immunoinformatics:
or
computational immunology, is an emerging area that provides fundamental
methodologies in the study of immunomics, that is, immune-related genomics and
proteomics. The integration of immunoinformatics with systems biology approaches
may lead to a better understanding of immune-related diseases at various systems
levels. Such methods can contribute to translational studies that bring
scientific discoveries of the immune system into better clinical practice. One
of the most intensely studied areas of the immune system is immune epitopes.
Epitopes are important for disease understanding, host-pathogen interaction
analyses, antimicrobial target discovery, and vaccine design. The information
about genetic diversity of the immune system may help define patient subgroups
for individualized vaccine or drug development. Cellular pathways and host
immune-pathogen interactions have a crucial impact on disease pathogenesis and
immunogen design. Epigenetic studies may help understand how environmental
changes influence complex immune diseases such as allergy. High-throughput
technologies enable the measurements and catalogs of genes, proteins,
interactions, and behavior. Such perception may contribute to the understanding
of the interaction network among humans, vaccines, and drugs, to enable new
insights of diseases and therapeutic responses. The integration of immunomics
information may ultimately lead to the development of optimized vaccines and
drugs tailored to personalized prevention and treatment.
Methods
Mol Biol. 2010;662:203-20.
doi: 10.1007/978-1-60761-800-3_10. Immunoinformatics
and systems biology methods for personalized medicine.
Yan
Q.
http://www.ncbi.nlm.nih.gov/pubmed/20824473
See also Therapeutic areas: immunogenomics
in
silico
clinical trials: See
Clinical trials computer trials simulations
in
silico pharmacology
(also known as computational therapeutics, computational pharmacology) is a rapidly
growing area that globally covers the development of techniques for using
software to capture, analyse and integrate biological and medical data
from many diverse sources. More specifically, it defines the use of this
information in the creation of computational models or simulations that
can be used to make predictions, suggest hypotheses, and ultimately
provide discoveries or advances in medicine and therapeutics. add
citation.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978274/
laboratory
informatics:
the
specialized application of information technology aimed at optimizing laboratory
operations. It is a collection of informatics tools utilized within laboratory
environments to collect, store, process, analyze, report, and archive data and
information from the laboratory and supporting processes. Laboratory informatics
includes the integration of systems, the electronic delivery of results to
customers, and the supporting systems including training and policies. Examples
of laboratory informatics include: Laboratory Information Management Systems
(LIMS), Electronic Laboratory Notebooks (ELNs), Chromatography Data Systems
(CDS), and Scientific Data Management Systems (SDMS). ASTM E1578 Standard
Guide for Laboratory Informatics 2013 http://www.astm.org/Standards/E1578.htm
Wikipedia
http://en.wikipedia.org/wiki/Laboratory_informatics
Related term?:
Drug
discovery & development LIMS
LOINC Logical Observation
Identifiers Names and Codes:
The purpose of the LOINC database is to facilitate the exchange and
pooling of results, such as blood hemoglobin, serum potassium, or vital
signs, for clinical care, outcomes management, and research. Regenstrief
Institute Inc. Germany
http://www.loinc.org/
meaningful
use:
is using certified electronic health record (EHR) technology to: Improve
quality, safety, efficiency, and reduce health disparities, Engage patients and
family, Improve care coordination, and population and public health, Maintain
privacy and security of patient health information, Ultimately, it is hoped that
the meaningful use compliance will result in: Better clinical outcomes, Improved
population health outcomes, Increased transparency and efficiency, Empowered
individuals, More robust research data on health systems HealthIT.gov EHR
Incentives and Certification http://www.healthit.gov/providers-professionals/meaningful-use-definition-objectives
The overall goal of
the Meaningful Use program is to promote the widespread adoption of
electronic health records systems, ultimately creating an infrastructure
that improves the quality, safety and efficiency of patient care in the
United States. … To qualify for Meaningful Use incentive payments,
eligible providers must not only adopt an EHR, but also show that they are
"meaningfully using" their EHR by meeting a number of objectives designed
to have a positive impact on patient care. The Centers for Medicare &
Medicaid Services (CMS) has established these measures as part of their
mission to advance health care IT in the U.S. AthenaHealth
https://www.athenahealth.com/knowledge-hub/meaningful-use/what-is-meaningful-use
CDC, meaningful use
https://www.cdc.gov/ehrmeaningfuluse/introduction.html
Medbiquitous Consortium: ANSI-accredited developer of
information technology standards for healthcare education and quality
improvement. http://www.medbiq.org/index.html
medical bioinformatics:
Linking clinical data to patient gene profiling. Covers haplotyping,
genotyping, population genomics, gene expression profiling,
particularly for use in diagnosis, prognosis and therapeutic stratification of
patients. Related
terms: Biomarkers, Expression,
Microarrays and protein chips
medical informatics:
The field of information science concerned with the analysis and dissemination of medical data through the application of computers to various aspects of health care and medicine.
MeSH, 1987
An emerging discipline that has been defined as the study, invention, and implementation of structures and algorithms to improve communication, understanding and management of medical information. The end objective of biomedical informatics is
the coalescing of data, knowledge, and the tools necessary to apply that data and knowledge in the decision- making process, at the time and place that a decision needs to be made. The focus on the structures and algorithms necessary to manipulate the information separates Biomedical Informatics from other medical disciplines where information content is the focus.
Medical Informatics FAQ, 1999 http://www.faqs.org/faqs/medical-informatics-faq/
MedDRA Medical Dictionary
for Regulatory Activities:
In the late 1990s, the International Council for Harmonisation of Technical
Requirements for Pharmaceuticals for Human Use (ICH) developed MedDRA, a rich
and highly specific standardised medical terminology to facilitate sharing of
regulatory information internationally for medical products used by humans.
https://www.meddra.org/
meta-analysis:
The
use of statistical techniques in a systematic review to
integrate the results of included studies. Sometimes misused as a synonym for
systematic reviews, where the review includes a meta- analysis. Cochrane Collaboration "Glossary
of terms in the Cochrane Collaboration, 2014 http://www.cochrane.org/glossary/5
A quantitative method of combining the results of independent studies (usually drawn from the published literature) and synthesizing summaries and conclusions which may be used to evaluate therapeutic effectiveness, plan new studies, etc., with application chiefly in the areas of research and medicine.
MeSH, 1989
meta-regression:
Meta-regression is an extension to subgroup analyses
that allows the effect of continuous, as well as categorical, characteristics
to be investigated, and in principle allows the effects of multiple factors to
be investigated simultaneously (although this is rarely possible due to
inadequate numbers of studies) (Thompson 2002). Meta-regression should
generally not be considered when there are fewer than ten studies in a
meta-analysis. General Methods for Cochran Reviews, Cochran
Collaborative http://handbook.cochrane.org/chapter_9/9_6_4_meta_regression.htm
mHealth :
(also written as m-health) is
an abbreviation for mobile health,
a term used for the practice of medicine and public health supported by mobile
devices.[1] The
term is most commonly used in reference to using mobile communication devices,
such as mobile phones, tablet computers and PDAs, and wearable devices
such as smart watches, for health
services, information, and data collection.[2] The
mHealth field has emerged as a sub-segment of eHealth,
the use of information and communication technology (ICT), such as computers,
mobile phones, communications satellite, patient
monitors, etc., for health services and information.[3] mHealth
applications include the use of mobile devices in collecting community and
clinical health data, delivery of healthcare information to practitioners,
researchers, and patients, real-time monitoring of patient vital
signs, and direct provision of care (via mobile telemedicine).[4]
While mHealth certainly has application for industrialized nations, the field has emerged in
recent years as largely an application for developing countries, stemming from the rapid
rise of mobile phone penetration in low-income nations. Wikipedia accessed 2018
March 15
https://en.wikipedia.org/wiki/MHealth
With
the emergence of new technologies such as mobile devices and wearables, the
pharma and biotech industry are poised to capitalize on these advancements to
innovate existing clinical trial processes and systems. Advancing technological
innovation in clinical trials coincides with the move toward greater
cross-industry clinical trial data sharing and clinical data transparency. Coupled together new technological advances and increased clinical trial data
sharing leads to more efficient clinical trials.
See also telehealth.
National Center for
Integrative Biomedical Informatics:
http://www.ncibi.org/
One of
eight National Centers
for Biomedical Computing (NCBC)
within the NIH Roadmap. The NCBC program is focused on building a universal
computing infrastructure designed to speed progress in biomedical research.
National Electronics Clinical Trials and Research
(NECTAR):
An enriched pipeline of biomedical discoveries, an infrastructure to facilitate
the translation of these discoveries from the laboratory to the clinic, and a
robust force of clinical investigators will make it possible to test new
therapeutic and preventive strategies in larger numbers of patients far sooner
than currently possible. These large studies are often best conducted through
networks of investigators who are equipped with tools to facilitate
collaboration and information sharing. Because of the vast number of therapies,
diagnostics, and treatments that must be evaluated through clinical trials, many
clinical research networks operate simultaneously, but independently, of each
other. As a result, researchers must sometimes duplicate data that already
exists because they are unaware of the data or do not have access to the data.
Standardizing data reporting would enable seamless data- and sample-sharing
across studies. By enhancing the efficiency of clinical research networks
through informatics and other technologies, researchers will be better able to
broaden the scope of their research. Reduced duplication of studies will leave
more time and funds to address additional research questions.
NECTAR, NIH Common Fund http://commonfund.nih.gov/clinicalresearch/overview-networks.aspx
neuroimaging:
Neuroimaging informatics tools and resources http://www.nitrc.org/
neuroinformatics:
a research field concerned with the organization of neuroscience data
by the application of computational models and analytical tools. These areas of
research are important for the integration and analysis of increasingly
large-volume, high-dimensional, and fine-grain experimental data.
Neuroinformaticians provide computational tools, mathematical models, and create
interoperable databases for clinicians and research scientists. Neuroscience is
a heterogeneous field, consisting of many and various sub-disciplines (e.g., cognitive
psychology, behavioral
neuroscience, and behavioral
genetics). Wikipedia accessed 2018 Oct 23
https://en.wikipedia.org/wiki/Neuroinformatics
NIH Blueprint for Neuroscience Research
https://neuroscienceblueprint.nih.gov/
Office of the National
Coordinator for Health Information Technology (ONC):
is at the forefront
of the administration’s health IT efforts and is a resource to the entire
health system to support the adoption of health information technology and the
promotion of nationwide health information exchange to improve health care.
ONC is the principal federal entity charged with coordination of nationwide
efforts to implement and use the most advanced health information technology and
the electronic exchange of health information.
https://www.healthit.gov/newsroom/about-onc
outcomes research:
The terms
"outcomes research" and "effectiveness research" have
been used to refer to a wide range of studies, and there is no single definition
for either that has gained widespread acceptance. As these fields evolved, it
appears that "outcomes research" emerged from a new emphasis on
measuring a greater variety of impacts on patients and patient care (function,
quality of life, satisfaction, readmissions, costs, etc). The term
"effectiveness research" was used to emphasize the contrast with
efficacy studies, and highlighted the goal of learning how medical interventions
affected real patients in "typical" practice settings (OTA,
1994). Effectiveness studies sought to understand the impact of health care
on patients with diverse characteristics, rather than highly homogeneous study
populations. While the terms may have different initial roots, there does not
appear to be much value in distinguishing these activities, and the field is
generally referred to as OER. .. OER evaluates the impact of health care
(including discrete interventions such as particular drugs, medical devices, and
procedures as well as broader programmatic or system interventions) on the
health outcomes of patients and populations. OER may include evaluation of
economic impacts linked to health outcomes, such as cost- effectiveness and cost
utility. OER emphasizes health problem- (or disease-) oriented evaluations of
care delivered in general, real- world settings; multidisciplinary teams; and a
wide range of outcomes, including mortality, morbidity, functional status,
mental well- being, and other aspects of health-related quality of
life. Outcome of Outcomes Research at AHCPR: Final Report, Agency
for Health Care Policy and Research, AHCPR Publication No. 99-R044 https://archive.ahrq.gov/research/findings/final-reports/outcomes-research/introduction.html
Related term: comparative effectiveness research
pathology informatics:
involves collecting, examining, reporting, and storing large complex sets of
data derived from tests performed in clinical laboratories, anatomic pathology
laboratories, or research laboratories in order to improve patient care and
enhance our understanding of disease-related processes. … The data sets used in
pathology informatics include clinical tests, anatomic pathology reports, image
files, telepathology data, and large-scale experiments including gene, proteomic
and tissue array studies. Association for Pathology Informatics
https://www.pathologyinformatics.org/about_api.php
patient
engagement: Surgeon General C Everett Koop once said “Drugs don’t
work in patients who don’t take them.” I’ll offer a corollary of my own:
Patients who aren’t engaged don’t comply with therapies or report
complications. Enabling Patient Engagement and Healthcare Innovation, FDA
Testimony Healthcare Innovation DDMAC Public Hearings on Internet & Social
Media #FDASM Zen Chu, 2009 http://www.slideshare.net/MedicalVentures/zen-chu-healthcare-innovation-fda-testimony-ddmac-public-hearings-on-internet-social-media
patient reported
outcomes:
the PROMIS (Patient-Reported Outcomes Measurement Information
System) initiative is developing new ways to measure patient-reported outcomes
(PROs), such as pain, fatigue, physical functioning, emotional distress, and
social role participation that have a major impact on quality-of-life across a
variety of chronic diseases. Clinical measures of health outcomes, such as
x-rays and lab tests, may have minimal relevance to the day-to-day functioning
of patients with chronic diseases. Often, the best way patients can judge the
effectiveness of treatments is by changes in symptoms. The goal of PROMIS is to
improve the reporting and quantification of changes in PROs. PROMIS Patient
Reported Outcomes, NIH Common Fund http://commonfund.nih.gov/promis/overview.aspx
Personal
Health Record PHR:
The PHR is a tool that you can use to collect,
track and share past and current information about your health or the health of
someone in your care. Sometimes this information can save you the money and
inconvenience of repeating routine medical tests. Even when routine procedures
do need to be repeated, your PHR can give medical care providers more insight
into your personal health story. AHIMA, MyPHR - http://www.myphr.com/startaphr/what_is_a_phr.aspx#sthash.gyUVxDmV.dpuf
pharmacoepidemiology:
the science that applies epidemiologic
approaches to studying the use, effectiveness, value and safety of
pharmaceuticals. The International Society for Pharmacoepidemiology
(ISPE) is an international organization dedicated to advancing the health
of the public by providing a global forum for the open exchange of
scientific information and for the development of policy, education, and
advocacy for the field of pharmacoepidemiology, including such area as
pharmacovigilance, drug utilization research, comparative effectiveness
review, and therapeutic risk management. International Society of
Pharmacoepidemiology
https://www.pharmacoepi.org/about-ispe/overview/
population health:
has been defined as "the health outcomes of a group of individuals,
including the distribution of such outcomes within the group".[1] It
is an approach to health that
aims to improve the health of
an entire human population. This concept does not refer to animal or plant
populations. It has been described as consisting of three components.
These are "health outcomes, patterns of health determinants, and policies
and interventions".[1] A
priority considered important in achieving the aim of Population Health is
to reduce health inequities or disparities among different population
groups due to, among other factors, the social
determinants of health,
SDOH. ... From a population health perspective, health has been defined
not simply as a state free from disease but
as "the capacity of people to adapt to, respond to, or control life's
challenges and changes".[5] The World
Health Organization (WHO) defined health in its broader
sense in 1946 as "a state of complete physical, mental, and social well-being and
not merely the absence of disease or infirmity."[6][7]
Wikipedia accessed 2018 Feb
20
https://en.wikipedia.org/wiki/Population_health
predictive genomics: Wayne
D. Hall1,+, Katherine I. Morley1,2 and Jayne C. Lucke1,
The prediction of disease risk in genomic medicine: Scientific prospects
and implications for public policy and ethics EMBO reports vol. 5 | Suppl 1 | pp
S22-S26 | 2004 DOI: 10.1038/sj.embor.7400224 See also Pharmacogenomics
predictive pharmacogenomics
prognosis:
The probable outcome or course of a disease; the chance
of recovery. [ORD]
Not a major emphasis in clinical medicine today. Nicholas Christakis'
Death
Foretold is an eloquent book about the delicate balance between medical reality
and optimism, and how seldom this is discussed in either classrooms or
hospital rooms today.
public
health informatics:
The systematic application of
information and computer sciences to public health practice, research, and
learning. It is the discipline that integrates public health with information
technology. The development of this field and dissemination of informatics
knowledge and expertise to public health professionals is the key to unlocking
the potential of information systems to improve the health of the nation. www.nlm.nih.gov/pubs/cbm/phi2001.html
MeSH 2003
is
the application of informatics in areas of public health, including
surveillance, prevention, preparedness, and health promotion. Public health
informatics and the related population informatics, work on information and
technology issues from the perspective of groups of individuals. Public health
is extremely broad and can even touch on the environment, work and living places
and more. Generally, AMIA focuses on those aspects of public health that enable
the development and use of interoperable information systems for public health
functions such as biosurveillance, outbreak management, electronic laboratory
reporting and prevention.
AMIA Public Health Informatics http://www.amia.org/applications-informatics/public-health-informatics
Real World
Data RWD: anything OTHER than RCT
[randomized controlled trails] generated data…data derived from:
Prospective observational studies, Non-interventional observations,
Database studies, Prospective registries create a database, Retrospective
databases created for other reasons, Medical records, Data abstraction. In
general, “real world data” are observations of effects based on what
happens after a prescriptive (treatment) decision is made where the
researcher does not or cannot control who gets what treatment and does not
or cannot control the medical management of the patient beyond observing
outcomes. Using Real World Data in Pharmacoeconomic Evaluations:
Challenges, Opportunities, and Approaches. Andreas M. Pleil, Pfizer https://pharmacy.ucsd.edu/faculty/AppliedPEForum/docs/Andreas_M_Pleil.pdf
the data relating to patient health
status and/or the delivery of health care routinely collected from a
variety of sources. RWD can come from a number of sources, for example:
Electronic health records (EHRs), Claims and billing activities, Product
and disease registries, Patient-generated data including in home-use
settings, Data gathered from other sources that can inform on health
status, such as mobile devices.
US FDA Real World Evidence Science and Research
https://www.fda.gov/scienceresearch/specialtopics/realworldevidence/default.htm
Makady A, van Veelen A, Jonsson P, et al. Using Real-World Data in Health
Technology Assessment (HTA) Practice: A Comparative Study of Five HTA
Agencies. Pharmacoeconomics. 2018;36(3):359-368. doi:10.1007/s40273-017-0596-z.
Real world data can
be gathered from retrospective
or prospective studies in which the investigator observes
natural events without intervention (e.g. audits, cohort or case–control
studies).
https://www.openhealth.co.uk/news/07-11-2017/the-use-of-real-world-data-in-nice-decision-making/
GetReal Project No 115546 WP1 Deliverable D1.3
Glossary of Definitions of Common Terms
2009
[PDF]
WP1: Deliverable D1.3 Glossary of
Definitions of Common Terms ...
Real World
Evidence RWE: While
the definition of Real
World Evidence is still evolving, most proponents associate such as
insurance claims data and clinical data from electronic health records.
Real World Evidence - The Network For Excellence In Health Innovation
the clinical evidence
regarding the usage and potential benefits or risks of a medical product
derived from analysis of RWD. US FDA Real World Evidence Science and
Research
https://www.fda.gov/scienceresearch/specialtopics/realworldevidence/default.htm
FDA, Framework for Real World Evidence Program
2018 Dec
https://www.fda.gov/downloads/ScienceResearch/SpecialTopics/RealWorldEvidence/UCM627769.pdf
SNOMED
Systematized Nomenclature of Medicine:
SNOMED International determines global standards for health terms.
https://www.snomed.org/
systems
medicine: an interdisciplinary field of
study that looks at the systems of the human body as part of an integrated
whole, incorporating biochemical, physiological, and environment interactions.
Systems medicine draws on systems
science and systems
biology, and considers complex interactions within the human body in light
of a patient's genomics,
behavior and environment.[1]
The earliest uses of the term systems
medicine appeared in 1992, in an article on systems medicine and
pharmacology by B.J. Zeng [2] and
in a paper on systems biomedicine by T. Kamada.[3]
Wikipedia accessed 2018 Sept 2
https://en.wikipedia.org/wiki/Systems_medicine
syndromics,
syndromic systems: Systems
of information for the detected of occurrences of syndromes. Edilson Damasio,
Systems of information and surveillance of occurrences in bioterrorism, 9th
World Congress on Health Information and Libraries, Brazil, Sept. 20-23, 2005 http://www.icml9.org/program/track3/activity.php?lang=en&id=20
telehealth:
Wikipedia http://en.wikipedia.org/wiki/Telehealth
telemedicine: http://en.wikipedia.org/wiki/Telemedicine
translational
bioinformatics:
is
the development of storage, analytic, and interpretive methods to optimize the
transformation of increasingly voluminous biomedical data, and genomic data,
into proactive, predictive, preventive, and participatory health. Translational
bioinformatics includes research on the development of novel techniques for the
integration of biological and clinical data and the evolution of clinical
informatics methodology to encompass biological observations. The end product of
translational bioinformatics is newly found knowledge from these integrative
efforts that can be disseminated to a variety of stakeholders, including
biomedical scientists, clinicians, and patients. AMIA Translational
bioinformatics http://www.amia.org/applications-informatics/translational-bioinformatics
PLOS Computational
Biology Translational Bioinformatics
http://www.ploscollections.org/article/browseIssue.action?issue=info:doi/10.1371/issue.pcol.v03.i11
UMLS Unified Medical Language System:
an interdisciplinary field of
study that looks at the systems of the human body as part of an integrated
whole, incorporating biochemical, physiological, and environment interactions.
Systems medicine draws on systems
science and systems
biology, and considers complex interactions within the human body in light
of a patient's genomics,
behavior and environment.[1]
The earliest uses of the term systems
medicine appeared in 1992, in an article on systems medicine and
pharmacology by B.J. Zeng [2] and
in a paper on systems biomedicine by T. Kamada.[3]
Wikipedia accessed 2018 Sept 2
https://en.wikipedia.org/wiki/Systems_medicine
uncertainty
factor:
Mathematical adjustments for reasons of
safety when knowledge is incomplete. For example, factors used in the
calculation of doses that are not harmful (adverse) to people. These factors are
applied to the lowest-observed-adverse-effect-level
(LOAEL) or the no-observed-adverse-effect-level
(NOAEL) to derive a minimal
risk level (MRL). Uncertainty factors
are used to account for variations in people's sensitivity, for differences
between animals and humans, and for differences between a LOAEL and a NOAEL.
Scientists use uncertainty factors when they have some, but not all, the
information from animal or human studies to decide whether an exposure will
cause harm to people [also sometimes called a safety factor].
Universal Trial Number UTN:
The aim of the Universal Trial Number
(UTN) is to facilitate the unambiguous identification of clinical trials.
The UTN is not a
registration number.
The UTN is a number that should be obtained
early in the history of the trial.
WHO
International Clinical Trials Registry Platform
(ICTRP)
The Universal Trial Number (UTN)
http://www.who.int/ictrp/unambiguous_identification/utn/en/
wearable technologies, wearables:
Biomaterials & Medical devices
Clinical informatics resources
AMIA American Medical Informatics Association,
Glossary of Acronyms and Terms commonly used in informatics, 2013
https://www.amia.org/glossary
ASHP, SOPIT Glossary of Informatics Terms
https://www.ashp.org/-/media/assets/pharmacy-informaticist/docs/sopit-terminology-glossary.ashx?la=en
CAP College of American Pathologists, Glossary of clinical Informatics terms
http://www.cap.org/ShowProperty?nodePath=/UCMCon/Contribution%20Folders/WebContent/pdf/clinical-informatics-acronym-glossary.pdf
Coiera, Enrico, Health Informatics Glossary
http://coiera.com/textbook-resources/glossary/
MedDRA Medical Dictionary for Regulatory Activities, Maintenance and Support
Services Organization. An international medical terminology designed to support
the classification, retrieval, presentation, and communication of medical
information throughout the medical product regulatory cycle. http://www.meddra.org/
SNOMED https://www.snomed.org/
Informatics Conferences
http://www.healthtech.com/conferences/upcoming.aspx?s=NFO
BioIT World Expo
https://www.bio-itworldexpo.com/
Molecular Medicine Tri Conference BioIT World West
https://www.bio-itworldexpowest.com/ Molecular Medicine Conference
Digital Health
https://www.triconference.com/digital-health
BioIT World magazine
http://www.bio-itworld.com/
BioIT World archives http://www.bio-itworld.com/BioIT/BioITArchive.aspx
Clinical Research News
http://www.clinicalinformaticsnews.com/
How
to look for other unfamiliar terms
|