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The Resource Health care engineering, Part II, Research and development in the health care environment, Monique Frize, (electronic book)

Health care engineering, Part II, Research and development in the health care environment, Monique Frize, (electronic book)

Creator
Author
Summary
Chapter 7 presents some statistics on the occurrence of medical errors and adverse events, and includes some technological solutions. A chapter on electronic medical records follows. The knowledge management process divided into four steps is described; this includes a discussion on data acquisition, storage, and retrieval. The next two chapters discuss the other three steps of the knowledge management process (knowledge discovery, knowledge translation, knowledge integration and sharing). The last chapter briefly discusses usability studies and clinical trials. The two parts consolidate material that supports courses on technology development and management issues in health care institutions. It can be useful for anyone involved in design, development, or research, whether in industry, hospitals, or government
Language
eng
Work
Publication
Extent
1 PDF (xviii, 65 pages)
Contents
  • 7. Adverse events, medical errors, and the role of information technology in reducing them -- 7.1 Some statistics on medical errors and adverse events -- 7.2 Types of medical errors -- 7.3 Information technologies that can help reduce errors and adverse events --
  • 8. The electronic medical record (EMR): design, safety, and meaningful use -- 8.1 What is an EMR -- 8.2 Benefits regarding the use of EMRs -- 8.3 Concerns regarding the use of EMRs -- 8.4 Historical development -- 8.5 Rate of adoption in western countries -- 8.6 Barriers to adoption of the EMR -- 8.6.1 Financial -- 8.6.2 Technical -- 8.6.3 Time -- 8.6.4 Psychological -- 8.6.5 Social -- 8.6.6 Legal -- 8.6.7 Organizational -- 8.6.8 Change process -- 8.6.9 Resistance to change -- 8.6.10 Comments by physicians -- 8.7 Incentives to establish an EMR system in physician practices -- 8.7.1 United States -- 8.7.2 Canada -- 8.8 Desirable design characteristics of EMRs -- 8.9 Patient safety -- 8.10 Ethical considerations -- 8.10.1 Autonomy -- 8.10.2 Beneficence and non-maleficence -- 8.10.3 Justice --
  • 9. Knowledge management (KM) in a clinical environment: data acquisition, storage, and retrieval -- 9.1 The importance of integrating knowledge management (KM) into clinical care -- 9.2 The health care knowledge management (KM) process -- 9.2.1 Step 1: access to clinical data: data collection, storage, and retrieval -- 9.2.2 Step 2: knowledge discovery (KD) -- 9.2.3 Step 3: knowledge translation (KT) -- 9.2.4 Step 4: knowledge integration and sharing (KIS) -- 9.3 Clinical data repository design -- 9.4 Example of perinatal databases used in a research project -- 9.4.1 The perinatal partnership program of eastern and southeastern Ontario (PPESO) database -- 9.4.2 PRAMS (pregnancy risk assessment monitoring system) database -- 9.4.3 The Canadian neonatal network (CNN) database --
  • 10. Knowledge discovery (KD): data analysis and data mining tools -- 10.1 Scoring systems to estimate outcomes -- 10.2 Examples of knowledge discovery tools -- 10.2.1 Brief description of artificial neural networks (ANNs) -- 10.2.2 Case-based reasoning (CBR) system --
  • 11. Knowledge translation (KT), integration, and sharing (KIS) in a clinical environment -- 11.1 Clinical decision support systems (CDSS) -- 11.1.1 Design of a CDSS for the obstetrical environment -- 11.1.2 Estimating neonatal intensive care outcomes -- 11.2 Knowledge translation to users -- 11.3 Knowledge integration and sharing --
  • 12. Clinical trials and usability studies in a medical environment -- 12.1 Usability testing -- 12.1.1 Heuristic evaluation -- 12.1.2 Cognitive walkthrough -- 12.1.3 Videotaped evaluation -- 12.2 Clinical studies and trials -- 12.3 Conclusion -- Author biography
Isbn
9781627050739
Instance
Label
Health care engineering, Part II, Research and development in the health care environment
Title
Health care engineering
Title number
Part II
Title part
Research and development in the health care environment
Statement of responsibility
Monique Frize
Title variation
Research and development in the health care environment
Creator
Author
Subject
Language
eng
Summary
Chapter 7 presents some statistics on the occurrence of medical errors and adverse events, and includes some technological solutions. A chapter on electronic medical records follows. The knowledge management process divided into four steps is described; this includes a discussion on data acquisition, storage, and retrieval. The next two chapters discuss the other three steps of the knowledge management process (knowledge discovery, knowledge translation, knowledge integration and sharing). The last chapter briefly discusses usability studies and clinical trials. The two parts consolidate material that supports courses on technology development and management issues in health care institutions. It can be useful for anyone involved in design, development, or research, whether in industry, hospitals, or government
Member of
Cataloging source
CaBNVSL
http://library.link/vocab/creatorDate
1942-
http://library.link/vocab/creatorName
Frize, Monique
Dewey number
610.28
Illustrations
illustrations
Index
no index present
LC call number
R855.3
LC item number
.F7542 2014
Literary form
non fiction
Nature of contents
  • dictionaries
  • abstracts summaries
  • bibliography
http://library.link/vocab/subjectName
  • Medical technology
  • Biomedical engineering
  • Medical records
  • Knowledge management
  • Clinical trials
  • Medical care
  • Medical care
  • Biomedical Technology
  • Biomedical Engineering
  • Electronic Health Records
  • Knowledge Management
  • Clinical Trials as Topic
  • Delivery of Health Care
  • Delivery of Health Care
Target audience
  • adult
  • specialized
Label
Health care engineering, Part II, Research and development in the health care environment, Monique Frize, (electronic book)
Instantiates
Publication
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type MARC source
rdacontent
Contents
  • 7. Adverse events, medical errors, and the role of information technology in reducing them -- 7.1 Some statistics on medical errors and adverse events -- 7.2 Types of medical errors -- 7.3 Information technologies that can help reduce errors and adverse events --
  • 8. The electronic medical record (EMR): design, safety, and meaningful use -- 8.1 What is an EMR -- 8.2 Benefits regarding the use of EMRs -- 8.3 Concerns regarding the use of EMRs -- 8.4 Historical development -- 8.5 Rate of adoption in western countries -- 8.6 Barriers to adoption of the EMR -- 8.6.1 Financial -- 8.6.2 Technical -- 8.6.3 Time -- 8.6.4 Psychological -- 8.6.5 Social -- 8.6.6 Legal -- 8.6.7 Organizational -- 8.6.8 Change process -- 8.6.9 Resistance to change -- 8.6.10 Comments by physicians -- 8.7 Incentives to establish an EMR system in physician practices -- 8.7.1 United States -- 8.7.2 Canada -- 8.8 Desirable design characteristics of EMRs -- 8.9 Patient safety -- 8.10 Ethical considerations -- 8.10.1 Autonomy -- 8.10.2 Beneficence and non-maleficence -- 8.10.3 Justice --
  • 9. Knowledge management (KM) in a clinical environment: data acquisition, storage, and retrieval -- 9.1 The importance of integrating knowledge management (KM) into clinical care -- 9.2 The health care knowledge management (KM) process -- 9.2.1 Step 1: access to clinical data: data collection, storage, and retrieval -- 9.2.2 Step 2: knowledge discovery (KD) -- 9.2.3 Step 3: knowledge translation (KT) -- 9.2.4 Step 4: knowledge integration and sharing (KIS) -- 9.3 Clinical data repository design -- 9.4 Example of perinatal databases used in a research project -- 9.4.1 The perinatal partnership program of eastern and southeastern Ontario (PPESO) database -- 9.4.2 PRAMS (pregnancy risk assessment monitoring system) database -- 9.4.3 The Canadian neonatal network (CNN) database --
  • 10. Knowledge discovery (KD): data analysis and data mining tools -- 10.1 Scoring systems to estimate outcomes -- 10.2 Examples of knowledge discovery tools -- 10.2.1 Brief description of artificial neural networks (ANNs) -- 10.2.2 Case-based reasoning (CBR) system --
  • 11. Knowledge translation (KT), integration, and sharing (KIS) in a clinical environment -- 11.1 Clinical decision support systems (CDSS) -- 11.1.1 Design of a CDSS for the obstetrical environment -- 11.1.2 Estimating neonatal intensive care outcomes -- 11.2 Knowledge translation to users -- 11.3 Knowledge integration and sharing --
  • 12. Clinical trials and usability studies in a medical environment -- 12.1 Usability testing -- 12.1.1 Heuristic evaluation -- 12.1.2 Cognitive walkthrough -- 12.1.3 Videotaped evaluation -- 12.2 Clinical studies and trials -- 12.3 Conclusion -- Author biography
Control code
201310BME051
Dimensions
unknown
Extent
1 PDF (xviii, 65 pages)
File format
multiple file formats
Form of item
online
Isbn
9781627050739
Issn
1930-0336
Media category
electronic
Media MARC source
isbdmedia
Other control number
10.2200/S00540ED1V01Y201310BME051
Other physical details
illustrations.
Reformatting quality
access
Specific material designation
remote
System details
System requirements: Adobe Acrobat Reader
Label
Health care engineering, Part II, Research and development in the health care environment, Monique Frize, (electronic book)
Publication
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type MARC source
rdacontent
Contents
  • 7. Adverse events, medical errors, and the role of information technology in reducing them -- 7.1 Some statistics on medical errors and adverse events -- 7.2 Types of medical errors -- 7.3 Information technologies that can help reduce errors and adverse events --
  • 8. The electronic medical record (EMR): design, safety, and meaningful use -- 8.1 What is an EMR -- 8.2 Benefits regarding the use of EMRs -- 8.3 Concerns regarding the use of EMRs -- 8.4 Historical development -- 8.5 Rate of adoption in western countries -- 8.6 Barriers to adoption of the EMR -- 8.6.1 Financial -- 8.6.2 Technical -- 8.6.3 Time -- 8.6.4 Psychological -- 8.6.5 Social -- 8.6.6 Legal -- 8.6.7 Organizational -- 8.6.8 Change process -- 8.6.9 Resistance to change -- 8.6.10 Comments by physicians -- 8.7 Incentives to establish an EMR system in physician practices -- 8.7.1 United States -- 8.7.2 Canada -- 8.8 Desirable design characteristics of EMRs -- 8.9 Patient safety -- 8.10 Ethical considerations -- 8.10.1 Autonomy -- 8.10.2 Beneficence and non-maleficence -- 8.10.3 Justice --
  • 9. Knowledge management (KM) in a clinical environment: data acquisition, storage, and retrieval -- 9.1 The importance of integrating knowledge management (KM) into clinical care -- 9.2 The health care knowledge management (KM) process -- 9.2.1 Step 1: access to clinical data: data collection, storage, and retrieval -- 9.2.2 Step 2: knowledge discovery (KD) -- 9.2.3 Step 3: knowledge translation (KT) -- 9.2.4 Step 4: knowledge integration and sharing (KIS) -- 9.3 Clinical data repository design -- 9.4 Example of perinatal databases used in a research project -- 9.4.1 The perinatal partnership program of eastern and southeastern Ontario (PPESO) database -- 9.4.2 PRAMS (pregnancy risk assessment monitoring system) database -- 9.4.3 The Canadian neonatal network (CNN) database --
  • 10. Knowledge discovery (KD): data analysis and data mining tools -- 10.1 Scoring systems to estimate outcomes -- 10.2 Examples of knowledge discovery tools -- 10.2.1 Brief description of artificial neural networks (ANNs) -- 10.2.2 Case-based reasoning (CBR) system --
  • 11. Knowledge translation (KT), integration, and sharing (KIS) in a clinical environment -- 11.1 Clinical decision support systems (CDSS) -- 11.1.1 Design of a CDSS for the obstetrical environment -- 11.1.2 Estimating neonatal intensive care outcomes -- 11.2 Knowledge translation to users -- 11.3 Knowledge integration and sharing --
  • 12. Clinical trials and usability studies in a medical environment -- 12.1 Usability testing -- 12.1.1 Heuristic evaluation -- 12.1.2 Cognitive walkthrough -- 12.1.3 Videotaped evaluation -- 12.2 Clinical studies and trials -- 12.3 Conclusion -- Author biography
Control code
201310BME051
Dimensions
unknown
Extent
1 PDF (xviii, 65 pages)
File format
multiple file formats
Form of item
online
Isbn
9781627050739
Issn
1930-0336
Media category
electronic
Media MARC source
isbdmedia
Other control number
10.2200/S00540ED1V01Y201310BME051
Other physical details
illustrations.
Reformatting quality
access
Specific material designation
remote
System details
System requirements: Adobe Acrobat Reader

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