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Sharing Clinical Research Data: Workshop Summary [Mīkstie vāki]

  • Formāts: Paperback / softback, 156 pages, height x width: 280x216 mm
  • Izdošanas datums: 07-Jun-2013
  • Izdevniecība: National Academies Press
  • ISBN-10: 0309268745
  • ISBN-13: 9780309268745
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  • Mīkstie vāki
  • Cena: 48,21 €
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  • Formāts: Paperback / softback, 156 pages, height x width: 280x216 mm
  • Izdošanas datums: 07-Jun-2013
  • Izdevniecība: National Academies Press
  • ISBN-10: 0309268745
  • ISBN-13: 9780309268745
Citas grāmatas par šo tēmu:
Pharmaceutical companies, academic researchers, and government agencies such as the Food and Drug Administration and the National Institutes of Health all possess large quantities of clinical research data. If these data were shared more widely within and across sectors, the resulting research advances derived from data pooling and analysis could improve public health, enhance patient safety, and spur drug development. Data sharing can also increase public trust in clinical trials and conclusions derived from them by lending transparency to the clinical research process. Much of this information, however, is never shared. Retention of clinical research data by investigators and within organizations may represent lost opportunities in biomedical research. Despite the potential benefits that could be accrued from pooling and analysis of shared data, barriers to data sharing faced by researchers in industry include concerns about data mining, erroneous secondary analyses of data, and unwarranted litigation, as well as a desire to protect confidential commercial information. Academic partners face significant cultural barriers to sharing data and participating in longer term collaborative efforts that stem from a desire to protect intellectual autonomy and a career advancement system built on priority of publication and citation requirements. Some barriers, like the need to protect patient privacy, pre- sent challenges for both sectors. Looking ahead, there are also a number of technical challenges to be faced in analyzing potentially large and heterogeneous datasets. This public workshop focused on strategies to facilitate sharing of clinical research data in order to advance scientific knowledge and public health. While the workshop focused on sharing of data from preplanned interventional studies of human subjects, models and projects involving sharing of other clinical data types were considered to the extent that they provided lessons learned and best practices. The workshop objectives were to examine the benefits of sharing of clinical research data from all sectors and among these sectors, including, for example: benefits to the research and development enterprise and benefits to the analysis of safety and efficacy. Sharing Clinical Research Data: Workshop Summary identifies barriers and challenges to sharing clinical research data, explores strategies to address these barriers and challenges, including identifying priority actions and "low-hanging fruit" opportunities, and discusses strategies for using these potentially large datasets to facilitate scientific and public health advances.
Acronyms xxi
1 Introduction and Themes of the Workshop
1(8)
Organization of the Report
2(2)
Themes of the Workshop
4(5)
2 The Benefits of Data Sharing
9(10)
The Uses of Shared Participant-Level Data
11(1)
The Rationale for Data Sharing
12(5)
Cautions on Data Sharing
17(2)
3 Barriers to Data Sharing
19(8)
Legal Issues Relating to Patient Privacy
20(2)
Cultural Barriers
22(3)
Technical Challenges
25(2)
4 Models of Data Sharing
27(16)
ClinicalTrials.gov
28(3)
The DataSphere Project
31(1)
The Yale-Medtronic Experience
32(4)
The Biomarkers Consortium
36(1)
The NEWMEDS Consortium
37(2)
PatientsLikeMe
39(1)
Distributed Systems for Clinical Research Information Sharing
40(3)
5 Standardization to Enhance Data Sharing
43(14)
How Standards Benefit Sharing
44(3)
Developing Standards to Enable Data Sharing
47(3)
Retrospective Versus Prospective Approaches to Data Standardization
50(1)
Data-Sharing Approaches That Have Benefited from the Use of Standards
51(3)
Governance Issues
54(3)
6 Changing the Culture of Research
57(16)
The Role of Regulators
58(2)
The Role of Journals
60(1)
The Role of Funders
61(2)
Incentivizing Change by Ensuring Credit
63(2)
Protecting Against Misuse of Shared Data
65(1)
Patient-Driven Sharing of Clinical Research Data
66(7)
7 Final Reflections On Sharing Clinical Research Data
73(8)
Low-Hanging Fruit
74(1)
The Boundaries of Precompetitive Collaboration
75(1)
Partnering with Patients
76(5)
REFERENCES
81(4)
APPENDIXES
A Workshop Agenda
85(16)
B List of Data-Sharing Initiatives
101(4)
C Participant Biographies
105