Motivation and Overview on STARE-HI

3. STARE-HI - Guidelines for authors of
IT evaluation studies
a) Why STARE-HI (Jan Talmon)
b) STARE-HI: Guidelines for authors
Motivation
• Good reports will be referenced
• Good reports have influence on the
standing of the journal (IF)
• IJMI welcomes papers that evaluate HI in
a clinical setting
Current Situation
• Variability in reporting
• Nearly all papers fall short on a few
accounts
• Studies may be valid, but papers often
raise more questions then being answered
by the study
Main problems
•
•
•
•
Status of system unclear
Functionality of system unclear
No account for sample size (power)
Poor motivation for study design and
methods chosen
• Poor discussion, no critical attitude
• Not clear what lessons are learnt
3. STARE-HI - Guidelines for authors of
IT evaluation studies
a) Why STARE-HI
b) STARE-HI: Guidelines for authors
Aim of STARE-HI
•
STARE-HI = Standards for Reporting of Evaluation Studies in
Health Informatics
•
Provide guidelines on how to write an IT evaluation paper (a
paper reporting on an IT evaluation study).
•
To support
• Authors when writing a paper
• Reviewers and editors when assessing a paper
Development of STARE-HI (1/3)
•
Only adaption of CONOSRT or comparable guidelines for RCT?
•
Not really a solution, because
• There is more than RCT
• Socio-technical assessment
• Qualitative studies
• Specific issues of health informatics evaluaiton studies
Development of STARE-HI (2/3)
•
Input for STARE-HI draft:
•
Other recommendations such as CONSORT (RCT papers),
STARD (studies of diagnostic accuracy), INAHTA (HTA
reports), QUORUM (meta-analysis) etc.
•
Own experiences as authors, reviewers and editors
Development of STARE-HI (3/3)
•
Writing team of IT evaluation experts
• EFMI WG
• IMIA WG
• AMIA WG
Structure STARE-HI
•
Describes items that should be contained in the various sections
of an IT evaluation paper
•
•
•
•
•
•
Title and Abstract
Introduction
Method
Results
Discussion
Conclusion
Content of STARE-HI
•
•
•
•
•
1. Title
2. Abstract
3. Keywords
4. Conflict of Interest
5. Introduction
–
–
–
•
6.1 System details
6.2 Location
6.2 Study constraints, conditions and
context
7. Method and material
–
–
–
7.1 Study design/method description
7.2 Frame of reference
7.3 Participants
7. Method and material (cont)
–
–
–
–
•
•
8.1Baseline data
8.2 Study flow
8.3 Unexpected events
8.4 Outcome data
9. Discussion
–
–
•
•
•
7.4 Study duration
7.5 Outcome
7.6 Data acquisition
7.7 Data analysis
8. Results
–
–
–
–
6. Study context
–
–
–
•
5.1 Scientific background
5.2 Rationale for the study
5.3 Ojectives of the study
•
9.1 Discussion of Findings
9.2 Discussion of Methods
10. Conclusion
11. References
12. Appendices
How to proceed
•
•
•
•
•
•
•
•
•
•
Discussion at MIE2006
Revision 1
Discussion through EFMI-WG/IMIA-WG website
Revision 2
Discussion at AMIA2006
Solicit comments of editors of MI and general medicine
journals
Revision 3
Final round for comments
Final version
Submission to MI and general medicine journals