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Systematic Review Data Repository (SRDR™)
The Systematic Review Data Repository (SRDR™) was developed by the Tufts Evidence-based Practice Center (EPC), Boston, Massachusetts, under contract with the Agency for Healthcare
Research and Quality (AHRQ), Rockville, MD (Contract No. HHSA 290-2007-10055-I).
What Is the Systematic Review Data Repository
(SRDR)?• SRDR is a powerful and easy-to-use, Web-
based tool for conducting systematic reviews.
• Searchable archive of key questions from included systematic reviews, and of data from their associated studies.
2http://srdr.ahrq.gov
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A repository for SR data will improve efficiency, data quality, transparency, and usability.
Why SRDR?
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Potential SRDR User
http://srdr.ahrq.gov
Funders of ResearchPatients
Policy Makers, Stakeholders
Independent Researchers
Research Centers
System Status
• System has been in development for 2 years • Launched in June 20th 2012• Hosted on the AHRQ server • Trademarked as Systematic Review Data Repository
(SRDR)• SRDR is committed to a policy of Open Access. All
completed systematic review projects deposited in the SRDR archive are publically available under the terms of a Creative Commons license.
• Initial data contributors will be members of the EPC and other participating organizations
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Privileges of SRDR UsersPublic
• Can view any study within the database, but cannot post comments.
Commentator• Privileges of public viewer • Can post comments on studies
Contributors• Privileges of commentator• Can modify any study they create under the project they collaborate on• View other studies within their project but cannot edit them• See project details but cannot edit them• View the extraction form but cannot edit it
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Current Features • Interfaces for creating extraction forms and extracting study data are in
place, with improvements being continually implemented• Certified data contributors may create extraction form templates and
extract data into the system• Upon completion of a systematic review project, users may choose to
release their extraction forms and corresponding data to the public • Tools for data retrieval/summarization and sharing have been
developed, with new features in the pipeline• Training materials including user manual, instructional videos, and an
FAQ are available in the Help section linked to the SRDR homepage• Certification procedures and training for data contributors are in place• Plans for user support and data backups have been put into practice
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SRDR Home Page AHRQ banner
Latest published projects Data
Commentator and Contributors login
Link to ‘Testing Site’
Steps for Data Contributor
Create Project
Enter Key Question(s)
Create Extraction Form(s)
Extract Study Data
Review and Publish Report Data
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System Structure
• Project: All data deposited within the SRDR are organized as individual projects. A project contains all information related to one systematic review (e.g., extraction forms, key questions, extracted studies, etc.)
• Key Question(s): The specific scientific queries an SRDR project is intended to address. All projects must include at least one key question
• Extraction Form: The user-defined dialogue by which collaborators extract data from relevant publications into an SRDR project
• Study: An individual publication extraction, consisting of one instance of a filled out extraction form
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Data Contributor Certification Process
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Step 1
•Attend training session conducted by the SRDR team
Step 2
•Enter 2 training cases into SRDR training site
Step 3
•Have the first few records entered to the production site reviewed by SRDR team prior to ‘publication’ in the system.
Step 4
•Change the status from ‘New user’ to ‘Certified user’
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Support Plan
Online support • The SRDR system will offer free online support to all user types along
with a user manual and instructional videos. • Another support platform is the user-supported forum where reviewers
are encouraged to post, as well as answer questions. The SRDR Support Team will also monitor the forums and answer questions.
Direct Support• Direct support is also available at no cost to the user.• Direct support would provide guidance for activities such as setting up
the review, importing of search results, and reviewing specific help/suggestions about optimal use of the software.
• Technical and content questions/issues will be referred to the Technical Team via the following methods:• Automatically – user will use the FEEDBACK feature in the system• Phone/email – individual user and/or ‘SRDR Administrator’ will refer the
question/issue to the SRDR Support Team15http://srdr.ahrq.gov
What Are the Benefits of SRDR?
SRDR can save valuable time by:
• Downloading study information from PubMed® (and from other databases in the near future) automatically.
• Quickly creating complex extraction forms, which can accommodate any study design or research question via the form design tool’s powerful and flexible “question builder” capability.
• Enabling easy comparison and reconciliation of double data extractions.
• Seamlessly saving all data online. (You can also export your data in a variety of formats for local backup, printing, or analysis using your favorite software package.)
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Other Benefits
• SRDR’s built-in messaging and commenting system makes it easy to coordinate with team members.
• SRDR can be easily incorporated into workflow. • Plan to integrated with other systematic review tools
such as Abstracker and OpenMeta.• In addition to creating and managing systematic
review projects, you can search completed projects that have been submitted to the public archive, and easily update your files, copying previously extracted study data into your own.
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How Can We Get Started?
The SRDR Web site contains a user’s manual as well as instructional videos to help you get the most out of
this powerful tool. To get started, or to learn more, just visit
www.srdr.ahrq.gov
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