Linking SDTM / ODM for better FDA Submissions of clinical data
A forum for discussing topics related to Electronic Data Capture and Clinical Data Management.
Thursday, April 1, 2010
If this is not already underway, I think it is time that we examined how we can do a better job of combining SDTM data submissions with ODM data and metadata. The following commentary is hopefully going to raise some comments, and, ideas as to next steps.
CDISC SDTM - the standard for the Submission of Clinical Data for New Drug Applications - is challenging to work with for a number of reasons. Data is structured per Domain, rather than per CRF - quite rightly in my view - however, this re-modeling does create a number of issues that deserve to be addressed.
First of all - getting the data into this format in the first place. In a typical EDC system, you have data captured across many pages. Often these pages contain 1 or more domains for data. Data is presented in nice friendly CRF Page like formats, with quick links to audit trails, queries, comments etc. In the SDTM world, things are not quiet as friendly. You have long lists of records structured by domain. You cannot see the audit trail. You struggle to relate the comments. The queries may not even exist.
Now - ok - maybe the audit trail and query log should be of no significant relevance to the Medical Reviewers... It is supposedly more evidence of the data cleaning process having taken place. Maybe that is just a carry over from working with paper CRF's for decades. However,I would argue that data is never 100% clean. It is sufficiently clean to merit safe statistical analysis. Reviewers may feel that in a position of doubt, that they would like to see context behind the data being recorded, and therefore see the query and audit logs.
So - after that short ramble - how could we make the life for Reviewers better?
Combining ODM with SDTM
Well, first of all, why not leverage the standards we already have for clinical data - ODM and SDTM - but combine them in a more effective way to offer SDTM directly linked to ODM?
What I mean by this - and I am sure XML4Pharma will point out that this has been suggested previously - is that we extend the ODM specification to accommodate SDTM Domains within the ODM spec, AND that we provide the means to link the SDTM domain content with the associated eCRF data & metadata in the present ODM.
To the end user - this would result in a mechanism to switch between a tabular SDTM view of data to an eCRF view of data, with ready access to the audit trail and queries, as well as potentially a better context of the data in the way it was captured.
Easy to achieve?
Sponsors struggle to create SDTM today. However, I am not certain that this is due to underlying faults in SDTM itself. I think the tools will mature, the standards will mature, and sponsor companies will simply get better at it.
Creating related ODM is also not too difficult. Any EDC vendor for instance that wish to be credible in the marketplace need to be able to offer data and metadata in the CDISC ODM format.
Programmatically linking the SDTM and ODM is probably the hardest part.
In theory, you could have a situation where every field that exists on a SDTM records belongs to a separate ODM page instance. The problem can be solved, but, it is not going to be easy.
Delivering SDTM data in a ODM style format, and creating a means to link the SDTM/ODM to the present ODM data and metadata will create data that is considerably more useful for both analysis, submission and archiving.
Posted by EDC Consultant at 10:38 AM