- From: Carini, Simona <Simona.Carini@ucsf.edu>
- Date: Fri, 2 Aug 2013 19:03:32 +0000
- To: "Andrea Splendiani" <andrea.splendiani@iscb.org>
- cc: HCLS <public-semweb-lifesci@w3.org>
- Message-ID: <4F5C368E3BADAF479EE3B307344FA3C90CFD3745@ex08.net.ucsf.edu>
Hello Andrea, in this paper: Ross J, Tu S, Carini S, Sim I. Analysis of eligibility criteria complexity in clinical trials. http://www.ncbi.nlm.nih.gov/pubmed/21347148 we describe the results of analyzing a sample of 1000 eligibility criteria extracted for ClinicalTrials.gov. (I don't see it in the list generated by Google Scholar.) Regards, Simona ________________________________ From: Michel Dumontier [michel.dumontier@gmail.com] Sent: Tuesday, July 23, 2013 12:43 AM To: Andrea Splendiani Cc: Kathrin Dentler; HCLS Subject: Re: Standards for inclusion/exclusion criteria ? Google Scholar says: http://scholar.google.ca/scholar?cites=18026669919486573499&as_sdt=2005&sciodt=0,5&hl=en m. On Mon, Jul 22, 2013 at 5:09 PM, Andrea Splendiani <andrea.splendiani@iscb.org<mailto:andrea.splendiani@iscb.org>> wrote: HI, thanks and sorry for the late reply. I have been doing a bit of reading. Let's say I am up2date until more or less the date of your review (2007). First, I wonder if something new come out since then (rather than evolutions of approaches/standards already existing). Second, I got the impression that rationales to standardize clinical trials criteria vary a lot. Mining EHRs for candidates has different requirements from criteria re-use, which in turns has different requirements from (trials) discovery. I was looking for some sampling of criteria in use in clinical trials. Could not find anything (at least open). Does anybody have some pointer in this direction ? best, Andrea Il giorno 15/lug/2013, alle ore 07:21, Kathrin Dentler <k.dentler@vu.nl<mailto:k.dentler@vu.nl>> ha scritto: > Hi Andrea, > > For a first broad overview, this paper is a good starting point: > Formal representation of eligibility criteria: A literature review > http://www.sciencedirect.com/science/article/pii/S1532046409001592 > > For CDISC, there is ongoing work on OWL/RDF formats: > http://www.cancer.gov/cancertopics/cancerlibrary/terminologyresources/cdisc > http://kerfors.blogspot.nl/2012/05/semantic-models-for-cdisc-based.html > > Best, > Kathrin > > > > Op 7/15/13 1:34 AM, Andrea Splendiani schreef: >> Hi, >> >> I was wondering if somebody could provide some pointer to work going on in an area that is related to clinical trials: inclusion and exclusion criteria. >> (I have followed the recent thread on encoding Hamilton Disease and pointers). >> >> In, particular, I am interested in two things: >> Standards with substantial uptake (sub question: is CDISC's uptake actual or perspective ?). >> >> Modeling of inclusion/exclusion criteria, but with a particular twist: not modeling the questions, but the facts that are queried. Basically I am interested in modeling patients and conditions (to the level of detail required "usually" required by clinical trials). The subject itself can be very vast, but is there a framework which provides at least an upper perspective on how to model subjects's features, diseases, interventions, samples (also respect to time) ? >> >> Any pointer is welcome! >> >> best, >> Andrea Splendiani >> >> > > > -- > Kathrin Dentler > > AI Department | Department of Medical Informatics > Faculty of Sciences | Academic Medical Center > Vrije Universiteit | Universiteit van Amsterdam > k.dentler@vu.nl<mailto:k.dentler@vu.nl> | k.dentler@amc.uva.nl<mailto:k.dentler@amc.uva.nl> > > http://www.few.vu.nl/~kdr250/ > > -- Michel Dumontier Associate Professor of Bioinformatics, Carleton University Chair, W3C Semantic Web for Health Care and the Life Sciences Interest Group http://dumontierlab.com
Received on Sunday, 4 August 2013 11:53:13 UTC