Aims
The only way to fill the gap between the need for clinical research and the availability of robust data is to directly extract such data from the ED’s Electronic Health Records (EHRs), avoiding dedicated, time-consuming data collection. Achieving this goal would enable distributed clinical research and allow clinical information to be leveraged to address a multitude of research questions.
Nonetheless, obtaining consistent data from EHRs is a complex task. While part of the data registered in EHRs is structured (as lab test results and vital parameters), most useful patient information is variably contained in free text (e.g. presence of signs and symptoms, suspected and confirmed diagnosis, anamnesis, etc.).
Moreover, as proactive follow-up of ED patients is also unfeasible for the above reasons, relying on existing different data sources is also needed to measure patients’ outcomes at the most appropriate time interval for the research question of interest. eCREAM closely adheres to the Open Science paradigm and is fully committed to putting FAIR principles (i.e., making data Findable, Accessible, Interoperable, and Re-usable) into practice, advocating the importance of data as a public good. We will consider the different data access needs of various end-users: clinicians, researchers, health policymakers, and citizens. Thus, eCREAM will implement different methods to make data readily available and re-usable by different stakeholders.
First, eCREAM will study the propensity of the ED to hospitalise patients. Second, eCREAM will exploit ED data to develop a dashboard to inform citizens in real-time about ED overcrowding and other characteristics, and policymakers about the possible emergence of specific epidemiological phenomena.
Project breakthrough
eCREAM will develop relevant lines of work with the following aims: