| Search de-identified data from clinic visits at several Harvard-affiliated hospitals. | SHRINE |
The Shared Health Research Information Network (SHRINE) helps researchers overcome one of the greatest problems in population-based research: Compiling large groups of well-characterized patients. Eligible investigators may use the SHRINE web-based query tool to determine the aggregate total number of patients at participating hospitals who meet a given set of inclusion and exclusion criteria (currently demographics, diagnoses, medications, and selected laboratory values). Because counts are aggregate, patient privacy is protected.
These data will be most useful for investigators interested in:
In June of 2011, SHRINE held its first annual conference entitled "Guiding the Emergence of Bottom-up EHR-Driven National Research Networks." Nearly 100 people, representing over 50 different institutions from 20 states across the US and 5 European countries, convened in the Countway Library on the HMS campus to discuss the technical and regulatory/ethical aspects of shared health research Information networks. The sessions' presentations are available at the conference website, where you can also find a link to SHRINE as open source code.
A pilot implementation of SHRINE as a demonstration of the feasibility of a national research network.
Of leading experts discussing SHRINE at the 2011 conference.