In NZ Optics April 2018 issue, a frustrated Chalkeyes pondered: “Imagine if our clinical data could be anonymous and pooled. What learning is hidden in those little boxes on our screens from all our patients across the country or even the world¹?”
I couldn’t agree more. Why are we wasting all this useful data? Is it just mutual mistrust that makes the main players in our eyecare world so reluctant to share?
There is, however, one project which does pool this data. Sydney eye surgeon Professor Mark Gillies and his Fight Retinal Blindness! (FRB) team already use data from clinical examinations to run medical research and clinical audits². They have a web-based application, which was developed using freely available tools, allowing anyone with a decent web browser to access an ‘on screen’ form to be completed at the clinical interview. The results are then sent automatically to, and analysed by, the University of Sydney.
From this wealth of data, 15 clinical papers have already been penned³ and their data definitions shared publicly via the International Consortium for Health Outcomes Measurement (ICHOM) project. At present FRB uses CSV (comma separated values) as the import/export medium for their data.
So, are there not other standard ways of sharing more of our data? Yes, but there are issues of data ‘ownership’ here, and this has become very topical, especially with the implementation of the European Union’s data standards on 25 May 2018. Europe’s General Data Protection Regulation (GDPR) affirms that the protection of natural persons in relation to the processing of personal data is a ‘fundamental right’ and that any ‘processing of personal data should be designed to serve mankind’. This has had a ripple effect worldwide and is fast becoming the de facto global standard.









