Standardising data collection across High-Risk Foot Services (HRFS) nationally has created unprecedented opportunity for audit, benchmarking and collaborative research. Routine collection of data presents a challenge for most services, primarily due to the time and resources required to establish a database. This became increasingly apparent following the introduction of formalised service accreditation in 2019 by the National Association of Diabetes Centres (NADC).
To realise the implementation of a national database, a minimum dataset was developed by several clinicians involved in Australian HRFS, integrating recommendations previously published by Diabetes Feet Australia. The dataset was developed into user-friendly, accessible and free electronic data collection forms. With uptake of this platform across Australia we are realising the potential to create a registry of international standing. Further, participating services have the means to evaluate service efficacy and resource allocation, and to direct quality improvement. A suite of online resources is available to support the quality improvement cycle.
By participating your service is joining a national collaboration of future-ready, likeminded, and enthusiastic clinicians. This investigative community has become a unique strength of the project and feeds its ongoing evolution. Access is provided to virtual meetings, an online communication portal and the database resource library, with sharing of thoughts and knowledge encouraged.