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.

This project is a testimony to the power of collaboration. The enthusiastic involvement of a range of services across the country in this project and commitment to improving clinical care is sincerely appreciated. In addition to the people with diabetes-related foot disease who are represented in the data.