Standardising data collection across High-Risk Foot Services (HRFS) nationally will create unprecedented opportunity for audit, benchmarking and collaborative research. However, routine collection of data is 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 there is potential to create a database of international standing. Further, services will have the means to evaluate service efficacy and resource allocation, and to direct service improvement.