Following initial discussions with Outcomes Managers at NOA member trusts WWL and RJAH, this meeting explored the creation of an NOA working group dedicated to Outcomes.
Outcomes data collection can mean different things to different people, ranging from PROMs data collection to national registries submission, to local data collection initiatives. The process needs clinical support and guidance, but the administrative support cannot be underestimated. Many decisions regarding data collection and registries are taken nationally with little consultation from Providers.
If you are interested or have any comments please email email@example.com.