Dataset version 5 feedback

Thank you to everyone who provided feedback on the proposed version 5 of the UKRR dataset.

Our responses to key queries can be found below.

The full list of feedback and responses can be viewed here


Thank you. Full details are at

In brief – for items such as medication, the entire list is sent in each file.

The UKRR will drop any existing list and replace it with the new submission.

For Observations and LabOrders it works like PatientView (with new data submitted between two dates sent in the submission file).

This took longer to finalise than we expected, so we added it in mid-November and extended the consultation by two weeks.

We will add specific new items consistent with LOINC, and retain the current one for historical values where we do not know the method or ethnicity correction.

We have tried to contact the author by email to explore this concern.

At the UKRR, we believe that the 'future care intentions' items allow people to be identified as preferring supportive rather than dialysis care in the future and that the definition here is to give centres a chance to identify ESRD not treated with dialysis.

We have had discussions with the main system suppliers and are advertising that we are keen to work with any who wish to develop a UKRDC feed.

We are pleased that we are getting an increasing number of enquiries from system suppliers to work with us.

Commissioning is changing to ICB(S) who will have a greater interest in the whole pathway.

Others within the UKKA, and respondents to the consultation, have welcomed the inclusion of CKD4/5 under the care of renal centres.

We are also well aware that if we wish centres to improve the quality of the data in the UKRR feed, they will need to identify where those errors are to allow them to amend the data in their renal centre system.

We are scoping tools to do this, starting with a tool to allow centres to see which and why files failed to load.

The UKRR are trying to provide a means to compare treatment between centres.

It is likely to be for others (esp. the commissioners guided by clinicians) to mandate/encourage data collection.

Any new validation will only be on recent items.

We have reduced the number of items and are no longer collecting derived items (which so often cause problems). Overall we do not intend to increase the number of queries.


NICE accredited clinical practice guidelines 

Available here

23rd Annual Report

Analyses about the care provided to patients at UK renal centres.

Read the report


A report on the nationwide collection of AKI warning test scores. 

Read the report