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Publication

[MI] National Data Opt-Out, February 2019

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Publication date:
Geographic coverage:
England
Geographical granularity:
GP practices, Clinical Commissioning Groups, Sustainability and Transformation Partnerships, Clinical Commissioning Regions, Regions, Country, Local Authorities
Date range:
Snapshot on 04 Feb 2019

Summary

This publication provides statistics on the number of unique NHS numbers with an associated national data opt-out. The national data opt-out was introduced on 25 May 2018. It was introduced following recommendations from the National Data Guardian. It indicates that a patient does not want their confidential patient information to be shared for purposes beyond their individual care across the health and care system in England. The service allows individuals to set a national data opt-out or reverse a previously set opt-out. It replaced the previous type 2 opt-outs which patients registered via their GP Practice.

Previous type 2 opt-outs have been converted to national data opt-outs each month, until November 2018. This is why the monthly increase in opt-outs decreases from December 2018 onward.

This publication includes the number of people who have a national data opt-out, broken down by age, gender and a variety of geographical breakdowns.

Key facts

NDOP Key Facts.  1,638,667 national data opt outs were registered as at 4 February 2019, 857 more than at 1 January 2019.

Resources

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Last edited: 22 February 2019 2:25 pm