Cookie policy notice

By continuing to use this site you agree to our cookies policy below:
Since 26 May 2011, the law now states that cookies on websites can ony be used with your specific consent. Cookies allow us to ensure that you enjoy the best browsing experience.

This site is intended for health professionals only

At the heart of general practice since 1960

GPC calls for publicity campaign over 'fundamental change' in use of patient data

Exclusive The Government should launch a publicity campaign to ensure patients are aware of the ‘fundamental change’ that is being planned in the use of their personal medical data, the GPC has said.

Dr Paul Cundy, chair of the the GPC’s ICT subcommittee, said that patients needed to understand that identifiable and anonymised data from their GP records was going to be used for purposes other than their care.

Dr Cundy argued that the General Practice Extraction Service (GPES) - which will be used to extract patient data from GP systems routinely to manage the NHS and be available to regulators and private companies - marked a sea-change in the way patient data was used over the past 60 years.

But the NHS Commissioning Board said the use of patient data in GPES was ‘nothing new’ and rebuffed concerns that it would be used for performance management of GPs.

The GPES Information Governance Principles, which were agreed by the GPC and the HSCIC to lay out patients’ rights, said that using patient’s data for ‘secondary uses’ should be publicised through a ‘public website’, as well as general information about GPES being ‘available in practices’.

They add that a mechanism will be introduced into the GPES system so that a patient’s preference to be excluded from extracts by general practices for secondary uses will be captured.

But Dr Cundy says this does not go far enough and that the data could be used to performance manage GPs and said surveys have shown patients do not want their data to be used in this way.

He says: ‘There’s a great move at the moment to say that patient data in the NHS is there for use by the NHS, but that’s not the way data has been used for the past 60 years. That’s a fundamental change and patients need to understand that.

‘Most patients do not understand that their information may be used to police CCGs, trusts, GPs. If you ask patients, if you do MORI polls they say “No- I don’t want my information to be used in that way”’.

‘If we’re going to be moving to an area where it’s being used to routinely managed what’s going on in the NHS- which is a legitimate aspiration- then patients need to understand that.’

Related articles

As the DH consult on changing the NHS Constitution to make patients’ rights in relation to their data more clear, Dr Cundy called for a public information campaign so patients understand their data will be used for ‘secondary purposes’.

He said: ‘So I think were on the verge of a public information campaign for the populations which says that when you go to see your GP or go to A&E or to hospital- the information that’s been taken will not be used just for your personal care but for other things too.’

Dr Paul Thornton, a GP from Staffordshire and campaigner for patient privacy, said a publicity campaign could remind patients that they have not actually consented for their records to be used by GPES.

He said: ‘These are another example of patient data being given to third parties without the patients’ knowledge.

‘It’s a substantial erosion of the doctor/patient partnership. Perhaps patients will start to demand that obligations about data protection and confidentiality contained in the Data Protection Act are met.’

A spokesperson for the Health and Social Care Information Centre (HSCIC) said: ‘Keeping patients informed about who has access to patient data and how this information may be used has always been central to the GPES project.  Communication materials for patients are currently being developed and will be published online and in general practices in March 2013.’

A spokesperson from the NHS Commissioning Board said: ‘The collection and analysis of anonymised data for the improvement of patient care is nothing new and happens throughout the NHS.

‘High-quality, large-sample statistical data is of course vital for ensuring all commissioning and clinical decisions are based on evidence.

‘The Board is simply working to ensure available NHS data is collated and used to the best possible impact in delivering evidence-based care. The Board will not receive any identifiable data and has not requested this. The data will not be used for performance management.’

Readers' comments (2)

  • The logical extension of this is that patient IDENTIFABLE data will then be sold to the big private players who are coming in to replace the apparently not fit for purpose (HMG clueless because they can' t measure quality properly and there is the bigger agenda of privatisation by stealth) 'cottage industry' of current NHS General Practice; this data will then inform insurance premiums with high risk being uninsurable and the low risk being cherry picked by the private companies to make them lots of money- effectively the end of the NHS- what amazes me is that the Govt have managed to get so far a long this route without the media realising the implications..

    Unsuitable or offensive? Report this comment

  • This could be a fantastic way for the NHS to do cheap research on the effectiveness and safety of pharmaceutical products and medical devices.

    Examples

    > When women are prescribed Sodium Valproate and other anti convulsants how many women have children with special needs and disabilities, on what medication and on what dose? Fetal Anti Convulsant Syndrome.
    More information on FACS go to Organisation for Anti Convulsant Syndrome registered charity number: 1116497.

    > How many children prescribed antipsychotics go on to commit suicide compared to those who receive behavioural therapies?

    > What drugs given to premature babies cause complications and at what dose?

    Evidence based research conducted by professionals and endorsed by the Cochrane Institute should be encouraged.

    All patients should consent before information is shared.

    I want to be paid and asked for consent if my information is used by anyone other than the public parts of the NHS.

    My fear is that this is another way of making money. Information will be (at some point) sold on to pharmaceutical companies and misrepresented in journals in order to market, license and sell new products.
    The MHRA is not doing an adequate job in safeguarding public health as it is and this will be a further burden on an organisation not fit for purpose.

    Unsuitable or offensive? Report this comment

Have your say