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Better Information Means Better Care: NHS contacts all English households from today
Since this news item published, certain details have now been superseded. Please see the care.data page for the most recent and up to date information.
Leaflets explaining how the NHS uses patient information will begin landing on the doormats of England’s 26.5 million households from today.
Over the next four weeks, every household in England will receive “Better Information Means Better Care”, a leaflet explaining the benefits of sharing information about the care they have received. Sharing information helps ensure that the quality and safety of services is consistent across the country and can also highlight different diseases and conditions that may require more NHS investment.
Households in the North of England will receive their leaflets this week, with the rest of England to follow during January, as announced in October.
As explained in the leaflet, patients have the right to object to their data being used for purposes other than their direct care. If patients wish to restrict their data being used then they should talk to their GP.
An information line has been set up for patients to call if they have any questions or concerns about how their data are used. The number is 0300 456 3531.
One of the great strengths of the NHS is that we treat millions of patients every week. Modern data techniques allow us to analyse the characteristics of all those patients, their treatments, and experiences to help us improve the quality of care for all. Using this combined information, we can now obtain low-cost answers to questions about the quality of care that would have been difficult or impossible to answer only a few years ago.
Dr Imran Rafi, Chair of the Clinical Innovation and Research Centre at the Royal College of General Practitioners said: “I fully support this initiative. GPs understand the importance of sharing information appropriately both as part of delivering clinical care and for wider uses, such as research and for planning NHS services. It is important that patients understand how the NHS uses and shares their information, and that they feel they have been given a proper choice to participate. The spin-off is the potential for all NHS patients to benefit
Dr Mark Davies, Medical Director at the Health and Social Care Information Centre, said: “The Health and Social Care Information Centre was set up as the legal ‘safe haven’ for protecting and managing patient information. We want everyone to feel confident that their information is kept private and used in non-identifiable form to improve the quality of health and social care for everyone. Equally important is that everyone knows that they have a choice and can raise an objection by simply talking to their GP.”
Dr Geraint Lewis, Chief Data Officer at NHS England, said: “The NHS has been collecting information like this from hospitals for decades but until now we’ve been missing information about the quality of care provided outside hospital. This initiative is about upgrading our information systems to get a more complete picture of the quality of care being delivered across all parts of the NHS and social care”
Dr Geraint Lewis, NHS England’s Chief Data Officer, explains why patients can be confident in agreeing to allow their health records to be shared:
Over the course of the next four weeks, every household in England will receive a leaflet, ‘Better Information Means Better Care’.
The leaflet explains how the NHS is upgrading its data systems and what people should do if they have any questions or concerns.
If you believed everything you read in the newspapers about this upgrade, you would think the NHS was either about to give away everyone’s confidential data free of charge or flog it to the highest bidder. Needless to say, we are doing no such thing: to do so would be unethical, illegal, and unconstitutional. But what actually is the plan?
Upgrading our Existing Data Systems
As the OECD reported recently, the NHS has some of the best health information systems in world. Dating back to the 1980s, we have been collating information about every hospital admission, nationwide. By pulling this information together and then analysing it in de-identified formats, analysts can compare the safety of different NHS hospitals, monitor trends in different diseases and treatments, and use the data to plan new health services.
At the moment, we are missing this type of information for much of the care provided outside hospital. We do not collect it nationally from all GP practices, for example, nor from ambulance trusts or community health services. As a result, we know worryingly little about how all the different parts of the NHS are working together to provide safe, joined-up care for patients. As the Chief Inspector of Hospitals put it, the NHS is currently “flying blind” in this regard.
So the purpose of the care.data project, which has secured support from the BMA and the RCGP, is to address these shortcomings. Building on the successes of our existing hospital episode statistics (HES) system, we will bring together all of this missing information in order to obtain a more rounded and more complete picture of the care being delivered by the health service.
As we’ve been doing for decades with hospital data, information from GP practices and other care settings will only be extracted as a series of codes, not as words and sentences. These codes will then be linked with a patient’s hospital codes using an automated system before being made available in three different data formats (see below). Each format is protected by a different suite of privacy safeguards as specified by the Information Commissioner’s code of practice on anonymisation. For simplicity, I refer to these formats as green, amber and red data, although their technical names are “anonymous or aggregated data”, “pseudonymised data”, and “personal confidential data”, respectively.
Green, Amber, and Red data
Green data are where we will publish the average values for large groups of patients or completely anonymous figures. For example, we might compare Ashford versus Bury in terms of the average time between presenting to a GP with bowel symptoms and having an operation for colon cancer. Green data are published free of charge for all to see. So before publishing green data, we take extra care not to publish information about rare conditions or any combinations of characteristics that might identify individuals from the data.
Amber data are where we remove each patient’s identifiers (their date of birth, postcode, and so on) and replace them with a meaningless pseudonym that bears no relationship to their “real world” identity. Amber data are essential for tracking how individuals interact with the different parts of the NHS and social care over time. For example, using amber data we can see how the NHS cares for cohorts of patients who are admitted repeatedly to hospital but who seldom visit their GP. In theory, a determined analyst could attempt to re-identify individuals within amber data by linking them to other data sets. For this reason, we never publish amber data. Instead, amber data are only made available under a legal contract to approved analysts for approved purposes. The contract stipulates how the data must be stored and protected, and how the data must be destroyed afterwards. Any attempt to re-identify an individual is strictly prohibited and there is a range of criminal and civil penalties for any infringements.
Over the years, many of the most innovative uses of amber hospital data have come from outside organisations, including universities, think-tanks and data analytics companies. We think it would be irresponsible not to make the maximum use of amber data for the benefit of patients. In future, we want charities and small academic units to be able to use amber data for the benefit of patients. Likewise, we think it would be wrong to exclude private companies simply on ideological grounds; instead, the test should be how the company wants to use the data to improve NHS care. And, as Polly Toynbee put it, if “it aids economic growth too, that’s to the good.”
Finally, in a few exceptional circumstances the HSCIC will make red data available where legally required to do so, for example in a public health emergency such as an epidemic. In the future, red data may also be made available to an organisation that has obtained the patient’s explicit consent or has been granted legal approval by the Secretary of State for Health or the Health Research Authority following independent advice from the Confidentiality Advisory Group (CAG).
CAG considers each application in great detail against the legal framework and recommends whether approval should be provided together with any conditions. Applicants for red data would need to demonstrate (i) that the research was in the public interest and for the benefit of the health service; and (ii) that it is not possible to use information that does not identify patients; and (iii) it is not possible to ask patients for their permission.
Patients have a choice
We want to make the most of the information that the NHS already collects. By drawing it together from all parts of the health service, not just hospitals, we will better be able to understand the causes of ill health, learn how to treat patients more efficiently, and find out what happens to patients after they leave hospital.
However, we are giving people a choice. If a patient is happy for their information to be used for these purposes then they do not need to do anything: there are no forms to complete and there is nothing to sign. But if they have any concerns, they can talk to their GP or contact the dedicated patient information line on 0300 456 3531
Ultimately, this is an opportunity for all of us to help the NHS deliver high quality care for all by making the most of the information collected about us.
- More information on the care.data programme is available here .
Geraint Lewis, FRCP FFPH is the Chief Data Officer of the National Health Service in England.
He trained in medicine at the University of Cambridge, and holds a Masters in Public Health from the London School of Hygiene and Tropical Medicine.
Dr Lewis worked in acute medicine and emergency medicine in the UK and Australia before specialising in public health.
He is the author of Mastering Public Health (a leading postgraduate text book on population health), as well as many peer-reviewed papers in journals such as Health Affairs, Milbank Quarterly and the British Medical Journal.
Dr Lewis was a 2007-08 Harkness Fellow in Health Care Policy and Practice based in New York. In 2008, he was awarded the National Director’s Award at the U.S. Department of Veterans’ Affairs and he was the 2011 recipient of the Bradshaw Lectureship of the Royal College of Physicians of London.
Dr Lewis was previously Senior Director for Clinical Outcomes and Analytics at Walgreens in Chicago, and was a Senior Fellow of the Nuffield Trust, a leading health policy think-tank based in London.
Have just discovered this website on 6 June. I am appalled that I have not received any information about this either from NHS or from my local practice. What ever have you been doing since January?
The implications of this development are both unethical and potentially damaging to all patients in UK. “Sharing” is just a euphemism for “selling”.
If it is so open; firstly why have we not received the leaflet (not has other people I know); and why does it need to be ‘opt out’ – how can you opt out if you haven’t had the leaflet.
In my opinion there is a massive smoke screen over how our data will be abused and sold so I will be opting out.
If companies want to use my data they can ask me and pay me.
Finally; there is too much big brother, casting privacy to the wind and I think it stops here.
I don’t want my data shared or sold to anyone
In my view, the term ‘sharing’ is being used a little inaccurately here as this initiative is really more about aggregation of data for internal (NHS) analysis in the expectation that there will be benefits to the quality of healthcare delivery. That may well be true and something that should be supported – bringing together all the silos of data is long overdue.
However, whilst this aggregated analysis is useful from a national, regional and local healthcare perspective, it misses out the individual. The rationale for undertaking this initiative equally well applies to each individual’s personal information as the availability of that in a single repository has numerous benefits. This should have been an essential part of this programme.
While welcoming this move I cannot help but note that this was first mentioned as going to be done about three – four months ago. I therefore find it strange that this is being portryed as something that is just now happening. Why was this campaign not done back in September when the idea was originally proposed?
Will NHS England/NHS Information Centre catagorically confirm that any health data collected will NOT be transferred overseas to be handled by agencies/call centres not based in the UK?