Author Archives: medcon

[PRESS RELEASE] Partridge Review: Patients need proof to restore confidence

For immediate release – Thursday 19 June 2014

In case you missed it, medConfidential’s initial response to the Partridge review is here: https://medconfidential.org/2014/press-release-patching-hscics-holes-medconfidential-initial-response-to-the-partridge-review/

Detailed analysis of the Partridge Review, published earlier this week [1], reveals a more disturbing picture than has yet been reported. While Sir Nick Partridge’s recommendations are to be welcomed and have been accepted, they have yet to be implemented and – more importantly – evidence must be provided that they are working. Such evidence will be essential to public confidence in the handling of NHS patient data.

The fact is that during a period when ministers and officials have been pushing for a massively increased amount of identifiable patient data to be extracted from the GP records of every man, woman and child in England to the Information Centre under the care.data scheme, serious issues at the Centre itself were either unknown or unresolved.

The largest single data breach in NHS history?

One of the more extraordinary revelations is that in at least two instances – as the list of releases cannot be guaranteed complete – the Information Centre cannot say where it sent patient data. Given that the instance involving the release of HES data was in 2010/11, the year after administration of HES releases was taken in-house, the suggestion that this may have been “an internal Northgate request for data” [6] seems inconsistent with the information provided.

Similarly, no evidence is provided to substantiate the assertion that “no identifiable or potentially identifiable data went missing” [7]. Indeed, the PwC report confirms only that the release in question “was not flagged as containing sensitive or identifiable data”; HES data is commonly provided as pseudonymised patient-level information, i.e. in re-identifiable form [8]. As no information has been provided as to the size of each HES release – which could be a partial extract or a year’s-worth of hospital episodes (tens of millions of dated events) – it is impossible to quantify the number of patients’ records involved.

That “no individual ever complained that their confidentiality had been breached as a result of data being shared or lost by the NHS IC” is beside the point. Up until now no-one knew their data had been lost and it is unlikely that most patients could determine the effects of inappropriate sharing or abuse. In fact there are cases, such as that of Helen Wilkinson [9], which show just how difficult it can be to remove stigmatising errors once propagated by central systems.

It is incorrect to state that no complaints have been made to the Information Commissioner’s Office. medConfidential and others made a complaint regarding the inappropriate and possibly unlawful uploading of 10 years’-worth of HES by PA Consulting (entry 1292 in the spreadsheet of 3,059 releases) to Google’s BigQuery servers [10], and a number of other ‘high profile cases’ are currently under investigation.

Insurers / re-insurers and commercial exploitation

The Secretary of State has repeatedly stated that use of NHS patient data “for commercial insurance or other purely commercial purposes” will be prohibited [11]. While it is to be welcomed that the HSCIC’s Chief Executive has written to three of the re-insurers who hold HES data asking them to delete it, we do not know whether those companies have even replied, much less complied with the request.

Assuming that deletion was part of the contract with the five other insurance companies listed [12], and every other release, it is concerning that the Review does not point to a single instance of an audited deletion of data. Specific mention is made of the suspension of research use, but no such action appears to have been taken in the case of commercial users (or re-users) of NHS patient data, which one can only assume still hold and process data [13].

Systemic failure

It has been claimed that failures were “not systemic”, but the evidence suggests otherwise. The clearest example of this is that when one study within the sample tested – 60 out of 591 MRIS releases – proved not to have the required ONS Legal Gateway approval, investigation of the remaining 90% revealed a further eight instances [2]. Sometimes the Information Centre followed policy and procedure, sometimes it didn’t; that is a systemic failing.

PwC confirms it used a “haphazard sampling” methodology [3] and clearly states there are too many “unknowns” to give “formal assurance or opinion” [4]. Because of failures in record keeping, and in some instances destruction of records, it cannot guarantee the “completeness of the data release list” nor whether the data released “has been used for the intended/stated purpose” [5].

We note that other instances of failure identified within chosen samples did not lead to similar investigations as with MRIS releases, or follow-up action. While we accept that time and resources were limited for this Review, it would be unsafe to conclude anything other than in quite a number of cases – certainly more than are listed in the PwC report, possibly ten times more, given the 10% sample – we simply don’t know what has happened to our data.

Phil Booth, coordinator of medConfidential [14], said:

“We welcome Sir Nick Partridge’s recommendations, but patients need to see the evidence that they’ve been acted on. Public confidence depends on actions, not just words.

“If patients are to trust that procedures and audit are working they must be provided proof of who has their own data, what they are using it for and when it has been deleted. If the systems being constructed for a 21st century NHS cannot provide these answers, they are not fit for purpose.

“Research has been a convenient fig leaf for NHS England when proposing the care.data scheme, but a picture is emerging of commercial companies who get preferential treatment at the head of the queue, while academics patiently languish on waiting lists.”

Notes for editors

1) Partridge Review documents: http://www.hscic.gov.uk/datareview

2) pp36-39, HSCIC Data Release Review PwC Final Report:http://www.hscic.gov.uk/media/14246/HSCIC-Data-Release-Review-PwC-Final-Report/pdf/HSCIC_Data_Release_Review_PwC_Final_Report.pdf

3) p81, HSCIC Data Release Review PwC Final Report: “Haphazard selection, in which the auditor selects the sample without following a structured technique… Haphazard selection is not appropriate when using statistical sampling.” This is not to suggest that such an approach was inappropriate in the time given for the review, more to indicate that conclusions cannot reliably be drawn since it is not a statistically based sampling methodology. Amongst auditors this form of testing is considered of minimal value since there is no assurance findings are representative.

4) p4, HSCIC Data Release Review PwC Final Report: “Given the number of ‘unknowns’ associated with this review due to the time period in question and the availability of historical records/evidence, no formal assurance or opinion have been provided over the findings that may be used by the HSCIC to publish their overall conclusions.”

5) pp4-5, HSCIC Data Release Review PwC Final Report.

6) p7, HSCIC Data Release Review PwC Final Report: “This left 2 data releases where it was not possible to identify the organisation that received the data based on the information retained by the NHS IC. One release related to HES data post April 2009. Further discussion with Northgate has indicated that this could relate to an internal Northgate request for data; however this could not be confirmed.”

7) Paragraph 15, Sir Nick Partridge’s summary of the Review:http://www.hscic.gov.uk/media/14244/Sir-Nick-Partridges-summary-of-the-review/pdf/Sir_Nick_Partridge%27s_summary_of_the_review.pdf

8) For an illustration of the information contained in HES and what can be done with it, see: https://medconfidential.org/2014/commercial-re-use-licences-for-hes-disappearing-webpages/

9) Helen Wilkinson was stigmatised as an alcoholic due to a coding error:http://www.theguardian.com/society/2006/nov/02/health.epublic And as debated in Parliament: http://www.theyworkforyou.com/debates/?id=2005-06-16b.495.0&s=helen+wilkinson#g495.2

10) medConfidential, FIPR & Big Brother Watch complaint re. upload of HES to Google servers: http://medconfidential.org/wp-content/uploads/2014/03/2014-03-13-ICO-PA-FIPR-complaint.pdf

12) As widely reported in February, e.g. the Guardian on 28/2/14:http://www.theguardian.com/society/2014/feb/28/nhs-data-will-not-be-sold-insurance-companies-jeremy-hunt

11) List of insurers and re-insurers who may still be holding HES and SUS data:

  • 143 Actuarial Profession Critical Illness Working Party – HES, 2011/12;
  • 602 FirstAssist – HES, 2012/13;
  • 603 Foresters Friendly Society – HES, 2007/8;
  • 1293 Pacific Life – HES, 2012/13;
  • 1339-42 RGA UK Services Limited – HES, 2009-2013 (Reinsurance Group of America);
  • 1381 Scottish Re – HES, 2008/9 (re-insurer, headquartered in the Cayman Islands);
  • 1517 Scor Global Life UK – HES, 2012/13 (re-insurer);
  • 2676 Milliman – SUS, 2012/13

13) Many of the websites of the commercial companies listed indicate that they are still offering services based on NHS data, e.g. Beacon Consulting, CHKS, Harvey Walsh, NHiS, etc.

14) medConfidential campaigns for confidentiality and consent in health and social care, seeking to ensure that every flow of data into, across and out of the NHS and care system is consensual, safe and transparent. Founded in January 2013, medConfidential is an independent, non-partisan organisation working with patients and medics, service users and care professionals.

For further information or for immediate or future interview, please contact Phil Booth, coordinator of medConfidential, on 07974 230 839 orphil@medconfidential.org

– ends –

[PRESS RELEASE] HSCIC’s lack of transparency is not so “innocent” after all

For immediate release – Wednesday 3 April 2014

The Health and Social Care Information Centre’s register of data releases, published at noon today, is incomplete and fails to reveal some of the most potentially embarrassing and damaging releases of patient data.

The register does list dozens of commercial companies that have received patient information in various forms over the past year, but fails to list companies known to be holding significant amounts of patient data under ongoing commercial licences.

For example, PA Consulting was awarded a licence for HES data in 2011 which was extended in 2012 to last until November 2015 [1]. The Information Commissioner’s Office is currently investigating a complaint by medConfidential, the Foundation for Information Policy Research (FIPR) and Big Brother Watch on PA Consulting’s uploading of this data to Google’s BigQuery cloud servers [2] so it is inconceivable that HSCIC is not aware the licence remains active.

Another significant omission is the lack of any Police Forces in the register. A Freedom of Information request revealed that Police Forces routinely request data about patients from HSCIC, and that data has been released in dozens of instances within the last year [3].

Phil Booth, coordinator of medConfidential, [4] said:

“Despite saying it has turned a new leaf, HSCIC is deliberately concealing releases of data that might cause itself, or ministers or other officials, embarrassment or political damage. The Information Centre’s lack of transparency is clearly not as “innocent” as its Chair has claimed. [5]

“HSCIC continues in its ridiculous assertion that pseudonymised data is not sensitive or identifiable when tools its customers have built show you can track individuals visit by visit through hospital – and with information published in press reports, social media posts or the date your child was born make it possible to pick out a named individual and read off their entire record. [6]

“Billions of patient records continue to be sold for commercial use without patients’ knowledge or consent, using as justification the very law that minsters have said provides additional safeguards. How long does HSCIC think it can get away with ignoring Jeremy Hunt’s promise to stamp out the commercial exploitation of NHS patients’ information?”

Notes for editors

1) See http://www.hscic.gov.uk/article/3948/Statement-Use-of-data-by-PA-consulting

2) See http://medconfidential.org/wp-content/uploads/2014/03/2014-03-13-ICO-PA-FIPR- complaint.pdf for medConfidential, FIPR and Big Brother Watch’s complaint to the ICO and http://www.theregister.co.uk/2014/03/04/tripleheaded_nhs_privacy_scare_after_hospital_data_rea ch_marketers_google/ for a description of what happened.

3) The FOI response states: “The Health & Social Care Information Centre (HSCIC) was formed on the 1 April 2013. Since the HSCIC was formed there have been 472 requests received from British Police Forces for information.” A spreadsheet detailing just 180 of these requests shows that 51 releases were made during the period covered by today’s register, all but 3 of which were made under Section 29(3) of the Data Protection Act – not under warrant or Court Order.

4) medConfidential campaigns for confidentiality and consent in health and social care, seeking to ensure that every flow of data into, across and out of the NHS and care system is consensual, safe and transparent. Founded in January 2013, medConfidential is an independent, non-partisan organisation working with patients and medics, service users and care professionals.

care.data opt out forms and letters available here: www.medconfidential.org/how-to-opt-out/

5) “Quite rightly however, the public are suspicious that these arrangements are in some way unfairly tipped in favour of the profit makers. This suspicion has been fuelled by our innocent lack of transparency.” Full text of Kingsley Manning’s speech at HC2014 conferencefile was (re)moved by HSCIC following this press release. This link is to a copy downloaded by medConfidential on 24/3/14.

6) See http://medconfidential.org/2014/commercial-re-use-licences-for-hes-disappearing-webpages/ for a screen grab and explanation of a tool developed by OmegaSolver – one of the companies listed in the register of releases – for use by pharmaceutical marketers.
For further information or for immediate or future interview, please contact Phil Booth, coordinator of medConfidential, on 07974 230 839 or phil@medconfidential.org

– ends –

 

HSCIC Board papers

The Board of the Health and Social Care Information Centre (HSCIC) rather unhelpfully publishes all of its documents within a single zip file, which makes them very hard to google. From November 2014, original documents are available on gov.UK. For your convenience and to assist HSCIC in its drive to become transparent, here is a copy of all of the Board papers, expanded:

June 2015 papers are provided as a published PDF (not zipped)

April 2015

March 2015:

28 January 2015:

27 November 2014

From November 2014 onwards, it seems the interesting material is all in “part 2” of the meeting,  in secret.

3rd September 2014

There was no August 2014 meeting

2 July 2014

4 June 2014

14 May 2014

 

03 April 2014

05 March 2014

 

05 February 2014

15 January 2014

4 December 2013

23 October 2013

September 2013

29 August 2013

19 June 2013

30 May 2013

26 April 2013

3 April 2013

 

care.data: the creep begins

If there were ever any doubts that NHS England’s first care.data upload, planned for next March, is anything more than a toe in the door, recent developments should quash them. Speaking at the BCS Primary Health Care Specialist Group’s annual conference a couple of weeks ago, Geraint Lewis (Chief Data Officer at NHS England) said that the current data spec would not yield enough information to be of use to researchers. In other words, it’s going to need some significant expansion.

And now, recently-published minutes of the Information Advisory Group (IAG) show that before the programme has even started, the Health and Social Care Information Centre has already been back for more. In an addendum to the first care.data request, they have sought to expand the range of agencies with access to ‘potentially identifiable’ patient data. Currently this data is available to commissioning bodies. HSCIC now wants to include ‘research bodies, information intermediaries, companies, charities’… oh, and ‘others.

The IGA that accompanies the application provides the following caveat:

This information governance assessment of the addendum is not classified in the summary sheet as either identifying or non-identifying because no assessment is made, or can reliably be made, of all of the possible additional disclosures of data to the wide variety of recipients that could result from this proposal

Ah, so this is all a bit of a shot in the dark then.

The HSCIC’s application, which can be seen here, further suggests that they could avoid troubling the IAG further by in future deciding for themselves on a case-by-case basis who can have access.

The IAG has firmly knocked back the application and sent the HSCIC away to think about it. It’s worth reading the IAG minutes in full because underneath the specific issue of the care.data addendum, the small nuances in the wording reveal a welter of problems and irritations.

Don’t take our word for it!

On the pages of this site you’ll find information about the planned extraction of medical records from GP surgeries. In particular we recommend that you read the whole of ‘What’s the Story?’ and follow up the links that we provide. All of these are to reputable sources, and mainly to NHS England’s own documents or those of their new Health and Social Care Information Centre.

Our aim has been to bring together the facts so that the public can understand what’s going on, and journalists can ensure that everything they write is based on the available evidence. We hope to save everyone the research leg-work that would otherwise be necessary in order to understand a dauntingly complex story.

Politicians and NHS England have repeatedly stressed that all patient information will be anonymised. Recently one or two journalists have been quick to pick up on this mantra. But if you read ‘What’s the Story?’ you will see that this is not true. What they really mean is that patient data will be anonymised unless there is a legal exemption that allows the use of identifiable information. NHS England has obtained just such an exemption.

But don’t simply take our word for it. Please take a bit of time to read the detailed information and if you think it isn’t accurate, let us know and send us all relevant links so that we can correct it where necessary.

If you’re new to this whole issue, there is a simplified FAQ sheet here but note that this doesn’t contain any links.

NHS #1: What’s happening in England? The new legislation

You’ve probably gathered that a lot of reorganisation is going on within the NHS. The most obvious changes and difficulties have been well-reported, but others are passing pretty much unremarked. In particular changes to the way that patient information in England is collected, passed around and processed fundamentally alter the concept of doctor-patient confidentiality. That isn’t hyperbole.

It’s been quite difficult to write the blogs that follow because it’s so interwoven. Please read all of the blog posts in sequence and bear with us if the story loops back on itself or if we haven’t explained something clearly enough.

For the time being we have switched comments off. When we’ve finished our outline of the current state of play, we will put them back on so that you can leave your views, ask questions and tell us if you think we’ve got something wrong – for which we apologise in advance. The situation is changing all the time and all we can do is set out our current understanding of it. Once we have set out the basic framework, we will discuss some of the elements in greater detail and with a wider range of links.

And now to get down to business. The first step is to look at the legislative framework that allows your medical records to be used in surprising new ways.

The Health and Social Care Act 2012, which came into force on April 1st 2013, made some fundamental changes to the structure of the NHS. The ones that are of particular interest here are:

1)    The creation of the ‘NHS Commissioning Board’

2)    The creation of ‘Clinical Commissioning Groups’

3)    New powers that change the ‘Regulation of health care and associated professions’ into the ‘Regulation of health professions, social workers, other care workers etc’ – in other words, the creation of a new over-arching Health and Social Care Service

4)    And finally, the whole of Part 9 of the Act.  This creates another new body: ‘The Health and Social Care Information Centre’. It also sets out various powers and duties relating to the establishment of information systems (e.g. databases) and the central collection and dissemination of health and social care information about every individual in England.

Tomorrow we’ll explain how this new structure actually works.

NHS #2 The new structure

At the top of the new pyramid sits the National Health Service Commissioning Board (NHSCB). This is an arms-length body of the Department of Health responsible for spending the £95.6 billion budget of the NHS. Actually, it has now changed its name to ‘NHS England’ – the reasons for this change are set out in this letter from NHSCB to the Secretary of State – so if you see any reference to NHSCB or NHS England, it should be taken as meaning the same thing.

Primary Care Trusts have been abolished and their staff have been moved across to local authorities and 19 regional Commissioning Support Units (CSUs). Or made redundant. In theory, decisions about the provision of services in your area will now be made by Clinical Commissioning Groups (CCGs). These are local groups made up of representatives of every GP practice in the area, a nurse, a hospital doctor and other healthcare practitioners. In practice, many decisions will still be made centrally by NHS England or one of its 27 Local Area Teams (LATs).

The NHS Information Centre – up until now principally a statistical data warehouse – has been renamed the Health and Social Care Information Centre (HSCIC) that is now to act as a ‘hub’ for data flows inside and out of the NHS.

As the legislation shows, the HSCIC:

  • can be directed by NHS England (or the Secretary of State) ‘…to establish and operate a system for the collection or analysis of information of a description specified in the direction.’  (s254)
  • can require health and social care bodies, and any of their sub-contractors, to provide it ‘with any information which the Centre considers it necessary or expedient for the Centre to have…’ (s259)
  • can request information from anyone else
  • must publish statistical information that does not identify individuals and
  • ‘may disseminate (other than by way of publication), to any such persons and in such form and manner and at such times, as it considers appropriate’ any other information – including identifiable patient information – that it receives (s261)

The National Information Governance Board (NIGB) – the independent statutory body responsible for data handling procedures and practices across the NHS – has been abolished, leaving responsibility for how your confidential information is treated spread across a number of different groups: the Confidentiality Advisory Group (CAG), the Data Access Advisory Group (DAAG) and other Independent Advisory Groups, such as GPES IAG*. You will need more information about how the new structure works in order to understand their functions, so we will deal with them later.

For further reading about the changes, you may find this BMA explanation helpful.
An overview of the current trusts and authorities in the English NHS can be found here.

*@Bigjoe498 adds: The Confidentiality Advisory Group and the Health Research Authority are the only ones that can advise the Secretary of State to grant s251 approval for the release of identifiable data. The Data Access Advisory Group only deals with sensitive data items, which for HES (Hospital Episode Statistics) includes things like consultant code, referrer and census area. DAAG also look at consent forms to make sure they are explicit enough to release identifiable data for those who have consented using each form. The GPES Independent Advisory Group only advises the HSCIC about whether they should allow an extraction of GP data using GPES. The IAG has no standing in law to decide whether or not identifiable data can be shared outside the HSCIC.

NHS #3: General Practice Extraction Service – GPES

The next thing you need to know about at this stage is something called the General Practice Extraction Service or GPES. This is a tool for extracting patient data directly from the records held on GP surgery systems and transferring it to central HSCIC systems.

Sending data from a GP practice to an Information Centre is not new. Information about specific groups of patients – e.g. those with mental health problems – has been submitted in anonymised form for some time. The difference now is that, for the first time, information that identifies you will routinely be extracted from your GP-held records – even if that information was gathered elsewhere.

Details of diagnoses and treatments will be collected together with each patient’s NHS number, date of birth, postcode, gender, ethnicity and other information. It may be processed in regional Data Management Integration Centres (DMICs) or be sent directly to the HSCIC, still in identifiable form, to be processed, stored and disseminated to others.

The data will be made available to researchers in universities and hospitals, but also to private companies – in fact, to anyone who can make a case for access to the data. Although the precise arrangements for charging are not yet entirely clear, the existence of a pricing structure indicates that there will be a charge for this data.

NHS England repeatedly insists that the information will be ‘anonymised’ before release. In reality, the standard they are using requires that they ‘…ensure that, as far as it is reasonably practicable to do so, information published does not identify individuals.’ In other words, they will do their best to ensure that information cannot be re-identified as being about a specific patient, but there can be no guarantee.

It’s also clear that there are times when identifiable data (aka ‘Patient Confidential Data’ or PCD) will be made available – we will come back to that later. The next step here is to discuss what ‘anonymisation’ means and why it is such a misleading term.

NHS #4 ‘Anonymisation’

If you’ve ever played ‘twenty questions’, you will already know how easy it can be to identify an individual from a relatively small amount of information. Each question narrows down the field, and the more unusual the person’s attributes, the easier it becomes to guess who it is.The same principle applies to data. If we say that someone is male, that tells us only that he belongs to a group that represents one half of the population. By adding that he is aged 42 we reduce the size of that group, but we’re still not going to guess his identity.

Such general information isn’t likely to be of much use to researchers either. They are approaching their research from a different angle: they are likely to be investigating the unusual and are therefore looking for certain characteristics in their study subjects. The rarer those characteristics or the more of them in combination, the easier it becomes to identify individuals within the study. Consider, for example, a study examining the prevalence of skin disorders caused by exposure to the sun in red-headed males aged 40-45 who live in Devon and Cornwall.

The more data that can be linked together about an individual, the easier it becomes to find out who they are. Journalists and private investigators already know this – and so do large companies. There is a huge industry around data-matching aimed at identifying those who can be targeted with specific advertising and products.

Removing or obscuring pieces of information that most obviously identify a person doesn’t make data about them ‘anonymous’. And in any case, despite claims it will only ever share ‘anonymised’ data, NHS England has already applied for and been granted permission to pass around patient data in identifiable form. (We’ll explain more about that later)

So does it matter if you can be identified? Your answer might well depend on whether you suffer from a condition, or live in circumstances, that you would prefer to keep as a secret between you and your doctor. It might also depend on whether you are actually asked if you will participate in a research study. Probably most red-headed 42-year-olds would be happy to contribute to research that could conceivably help them, although even then they might want to draw some lines about what exactly is released.

The point is, people generally regard their medical records as private and want to keep control of access to them. They can talk to their doctors about highly sensitive and embarrassing things like sexual health problems, worries about their erratic moods or their alcohol intake precisely because they believe they are talking in confidence. If they are to continue talking to their doctors, they need to know that they will be asked for permission before that confidence is breached.

NHS #5: Consent

The burning question, then, is: ‘will your permission be asked before your medical information is uploaded?’ To which the answer is a straightforward ‘no’. The default position is that the uploads will go ahead unless you do something to stop them.

The original plan was that nobody would have any say about the use of their data. After concerns were expressed by doctors, NHS England agreed that there could be a ‘right to object’. Following our meeting with the health minister Jeremy Hunt, he announced that there would be a right to ‘opt out’ and that the 750,000 patients who had already opted out of the Summary Care Record would automatically have their existing opt-out respected.

On 29th May, NHS England published its guidance to GPs  which makes it clear that existing opt-outs will not be respected. Those who opted out of the previous, more limited upload of their Summary Care Record will now need to opt out all over again.

NHS England is currently in discussions with the Information Commissioner. The Information Commissioner’s Office is obviously concerned that patients should be made aware of the data-upload plans, informed of their ability to opt-out and given sufficient time to exercise it. It should be noted, though, that the ICO’s powers are limited by the way in which the legislation has been framed.

NHS England has prepared posters and leaflets for GPs to display in their surgeries. You may feel that these are short on detail. More informative is the patient leaflet prepared by EMIS one of the main suppliers of GP surgery systems.

Pilots of the care.data system are imminent. They will be taking place in 82 GP surgeries dotted around England. Meanwhile, all GP practices in the north of England have been told to be ready for the full roll-out within the next 8 weeks.