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August 22, 2010

Dr Phil’s Private Eye Column Issue 1269 20.8.10
Filed under: Private Eye — Tags: , , — Dr. Phil @ 1:01 pm

Rewarding Whistleblowers

Well done Channel 4 News and the Bureau of Investigative Journalism for their exposure of the widespread use of taxpayers’ money to silence NHS whistleblowers (Ch 4 news, 2.8.10). Many employment contracts still have gagging clauses and most doctors who invoke the Public Interest Disclosure Act (PIDA) to raise concerns about unsafe or fraudulent practice reach a settlement with their employer to prevent concerns being made public. Superficially, this smells of whistleblowers bottling it and taking the money, but when you look at the experience of those who refuse to be silenced, there’s no great incentive to do the right thing.

The NHS’s most famous whistleblower, Dr (now Professor) Stephen Bolsin, was praised in Parliament for raising concerns about standards of child heart surgery in Bristol nearly 20 years ago, and his actions were fully vindicated by a Public Inquiry. Yet he became unemployable in the NHS and relocated to Australia, where he continued his excellent work in monitoring clinical outcomes. Had Bolsin remained in the NHS, it is inconceivable that small units would have been allowed to continue operating and the Oxford heart scandal would have been avoided (Eye last).

If Andrew Lansley is genuine in his desire to support whistleblowers, he should consider formal recognition of Bolsin’s bravery1. The Mid Staffs inquiry will doubtless show that staff were either too afraid to blow the whistle, or too easily silenced, despite the many avoidable deaths occurring around them. NHS whistleblowers are vulnerable and isolated, and have few role models. The public recognition of Bolsin’s legacy would go some way to making it acceptable to speak up.
For whistleblowers who want to go the distance, the best chance of being heard is to go to court. In the UK, any payouts tend to be swallowed up by legal expenses and loss of earnings. But in the US, whistleblowers are rewarded handsomely if they help the government bring a successful case. In May, the New England Journal of Medicine followed up 26 successful whistleblowers from the pharmaceutical industry 2. On average each received $3 million for speaking up, with the range going from $100,000 to $42 million. Last September, Pfizer paid $2.3 billion to settle allegations that they illegally marketed a painkiller, Bextra, which has now been withdrawn. A proportion of the settlement was divided between the 6 whistleblowers.

Whistleblowers are rarely motivated by money, and nearly all try to ‘go through the correct channels’ first before going public. And even a large payout is scant consolation for the emotional exhaustion and stress of speaking out. In May, an employment tribunal found that John Watkinson, a former chief executive of the Royal Cornwall NHS Trust, was sacked for blowing the whistle on the failure of the Trust and Strategic Health Authority to consult the public adequately before moving cancer services. An independent review has now agreed that public consultation was inadequate, but the Trust is appealing against the tribunal findings. They accept that Watkinson was unfairly dismissed but challenge that he was a whistleblower, wary off the unlimited damages that are supposed to be awarded to sacked whistleblowers under PIDA. In the meantime, Watkinson remains unemployed – and like Bolsin, probably unemployable in the NHS.

As well as publically recognizing whistleblowers, Lansley needs to place a statutory duty on all NHS employers to report all serious concerns about patient safety or fraud to the Care Quality Commission (CQC) and Monitor for investigation and publication. Gagging clauses, and attempts to buy the silence of public sector workers raising genuine concerns in the public interest, must be outlawed. Whether the CQC and Monitor have the independence, expertise and resources to deal with all the NHS’s dirty secrets remains to be seen, but the practice of damage limitation, either by paying off staff or ordering secret ‘independent’ inquiries that never see the light of day, must end.

1 www.steve-bolsin.com/ 2 www.nejm.org/doi/full/10.1056/NEJMsr0912039



  • http://lookingatlyme.blogspot.com/ J Drayson

    CQC now there’s a thought but having just tried them got nowhere so where now?

    My problem is like many hundreds more in the UK trying to access appropriate treatment in the UK for Lyme Disease.

    Sadly the response from the ‘expert’ at HPA seems to follow a very restricted view, that by the discredited 2006 Guideline authors. Who say there is no such thing as chronic lyme or persistent infection when it comes to their guidelines for treating patients despite the fact they wrote research to the contrary and acknowledged Chronic Lyme and persistent infection when applying for patents on vaccines.

    The problem is that they are ‘guidelines’ which are being used by the ‘expert’ as mandatory here in the UK so that doctors are told not to treat on long term antibiotics ( the fact that Borrelia a sirochetal illness like syphilis but far more complex, is as complex as TB and Leprosy, who ever would treat any of those illnesses on just a couple of weeks antibiotics).

    In fact the ‘expert’ goes even further and threatens doctors that they risk their license by treating us following International Lyme and Associated Disease Society http://www.ilads.org

    She has even reported doctors to GMC for not following HPA guidelines although in the case of my doctor there was found no case to answer.

    So any advice as to where we go to get this investigated letters to HPA from patients, doctors, patient advocates and politicians have got us no where, any suggestions would be welcome.

    I am one of the few lucky people whose GP treated me despite the ‘expert’ advice and I have recovered following ILADS treatment by my GP and supporting private doctor. At my worst I had difficulty standing and walking across a room I was not able to walk up or down starirs properly for 3 1/2 years due to arthritis and muscle weakness, was Retired early from the Civil Service on Ill Health Grounds but now after many months antibiotics I can cycle and garden I have no pain and no disability life is a joy.

    My story is like so many more but not everyone gets diagnosed and not everyone can afford private treatment or has such an enlightened GP as me.

    So any advice would be welcomed.

    http://lookingatlyme.blogspot.com/

  • D Havercroft

    For the regulators CQC and Monitor to deal with the NHS’s dirty secrets requires them first to ferret them out. What hope is there when, in the case of the Bristol Histopathology Scandal, Monitor was only informed of the misdiagnoses allegations in a routine phone call with John Savage the UHB Chair on 1st June 2009, conveniently only 9 days before Dr Phil broke the story in Private Eye?

    Around the same time as the Foundation Trust Governors were informed, I believe.

    I have a Freedom of Information response due from CQC by 13th September to find out when they knew about the allegations, and by what means.