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271WH<br />
Candour in Health Care<br />
1 DECEMBER 2010<br />
Candour in Health Care<br />
272WH<br />
[Mr Robert Syms]<br />
into force in April 2010. That introduced a statutory<br />
requirement on health care organisations to report<br />
anonymously incidents that caused harm to the national<br />
incident reporting system. However, it did not include<br />
an equal requirement on the organisation to inform the<br />
patient or their relatives.<br />
T<strong>here</strong>fore, an organisation is not currently in breach<br />
of the regulations if it covers up an incident from<br />
patients or relatives. It may be bad practice, but t<strong>here</strong> is<br />
no real sanction as long as it sends an anonymous<br />
report to the system. An organisation will be ticked off<br />
if it does not send a report for the purposes of national<br />
measurement, but it will not be ticked off it fails to be<br />
open and honest with a patient or their relatives. Let me<br />
draw the Chamber’s attention to a document produced<br />
by Action against Medical Accidents entitled “The<br />
need for a statutory duty of candour in healthcare.” It is<br />
a good article for those who want to look at the more<br />
detailed requirements involved.<br />
I pay tribute to my constituents, Derek and Joan Bye.<br />
As MPs, we deal with many constituents, but Mr and<br />
Mrs Bye have had to put up with a horror story following<br />
the death of their daughter, Helenor Bye, who died on<br />
27 April 1978 in south Wales. T<strong>here</strong> was a catalogue of<br />
medical errors. The parents were lied to, records were<br />
altered and their MP, John Morris, then the right hon.<br />
Member for Aberavon, held a debate in the House of<br />
Commons on 27 November 1979, volume 974, columns<br />
1253-64. He called for a public inquiry, although that<br />
was turned down.<br />
The situation was compounded by the fact that body<br />
parts were taken from Helenor Bye, some of which have<br />
been returned over the years. The last time body parts<br />
were received by the parents was in 2005. They have<br />
been through the most horrific period because of what<br />
happened to their daughter, what happened subsequently<br />
and, more importantly, because all along the line they<br />
felt that they were being lied to and that people were not<br />
being open and honest. Mr and Mrs Bye have become<br />
doughty campaigners for a more honest and honourable<br />
system of health care. They have also campaigned on<br />
their concerns about the drug Epilim. I cannot do<br />
justice to that campaign today, but if any journalist<br />
wants to know what can go wrong, I advise them to<br />
look at the case of Mr and Mrs Bye. They have had a<br />
very rough time.<br />
Action against Medical Accidents calls for a change<br />
in the law and the introduction of a statutory duty of<br />
candour. It is called “Robbie’s law” because of the case<br />
of Robert Powell, who died on 17 April 1990, aged 10.<br />
His parents have campaigned for over 20 years to try<br />
and get justice. Similar things happened to them, such<br />
as changed medical records, and t<strong>here</strong> was a catalogue<br />
of events, but they still do not feel that they have justice.<br />
Their campaign has continued under several Secretaries<br />
of State. The case is currently with the Welsh Assembly,<br />
and Mr and Mrs Powell are waiting to hear whether<br />
t<strong>here</strong> will be a public inquiry into what happened to<br />
Robbie. Will Powell, who feels passionately about putting<br />
right what happened to his son and getting to the truth,<br />
has been a doughty campaigner for a long time. I pay<br />
tribute to him.<br />
All the people whom we are talking about are, in their<br />
own way, fighting for the truth, not only to find out<br />
what happened to their loved ones, but so that such<br />
things do not happen again to someone else. This<br />
debate is about setting out a context and a better way of<br />
doing things, so that we have a much more honest and<br />
honourable system and families do not have to spend<br />
10, 20 or 30 years going through absolute hell. Mr Bye<br />
told me that the start of the healing process is learning<br />
the truth and knowing what has happened to one’s<br />
relative. That is a very important point.<br />
The Government have two options to consider. They<br />
can go for an explicit duty or for more guidance. Ministers<br />
often go down the guidance route. When the NHS<br />
constitution was being debated in the previous <strong>Parliament</strong>,<br />
the then hon. Member for Wyre Forest, Dr Richard<br />
Taylor, who served with me on the Health Committee,<br />
raised the issue of openness and whether we could go<br />
further down that route. He was informed by the then<br />
Minister of State, Mike O’Brien, “No, we can do it all<br />
through guidance,” yet guidance so far has not produced<br />
the results that we need.<br />
Department of Health officials met representatives<br />
of Action against Medical Accidents and other stakeholders<br />
on 16 November 2010, when the two options were<br />
discussed in some detail. I shall go through the pros and<br />
cons of both. Option 1 is no new statutory duty but<br />
refreshed guidance in respect of the existing CQC<br />
regulations. The pros of that are that it would require<br />
no new legislation or change in the regulations.<br />
Dr John Pugh (Southport) (LD): Is not the difficulty<br />
with guidance the fact that guidance is already in place<br />
and any other guidance would simply reiterate what it<br />
says? Clearly, guidance by itself is not doing the trick in<br />
this case.<br />
Mr Syms: The hon. Gentleman makes a very important<br />
point, because we have to change the whole culture of<br />
the national health service and I am not sure whether<br />
guidance will do that.<br />
An argument can be made that the existing CQC<br />
regulations, backed up by clearer guidance, could be<br />
interpreted as making it a requirement to be open. For<br />
example, regulation 17 has been cited. It says that<br />
service users should be provided with adequate information<br />
and support in relation to their care or treatment. The<br />
guidance could clarify that that includes telling them if<br />
something has gone wrong. However, one of the cons is<br />
that, as the hon. Member for Southport (Dr Pugh) said,<br />
that would be in effect no different from the current<br />
situation. Such guidance and the existing regulations<br />
already existed when the policy to introduce a requirement<br />
was agreed. They were clearly not seen as sufficient<br />
then.<br />
Given that the Department of Health was of the firm<br />
opinion previously that the existing regulations, even<br />
with the guidance alongside them, did not constitute a<br />
statutory duty to be open with patients when things go<br />
wrong—because at that stage they were not supporting<br />
a statutory duty—it is hard to see how that could be<br />
credible now.<br />
Such a measure would be unlikely to be enforceable.<br />
Lawyers would no doubt have a field day if, given the<br />
above, the CQC tried to impose sanctions on a trust<br />
based on such a tortuous and dubious interpretation<br />
when the opportunity to be clear and specific had not<br />
been taken. Even if such a measure were enforceable,<br />
the CQC would be unlikely to give it a high priority,