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3 Apr 2003 : Column 1157continued
Mr. David Amess (Southend, West): I have the honour to present a petition from Doctor, which has organised a campaign called "Save our single-handers". Signatures have been gathered from all over the country, and the petition involves many local practitioners whose patients value their work and are very upset by what the Prime Minister said in the House a year ago.
The petition reads as follows.
The Humble Petition of Doctors supported by those signatories whose signatures are appended.
Sheweth,
Their concern at the comments of the Prime Minister and First Lord of the Treasury during Prime Minister's Questions on 3rd July 2002 to the effect that "There has been a move over time away from single-handed practices so as to improve the quality of care that people receive", and also their concern that he has not been able to cite any evidence to support his supposition.
Wherefore your petitioners pray that your honourable House urge the Prime Minister and First Lord of the Treasury to apologise for his aforementioned comments of 3rd July 2002 which have caused discontent amongst patients and General Practitioners.
And your petitioners, as in duty bound, will ever pray, etc.
Bob Spink (Castle Point): I have the honour to present a petition on behalf of all people with hearing impairment, particularly those living in south-east Essex. We must listen to what these worthy and caring people have to say, and promote equal access for disabled people and inclusive design to make television, radio and telephone equipment useful for those with impaired hearing without adaptation. I warmly congratulate the members of the Benfleet hard of hearing club on their community-spirited action in collecting signatures for the petition, which reads as follows.
The Humble Petition of Mrs. Irene Haylock, Ashleigh Sharp, Jessica Arnold, members of the Benfleet Hard of Hearing Club, and others of like disposition sheweth
That there are some 8.7 million hearing impaired people in the UK and without changes in legislation, and particularly in the Communications Bill, technology and commercial developments will leave them under increasing disadvantages and will increase the extent of the digital divide whereby disabled people will be left further behind and more seriously discriminated against.
Wherefore your Petitioners pray that your Honourable House shall urge the Government to implement changes in the Communications Bill to end exclusion for hearing impaired people from digital TV, Radio and telephone services.
And your Petitioners, as in duty bound, will ever pray, etc.
Motion made, and Question proposed, That this House do now adjourn.[Joan Ryan.]
Mr. Peter Duncan (Galloway and Upper Nithsdale): I welcome the Minister. We have not met before on the occasion of a health debate. As she knows, in Scotland health matters have been devolved to the Scottish Parliament. This, however, is a particularly unusual case which has given me a constituency interest in health services in England.
A couple of Members, having seen the Order Paper, naturally asked me "Who is Tom Cooke?" They wondered whether he was an important person of whom they should have heard. I told them that, having read the report of this debate in Hansard, they would probably appreciate the significance that Tom Cooke might have, and realise that he would prove in due course to be a very important person.
As you will know, Mr. Deputy Speaker, Members are often presented with tragic cases by constituents. Many of those cases seem to involve injustice on a disturbing scale. The sad death of Tom Cooke and the issues raised by his death combine both. Tom's mother and father, Lauren Devine and Gordon Cooke have sought my involvement to bring a focus on Tom's case and draw attention to their plight as they strive to deal with the ongoing consequences more than two and a half years after his death in June 2000.
Tom's birth and short nine-day life were beset with negligence on behalf of the United Bristol Healthcare TrustUBHTand covering up by that organisation when challenged. That this cover-up culture persisted, after the Bristol heart inquiry and the Kennedy report were supposed to have brought it to an end, is a scandal in itself. The Kennedy report highlighted a culture of failure and cover-up in Bristol. There was clearly organisational failure and a culture that was developed in the interests of the trust, and not of the patients in their Bristol hospitals.
The Secretary of State, in responding to a debate in the House, accepted Kennedy's recommendations and sought to reassure the public that the Government would address the failures. He said:
Lauren and Gordon had two children already before Tom. Both are healthy and happy and are now attending primary school in my constituency. Tom was born with catastrophic brain injury after antenatal care for Lauren went badly wrong. As a measure of that failure of care, Lauren's period of labour extended to some 62 hours, but UBHT midwifery staff failed to accelerate her care in proportion to the danger faced by both mother and baby.
That the antenatal care fell below the standards that should be accepted is clear. What is also clear is that UBHT sought to brush the tragedy under the carpet.
Some months later, long after Tom had died, Lauren still had possession of her antenatal case notes. They had never been collected, never been checked and never been analysed to learn the lessons. Lauren had to return copies voluntarily so that Tom's file at the hospital might be completed. Put simply, the instinctive reaction of UBHT was to deny, evade and deflect possible criticismexactly the same denials, evasions and deflection that had characterised the previous scandal in Bristol.Tom was born on 20 June 2000, severely handicapped and with significant brain damage. Lauren was also severely weakened by the birth and a traumatic labour. At this stage, significant confusion and, perhaps, obfuscation developed between the two roles of treatment and research. In the immediate aftermath of the birth, was Tom being treated for his condition, or was he being researched as part of a trial? It has since emerged that consent was gained from Lauren for Tom's entry into a research programme. At the time, Lauren had a haemoglobin level of 6.4half the normal valueand was clearly in no fit state to make any decisions of that nature. Her assent to treatment was obtained, when in fact it was a research programme into brain cooling equipment. Despite the treatment being presented as being necessary to help her son, it has since emerged that in fact Tom was to be used in the research as a control. He was to be given no treatment.
Equally reprehensibly, Gordon and Lauren were kept away from their son during this period. As a parent myself, I cannot begin to contemplate the isolation that was inflicted upon them, at such a desperate time. Further, Lauren's consent to the recording of a video of Tom's "treatment" was sought. She declined to give that agreement, but the video was produced in any case. This kind of appalling side-stepping and reversal of the express wishes of parents shows what failure remained at UBHT. Action is now required to ensure it cannot happen again.
Tom died nine days after his birth, at a point when relations between the parents, the doctors and the research team had reached a low point. Lauren and Gordon were given Tom to take home, as they were told he was going to die that day. No advice was given as to how to make his remaining hours comfortable, and no real guidance was given as to why Tom should have been taken home to die. No instructions were given on how to feed him liquids. The House should remember that this was a childa personwho could not swallow.
It is now clear that when Tom died, some 10 hours after leaving the hospital, he was probably malnourished, and deprivation of liquids clearly played a significant part in his passing.
That this case is tragic is not in doubt. The Department of Health must address the following questions. What action has been taken to learn the lessons of the midwifery failure that contributed in large part to this tragedy? Why are the procedures for obtaining parental consent for research trials so routinely bypassed, and why is the division between research and treatment so obviously blurred? What can be done to bring an end to the attempts by UBHT to airbrush out inconvenient patient episodes?
As I mentioned earlier, it was five months before Lauren contacted the hospital to inquire what lessons had been learneda perfectly reasonable request. The error of the hospital's failure to reclaim Lauren's case notes came to light during that conversation. They are always held by the patient during antenatal care, but should always be returned afterwardsUBHT knew that, but the airbrush had been used to fine effect.
The fact that Lauren is a qualified barrister obviously raised suspicions that she would not be easily placated. The ongoing heart inquiry, leading to the Kennedy report, meant that her silence was vital. After she was warned to keep quiet, the story takes a turn for the worse.
In order to silence Tom's parents, the totally unfounded allegation subsequently proven to be inaccuratewas made that Lauren had threatened to harm her other children. It was absurd. It was highly damaging to the family, and the allegation was subsequently rejected.
These allegationsinvolving child protection issuesare covered by the Children Act 1989. Quite properly, the legislation seeks to allow the holding of information on those deemed to be a threat to children. But surely the allegations that are recorded must be accurate. I refer to an answer that I received to a written question in which I asked what guidance was given to Government Departments in dealing with information on individual files that have been accepted as inaccurate. The reply was:
The allegations remain on file. Indeed, should Lauren or Gordon seek to request details on their child protection allegations on file, their inquiries themselves would be treated as further incidents of concern.
These inaccurate allegations spread like wildfire throughout the social services and healthcare network. Lauren and Gordon found their other children affected at their schools, and they were affected at their work. All of that was based on deliberate inaccurate allegations, and all of it deliberately designed to maintain Lauren's silence. It is worth noting that those allegations were distributed on an unsolicited basisthey were even sent to my region, Dumfries and Galloway, the family's new home, when there was no reason for that to happen. It is not in doubt that there was systemic failure at UBHT. Kennedy made that clear. It also made it clear that this is an organisation that will do absolutely anything to cover up bad news.
As I said, Lauren is a barrister. She is a specialist in child protection issues, so she knows her and Gordon's rights as Tom's parents. Surely the Data Protection Act
1998 would force the release of their records from UBHT and allow proper scrutiny of the facts. In fact, the trust has even evaded its responsibility to hold and release information as it is required to by law. Some limited releases are only now being made. One of the items that couldindeed, shouldhave been released is the video that was made of the research trial against the express wish of Tom's mother. That was prevented by Department of Health officials breaching confidence and relaying the subject of a private meeting with the DOH's investigation and inquiry unit to the hospital. The video was destroyed by the trust. That is unbelievable deception and an extraordinary failure of the system.This raises serious questions. If the Department of Health's own inquiry team cannot be depended upon for action, who can? In the system for scrutiny after the Bristol heart scandal there were supposed to be new channels to ensure independent scrutiny of failures. In fact, for my constituents, there seems to be no such independent channel. An inquiry was offered to Tom's parents, but only by someone overseen by the chief executive of UBHT. That is no way to ensure patient confidence. Given the nature of their treatment over the past months, is it any wonder that Lauren and Gordon would have no confidence in such an option? Where, after the Kennedy report, is the new openness and accountability? Where is the confidence-building independent scrutiny? Many quangos have been created, but none is delivering material improvement in the system of governance and inquiry.
It is obvious that the system is failing in forcing compliance on errant trusts. How can the Secretary of State for Health, who has ultimate responsibility, ensure that trusts comply with his wise words and his directives? It was impossible to force UBHT to release that research videoinstead, they destroyed it. The Secretary of State is the legal owner of trust records and files, yet has no power to ensure that they are held and used properly. The Department has long been aware of the scale of injustice that has been inflicted on Lauren and Gordon and their children. It now needs now to do something about it.
Closure is required for this family. The best form of closure would be the knowledge that a tragedy like theirs could not happen again. During the time since Tom's death, that has been at the forefront of my constituents' minds. Confrontation has been, and will remain, the last resort. The family have offered to engage constructively with the Department to work through the issues involved, and I hope that the Minister will seize that initiative today.
The Minister has to address three fundamental issues on which the case rests, as well as many other issues. How can the Department of Health be sure that it cannot happen again? Why is there is no independent mechanism for governing such disputes? How can false allegations stay on file? The Kennedy report had fine objectives. It made 198 recommendations which together and over time would help change the culture of the NHS, which according to the inquiry needs to be
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