The government said it was taking steps to address the problems.
The ombudsmen investigated the cases after they were highlighted by the charity Mencap.
They looked into complaints made by the families of the six people who died between 2003 and 2005.
Allan Cannon, father of Mark, said: "The hospital killed him with neglect and malpractice."
In total, the role played by 20 different bodies in the cases was investigated.
|
|
|
|
But Mencap chief executive Mark Goldring said the findings were "damning".
>
Nearly half of NHS staff feel so overstretched they fear they cannot do their jobs properly, a survey shows.
The Healthcare Commission poll of 160,000 workers across England also showed many did not feel valued.
Unions said the figures were worrying as under-staffing was one of the key problems highlighted in the critical report on Stafford Hospital last week.
But ministers said more people than ever were being employed by the NHS and the problems reported were improving.
|
Karen Jennings, of Unison
|
The poll, which is carried out each year by the regulator, covers the full range of NHS staff from doctors and nurses to support staff.
Some 47% of staff said they did not feel there were enough people to do the job, down from 51% in 2007.
A third said they did not feel valued by bosses and just over a quarter had experienced work-related stress - however both of these had fallen slightly in the previous year.
The poll also revealed that half of ambulance staff had said the vehicles were not kept in a good state of repair.
Anna Walker, chief executive of the commission, said progress was being made but more work was needed.
"There are real lessons to be learned from this survey about leadership, management and team work."
'Worrying'
Karen Jennings, head of health at Unison, said the findings were worrying, pointing out that inadequate staffing levels were at the heart of the critical report into Stafford Hospital's emergency care where death rates were significantly above average.
"NHS employers need to listen to staff and must act when they are told they do not have enough time or people to do their jobs properly and deliver quality patient care."
But the survey has been published as the latest workforce census showed that NHS staffing levels have hit a record high.
There are now nearly 1.4m staff employed in England - a rise of over 25 percent in the past decade.
Health minister Ann Keen said it was clear working in the health service was a "rewarding career" as many more nurses, matrons, consultants and GPs were now being employed.
She said staff across the NHS were helping "deliver high quality patient care to all".
But the Tories accused the government of creating too much bureaucracy as the figures also showed that the rise in managers was outstripping that of many clinical staff.
Shadow health secretary Andrew Lansley said: "These spiralling management costs show that Labour's repeated pledges to spend NHS money on the things that matter most were just empty rhetoric."
More than 240 patients a year die of starvation on hospital wards, shocking figures reveal today.
The damning death toll comes to 261 when private and public care homes are considered. And over a decade 2,656 patients have lost their lives through being under-fed while supposedly being looked after by health professionals.
The Tories, who unearthed the statistics, yesterday condemned the scandal. Shadow health minister, Stephen O'Brien said: "The Government is presiding over a culture of carelessness and rising deaths.
"The least patients should be able to expect is to be fed properly when they go into hospital for treatment." Mr O'Brien said part of the problem was NHS staff overburdened with red tape. He urged: "They must be released to do the job they are there to do - help people - or risk more unnecessary and needless deaths."
The data, which covers England and was compiled by the UK Statistics Authority, shows how the crisis has grimly worsened over a decade.
The 242 hospital deaths in 2007 was 16 per cent up on 1997. And more than 139,000 patients were discharged from hospitals with malnutrition in 2007, an 85 per cent rise. The worst death tolls over the decade were in the West Midlands, 409, and the South-East, 388.
The Department of Health said: "The majority of patients are satisfied with the food and we're working to drive care standards further. It is crucial that everyone is treated with dignity."
2,311 The number who starved to death in hospital wards in England from 1997-2007
16%The shock rise in the death toll over 10yrs
409 Number who perished in West Midlands, the worst performing NHS region
http://www.mirror.co.uk/news/top-stories/2009/04/08/240-patients-starve-...
Hundreds of people are dying every year while sectioned under the Mental Health Act, the Observer can reveal.
New figures released by the Ministerial Council on Deaths in Custody show that in the past 10 years 3,540 of those detained in NHS facilities, including high-security psychiatric hospitals, have died.
The figures have been condemned as "horrific" by the Howard League for Penal Reform, which will launch a campaign tomorrow called Lost Daughters, calling for fewer women and girls to be held in custody. As part of its campaign, the charity will place a memorial advert in the Observer every time there is a death.
"These numbers are horrific," said Frances Crook, director of the Howard League. "These are closed institutions. These deaths are happening away from the public eye. We need to scrutinise exactly what's going on in this shadowy, hidden world."
The figures reveal that more than 800 of the 1,979 male deaths and almost 300 of the 1,561 deaths among women over the 10-year period were from unnatural causes, including suicides and accidents.
These patients were largely middle-aged, with about half dying outside the hospital, either during home leave or during periods when they were absent without permission.
Anna Savage, from Thundersley, Essex, took the South Essex Partnership NHS Foundation Trust to court last year, arguing that it had taken insufficient care to protect her mother, who committed suicide after walking out of hospital. Hospitals must now take reasonable measures to avoid harm to patients who have been sectioned.
Paul Corry of Rethink, a mental health charity, said that the figures revealed a "hidden scandal". He added that many of the deaths attributed to natural causes could be prevented.
"We assume that because these people are being kept in so-called 'hospitals', whether they are secure or psychiatric, they are receiving a satisfactory level of physical care," he said. "This is often far from the case.
"Psychiatric hospitals have far fewer facilities than normal hospitals, so patients don't get the day-to-day help they need. In addition, transferring patients with serious health issues to normal hospitals can be very difficult, because doctors often don't want to have these people on their wards."
Helen Shaw, co-director of Inquest, which offers advice to bereaved families about deaths in custody, said the current investigation system into these deaths is "not fit for purpose".
"These deaths do not receive sufficient public scrutiny and contentious deaths are escaping any public scrutiny," she said. "As a vulnerable group, mentally ill detained patients are deserving of protection, and failure to implement preventative measures against their heightened risk of suicide and self-harm could lead to a breach of the European convention on human rights."
http://www.guardian.co.uk/society/2009/jul/12/hundreds-die-mental-hospitals
Many NHS doctors and nurses are inadequately prepared to spot and act upon signs of child abuse or neglect, a damning report on the aftermath of the Baby P scandal warns.
The detailed survey by the Care Quality Commission exposes a failure inside the health service even among some paediatric specialists and GPs to get to grips with the challenges of safeguarding children.
It says many clinicians have not received up-to-date mandatory training in child protection, while health visitors are overwhelmed by excessive case loads.
The review was ordered after it emerged that NHS staff in Haringey, north London, including some employed by Great Ormond Street children's hospital, saw Baby Peter, as he is now known, on 35 separate occasions in his short life and, on all but one occasion, failed to realise he was in danger.
Highlighting the inadequate response by health trusts, Cynthia Bower, the commission's chief executive, said: "Immediately after the Baby P tragedy, everyone agreed that everything possible must be done to prevent a recurrence. This must not prove to be hollow rhetoric. The NHS has got to play its part by getting these safeguarding measures in place.
"It is clear that safeguarding has not been as high on the agenda of trust boards as it should have been ... In some cases NHS staff have not been given the support they need in terms of training and clear procedures for handling concerns. If that were to change, it would be an appropriate legacy for Baby Peter."
The 17-month-old Baby Peter, who had been also monitored by social workers and police, was seen by a consultant paediatrician, Sabah Al-Zayyat, two days before he died in Haringey in early 2007. She had not been not given the full picture of Peter's history before the examination, although a subsequent internal Great Ormond Street inquiry said she should have identified his injuries as signs of abuse.
After he died, Peter was found to have serious injuries including a broken back and fractured ribs. His mother, her boyfriend and a lodger were later sentenced for causing or allowing the child's death.
The report says that only 54% of eligible NHS staff have received basic child protection training, a "worryingly low" proportion. According to the inspectors, in 20 of the primary care trusts surveyed, as few as 10% of GPs were up-to-date with what was said to be a "basic" level of training.
On health visitors, the investigation discovered that 29 out of 152 primary care trusts were dealing with caseloads of more than 500 children each, "well above [the] recommendation of 400".
Among other findings were that only 37% of trusts have a dedicated budget for training staff in child protection issues, while 65% of GPs either do not have appropriate training or there is no data to say whether they do or don't. Only 58% of A&E or urgent care staff have adequate training in child protection.
Last year about one in 10 GP consultations were with children aged 14 or under; nearly three million children under 16 attend A&E departments ever year.
In 2008-09, the year that the Baby P scandal erupted, more NHS trusts did admit that they could not comply with national core standards – one of which deals with child protection. The numbers declaring compliance fell marginally from nearly 97% to 94% – suggesting a slight increase in self-criticism.
More than one in 10 trusts "did not appear to comply with the statutory requirement to carry out criminal records bureau checks for all staffemployed since 2002," the report said. "We are particularly concerned with the large proportion of trusts that do not have a process for following up children who miss outpatient appointments."
Commenting on the findings, Jo Webber, deputy director of policy at the NHS Confederation, said: "Despite the progress many NHS organisations have made, and the commitment of individuals working in the health service, there is clearly much more that can be done to make sure children are protected properly. This means promoting a culture of questioning amongst staff."
The Liberal Democrat health spokesman, Norman Lamb, said: "It's disgraceful that some parts of the NHS are still failing to comply with basic child protection requirements like carrying out criminal record checks on staff."
The health secretary, Andy Burnham, said: "I want trusts and PCTs to use this report to support a coordinated programme of action to assure and sustain essential levels of safeguarding in activities relating to children."
http://www.guardian.co.uk/society/2009/jul/16/baby-p-child-protection-nhs
Britain's highest court issued a historic judgment today that could finally remove the fear of prosecution from people who travel abroad to support relatives seeking an assisted suicide.
In a unanimous ruling, the law lords ordered the director of public prosecutions to immediately draw up a policy that would spell out when prosecutions would and would not be pursued.
The ruling was strongly in favour of Debbie Purdy, 46, who has multiple sclerosis and who has been fighting to protect her husband, Omar Puente, should he accompany her to a clinic in Switzerland that specialises in euthanasia. She had argued that the law was unclear and uncertainty surrounding the issue breached her human rights.
Debbie Purdy on assisted suicide victory: 'This means my life will be longer' Link to this audio
Speaking outside the House of Lords after the judgment, Purdy, from Bradford, said she was "ecstatic".
"I am eagerly awaiting the DPP's policy publication so that we can make an informed decision to make sure what we do does not risk prosecution. I feel like I have my life back," she said. "I want to live my life to the full, but I don't want to suffer unnecessarily at the end of my life. This decision means that I can make an informed choice, with Omar, about whether he travels abroad with me to end my life because we will know exactly where we stand."
Moments after the decision was made public Keir Starmer, the DPP, said he had set up a team of lawyers to review the issue and promised to conduct a public consultation before setting out a fresh policy.
"This is a difficult and sensitive subject and a complex area of the law. However, I fully accept the judgment of the House of Lords," Starmer said. "The CPS has great sympathy for the personal circumstances of Ms Purdy and her family. We will endeavour to produce an interim policy as quickly as possible which outlines the principal factors for and against prosecution."
The decision, the last by the House of Lords before reconvening as the supreme court in October, was described as a far-reaching precedent by lawyers representing Purdy. Saimo Chahal, one of her legal team, said: "I always knew we would have to go to the House of Lords to get a judgment that was reasoned and considered. I hope that it will go a long way towards indicating that there are very many factors against prosecution in the public interest in cases involving assistance to a person who is mentally capable … and decides to have an assisted suicide in a country where it is legal."
Lord Lester QC, one of the peers who supported a recent bill that would have removed the threat of prosecution for relatives in assisted suicide cases, said: "It is up to the government to show leadership. People need to know whether their conduct is or is not going to be criminal, but there is a need for legislation."
At least 115 Britons have travelled abroad for an assisted suicide since 2002. Nearly 800 people from the UK have become members of Dignitas, the assisted suicide group based in Switzerland, since it was established in 1998. A report last month from campaign group Dignity in Dying, which has supported Purdy's case, said a further 34 Britons were in the final stages of preparing to follow.
In their ruling, the law lords recognised that Purdy was one of a growing number of people likely to want to travel abroad to die.
"The cases that have been referred to the DPP are few, but they will undoubtedly grow in number," said Lord Hope. "Decisions in this area of the law are, of course, highly sensitive to the facts of each case … But I would not regard these as reasons for excusing the DPP from the obligation to clarify what his position is."
Another of the law lords, Lady Hale added: "If we are serious about protecting autonomy we have to accept that autonomous individuals have different views about what makes their lives worth living. In additudinal surveys the British public have consistently supported assisted dying for people with a painful or unbearable incurable disease".
But the law lords were careful to avoid appearing to attempt to influence a change in the law. "It must be emphasised at the outset that it is no part of our function to change the law in order to decriminalise assisted suicide," Lord Hope said.
"No one who listened to the recent debate in the House of Lords … can be in any doubt as to the strength of feeling on either side or the difficulties that such a change in the law might give rise to".The Ministry of Justice said there was no need to change the law in the light of the Law Lords' ruling because the judgment related to the way the law was implemented by prosecutors, not the actual law itself.
The Ministry of Justice said there was no immediate need to change the law because the ruling related to the way prosecutors implemented it.
"The government believes that any change to the law in this area is an issue of individual conscience and a matter for parliament to decide, rather than government policy," it said.
http://www.guardian.co.uk/society/2009/jul/30/debbie-purdy-assisted-suic...
The state can do terrible things to people. While libertarians worry about big brother CCTV cameras, information stored on computers or the shameful power to lock people up without trial for 28 days, even worse happens behind closed doors at the state's behest.
Every day in hospitals, nursing homes and at home, the state not only permits but orders the torture of the terminally ill. Confined within bodies too frail to help themselves, people are denied assistance from doctors to end their lives peacefully. If anyone counted up the numbers of the dying and the months of agony they suffer against their will in the many dying rooms of the nation's institutions, then the 1961 Suicide Act would emerge as the cruellest torture instrument.
Because dying happens far from the public eye, the sheer scale of suffering is a secret garden the medical profession prefers to keep hidden, denying doctors' limited skills to prevent thousands ending up in a state everyone hopes will never happen to them. (Doctors, though, are among those most likely to kill themselves when terminally ill, knowing what lies ahead).
Let's be graphic: morphine (and its derivatives) is no wonder drug, though it is the only effective painkiller available. It usually dulls pain, but not always. At high enough doses it can induce unpleasant hallucinations. It is a depressant: don't imagine you end life on some glorious high, floating away in a cloud of pleasurable dreams. It causes acute constipation, so the dying spend their last weeks thinking mostly of their bowels, of laxatives and enemas punctuated by explosive "accidents". Elevated end-of-life thoughts and feelings are often banished by pain and the indignity of bodily functions.
Palliative-care doctors and nurses can be wonderful: I have seen them at their best, caring for my mother and for others close to death. But collectively they strongly oppose giving their patients the right to die – and their voice carries extra weight inside and outside the medical profession because they are the experts in death. They tend to claim that with the best care, anyone can live out their last days with enough comfort and dignity not to want a mercy killing. But following in the footsteps of Mother Theresa and Dame Cicely Saunders, this is a branch of medicine exceptionally heavily dominated by the deeply religious who believe only God disposes. Either they deceive themselves or else they deny the evidence of their own eyes and ears about many patients' experience. Their influence in this debate has been immense – and baleful.
They are right that too few people get good end-of-life care; the Dying Matters coalition, set up by the National Council for Palliative Care, reports that the least affluent get the least care, as in life. But many, like my family, report excellent care that still can't save a dying person from dreadful last days.
It was a cabal of bishops, rabbis and assorted religious enthusiasts who wrecked the Joffe bill in the Lords through a devious putsch that broke Lords' procedural practice, denying the bill a Commons debate. Even more spurious were their arguments, summarised by the Bishop of Oxford's opinion that "we are not autonomous beings" and so must wait for God to release us.
This week the law lords opened the door to a gentler way of death by a small chink, after the admirable Debbie Purdy's long campaign for her own autonomy. Keir Starmer, the director of public prosecutions, must set out his interpretation of when people will be prosecuted for easing someone's exit. But it should not be for one man to determine what to do once a law has become redundant. It is for parliament to debate how to replace the Suicide Act, now hundreds of relatives of the terminally ill – and even of the severely disabled, but not terminal – have not been charged for assisting relatives to die. The Commons needs to bring forward a bill urgently. Every poll in the last decade has shown between 74% and 87% of the public want the terminally ill to have the right to ask a doctor for a peaceful death.
Safeguards are not hard to devise: someone in sound enough mind to write their will can be judged fit enough to choose when it's time to die, without undue duress from greedy relatives. Besides, the loss of independence and becoming a burden to others may be a valid part of the reason why someone feels life has become undignified and past bearing.
Each person has their own threshold, with their own sense of what makes life worth living. When my friend Jill Tweedie, late of this paper, was dying of motor neurone disease, she was driven to rage by sanctimonious people telling her to consider how Stephen Hawking found so much value in life despite severe disability. What mattered to her was what she found bearable. She took her own life while still mobile, probably far earlier than if she had been guaranteed assistance from a doctor at a later stage. Every one of us will die and many will not have a quick and painless death. Experience in Oregon shows that simply knowing you can call for an injection eases anxiety and makes it less likely people will end their lives prematurely.
The absurd state of the law now means only the well-off can fly to Zurich and many are probably still too well to need to die quite yet: 800 Britons are on the waiting list. When my mother in her last days begged me to take her to Switzerland, it was too late. But I would have dreaded taking her while she was still fit enough to travel, before the last stages. The very idea of a funereal last flight to a strange place is horrible to contemplate. The prospect of that tastefully anonymous Dignitas death chamber seems a desperately grim way to go, all because of the hypocritical British law. Most people want to know they can die at home, surrounded by family or friends at a time of their choosing, with an injection no more distressing than a pre-operative anaesthetic. We might never need it, we might never choose it, but to know there is an easeful escape is to take away fear of dying.
Surveys of candidates show the next parliament is set to be filled with a socially as well as politically conservative cadre of new MPs. There is not long left for this House of Commons to change the law. This is among many other progressive reforms Labour has neglected, but there is still time – just.
http://www.guardian.co.uk/commentisfree/2009/jul/31/assisted-suicide-law...
Patients who fail to keep hospital appointments cost the NHS more than £600 million a year, enough to run two medium-size hospitals, data has shown.
Between 2007 and 2008, 6.5 million appointments were missed in the UK, with hospitals losing around £100 per patient in revenue.
The Patients Association said missing an appointment was "unforgivable".
The Department of Health in England says initiatives such as text message reminders are being rolled out.
But Unison said patients were not always to blame as check-ups are often arranged months in advance and easily forgotten.
The public service trade union said primary care trusts should find ways of reminding patients of their appointments, which could include text or e-mail alerts.
Some are already doing this.
'Did not attends'
Young men in their early 20s are the worst offenders and people aged 70 to 74 are the most conscientious about keeping an appointment, the figures from UK health departments and analysts Dr Forster showed.
There has been a slight improvement in attendance over the last few years in England, Wales and Northern Ireland.
In Scotland, however, the figure is higher than in recent years.
Some clinics in the UK are now over-booking patients in anticipation of no shows.
|
Michael Summers,
Vice-chair of the Patients Association |
But Karen Jennings, Unison's head of health, warned: "Hospitals who go down the route of over-booking, based on previous experience of missed appointments, must ensure that it doesn't disadvantage patients if there is a 100% turn-out."
Michael Summers, vice-chair of the Patients Association, said: "It's unforgivable really.
"It doesn't take much to lift a phone and say that you have recovered or to apologise because you will have to miss an appointment.
"We owe a responsibility to our doctors to behave properly. Missed appointments waste healthcare professionals' time and a great deal of money."
Simon Jones: 'Worst offenders are young men'
A Department of Health spokesman said successful initiatives, such as text messages to remind patients, were on the rise.
He said the choose and book, which allows patients to select a chosen time, date and place for an appointment at their own convenience, was also helping reduce the number of missed appointments.
He added: "The NHS Constitution gives patients the right to access NHS services, but patients have responsibilities too - it is important to keep appointments, or cancel within reasonable time.
"Otherwise, receiving treatment within the maximum waiting times may be compromised."
Some chronically ill patients are so overburdened by treatment that it makes their health worse, according to a new study in the BMJ medical journal.
The paper, by clinicians from Glasgow and Newcastle universities, says badly co-ordinated care leads to "wasted resources and poor outcomes".
It calls for more "minimally disruptive medicine" that is tailored to the realities of patients daily lives.
The findings of the paper are based on 10 years of research.
The paper, led by Carl May, professor of medical sociology at Newcastle University, states that patients can be burdened by much more than drug management and self monitoring.
|
Professor Frances Mair
Glasgow University |
He said: "It includes organising doctors' visits and laboratory tests. Patients may also need to take on the organisational work of passing basic information about their care between different healthcare providers and professionals.
"In some countries, they must also take on the contending demands of insurance and welfare agencies.
"Patients are thus overwhelmed not just by the burden of illness, but by the ever present and expanding burden of treatment."
The paper highlights cases where patients have suffered due to such a burden.
Among these cases is that of a man treated for heart failure who rejected the offer to attend a specialist heart failure clinic to improve his condition.
He said that over a two-year period he had made 54 individual visits to specialist clinics for consultant appointments, diagnostic tests and treatment - the equivalent of one full day every two weeks.
'Wasted resources'
Frances Mair, professor of primary care research at Glasgow University and co-author of the paper, said the findings showed the need for "better co-ordination of care".
"Thinking seriously about the burden of treatment may help us begin to consider minimally disruptive medicine - forms of effective treatment and service provision that are designed to reduce the burden of treatment on users," she said.
"The treatment burden leads to poor adherence, wasted resources and poor outcomes.
"We are calling for minimally disruptive medicine that seeks to tailor treatment regimens to the realities of the daily lives of patients.
"Such an approach could greatly improve the care and quality of life for patients."
http://news.bbc.co.uk/1/hi/scotland/glasgow_and_west/8196928.stm
NHS care for patients with muscle-wasting disorders is often "inadequate and not acceptable", MPs and peers say.
The All-Party Parliamentary Group on Muscular Dystrophy inquiry found huge variations in life expectancy.
People with the disorders also often faced long waits for wheelchairs and having to pay for physiotherapy, the report said.
The government said it expected the local NHS to provide services to meet people's needs.
There are more than 60 different types of muscular dystrophy and related neuromuscular conditions, affecting some 60,000 people across the country.
They cause muscles to waste and weaken, making it hard to do even the most simple tasks and many of those affected do not make it to adulthood.
The diseases cause muscle weakness and wasting
|
The cross-party group of MPs and peers, which was supported by the Muscular Dystrophy Campaign in its inquiry, gathered evidence from doctors, patients and health managers.
It found there was a "postcode lottery" when it came to life expectancy, which politicians said would have been a national scandal if it had been related to cancer.
In the north east, sufferers can expect to live to 30 whereas elsewhere those with the condition struggled to reach 18.
The report also accused the NHS of relying on charities to provide support to families affected.
Dave Anderson, the MP who led the inquiry, lost a brother and sister to the disease. He said: "It is very clear that the standard of care provided to these patients by the NHS is often inadequate and not acceptable."
'Appalled'
Cross-bench peer Lord Walton, a founder of the Muscular Dystrophy Campaign, was one of the key members of the group and he said he was "appalled" by much of the evidence heard.
The report concluded by calling for official guidelines to be given to trusts to ensure high standards of care as well as a review of skills in the health workforce.
|
Philip Butcher, Muscular Dystrophy Campaign
|
It also recommended that each of the 10 health regions in England and Scotland, Wales and Northern Ireland should appoint a specialist to oversee services.
Phillippa Farrant has a seventeen-year-old son with a rare muscle-wasting condition and she said getting treatment on the NHS had been a struggle.
"You just feel as though you are battling the system the whole time and that your whole life is based around hospital appointments," she said.
"We have got something fairly local but in other parts of the country they are travelling hundreds and hundreds of miles to get to the specialist places, which is completely wrong."
'Meeting community needs'
Philip Butcher, chief executive of the Muscular Dystrophy Campaign, agreed that improvements were needed.
"I hope that the report will help to put pressure on the NHS to start providing the standard of care that these patients so dearly need and deserve."
A spokesman for England's Department of Health said it recognised the importance of providing high-quality, personalised care for people with long term conditions such as muscular dystrophy.
He added: "We expect the NHS to commission services to meet the needs of its local communities.
"However, muscular dystrophies are to be included in an updated list of specialised services to help local NHS organisations plan services."
A Welsh Assembly government spokeswoman said it was already taking action to improve muscular dystrophy services.
http://news.bbc.co.uk/1/hi/health/8212461.stm
The Care Quality Commission has published its in-depth analysis of the performance of England's 391 NHS trusts across a range of categories over the past year.
|
NHS RATINGS 2008
To find out more Care Quality Commission information for England, enter your full postcode here:
This search goes to an external site
|
The watchdog assessed the trusts on a series of criteria, focusing on their quality of service and use of resources.
Each trust was graded either excellent, good, fair or weak.
The services measured included patient access, safety and the way the services are run.
The ratings reflect how well the organisation met basic standards of care and how they performed against existing and new national targets.

The NHS is being praised for improving the services it provides.
The number of excellent performers has risen more than six-fold in the last two years. Meanwhile, just 5% are classed as weak.
The poorest performers will now be subject to monitoring by the Care Quality Commission.

Basically, this is a measure of how well trusts are managing their finances.
Again the figures show an improvement in recent years as the health service has turned its deficit into a healthy surplus.

Performance is generally up for each of the four types of trusts. However, primary care trusts, which oversee community services such as GPs, are still struggling to achieve excellent ratings.
This is probably because as largely management organisations they have more targets to hit.

|
READ THE FINDINGS IN FULL
Most computers will open this document automatically, but you may need Adobe Reader
|
Hospitals, in particular, have upped their game on financial management in recent years. Two thirds are now excellent or good.
But the watchdog has flagged up the lack of rigour seen among ambulance trusts. These have recently been merged, which could partly explain the lack of any excellent performers. NHS chiefs will be expecting this to improve in future years.
A patient lobby group is demanding an urgent review of basic hospital care after highlighting accounts of "appalling" NHS standards.
Relatives told the Patients Association how their loved ones, often elderly people, were left lying in faeces and urine and were not helped to eat.
The group's president Claire Rayner, an ex-nurse, called for "bad, cruel nurses" to be struck off.
The government said the cases were unacceptable but not representative.
The report focused on 16 stories from relatives of patients in England, which the association says are just a few of "hundreds and hundreds" of similar reports from across the UK.
It says self assessment allows too many health authorities to ignore problems that have been raised and is calling for regulator the Care Quality Commission to intervene.
Soiled bedding
The association insists accounts used in the report were reviewed critically before publication as it was aware complaints do "not necessarily reflect the reality".
But it stressed nearly all the accounts were concerned not about treatment but basic nursing and domiciliary care.
The Patients Association noted the latest inpatient survey found 43% rated the service they received as excellent, a significant increase from the previous year.
|
Chris Beasley
Government chief nursing officer |
But it stressed the 2% who deemed the service poor had not changed between 2002 and 2008, and that while the proportions were small they still represented thousands of patients.
Earlier this year, a report from the Healthcare Commission - now replaced by the Care Quality Commission - detailed grave lapses in standards of care at the Mid Staffordshire NHS Trust.
Families described "Third World" conditions, with some patients drinking water from vases and lying for hours in soiled bedding.
"Whilst Mid Staffordshire may have been an anomaly in terms of scale the Patients Association knew the kinds of appalling treatment given there could be found across the NHS," said Katherine Murphy, the association's director.
"This report removes any doubt and makes this clear to all. Two of the accounts come from Stafford, and they sadly fail to stand out from the others."
She said the stories were often about the most vulnerable elderly.
"We hope this report also encourages other people to get in touch with us and tell their stories. We plan to continue publishing accounts until we can be confident that every patient is secured dignity in their care," she continued.
|
Dr Peter Carter
Royal College of Nursing |
Relatives described how they found their loved ones dehydrated or lying in faeces, blood and urine, and told of problems in getting help from nurses. They also told how patients were left with sandwiches or drinks in packaging which they could not open.
Ron Kirk said his father, Leslie, was admitted to hospital in October 2007, having suffered a stroke, but that his treatment at the hands of some nurses amounted to cruelty.
His father had been fitted with the wrong catheter, leaving him in pain, but nurses took away his bedside alarm because they thought he was "pressing it too often", Mr Kirk said.
Claire Rayner said: "I am sickened by what has happened to some part of my profession of which I was so proud. These bad, cruel nurses may be - probably are - a tiny proportion of the nursing work force, but even if they are only one or two per cent of the whole they should be identified and struck off the Register."
Good 'overshadowed'
Government chief nursing officer Chris Beasley said: "All patients deserve the highest quality of care from the NHS and the poor care received in these cases is simply unacceptable."
But she said this was not representative of the picture across the NHS.
"The NHS treats millions of people every day and the vast majority of patients experience good quality, safe and effective care - the Care Quality Commission's recent patient experience survey shows 93% of patients rate their overall care as good or excellent."
The CQC said the registration system it was introducing for trusts next year would ensure they met key quality standards.
"It is absolutely right to highlight that standards of hospital care can vary from very good to poor," said chairman Barbara Young.
"Many people are happy with the care they receive, but we also know that there are problems.
"Matters related to the dignity of care are of particular concern to patients and their families.
"And poor basic nursing is a recurring theme in organisations that perform badly.
"I am in no doubt that many hospitals need to raise their game in this area."
Dr Peter Carter, chief executive of the Royal College of Nursing (RCN), said it would not condone nurses who behave in ways "that are contrary to the principles and ethics of the profession".
But he added: "This report is based on the 2% of patients who feel that their care was unacceptable.
"Two per cent is too many but we are concerned that this might undermine the public's confidence in the world-class care they can expect to receive from the NHS.
"Furthermore it could also dampen the morale of the millions of staff who work tirelessly to help their patients."
http://news.bbc.co.uk/1/hi/health/8223710.stm
Researchers have claimed the food provided in prisons is better than in NHS hospitals.
Experts from Bournemouth University examined the quality of food offered to prisoners and NHS patients.
They say people in hospital are losing out on nutrition because they are not being helped with eating or having their diet monitored.
A Department of Health spokesman said most patients were "satisfied with the food they receive in hospitals".
Professor John Edwards said about 40% of patients entering hospital were already malnourished, and this did not tend to improve during their stay.
"If you are in prison then the diet you get is extremely good in terms of nutritional content," he said.
"The food that is provided is actually better than most civilians have.
|
Norman Lamb, Liberal Democrat
|
"There's a focus on carbohydrates. Then there's the way they prepare the food; it's very healthy. They don't add salt and there's relatively little frying of food - if you have a burger then it goes in the oven.
"Hospital patients don't consume enough. If you are using food as a means of treatment then it's not working.
"And from the work we've done we know that people who sit round a table eat a lot more, but this doesn't happen in hospitals."
Professor John Edwards: ''People often need help with eating''
His fellow researcher Dr Heather Hartwell said fruit and vegetables were made available in hospitals "but this doesn't mean it's eaten".
She also said that patients suffered because they may have no appetite as a result of their illness, and might also not get help with eating and drinking.
The research suggests further problems are caused because meals are likely to be at a set time, when patients may be having tests or treatment.
"Hospital cutbacks are also seen in areas like catering budgets, rather that elsewhere," Dr Harwell said.
"Hospital food services also need to be less fragmented and more joined up."
'Improve services'
Liberal Democrat shadow health spokesman Norman Lamb said: "This study highlights the experience of too many patients in NHS hospitals.
"While there is excellent care in many places, there are a lot of examples of what is in effect neglect of vulnerable people.
"It's incredible that so many hospitals are failing to serve healthy meals. If prisons can serve good food then so can hospitals."
A Department of Health spokesman said: "Good quality food for patients improves their health and their overall experience of services.
"The majority of patients are satisfied with the food they receive in hospitals, and we are working to improve services further."
"Clinicians have a duty to ensure patients get the appropriate treatment for any condition, including malnutrition.
"We have also introduced the concept of 'protected mealtimes' where all non-urgent activity on the ward stops, so that patients can enjoy their meals."
The Patients Association has exposed awful hospital neglect. Our cherished healthcare system needs a dose of regulation
There has been an absolutely astounding response to the report the Patients Association released yesterday, detailing examples of neglect of elderly and vulnerable patients. While I was as ever hopeful that the people who so bravely volunteered to take part in this work would feel it had been worthwhile, the response has been staggering. I was shocked and touched reading the stories of patients' families who have suffered and it seems the rest of the country has been as well.
What is very worrying is that the Patients Association has been flooded with hundreds of calls and emails since the report was released from patients and their relatives up and down the country saying "add me to the list". Websites featuring stories on our report have comments left by readers saying the same thing.
We have to make sure that all this effort and public outcry gets real results. Though it's been somewhat lost in the storm, our report makes some very clear recommendations. I think the two most important ones are for changes to hospital regulation and changes to complaints handling. And I would like to add my particular concern about the effect of target culture on everybody giving frontline care. It must be reconsidered and where possible minimised.
First, hospital wards should be subject to independent checks. Bits of paper with tick boxes and statistics are not enough. Schoolteachers have inspectors who come and watch their lessons – those looking after people, often some of the most vulnerable people in our society, should face the same type of direct scrutiny.
Second, whenever a hospital has a complaint upheld against it, the regulators and ombudsman shouldn't be writing letters back and forth – they should be visiting the hospitals and seeing for themselves that changes have been made. The people that make legitimate complaints deserve an immediate response and expressions of regret.
The emphasis shouldn't be on knocking nurses in general, it has more to do with appalling NHS management; the pressure of targets and a nursing workforce overworked and overwhelmed by NHS bureaucracy.
Many years ago now it was decided by the government and others to use a light-touch approach to regulating our hospitals. It didn't work with the banks and it hasn't worked with the NHS. Lets us now all accept that very real change is needed and take positive steps towards it.
On a slightly separate note: since we at the Patients Association published our report, some people have said to me: "Won't all this publicity about cases of poor care have a bad effect on the NHS's reputation in the US, where they're already saying awful things about it and how much they don't want a similar system of their own?"
Much as I would like to respond to their ill-informed opinions with a crisp "Frankly, my dear, I don't give a damn what you think," let me instead point out that any intelligent American Republican should be able to see clearly that the anger we are expressing shows just how good the NHS normally is. And exposing the fact that we have a few rotten apples (so rare in the US, according to the self-aggrandising politicians I have heard slagging off our system) and are determined to seek them out and deal with them shows how much we care about our vulnerable, frail, and helpless elders.
I have no doubt that eventually this uproar will lead to the finding and application of the necessary remedies and ensure that future care for them will be what it should be – that is, gentle, dignity-protecting and life-extending as far as possible. If the national anger we are hearing in this country, where we love and value our NHS, doesn't prove to you that we don't have so-called "death panels" nothing will.
I have actually seen the sort of wards in which Americans currently put their poor. I almost threw up on the spot at the stench, the filth on the beds and floors where their wretched patients lay. American detractors of our system should go and see another truth in their own backyard.
http://www.guardian.co.uk/commentisfree/2009/aug/28/nhs-patients-associa...
Elderly and vulnerable hospital patients suffer neglect and cruelty, according to Patients Association dossier
Vulnerable and elderly NHS patients are being given poor-quality care and denied their basic dignity in hospitals across the UK, the Patients Association claims today.
The association, whose president is agony aunt Claire Rayner, has submitted a dossier of 16 cases in which it alleges elderly patients were let down and sometimes cruelly treated by health service staff to the inspectorate, the Care Quality Commission.
Almost all the case histories in the report, Patients Not Numbers, People Not Statistics, come from relatives of patients who died. Many of the allegations are made against nurses and include a lack of compassion and patients being left lying in faeces and urine and not receiving the help they need to eat and drink. There are also accusations of mistaken diagnosis, the wrong medication being given and treatment delays, as well as staff shortages.
The cases have all been referred to the NHS trusts involved and have been or are being investigated locally. Some of the allegations are disputed.
Claire Rayner, a former nurse, said that for too long the association's helpline had been receiving calls complaining of demeaning and poor treatment by nurses. "I am sickened by what has happened to some part of my profession of which I was so proud," she said. "These bad, cruel nurses may be – probably are – a tiny proportion of the nursing workforce, but even if they are only 1% or 2% of the whole they should be identified and struck off the register."
Katherine Murphy, director of the Patients Association, claims that the cases, and others that have been referred to it over the years, reveal that the appalling treatment given to patients in Mid Staffordshire, which became public earlier in the year, can be found across the NHS.
"This report removes any doubt and makes this clear to all. Two of the accounts come from Stafford, and they sadly fail to stand out from the others," she said.
"These accounts tell the story of the 2% of patients that consistently rate their care as poor. If this was extrapolated to the whole of the NHS from 2002 to 2008 it would equate to over 1 million patients. Very often these are the most vulnerable elderly and terminally ill patients – it's a sad indictment of the care they receive.
"These accounts reveal patients being denied basic dignity in their care – often left in soiled bedclothes, being given inadequate food and drink, having repeated falls, suffering from late diagnosis, cancelled operations, bungled referrals and misplaced notes. There are also worrying instances of cruel and callous attitudes from staff towards vulnerable and sometimes terminally ill patients."
Barbara Young, chair of the Care Quality Commission, said: "It is absolutely right to highlight that standards of hospital care can vary from very good to poor.
"Many people are happy with the care they receive, but we also know that there are problems. Matters related to the dignity of care are of particular concern to patients and their families. And poor basic nursing is a recurring theme in organisations that perform badly. I am in no doubt that many hospitals need to raise their game in this area.
"As the regulator, CQC is dedicated to helping eliminate poor practice and to ensuring care focuses on people as individuals and on their needs."
http://www.guardian.co.uk/society/2009/aug/27/patients-association-poor-...
People with Down's syndrome are particularly prone to dementia, an expert said today, and more needs to be done to help them.
Up to half of people in their 50s with Down's syndrome can be affected by dementia, yet campaigners say the problem was barely mentioned in a recent green paper on dementia care in England.
A chemical thought to play a key role in the onset of dementia tends to build up in the brains of people with Down's more quickly than in the rest of the population.
A leading neuroscientist, Professor Tony Holland, who specialises in learning disabilities, said sufferers of the dual condition had effectively been ignored by the government.
"We would like to see it acknowledged at a governmental level, and then clear strategies put in place – which may vary across the country – that ensure they have access to the right services," the Cambridge University professor told the BBC.
The sister of a Down's sufferer who died aged 52 after his memory started failing said she had to fight to get the right treatment.
"I think the levels of care now are becoming much more professional – it's very gradual, some areas are far more progressive than others," Nikke Lewis said. Her brother Andrew started showing symptoms of dementia in his 40s.
The care services minister, Phil Hope, said the green paper set out plans to redesign the care system so that it works better for everyone.
He said: "The green paper is based on making the system fairer, simpler and more affordable for everyone.
"Doing this will benefit people with Down's syndrome as much as any other group."
http://www.guardian.co.uk/society/2009/oct/05/downs-syndrome-dementia-help
Almost 40% of British people would put off seeing a doctor about suspected cancer symptoms because they did not want to bother them, according to a survey presented today.
The high numbers who would delay visiting their GPs – because they did not want to take up their time or because they were afraid to hear what they might say – are a big issue for cancer services. One of the main reasons UK survival rates lag behind some other European countries is that cancers are not detected early enough.
The presentation to the National Cancer Research Institute (NCRI) conference in Birmingham revealed that people delay making an appointment because they are embarrassed, scared or busy.
Women are more "worried about wasting their doctor's time" than men – 41% admitting they would delay the visit because they did not want to trouble the GP, compared to 36% of men.
Similar proportions – 40% of women and 34% of men – said they would put off an appointment because they were worried about what the doctor might find.
The national survey was carried out by Cancer Research UK's health behaviour research centre at University College London. It involved 3,600 people randomly selected from across the UK, 2,600 of whom were interviewed face to face.
"If we were to carry out this survey in other countries, I suspect that the results might be different – because it's typically British to think 'I mustn't bother the doctor,'" said Jane Wardle from the centre. "But when this etiquette stops us talking to the GP about potentially serious symptoms, it can be dangerous."
"A lot of work now needs to be done to help people feel like they can go to their doctor as soon as they find something that could be a symptom of cancer.
"Changes to public attitudes, along with changes within the healthcare system, will be fundamental to making a difference. Cancer is more likely to be treated successfully when it's spotted early, so it's crucial that we do something with the results of this survey quickly."
Reasons for delay varied by economic status. People from more deprived areas were more likely to say they were too embarrassed to see a doctor, or worried they might have cancer. More affluent people were more likely to say they were too busy or had other things to worry about.
"We believe that thousands of deaths could be avoided each year in the UK if cancers were diagnosed earlier. We wanted to find out why we were behind the best in Europe on early diagnosis," said Sara Hiom, Cancer Research UK's director of health information. The survey is part of the National Awareness and Early Diagnosis Initiative, which also involves the NHS and Department of Health.
"This survey will be a baseline for understanding why people sometimes put off such a crucial appointment, and for measuring the effect of any initiatives that aim to fix this problem."
http://www.guardian.co.uk/society/2009/oct/07/britons-cancer-symptoms-do...
Eleanor Cappell is the only "social entrepreneur in residence" in the UK. She is attached to, and paid by, NHS Birmingham East and North, a primary care trust (PCT) eager to demonstrate its pioneering credentials. Her business-like manner and BlackBerry-tapping enthusiasm do not suggest that Cappell, 27, is fazed by the uniqueness of her role. However, the ambitions and aspirations of many social theoreticians and progressive politicians rest on her young shoulders. Internationally, she is in the vanguard of an emerging profession.
Cappell's post involves identifying health needs, then developing innovative, not-for-profit services so that they become economically sustainable. Her agenda is radical: economic growth through health provision.
The Saheli Women's Centre in Balsall Heath, south Birmingham, is an example of what she hopes to achieve. As a group, Saheli has grown up over 10 years, developing sports and social activities for its predominantly Asian community. The aim is to provide fitness training in its hi-tech gym and health promotion regimes, mainly for women but also for men.
"Saheli" is the Hindu traditional term for a woman's best friend on her wedding day, the one who keeps her in touch with her native village. The Saheli centre has helped women become more active, encouraging them out of their homes and involving them in community life. Most members – who pay £10 a month – are referred on by GPs for exercise aimed at preventing serious conditions such as diabetes, coronary heart disease and kidney disorders. Here, as elsewhere in the NHS, disease prevention programmes are being belatedly but enthusiastically adopted.
Cappell's interest is in exploring whether she can reproduce this invigorating scheme in Washwood Heath, a deprived district in her PCT area where unemployment has rocketed since the closure of the van manufacturer LDV.
The centre's managers, Naseem Ahktar and Shebina Gill, exude energy and imagination, but can the Saheli centre, which grew out of community activism, simply be copied and recreated – and franchised – in inner cities across the UK?
With two years already spent developing social firms and community groups across the city in her previous role as business development manager for third sector organisation the Initiative for Social Entrepreneurs, Cappell is ideally placed to take on the challenge.
Selling point
"The USP (unique selling point) of this scheme," she says, "is that it's overcoming barriers within the Asian community. We are looking for local women to run it in Washwood Heath."
Another scheme she hopes to develop is called Start Again Football, using sport and exercise as a means of combating depression. "The passion of the man who runs it stems from him seeing his brother being sectioned," Cappell says. "He felt he wanted to do something about it, so we are looking at the viability of existing schemes to become social enterprises".
From her office in a corporate NHS tower block looking out on one of Birmingham's many inner ring roads, Cappell insists that she is not a management consultant working by consensus. "It's much more than that. For me, it's about passion. A social entrepreneur is somebody who's passionate, but with a good business head on their shoulders. It's about inspiring and motivating others to join your cause – about generating income to sustain and grow businesses that make a difference to the environment and people."
Her other employer is the Young Foundation, the long-established London-based centre for social innovation, which selected and placed her in the PCT. The foundation is developing new partnerships through its Health Launchpad team, investing in projects that are "radical in approach and with the potential to transform society".
Two of Cappell's other lead projects could prove more controversial. They involve spinning off in-house NHS services into social enterprises – an idea championed by cabinet office minister Liam Byrne, whose Birmingham Hodge Hill constituency overlaps the PCT area. If successful, employees could be encouraged to leave the comfort of the NHS and work for independent, not-for-profit operations exposed to the unpredictable buffeting of market forces.
"A lot of other PCTs are looking at this," Cappell explains. "We have identified two teams that want to do things differently. We haven't had any discussions [with staff] yet. We are looking at how the projects might add value and improve patient outcome." But she admits: "Staff would be apprehensive about what change means for their employment rights and pensions."
Cappell believes that as many as 15 other social entrepreneurs in residence (Seirs) could eventually be attached to NHS trusts, and that there is no reason why they couldn't be embedded within local authorities.
Joop Tanis, her boss at the Young Foundation, says the Seir approach is that of a venture capital operation. "Eleanor has already looked at 50 to 60 projects, and four of them are real runners," he says. "We had a visit recently from representatives of the top 200 civil servants, who were very interested in the idea of placing an entrepreneur in a public sector organisation."
Andrew Donald, chief operating officer at Cappell's PCT, and a former management consultant himself, is convinced that social entrepreneurs will transform the way the NHS operates. "One of our concerns is to reduce health inequalities," he says. "To do that, we need to do radically different things than are being done in the NHS now.
Exciting bit
"We are trying to develop a preventive system. If people live longer, it reduces the cost of NHS interventions. The exciting bit for me is that, through commissioning new health services, we may create jobs.
"The way we are going to deal with this period of economic austerity is to commission lots of preventive services, and if it reduces the number of acute care interventions it will dramatically reduce the pressure on the NHS budget."
The theory is alluring. If the numbers add up, social entrepreneurs will enhance their reputations as visionary professionals – not only Seirs but also seers.
As Cappell says: "We have health challenges as never before. This is an opportunity to empower people and motivate them. They have energy and passion that money can't buy."
http://www.guardian.co.uk/society/2009/oct/07/social-entrepreneur-nhs-pr...
More than 5,700 patients died or suffered serious harm due to errors and near misses in England, latest figures for a six-month period show.
The National Patient Safety Agency said there were 459,500 safety incidents from October 2008 to March 2009 - the highest rate since records began.
Patient accidents were the most common problem, followed by mistakes made during treatment and with medication.
Experts said the health service had to do more to eradicate errors.
The NPSA operates a voluntary reporting system whereby the onus is on hospitals, GPs and mental health units to record problems themselves.
|
Katherine Murphy, of the Patients Association
|
It has meant that ever since the programme was launched in 2003 the number of mistakes being reported has been rising as more and more trusts join the scheme.
The last six months have been no different with the overall figure representing a 12% rise on the period before.
The NPSA now has 382 of the 392 trusts on board.
A breakdown of the latest figures show that in two thirds of cases - 303,016 - there was no harm to the patient, while a quarter - 122,246 result in low harm.
Another 28,521 - or 6% - resulted in moderate harm and 5,717 - 1% - in death or severe harm, which is classed as permanent injury or disability.
NPSA chief executive Martin Fletcher said the involvement of most trusts showed that the health service was willing to learn from its errors.
"This will help build an even stronger safety culture of reporting and learning to prevent harm to future patients."
Katherine Murphy, of the Patients Association, agreed the increasing involvement was encouraging.
But she added some of the levels of mistakes being made were too high.
"Patients shouldn't have to face a postcode lottery on patient safety."
And Peter Walsh, of Action Against Medical Accidents, said the reporting of safety incidents should be made mandatory, adding: "Not to do so would be a travesty."
http://news.bbc.co.uk/1/hi/health/8295417.stm
The NHS is turning to no win, no fee legal representation - despite being a persistent critic of the practice.
The health service has spent the last few years complaining the no win, no fee culture has led to a rise in costs incurred in medical negligence cases.
But the NHS Counter Fraud Service is now embracing the system after reaching an agreement with a law firm in a bid to recoup more money lost to fraud.
Patient groups accused the NHS of double standards.
|
Joyce Robins, of Patient Concern
|
Half of the medical negligence cases the NHS deals with now are brought on a no win, no fee basis whereby lawyers get paid only if they win the case.
But in return for taking on such a risk, they increase their rates of pay and the practice has led to accusations they have tried to entice patients into legal action.
Nonetheless, the Fraud Service, which supports individual trusts in bringing action, believes the agreement with a law firm called Capsticks will help the service recoup money.
Under the terms of the scheme, Capsticks will provide expert advice and representation at a discounted rate.
About £6m a year is returned to the NHS following legal action against fraudsters - although the true value of the crime is much higher.
Fraud cases can run into hundreds of thousands of pounds with some of the biggest crimes involving companies with NHS contracts or health workers, such as GPs and dentists, incorrectly billing for work.
There are two routes open to the health service when tackling fraud - criminal and civil action - but both are fraught with difficulties.
In criminal cases a judge may not always order the return of funds and even when they do the case may have only been heard on a small sample of the fraud committed.
Civil action, because the evidence required is much lower, is in many ways a more attractive option.
But trusts have often been reluctant to start proceedings because of the time and resources needed.
As a result, there were just eight civil cases launched last year compared with 60 criminal proceedings.
Exploited
The Fraud Service believes the deal with Capsticks will make it easier to pursue civil action.
No cases have been brought yet as it was only finally signed off during the summer, but there is said to be a great deal of interest from trusts in the service.
Allan Carter, head of operations at the Fraud Service, said: "I don't think we would change our view on no win, no fee."
But he added there was no point ignoring a route that may, in the case of fraud, benefit the NHS.
|
NHS FRAUD
Private contractors - The health service has contracts with private firms for a variety of services, including cleaning, catering and procurement, which are all open to abuse
Dentists - There is scope in the dental contract for dentists to make out they are treating more NHS patients than they do
Pharmacists - They bill the NHS for each prescription they hand out and while many patients do pay for their medicines the fees do not cover the true cost of the treatment so pharmacists claim that back from the NHS. Again there is scope to cheat the system
GPs - Family doctors are now paid a bonus for hitting certain targets and while there is some independent assessment of whether these have been met, cases have begun to emerge where fraud is suspected
|
"We want to help get more funds back into the health service and I think this agreement will help us do that."
He also said that no win, no fee would probably represent only a minority of cases taken on under the deal with Capsticks.
As well as no win, no fee, Capsticks will also be operating under the more traditional hourly and fixed rates.
But despite the potential to recoup more money, there was some surprise at the move.
Joyce Robins, of Patient Concern, said: "They have a right to do it, but I find the attitude quite amusing when they have been so against it.
"I think there is a case of double standards here."
And Karen Jennings, head of health at Unison, said the NHS had been "exploited" by the no win, no fee culture.
But she added: "I can understand why they are looking to do this. With the introduction of the market in the NHS, there is going to be more and more scope for fraud."
http://news.bbc.co.uk/1/hi/health/8292897.stm
Over the last 50 years, there have been impressive social economic and health improvements in this country. People from every class and region are healthier and living longer than ever before. Unfortunately, not everyone is able to share the benefits of these improvements. It is essential that everyone is empowered and encouraged to do so.
Health inequalities are unacceptable. They start early in life and persist not only into old age but subsequent generations. Tackling health inequalities is a top priority for this Government, and it is focused on narrowing the health gap between disadvantaged groups, communities and the rest of the country, and on improving health overall.
Concerted action to reduce the health gap permeates our programmes within the Department of Health and is supported across Government. The Secretary of State for health has announced a new comprehensive strategy for reducing health inequalities, confirmed in the Our NHS Our future: NHS next stage review - interim report. The new strategy will challenge the NHS, as a key player, to live up to its founding and enduring values of universality and fairness addressing unjustified gaps in health status, fair access to NHS services for all and good outcomes for all.
Post-2010 strategic review of health inequalities (the Marmot Review)
On 6 November 2008, the Secretary of State for Health announced that Professor Sir Michael Marmot, Chair of the WHO Commission for Social Determinants, will lead a post-2010 strategic review of health inequalities. The review will be wide ranging and will require the Department of Health leadership across government to develop a joint approach to tackling health inequalities. Local government, the NHS, health and social care system and local community organisations will also be important partners with whom we will need to engage with to help us meet our challenge post-2010, as well as the advice of many experts to help shape our thinking.
Government Response to The Health Select Committee Report on Health Inequalities
This Command Paper sets out the Government's response to the conclusions and recommendations of the House of Commons Select Committee report on health inequalities which was published on 15 March 2009. The Government welcomes the Committee's support and commendation for taking specific action to tackle health inequalities, and for its support for the national health inequalities target
Tackling health inequalities: 10 years on
Published: 7 May 2009
This report reviews developments in health inequalities over the last 10 years across government - from the publication of the Acheson report on health inequalities in November 1998 to the announcement of the post-2010 strategic review of health inequalities in November 2008. It covers developments across government on the wider social determinants of health, and the role of the NHS. It provides an assessment of developments against the Acheson report, reviews a range of key data sets covering social, economic, health and environmental indicators, and considers lessons learned and challenges for the future.
Progress and Next Steps
Health Inequalities - Progress and Next Steps outlines the Government’s approach to hit the 2010 Health Inequalities PSA targets, assessing what has and hasn’t worked, and setting the direction of travel beyond 2010.
Programme for Action
Tacking Health Inequalities: A Programme for Action was launched in July 2003 and is the current Health Inequalities cross government strategy. Backed by twelve departments, the Programme lays the foundation for meeting the government's targets to reduce the health gap on infant mortality and life expectancy by 2010. Reversing this widening gap between social groups is a major challenge and the Programme emphasises the need to improve health and the factors that contribute to health faster in disadvantaged areas than elsewhere.
Status Report on the Programme for Action
Progress against the national strategy is set out in an annual Status Report on health inequalities. The report assesses progress against the target, against 12 cross governments headline indicators and the 82 government commitments included in the Programme for Action.
PSA target
The documents below show the latest monitoring data for the two specific objectives relating to the health inequalities national target - infant mortality and life expectancy. The latest data shows that the trend has widened since baseline, however, there are some signs of success. To review this data in a wider context, further information is available in Tackling health inequalities: 2004-06 data and policy update for the 2010 national target (via the link below).
Wider social determinants
Health inequalities are the result of a complex and wide-ranging network of factors. People who experience material disadvantage, poor housing, lower educational attainment, insecure employment or homelessness are among those more likely to suffer poorer health outcomes and an earlier death compared with the rest of the population.
Health inequalities useful links
External websites relevant to redressing health inequalities in the UK.
Health inequalities guidance and publications
Guidance documents and other publications about the Department of Health's drive to redress UK health inequalities.
http://www.dh.gov.uk/en/Publichealth/Healthinequalities/index.htm
One in eight NHS trusts has been told it must urgently improve the care it provides, by a new regulator publishing ratings on England's 392 trusts.
The assessments by the Care Quality Commission show a drop in the number of hospitals meeting basic standards in areas such as hygiene and safety.
But it also said more services than ever could be rated good or excellent.
From April, the CQC will gain new powers to be able to shut any of the 47 underachieving trusts down.
Rigorous assessment
The new commission, which took over the watchdog duties of the old Healthcare Commission earlier this year, pointed out a number of successes in its report.
These included what it called the notable achievement of most patients in England receiving hospital treatment within 18 weeks.
|
NHS RATINGS 2009
To find out more Care Quality Commission information for England, enter your full postcode here:
This search goes to an external site
|
The government said this was the most rigorous assessment the NHS had ever seen.
NHS Ratings Health Minister Mike O'Brien said the report showed improving standards across the health service.
"We have transformed the waiting experience for millions of patients and now have the shortest waits on record. MRSA and C. difficile infections have been significantly reduced and over three quarters of GP surgeries are providing extended opening hours, giving patients greater choice and more convenient access to GPs."
But shadow health secretary Andrew Lansley said the report showed the government was unable to "turn round poor performers".
"Many staff are doing a great job in keeping up high standards but we cannot allow that to obscure the fact that there has been poor performance in some very important areas in the NHS, such as maternity and stroke services.
"And it is unacceptable that the number of patients who have had their operations cancelled has risen so sharply."
|
PARTICULARLY POOR PERFORMERS
Royal Cornwall Hospitals NHS Trust
Great Western Ambulance Service NHS Trust
Yorkshire Ambulance Service NHS Trust
Maidstone and Tunbridge Wells NHS Trust
Barking, Havering and Redbridge Hospitals NHS Trust
|
The CQC looked at every type of NHS trusts, including acute, mental health, primary care and ambulance.
More than half of primary care trusts were rated good or excellent, with many patients reporting being able to get an appointment within two days and services such as chlamydia screening for young people improving.
There were, however, significant regional variations, with trusts in London performing particularly poorly on patient satisfaction with appointments and opening times.
Fewer mental health trusts were rated excellent or good, and some struggled to meet new criteria on collecting data about services. Ambulance services also failed to perform as well as last year, but the CQC nonetheless praised the general response to emergency calls.
But much of the focus is on hospitals: fewer acute and specialist trusts were rated excellent, with more receiving an unimpressive fair grading.

Based on a system of self-reporting, there was a significant drop in the number of acute trusts fully meeting basic standards such as those relating to hygiene, child protection and training: this was down to 59% of all trusts from 69% last year.
Many also failed to meet new performance targets, such as the collection of maternity data to help improve services, and stroke care.
The number of operations cancelled rose for the second year in a row - equating to 63,000 procedures called off at the last minute for non-clinical reasons.
However a higher proportion are now being rearranged within 28 days of the original appointment, and the figure also reflects the much higher number of people now receiving treatment.
Waiting times for treatment have fallen to 18 weeks or less this year, one of the achievements highlighted by the regulator.
It also noted that 98% of the 19 million patients who attended A&E waited less than four hours, while rates of the infections Clostridium difficile and MRSA had both fallen by about a third - despite hospitals themselves reporting failings in hygeine.
While a number of trusts were singled out for praise - including the Royal Marsden, which has scored excellent every year for both quality and finance - the CQC said the focus now had to be on those which had performed persistently poorly.
Twenty trusts scored weak for overall quality, while 27 others have now never scored higher than fair for either quality or finance in the four years since the ratings system was started.
'Nuclear option'
Some particularly poor performing acute trusts were highlighted: Barking, Havering and Redbridge hospitals received a double weak rating, while the Royal Cornwall Hospitals NHS Trust was deemed weak for the fourth year in a row.
Maidstone and Tunbridge Wells NHS Trust - which saw a deadly outbreak of clostridium difficile amid serious hygiene lapses between 2004 and 2006 - was rated weak for the third year in a row.
The CQC said it intended to work closely with these 47 trusts to sort out their problems ahead of April next year, when it will gain the power to intervene in every trust, from dealing out admonishments to potentially launching prosecutions and closing services down.
"But that would be the extreme nuclear option for any regulator," said CQC head Cynthia Bower.
"Trust are aware of what their issues are, so none of this is going to come as a surprise to them.
"There is an ongoing process of debate to sort these problems out by April, no-one is just waiting around."
The King's Fund chief executive Niall Dickson stressed that overall the report showed the NHS appeared to be performing well, but that it was unfortunate the ratings did not shed light on why some did well and some badly.
"Patients served by the hospitals and other services that consistently rank at the bottom have a right to know why these organisations are not providing the quality of services that is expected from them.
"We need to understand whether the problems are managerial or structural, and what is being done to help them raise their game."

Patients leaving hospital may be being put at risk of harmful reactions to drugs due to poor communication between hospitals and GPs, a study says.
The Care Quality Commission found hospitals often failed to fully pass on details of medication after polling 280 GPs and visiting 12 NHS trusts.
The regulator said it meant GPs could end up prescribing incompatible drugs.
But the CQC said GPs were also at fault for not sharing data when patients were first admitted to hospital.
|
Department of Health spokeswoman
|
While nearly all surgeries provided medicines information to hospitals for non-emergency cases, a quarter were not systematically providing details on previous drug reactions, 14% on existing illnesses and 11% of known allergies, the report said.
However, when the CQC asked GP practices about the quality of information given by hospitals when they discharge patients, 81% said details of medicines was incomplete or inaccurate 'all of the time' or 'most of the time'.
Nearly half of doctors also complained that it took too long for hospital discharge summaries to arrive, meaning patients were seen without a full set of records.
The report said primary care trusts, which are responsible for local health services, needed to do more to monitor and encourage hospitals and GPs to ensure drug information is shared properly.
Mistakes
Prescribing errors and a failure to review medication after a patient leaves hospital are known to cause harm to patients every year.
Such errors and near-misses were the fourth most commonly reported issue to the National Patient Safety Agency during 2008.
One study has estimated that around 4% of all hospital admissions are due to mistakes with medicines that could have been prevented.
CQC chief executive Cynthia Bower said: "It is important that basic systems to share essential patient details are working effectively to get the right information to clinicians at the right time to minimise risks.
"It is clear from this study that services have some way to go before this routinely happens in the way it should."
A Department of Health spokeswoman said the findings would be studied carefully and warned any trusts failing to meet standards could face sanctions from the CQC.
She added: "We acknowledge there is more to do and will continue to strive to make services even safer."
http://news.bbc.co.uk/1/hi/health/8326839.stm
Key areas of lung cancer care are still "woefully inadequate", a report by leading lung cancer experts says.
The UK Lung Cancer Care Coalition, an umbrella group composed of doctors, charities and private health firms, says UK care lags behind Europe.
It says too few patients are receiving treatment, such as chemotherapy or surgery, because of staff shortages.
The government says it already recognises that more needs to be done to improve lung cancer services.
|
Dame Gill Oliver, of UK Lung Cancer Care
|
Lung cancer kills about 34,000 people a year - more than breast, prostate, bladder and leukaemia versions of the disease combined.
Despite being labelled a "smoker's disease", one in eight people with lung cancer have never smoked.
The coalition draws on data from this year's official national audit as well as feedback from leading doctors.
The report says in some parts of the UK, as few as 10% of patients are receiving any form of treatment and nationally the figure is only 51%.
The coalition is calling for a target of 70% - recognising that for some patients further treatment is not advisable because the cancer has already spread too far.
It estimates this would save an extra 3,000 lives a year.
One of the major problems is a lack of access to surgeons - there are only 44 full-time positions for more than 240 separate teams.
The shortfall means that some patients who would be eligible for treatment are being turned down, the report adds.
'Vast inequalities'
Dame Gill Oliver , chairman of the coalition, says: "We are still letting lung cancer patients down.
"Our review shows there are still huge variations and vast inequalities in care across the country.
"We believe that whatever the cause of their disease patients deserve the best care and support."
Five-year lung cancer survival rates are still below 9% in the UK, compared with 12.3% across Europe on average.
But the coalition believes survival rates can be doubled by 2020 by making the disease a priority.
It says more money needs to be invested in diagnostic equipment and the workforce as well as encouraging GPs to refer at-risk patients for tests at an earlier stage.
A Department of Health spokesman said: "We know there is more to do on lung cancer.
"That is why we recently re-convened the Lung Cancer and Mesothelioma Advisory Group to look at many of the issues raised in this review, including access to surgery."
http://news.bbc.co.uk/1/hi/health/8334340.stm
Poor communication between hospital staff and with their patients is far too common and deeply damaging, experts have warned.
Patients left out of the loop and staff clocking on and off without a handover was commonplace, according to the findings of a confidential review.
The National Confidential Enquiry into Patient Outcome and Death looked at the care of over 3,000 terminal patients.
It revealed two-fifths received "sub-standard" care.
Change in the hospital team structure over recent years has seen individual clinicians become "transient acquaintances during a patient's illness rather than having responsibility for continuity of care", says the NCEPOD report.
Kept in the dark
It found a co-ordinated handover of patients between night and day staff only occurred in a quarter of the teams.
In 13.5% of cases lack of communication compromised continuity of patient care.
|
Katherine Murphy of the Patients Association
|
In just over half (53%) of cases there was an apparent lack of input from senior doctors "leading to delays in giving patients timely and appropriate care", report author and surgeon Ian Martin said.
And 30% of the patients were not seen by a consultant within the recommended 12 hours after admission.
In a fifth of patients who were not expected to survive on admission there was no evidence of any discussion between the health care team and either the patient or relatives on treatment limitation.
Many "do not attempt resuscitation" orders were signed by very junior trainee doctors.
NCEPOD chairman Professor Tom Treasure said the report vividly revealed the challenge medical teams face in making the transition between saving life and allowing natural death.
"It should be ensured that patients achieve the best quality of life until they die. Effective team working and communication with patients, relatives and carers are fundamental to getting this right."
Director of the Patients Association, Katherine Murphy, said: "These findings run the risk of undermining basic confidence in the NHS. Some of the examples are shocking.
"NCEPOD is the nearest the NHS has to airline 'near miss reporting'. Its findings must be acted upon, or problems will continue to plague vulnerable patients and their families."
Working time directive
John Black, president of the Royal College of Surgeons, said doctors had long been concerned that the loss of team working in hospitals had fuelled the risk of poor communication, and sub-standard patient care.
He said the implementation of a 48-hour working week under the European Working Time Directive almost certainly meant that the problem had got worse since the latest study was carried out.
Professor Black said the only way to address the problem was to opt out of the directive.
A Department of Health spokesperson said measures had been introduced to improve care - including an end of life strategy - since the report's survey was carried out.
"We are putting in place an extensive programme of health and social care training to support end of life care provision, including pilot projects to support the development of communication skills.
He added that evidence from hospitals already implementing a 48-hour week showed a drop in mortality and no evidence of harm to patients.
"Working together with the local NHS and the Royal Colleges we have set up a rigorous quality assurance process to give us an accurate picture of how EWTD is being implemented and so we can provide support where it is needed."
An outbreak of the Clostridium difficile (C. diff) bug has killed two hospital patients and contributed to the deaths of three more.
The patients were among a total of eight elderly people who contracted the infection at Ninewells Hospital in Dundee over an 18 day period.
All of those affected had been in the hospital's ward 31, which generally cares for geriatric patients.
Seven of the patients had contracted the more dangerous 027 strain.
NHS Tayside said it carried out regular testing in order to detect C. diff outbreaks early.
Dr Gabby Phillips, lead infection control doctor for Ninewells Hospital, said the ward remained closed to new admissions.
The hospital has been dealing with the outbreak since September, over a 10 week period.
The deaths occurred between 19 October and 6 November.
'Appropriate measures'
Dr Phillips added: "We have comprehensive infection monitoring procedures throughout our hospitals and these are able to rapidly identify any emerging trends of infection which then trigger a rapid response from our infection control teams.
"These cases of C. diff infection were detected very early which meant we were then able to identify the 027 strain rapidly and reinforce all appropriate infection control measures.
"There have been no new cases identified in the ward for 10 days. I am confident that all appropriate procedures to deal with this infection were put in place immediately."
She added that the hospital had sought external advice over its policies and procedures, and had been "reassured that our surveillance systems are robust".
http://news.bbc.co.uk/1/hi/scotland/tayside_and_central/8352612.stm



Investigators have criticised the standards of health care available to people with learning disabilities.
But will the joint Health Service and Local Government Ombudsmen report make a difference?
The care Martin Ryan received was shocking.
The 43-year-old, who had severe learning disabilities, Down's syndrome and epilepsy, suffered a stroke at the care home he was living at in November 2005.
He was admitted into London's Kingston Hospital, but in the 26 days he was there until his death he was not fed.
The stroke had affected his ability to swallow, but it was not until more than a fortnight after being admitted that his medical team decided tube feeding was needed.
Staff at the hospital said they found it difficult to assess and treat him - Mr Ryan could not talk - and communication with his carers had broken down.
But just before he was due to have the operation to insert the feeding tube, Mr Ryan developed pneumonia.
He was deemed too ill to undergo the surgery and four days before Christmas he died.
His mother, Vera, accused the hospital of "starving him to death" and complained about the standards of care at the hospital - there was no dedicated facilities for stroke patients.
Medical experts could not say for sure whether the failure to feed Mr Ryan had caused his death, but they said "undoubtedly placed him at considerable risk of harm".
Criticised
The lack of specialist services for stroke patients and leadership shown by doctors and senior staff was also criticised.
In short, the hospital had poor services which was compounded by the failure to properly deal with a patient with learning disabilities.
But this is not the only case where someone with learning disabilities had suffered at the hands of the NHS.
The ombudsmen report looked at five other cases. In one case, they ruled, the care given to man with learning disabilities contributed to his death.
There are also a number of other cases still under investigation and campaigners believe this is just the "tip of the iceberg".
Understandably, families and carers are now asking whether standards will improve.
The government has already published a three-year strategy, Valuing People Now, to improve services for people with learning disabilities across health, housing, employment and community care.
A new Public Health Observatory is being established to provide better data on the health of people with learning disabilities and feed into training courses for medical students and NHS staff.
Ministers have also promised an inquiry into premature deaths among people with learning disabilities.
But does this represent a watershed for people with learning disabilities?
The government hopes so as do councils which are so often involved in their care through their social services departments.
David Rogers, of the Local Government Association, said services are already reviewing the way they treat people and with the issue of personalisation of care at the top of the political agenda progress should soon be seen.
"People are quite rightly being viewed as individuals and this means they will be treated with more dignity and respect."
But Mencap, the charity which has campaigned long and hard on the issue, is not so sure.
Its response to the ombudsmen's report was noticeable for the fact that it did not think the investigators went far enough.
The charity said it wanted to see doctors named and shamed and is now threatening to refer some of those involved in the cases highlighted to the General Medical Council.
A Mencap spokesman said: "What we really need is for health staff to be aware that they have to provide people with learning disabilities the same quality of care as everyone else.
"It is not good enough for doctors to ignore their needs, but the only way we will get to that point is by making people accountable. They need to know that they will be in trouble if they don't."