Media
21
Jul 10

Dementia

Dementia

What is dementia?

Dementia is not a single illness. It is a group of symptoms caused by specific brain disorders. The most common cause is Alzheimer’s disease, but dementia can also be the result of a stroke or mini-strokes.

The main symptoms are:

•    loss of memory – such as forgetting the way home from the shops, forgetting names or places, or being unable to remember what happened earlier in the day

•    mood changes – because of damage to parts of the brain that control emotions, people can become frightened, angry  or sad more easily

•    communication problems – a decline in the ability to talk, read and write

Dementia is progressive – the symptoms will get worse over time. Although there is no cure, treatments can slow the progression of the disease, and there are ways of helping to keep it manageable.

 

Understanding dementia

In Ireland, it is estimated that some 38,000 people are likely to have dementia. Because our population is ageing, these figures are likely to reach between 80 000 and 100 000 over the next 30 years. Both men and women are affected.

Becoming forgetful does not necessarily mean that someone has dementia: memory loss can be a normal part of ageing, and it can also be a sign of stress or depression. If you know someone who is worried about their memory, encourage them to visit their GP. A proper diagnosis of dementia is essential. The doctor – either a GP or a specialist – will carry out a number of tests, looking at both memory and the ability to perform daily tasks. The doctor will also aim to rule out any illnesses that might have similar symptoms to dementia, including depression. The right diagnosis, whatever it may be, can help patients and those close to them prepare and plan for the future.

 

Five simple ways to help someone living with dementia

1   Respect and dignity : Focus on what the person can do, not what they can’t.

2   Be a good listener and be friendly :  Support and accept the person, be patient.

3   Do one little thing : Cook a meal or run an errand, it all helps.

4    Make time for everyone : Partners, children and grandchildren will be affected.  Could you do something to help one of them?

5   Find out more : Understanding dementia makes living with it easier.

 

Practical tips

Especially in the early stages, there are lots of simple things you can do to help someone with dementia maintain their independence.

•  encourage them to keep a notebook or diary for things such as appointments, To Do lists, thoughts and ideas

•  keep important things like money, glasses and keys in the same place

•  put labels on doors and cupboards

•  place important numbers by  the phone where they can be seen easily

•   put a note on the back of  the door as a reminder to  take keys

•   label family photographs, both on display and in albums

•  pin a weekly timetable to  the wall

•   mark a calendar with the date or get an electronic calendar that changes automatically

•  write reminders to lock the door at night, turn the gas off and put the rubbish out on a certain day

There are products you can buy which are designed to help with memory problems – telephones  where buttons are replaced with photos of people, and pill boxes with compartments for different days. An occupational therapist may be able to advise you on what things could be most useful (you can find an occupational therapist through your GP or social services).

 

Keeping active

People with dementia can continue to enjoy many activities, both individually and with others. Remaining physically and mentally active can help them focus on the positive and fun aspects of life.

Many beneficial activities can be simple everyday tasks, such as taking a walk, polishing a pair of shoes, listening to the radio or looking after a pet. Think about ways of adapting favorite activities (for example, reading magazines and newspapers rather than books), to help the person avoid feeling frustrated that they can’t tackle things they previously took for granted.

Keeping active can help the person feel better about themselves by providing a structure to the day and a sense of achievement.  

 

Showing you understand

A diagnosis of dementia can cause different emotions, many of them difficult to manage both for the person with the illness and those around them. There may also be a sense of relief: now that they know what the problem is, they can begin to deal with it.

A person with dementia will probably be sad or upset at times. In the earlier stages, they may want to talk about their anxieties and the problems they are experiencing. Try to understand how they feel, and don’t brush their worries aside. Listen, let them talk, and show that you are there for them. When someone has dementia, they need:

•  reassurance that they are still valued, and that their feelings matter

•  freedom from as much external stress as possible

•  appropriate activities and stimulation to help them to remain alert and motivated for as long as possible.

Many people who have dementia develop what appears to be unusual or inappropriate behavior. Remember their actions may be perfectly rational to them. You may need to think about how their altered view of the world may lead to different ways of thinking and behaving.

A person with dementia is not being deliberately difficult: often their behavior is an attempt to communicate. If you can establish what this is, you can resolve their concerns more quickly. Try to put yourself in their place and understand what they are trying to express and how they might be feeling.

 

Support services

It is worth thinking ahead about support available, so it  will be easier to organize if needed in the future.

•  Social services have a duty to assess the needs of people with dementia. Help may be in the form of home care assistants, laundry services, meals on wheels or nursing care

•  Day care centres are often run by voluntary organisations such as Alzheimer’s Society, or by social services. They can be a great source of support both to the person with dementia and those who are caring for them

•  Respite care is short-term care used as a temporary alternative to someone’s usual care. It gives the carer an essential break from looking after the person with dementia

Other sources of support include hospital care, sheltered housing and residential care. Your GP or social services will know what is available in your area.

 

Other useful information and organizations

The Alzheimer Society of Ireland
National Office: Temple Road, Blackrock, Co Dublin
Tel (01) 207 3800 // Fax (01) 210 3772 // Email info@alzheimer.ie

 

Dementia Services Information and Development Centre

Top Floor, Hospital 4,

St. James’s Hospital,

James’s Street,

Dublin 8, Ireland  

http://www.dementia.ie/

 dsidc@stjames.ie   +353 1 4162035

The Carers Association
Ireland’s national voluntary organisation for and of family carers in the home. Family carers provide high levels of care to a range of people including frail older people, people with severe disabilities, the terminally ill and children with special needs: www.carersireland.com

Health Service Executive
The Health Service Executive provides thousands of different services in hospitals and communities across the country. These services include public health nurses treating older people in the community. This website also includes published Nursing Home Inspection Reports: www.hse.ie

20
Jul 10

O’Reilly concern at care of elderly

DEAGLÁN DE BRÉADÚN Political Correspondent, in Glenties

Systems to provide long-term care for the elderly are largely chaotic, with many people confused about their rights and entitlements and subject to years of stress and crippling expense, Ombudsman Emily O’Reilly said today.

Although the newly-introduced “Fair Deal” Nursing Homes Support Scheme would improve things for many people, what effectively happened was the State now believed it had no further responsibility in this area.

Speaking to the MacGill Summer School Ms O’Reilly said she would shortly publish an investigation into the operation of this sector over the last number of years by the Department of Health and the Health Service Executive.

“It will tell of a largely chaotic ad hoc system, in which many people were not alone confused about their rights and entitlements but also suffered years of stress and crippling expense because of the deliberate failure of the system to clarify their rights to public care let alone provide for them.”

She added: “I am aware that the new system – the so-called Fair Deal system, the Nursing Homes Support Scheme – will make things a lot clearer and a lot better for very many people, but as my investigation will point out, what has effectively happened through the new legislation, is that the State believes it has now divested itself of the responsibility to provide nursing home care.”

She said while Irish people had fancied themselves as possessing “a great community sense” the fault-lines in the health and social services reflected the lack of a shared approach to the State’s responsibility to vulnerable groups.

Home Care

16
Jul 10

Ireland is ranked as fourth-best place to die in world

By Fiona Ellis

Friday July 16 2010

IRELAND has been ranked the fourth best country in the world in a new “quality of death” survey.

The survey, which measured the kind of care given to the dying, was carried out by the Economist Intelligence Unit.

It comes despite a recent damning audit by the Irish Hospice Foundation which examined end-of-life care in Ireland and found serious lapses in the kind of standards expected.

The audit revealed serious differences in the quality patients experienced in hospitals. It also uncovered horrific personal accounts from relatives of people who died in medical facilities.

Yesterday’s survey rated the countries according to the quality of provision of care for those who are at the end of their life.

Ireland beat other comparatively rich countries like the US, Norway, Luxembourg and Canada with a score of 6.8 out of 10. It fell to 17th place, however, for the quality of the healthcare environment, outranked by countries like Hungary and Slovakia.

Commenting on the findings Paul Murray from the Irish Hospice Foundation said, “We are very pleased that Ireland got such a good index marking. However, a lot still needs to be done in hospice care, palliative care and end-of-life care in Ireland.”

The UK came top of the table with Australia and New Zealand second and third, respectively.

- Fiona Ellis

Irish Independent

Home Care

16
Jul 10

Groups representing older people call for pension not to be reduced

GENEVIEVE CARBERY – Irish Times

CALLS FOR the pension not to be reduced in December’s budget were made by three groups representing older people yesterday.

They argued that pensioners had already experienced income and service cuts and such a move would place more older people below the poverty line.

Income reductions already experienced by older people included the loss of the Christmas bonus, dental benefit and optical benefit, as well as the introduction of prescription charges and increased fuel costs, said Mairéad Hayes, chief executive of the Irish Senior Citizens Parliament.

Many older people were “hovering around the poverty line” with one in 10 pensioners living in poverty, Eamon Timmins, head of advocacy at Age Action, said.

Despite a public perception that older people had escaped cuts “nothing could be further from the truth”, he added.

Recent service reductions which have made life more challenging for older people included rationing of home help and meals on wheels as well as the cessation of local authority home adaptation and mobility grants, he said.

Increases to the State pension since 2001 were just playing catch-up, said Patricia Conboy, director of the Older and Bolder campaign. Reductions in the cost of living were largely based on lower housing costs which was “not widely relevant to older people . . . In the areas that do affect them, costs have been increasing.” The inequity of private pension tax relief might be a more appropriate focus for analysis, she added.

Home Care

12
Jul 10

Exercise ‘may reduce dementia risk’

Exercise followed by a relaxing mug of tea might be a good tonic for the brain in old age, research suggests.

In two separate studies, US scientists found that physical activity and regular consumption of tea or coffee both protect against mental decline.

One team led by Dr Zaldy Tan, from Harvard Medical School, Boston, followed the progress of 1,200 elderly men and women with an average age of 76.

Health checks after an average of 10 years showed that those who engaged in moderate to heavy levels of exercise had a 40% lower risk of developing dementia than the least physically active.

The trend was more evident in men than in women, the International Conference on Alzheimer’s Disease in Hawaii was told.

Professor Clive Ballard, director of research at the Alzheimer’s Society, said: “Whether it be a round of golf, a brisk walk or a session on the treadmill, 30 minutes of exercise five times a week can be beneficial at any age. The best way to reduce your risk is to combine exercise with a healthy diet, not smoke, and have your blood pressure and cholesterol checked regularly.”

The second study, also presented at the conference, suggested that a regular cup of tea or coffee can stave off age-related mental decline.

Scientists led by Professor Lenore Arab, from the University of California at Los Angeles, monitored 4,800 people aged over 65 for more than 14 years.

Participants who drank tea regularly were between 17% and 37% less likely to suffer a reduction in mental ability than non-tea drinkers.

People who preferred coffee were also protected. Drinking coffee more than five times a week lowered the chances of mental decline by 20%.

Home Care

9
Jul 10

Inefficiencies in the Provision of Care

The recent publicity around cuts to disability services has brought to light some of the inefficiencies involved in delivering these services which in all probability exist in delivering similar services to other sectors such as children and the elderly.

The HSE delivers a lot of its care services through “not for profit” organisations which it funds partially or wholly with very significant amounts of money. It is vitally important that a proper supervision and cost analysis of these funds is carried out to ensure that the funds are efficiently spent and that the maximum percentage is funnelled towards the provision of frontline services rather than unnecessary administration and management services.

Presently in the disability sector over 200 organisations are providing services. This means an awful lot of doubled up administration costs that could otherwise be going directly to frontline services.

Some organisations have very top heavy organisational structures with several regional chiefs and their attendant bodies.

Where organisation providing care and support are getting state funding it is very often in the absence of detailed service provision agreements. The putting in place of these service agreements would be one way to get better value for money in conjunction with proper regular tendering between services providers and avoiding long term agreements. This would ensure competition between service providers.

The Minister is making headway with these type of issues but a lot more work needs to be done to ensure in these times of economic hardship that there is minimum disruption to frontline services.

Home Care

8
Jul 10

Depression linked to dementia

“Having depression may nearly double the risk of developing dementia later in life,” reported BBC news. It said that a 17-year study of nearly 1,000 elderly people, found that 22% of those who were depressed at the start went on to develop dementia, compared with 17% of those who were not depressed.

This is a well-designed study and was accurately reported by the BBC. It has several strengths and adds to the evidence of a link between the two conditions.

However, as the researchers say, this does not necessarily mean that depression causes dementia and the reason for the association between the two conditions is still unclear. It is unknown if depression is a risk factor for dementia, whether it is an early sign of cognitive decline or if certain changes in the brain are associated with both conditions. Also, certain lifestyle factors not measured by this study, such as poor diet, lack of physical activity and social interaction, may increase the risk of both depression and dementia.

Importantly, this study was in elderly people (average 79 years) and it is unknown if depression earlier in life would be associated with dementia in the same way. Further research is needed.

Where did the story come from?The study was carried out by researchers from the University of Massachusetts in Worcester, and Boston University in the US. It was funded by the US National Heart, Lung and Blood Institute, the National Institute on Aging and the National Institute of Neurological Disorders and Stroke. The study was published in the (peer-reviewed) medical journal Neurology.

The study was accurately reported on by the BBC, which was careful to explain that depression had not been proved to be a cause of dementia and that more research was needed to find out why the two conditions are linked. However, although the BBC mentions that the study was in elderly people, its story could be taken to imply that depression at any age is associated with dementia later. This study did not look at whether depression earlier in life is associated with later dementia.

The BBC also reported on another paper published in the same journal that found that the more times someone experienced depression, the higher their risk of dementia. This paper is not examined in this appraisal.

What kind of research was this?This was a prospective cohort study, which aimed to examine a possible association between depression and dementia. The participants were recruited from the Framingham Heart study, a long-running cohort study that began in 1948 and was initially set up to investigate risk factors for cardiovascular disease.

Cohort studies are useful for looking at potential risk factors for conditions because they are able to follow large groups of people for many years and to assess how certain events (in this case, depression) might impact their health later. As a prospective study, its results are more reliable than a retrospective study. This is because it tracks people forward in time and can establish any relevant information at the start of the study, as opposed to relying on previous medical records or personal recall. There is also added strength in that it ensured that participants were free from cognitive impairment at the time their depression was assessed.

The researchers point out that some, but not all previous studies have indicated a link between depression and cognitive impairment or dementia. Their research aimed to examine this possible association further over a longer follow-up period than previously achieved.

What did the research involve?This particular study began in 1990, when  1,166 members of the original Framingham cohort attended for assessment. A total of 949 attendees were identified to be free of dementia and were included in the study. Of these, about 64% were women and the average age was 79 years.

The participants were assessed for depressive symptoms, using a validated depression scale that has a score ranging from 0-60, with higher scores reflecting greater depressive symptoms. Based on established guidelines, a score of 16 or over was used to define depression. The researchers also recorded who was taking drug treatment for depression. Of the 949 participants, 125 (13.2%) were classified as depressed and a further 39 (4.1%) were taking anti-depressant medication.

The researchers followed up this group for up to 17 years (average follow up was eight years). Those participants that developed dementia were identified using regular examinations every two years. For this, a well-established questionnaire was used to screen for cognitive impairment, together with other relevant findings from the primary care physicians, medical records, observations from clinic staff and personal observations from the participant and their family. Those with possible dementia had further neurological tests and reviewed by a panel of specialists. Diagnoses of dementia were made using a validated diagnostic tool, and further assessments for Alzheimer’s disease made using established criteria.

The researchers used validated statistical methods to analyse any potential link between depression at the beginning of the study and the subsequent development of dementia. Their analyses also took into account many things that can affect the risk of dementia including age, sex, education, smoking habits, history of cardiovascular disease, diabetes and other relevant conditions.

What were the basic results?During the 17-year follow up, 164 participants developed dementia and 136 of these had. A total of 21.6% of participants assessed as depressed at the start of the study went on to develop dementia, compared with 16.6% of those who were not depressed.

Overall, a total 21.6% of depressed participants developed dementia compared to 16.6% of non-depressed participants. This was equivalent to a 72% increased risk of dementia if the person had depression (Hazard ratio [HR] 1.72, 95%, Confidence interval [CI] 1.04-2.84).

For each 10-point increase in depressive symptoms there was a 46% increase in the risk of dementia (HR 1.46, 95% CI 1.18-1.79) and a 39% increase in risk of Alzheimer’s disease (HR 1.39, 95% CI 1.11-1.75).

When the figures were further adjusted to take account of vascular risk factors such as stroke and diabetes, depressed participants were found to have double the risk of dementia (HR 2.01, 95% CI 1.20-3.31).

How did the researchers interpret the results?The researchers say that their findings support previous studies that have suggested depression is a risk factor for dementia and Alzheimer’s.

 home care

6
Jul 10

Avoiding Cuts To Frontline Services

Recently there has been significant media coverage of HSE cuts to frontline services because of reduced budgets. This has caused uproar, with various interested organisations claiming that the most vulnerable in our society are been made scapegoats as they are seen as easy targets.

We all realise that the same money is not available now as at the height of the Celtic Tiger and while it is a pity more was not invested to improve frontline health services and less dedicated to increasing back office resources, we have to live with the fact that savings have to be made.

However, we at Home Care Plus feel that before cutting frontline services we need to examine efficiencies within the delivery of health services, to see where we can in fact improve services without increased expenditure.

One area that is a central plank of HSE policy going forward is the provision of home care. It also impacts one of the vulnerable sectors of society, the elderly.

Presently the HSE spends about €330M per annum on home help and home care packages. The vast majority of this is provided for by the HSE directly and not for profit organisations which are funded directly by the HSE. Private providers cannot compete for the vast majority of this spend leading to a severe lack of competition.

A recent report carried out by the PA Consulting Group for the Irish Private Home Care Association showed the total cost of care carried out by the HSE to be over €29/hour when overheads are taken into account. The private sector can provide this care on average at rates of €21/hour. This translates into a saving of nearly 30%. Applying this to the HSE’s current spend mentioned above would result in a saving of around €90M per annum.

In addition, the private sector generally works to higher standards of care with garda vetting, proper reference checking, training and supervision all being carried out by the main private providers.

The current HSE procurement policy for home help and home care packages is not transparent and it is most certainly not getting the best value for money.

This type of analysis could surely be carried out in other areas within the HSE. In these times of financial crisis, transparent competition is the best way to ensure you are getting the maximum bang for your buck.

Home Care

6
Jul 10

Beyond Caring

The Irish Times – Tuesday, July 6, 2010

Beyond caring

HSE cutbacks are putting community health services under strain, causing widespread anguish, not just for the most vulnerable citizens of the State but also for those caring for them at home, writes MARESE McDONAGH 

INCONTINENCE PADS are being rationed, there are plans to put home helps on a stopwatch when showering elderly clients, and parents are fretting because some public health nurses are too stretched to carry out infant developmental checks.

Ward closures may grab the headlines, but advocacy groups are on red alert as HSE cutbacks put community health services under strain, causing widespread anguish, not just for the most vulnerable citizens of the State but for those engaged in the thankless task of caring for them at home.

Enda Egan of the Carers’ Association is not easily shocked, but he was appalled recently by the indignity inflicted on some of his members, in the name of saving the HSE a few euro.

Egan was horrified to learn that some carers who dared to ask for extra incontinence wear to make their loved ones more comfortable, were asked to bring in used “nappies” to be weighed.

A small number of so-called “incontinence managers” put carers through this trauma in a crude attempt to measure the amount of fluid passed, in order to calculate if they really did need more than the permitted quota of pads, he says.

“We have come across four cases in two months,” says the Carers’ Association chief executive, who has long waged a campaign to highlight the injustice of having incontinence wear subjected to the “luxury” 21 per cent VAT rate.

Egan believes the HSE is snipping away at community health services because, despite the lip service paid to the importance of caring for our elderly and infirm in the community, “it is an easy one to cut”.

His association estimates there are 160,000 carers in the State, most of them family members who provide three million hours of care per week. There are 40,000 full-time carers, slightly more than the 39,000 nurses in the Irish hospital system.

“Of course, you can’t spot them as easily,” says Egan, who believes the value of the 24-hour care provided by these people is incalculable – and worth a lot more than the maximum means-tested €212.50 weekly payment, which only a fraction of the carers get.

A study commissioned for the Jack and Jill Foundation earlier this year underlines that point. The independent Trinity College report, entitled There is No Place like Home , found that it is nine times more expensive to provide acute hospital care for children with severe intellectual and physical disabilities than to have them cared for at home.

The foundation supports 320 families who care for children at home. But just 19 per cent of its annual €3 million budget comes from the State – and recently it suffered a 6.5 per cent “value for money” cut. Last week, the Minister for Health allocated an extra nurse to the foundation.

But spokeswoman Carmel Doyle points out that recycled mobile phones are still its main source of income. While they have been a spectacularly successful source of revenue, she wonders how long vulnerable children, who in many cases cannot walk, talk, see or eat independently, will be able to depend on the nation’s cast-off phones in order to survive.

For financial reasons, the foundation can only support children up to the age of four but, according to Doyle, more revenue is urgently needed so that it can extend its remit to children aged up to six. “We don’t want to leave them high and dry at four.”

Sinéad Moran, paediatric co-ordinator with the Jack and Jill Foundation, said that 35 children on its books have reached or are about to reach the four-year-old threshold and negotiations are under way with a view to getting the HSE to replace the nursing hours these families are about to lose.

“Many just won’t cope if they don’t get this nursing care,” she says. Moran says there is also a huge issue now for parents of severely disabled children, who find that funding for specialist equipment is drying up.

“These children need special equipment, buggies which support their trunks, special chairs for feeding, walking frames which allow them to stand for maybe 20 minutes a day. They now have to wait months for these things and it is putting a lot of strain on families.”

The foundation provides a nurse two nights a week to the parents of Tommy Simon from Knockarush, Boyle, Co Roscommon, a severely disabled boy who requires round-the-clock care.

“They have been sent to us from heaven,” says Tommy’s father, Frank, who explains that without help at night he and his wife, Niamh, would never get any sleep.

“Our problem is that Tommy will be four in a few weeks’ time, so that is a big worry,” adds Frank. Other parents are worried too.

The Irish Nurses Midwives Organisation (INMO) has warned that the roll-out of the cervical cancer vaccine programme combined with staff shortages means that the ongoing problem of delayed developmental checks for babies will continue.

Labour’s Health spokeswoman, Jan O’Sullivan, says that in many parts of the State, checks which should be done at nine months and which are crucial for picking up hearing difficulties, are being delayed.

“We have also had reports that hearing and eyesight tests, which are usually done on junior infants, have not been done in some schools this year,” she says.

The abrupt closure of respite centres such as Bawnmore in Limerick is causing anguish for carers, many the elderly parents of intellectually disabled adults, who will now never get a break even when ill, she points out.

The closure of the Brothers of Charity facility, which catered for 63 families, has been described by the chaplain, Fr Joe Young, as “the greatest injustice I have experienced in 34 years as a priest”.

The HSE says no decision has been made that has an impact on developmental checks or routine vaccinations in order to facilitate the HPV programme, but some parents say there have already been significant delays.

The HSE acknowledges that last winter’s swine flu campaign, “the largest public health immunisation campaign ever undertaken in Ireland”, led to deferrals of some routine vaccinations and developmental checks. But it says catch-up campaigns have been in place since April.

Claire O’Connor, from Harold’s Cross in Dublin, says her son’s nine-month check is now a month and a half overdue and she is worried about his hearing because he has been getting repeated ear infections.

“I know I can bring him to the GP and I have done that,” she says. “But apart from the fact that it’s €55 every time and I am on unpaid leave from my job, GPs don’t specialise in paediatric care, and I was hoping to have him seen by someone with specialist training who would pick up any problems from a developmental point of view.”

The first time she rang her local health clinic she was told there was a huge backlog and to call back in a month if she was not called.

“I did that but the next time they did not even seem to have me on record and they were telling me that the check can be done any time from nine to 12 months,” she says.

Phil Ní Sheaghdha, director of industrial relations with the INMO, says that if the moratorium is not lifted, public health nurses, still playing catch up after last winter’s swine flu vaccination programme, will be so busy with the HPV vaccine that developmental checks will be further delayed, with potentially damaging consequences.

She stresses that PHNs doing these checks in the home also pick up on other serious issues such as post-natal depression and problems with breastfeeding.

Ní Sheaghdha says there could also be child protection implications if nurses are too stretched to visit vulnerable families. “Sometimes parents don’t want a social worker to call maybe because they are afraid of losing their children, but they don’t have a problem with a public health nurse,” she explains.

Ní Sheaghdha says staff shortages caused by the moratorium on recruitment means public health nurses are not calling to see vulnerable elderly people as often as they would like. “And we have been told that there is a waiting list for palliative care in Kildare. You cannot wait when you are dying,” she says.

Age Action Ireland recently highlighted proposed cuts to home help services, which many working in the sector say could actually put vulnerable people at risk.

The HSE draft guidelines proposed that home helps allocate just 10 minutes to getting older people up and dressed in the mornings, while 15 minutes was the recommended allotted time for helping someone shower.

Ten minutes should be spent getting breakfast and the home helps should spend their visit looking after the client’s “personal care” rather than doing housework or other tasks such as popping out for a litre of milk.

Public health nurses, who are themselves spending less time doing what they regard as essential “surveillance” work spotting potential health problems before they develop, are also horrified at the attempt to speed up home helps.

“How long would it take you to transfer someone from a wheelchair onto a shower seat and get them showered and back out again?” asks one nurse. “Apart from the stress this would put on any elderly frail person whether in a wheelchair or not, can you imagine the consequences if they slipped and fell and maybe broke a hip because someone was trying to meet a deadline?”

Noel Treanor, the INMO’s industrial officer in the northwest, says that early discharges from hospital means an explosion in the number of people requiring support in the community – at a time when the moratorium and the vaccine programmes mean PHNs are unable to do vital surveillance work.

“Not everyone is articulate enough to demand the assessment or the follow-up care they need,” says Treanor.

He points out that because manpower is so stretched, nurses in some regions have been given a list of priorities, which beg the question which services are being put on the back burner.

Maureen Kavanagh, chief executive of Active Retirement Ireland, says it is wrong to even contemplate putting a stopwatch on a home help who is assisting a frail elderly person to have a shower or to get dressed.

“I am concerned that these things are being done from an administrative point of view. Timing a shower is a paper exercise – it has nothing to do with the human.

“I would question whether we are losing the human touch in the health service. If we do, this will not be a good country to grow old in.”

Home Care

1
Jul 10

HSE – papering over the service cracks?

 Niall Hunter, Editor – www.irishhealth.com]

Our health service currently comes in two versions – the official one that tells us that real reform and progress is being made in delivering better care.

And then there’s the harsh reality that many of us are only too aware of, and which poses a major question mark over the safety of care being delivered.

Much of the HSE’s latest annual report read more like a glossy company report than an account of how a ‘patient-centred’ health service is being delivered. You cannot help but get the impression that there is more emphasis on financial rather than patient outcomes.

We are told that the HSE had delivered services 3% ahead of targets, extra services were provided within budget, that staff numbers came in below projected levels and that savings were achieved through efficiencies and cost containment measures.

The HSE trumpeted the progress it was making in (slowly) setting up primary care teams, in cutting waiting lists (although numbers are starting to rise again, which didn’t get a mention), in opening some new hospital units and services, and in treating 3.4 million outpatients, although again it was not mentioned that there are over 175,000 people on outpatient waiting lists.

However, HSE CEO Prof Brendan Drumm, in one of his valedictory statements as he enters the final lap of his tenure, also told us that staff were going that extra mile to provide ‘more care with less funding’. At first glance this sounds like a good thing – getting better healthcare value for money for our tax dollars.

And it cannot be denied that the HSE under Prof Brendan Drumm has had to live recently in straitened budgetary times, but has managed to root out some waste and inefficiency, as well as recording some successes such as re-organising cancer care.

However, might ‘staff going that extra mile to provide more care with less funding’ also mean ‘staff struggling to maintain safe and quality care with ever diminishing resources?’

Read another report, the latest HSE financial performance report, for the year up to the end of April, and you’d be inclined to take the more pessimistic view.

The report showed us that the HSE, which has suffered a massive €1.2 billion budget cut this year, is finding it difficult to deliver a reasonable standard of service within the unprecedented budgetary restraints it is now labouring under.

The situation is exacerbated by the fact that the pay cuts and income gathering targets aimed at meeting most of the deficit are not being met. The fact that the job reduction target is not being met means that new posts may be denied to vital new services in areas such as cancer.

The HSE’s financial report expressed concern about the effects of the recruitment moratorium on service delivery, indicating that vital frontline staff were not being replaced. The HSE’s deficit for the year is already exceeding €100 million, and while that is small in the context of a €14 billion allocation, in terms of a tight budgetary situation it can mean a lot. And further cuts may have to be made to deal with it.

The HSE has been learning to live on diminishing resources over the past few years. The obvious challenge is how much further can the budget cuts go before the HSE holds up the white flag and says it cannot guarantee a safe service for the money it has at its disposal.

Recent events would indicate that the level of cuts being imposed on the HSE are starting to compromise the delivery of safe and good quality care. And at this stage the warnings being given are not merely industrial relations or vested interest rhetoric.

These worrying developments include:
* Extra beds moved onto wards/beds on corridors to cope with increasing pressure on emergency departments (EDs). Traditional summer decrease in trolley numbers not taking place to any great extent.
* Ambulances delayed at a major Dublin hospital while their trolleys were used for the ED.
* Patients dispersed from an Alzheimer’s unit at a Dublin hospital.
* Some patients requiring MRI scans having to wait three to four months to get a scan.
* Delays in developmental check-ups for infants.
* Continuing cuts in acute bed numbers with no real evidence of transfer of resources to boost primary and community care.
* Growth in numbers on inpatient and day case waiting lists.
* Institute of Obstetricians indicating that maternity units may currently be prevented from sticking to best practice guidelines due to a shortage of staffing and resources.
* Threatened scuppering of plans to hire staff for new cancer services.
* HSE itself admits that it is concerned about the recruitment moratorium’s effect on service delivery.

The crisis the HSE faces in terms of delivering adequate services with less and less money will be the most immediate challenge facing new CEO, Cathal Magee, when he takes over on September 1.

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