Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Saturday, March 12, 2016

Insufficient knowledge of stroke patient’s last hours of life

Something to think about.

Insufficient knowledge of stroke patient’s last hours of life

 
Caregivers are displaying insufficient knowledge of how things are for stroke patients the week before they die – for example, staff have difficulties stating whether the patients had someone with them at their death, or if they were experiencing pain. Care for stroke patients therefore risks becoming worse compared to patients who die from cancer.
Nearly 20 percent of those who suffer a stroke die within one month, and 40 percent die within a year. With death so close, the care the patients get at the end of their lives is enormously significant.
But general palliative care for stroke patients has deficiencies, as new research from Linköping University shows.
“There seems to be ignorance among those caring for stroke patients about how things are for the patients the week before they die. For example, it’s not known whether the person dies alone, or if they are in pain. This is remarkable; we don’t see the same tendencies in cancer care,” says Heléne Eriksson, who worked as a nurse for 25 years and is now a PhD student.
Four researchers from Linköping University compared palliative care for stroke patients with that for cancer patients. The comparison was made using the Swedish palliative care register, to which caregivers report in the event of a death. What researchers reacted to was the remarkable differences in what the caregivers know about their patients in the last week of their lives. Caregivers for stroke patients know to a much lesser extent how things are for their patients before they die.
Registry data also shows that stroke patients, to a lesser extent than cancer patients, are stated as suffering from pain, from feeling sick, from confusion and anxiety, and from dyspnea (breathing difficulties) in their last week of life; on the other hand, they suffer more from rattling breath. Stroke patients seeming to suffer from fewer symptoms compared to cancer patients, however, need not tally with reality; it may be a result of the deficient insight of staff into how things were for the patient.
Death not talked about
The study also shows that care for stroke patients at the end of their lives is worse as regards information. The ‘turning point’ conversation – where people are told that a cure is not possible and that care will instead enter a palliative stage – is rarely held with stroke patients. Researchers do not know if this is due to the conversation not being prioritised or if the patient’s condition is too poor for it. Nor, after the patient has died, do those close to the stroke patient get a follow-up conversation to the same extent as those close to the cancer patient – something that could be important for them when the course of the illness can go quickly.
“Being given good care in the last hours of life is important for all people, even for those who don’t die of cancer. They should have as peaceful a death as possible, and avoid an emergency care environment where care staff and family members are running in and out to care for other patients in the same room,” Ms Eriksson says.
She argues that care for stroke patients at the end of their lives has the potential to be improved, and is looking for more training and routines that function, regardless of diagnosis.
The study, which is a part of a doctoral thesis, has been published in PLOS One. The authors are PhD student Heléne Eriksson, Professor Katarina Hjelm, reader Anna Milberg and reader Maria Friedrichsen, all of Linköping University.
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0147694#sec008

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