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.

Friday, November 10, 2017

Scientists have discovered why patients develop life-threatening infections after stroke

More work needed which that non-existent stroke leader should be told about to followup. IF we had ANY stroke leaders at all.

Scientists have discovered why patients develop life-threatening infections after stroke

Editors note: Having a stroke damages immune cells as well as affecting the brain.The findings help explain why patients have a greater risk of catching life-threatening infections, such as pneumonia, after having a stroke. This knowledge can now be used to generate targeted therapies.

Motivation behind the research

Stroke is a leading cause of death and disability worldwide and is most commonly caused by a blockage in an artery carrying blood to the brain. Currently, the only effective treatment is pharmaceutical or mechanical unblocking of the artery, and this is only available to a limited number of patients depending on the type of stroke and how quickly they are admitted to hospital. There are additional complicating factors of stroke that can worsen the damage in the brain and further impair the recovery of patients. Infection is the most common complication and can affect up to one-third of patients. Bacterial lung infections are the most common types of infections and are associated with increased death and reduced functional recovery of survivors. If we can understand why stroke patients are especially susceptible to these infections, we can identify new therapeutic targets to reduce the risk of infection and improve survival and recovery of patients after stroke.

The Discovery

Using an experimental model of stroke the in mice, research found that stroke results in the loss of a special population of antibody-producing immune cells in the spleen called “marginal zone B cells”. The antibodies produced by these cells are crucial for anti-bacterial defence. The numbers of marginal zone B cells and levels of their protective antibodies were greatly reduced after experimental stroke, and the animals developed bacterial lung infections. Signals from the brain to nerves in the spleen after stroke resulted in increased levels of the chemical noradrenaline, which was responsible for the loss of the marginal zone B cells.
Researchers blocked noradrenaline using a drug called propranolol. As a result, they successfully protected the cells after stroke, restored the antibody levels and reduced infection in the animals. Analysis of blood samples from stroke patients showed a similar reduction in protective antibodies which suggests the same loss of cells is also occurring in humans. Supporting this, patients who developed infections after stroke were those with the lowest levels of antibodies in their blood.

The Future

Identifying this previously unknown defect in our immune defences after stroke will give scientists and doctors a new target to try to restore the body’s own anti-bacterial defences and reduce infection levels in stroke patients. Targeting marginal zone B cells, or their functions, may provide a new approach to prevent infection in stroke patients. By preventing or minimising the impact of infection after stroke, researchers hope to improve survival of patients and reduce disability.
Research Article: Adrenergic-mediated loss of splenic marginal zone B cells contributes to infection susceptibility after stroke. Nature Communications 8, 5051 (2017). doi:10.1038/ncomms15051
Scientists bio: This article was written by Dr. Barry W. McColl, the lead investigator of this research. Barry is a principal investigator at the Roslin Institute, University of Edinburgh, UK.

No comments:

Post a Comment