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Is PSP life limiting?

These complications can be fatal. The rate of progression with PSP varies significantly from person to person. The average life expectancy after diagnosis is approximately seven years, which means that half the people with PSP will live longer, some up to 15 years, and half will live shorter, even as short as 3 years.
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How long can a person live with PSP?

PSP typically progresses to death in 5 to 7 years,1 with Richardson syndrome having the fastest rate of progression.
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Is PSP always fatal?

Although PSP isn't fatal, symptoms do continue to worsen and it can't be cured. Complications that result from worsening symptoms, such as pneumonia (from breathing in food particles while choking during eating), can be life threatening.
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What are the survival rates of PSP?

Results: The median survival of PSP patients (8.0 years; 95% CI 7.3 to 8.7) was significantly shorter than that of FTD patients (9.9 years; 95% CI 9.2 to 10.6). Corrected for demographic differences, PSP patients were still significantly more at risk of dying than FTD patients.
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What is the 4th stage of PSP disease?

Advanced stage: In the advanced stage of PSP, individuals may become wheelchair-bound and require assistance with daily activities such as eating, dressing, and bathing. Symptoms such as rigidity, spasticity, and involuntary movements become more severe.
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Current challenges in PSP management

What are the final stages of PSP disease?

Advanced stages

As PSP progresses to an advanced stage, people with the condition normally begin to experience increasing difficulties controlling the muscles of their mouth, throat and tongue. Speech may become increasingly slow and slurred, making it harder to understand.
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How fast does PSP progress?

PSP typically begins in late middle age and worsens over time, with severe disability occurring within three to five years of onset. The disease can lead to serious complications such as pneumonia, choking, head injury, and fractures.
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How does PSP cause death?

Eventually, swallowing food, and particularly liquids, can be poorly coordinated, leading to the leakage of food into the windpipe (dysphagia). This can result in pneumonia, the most common cause of death in PSP.
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Are PSP patients in pain?

Pain can be present as a direct result of PSP, or as part of any other conditions that you are experiencing.
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What are the 4 stages of PSP?

The four stages are: Early stage. Mid stage. Advanced stage.
...
End of life stage:
  • Severe impairments and disabilities.
  • Rapid and marked deterioration in condition.
  • Decisions with regard to treatment interventions may be required, considering an individual's previously expressed wishes (advance decisions to refuse treatment).
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Do PSP patients have dementia?

Progressive supranuclear palsy (PSP) is a condition that causes both dementia and problems with movement. It is a progressive condition that mainly affects people aged over 60. The word 'supranuclear' refers to the parts of the brain just above the nerve cells that control eye movement.
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What does PSP do to the brain?

Progressive supranuclear palsy (PSP) is a rare neurological condition that can cause problems with balance, movement, vision, speech and swallowing. It's caused by increasing numbers of brain cells becoming damaged over time.
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How can I help someone with PSP?

Physical therapy and occupational therapy, to improve balance. Facial exercises, talking keyboards, gait and balance training also can help with many of the symptoms of progressive supranuclear palsy.
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Does PSP run in families?

Most cases of progressive supranuclear palsy are sporadic, which means they occur in people with no history of the disorder in their family. However, some people with this disorder have had family members with related conditions, such as parkinsonism and a loss of intellectual functions (dementia).
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Do people with PSP go blind?

Involuntary eye closure is common in PSP. It can be mild and irritating or severe with functional blindness.
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What is the average age of onset for progressive supranuclear palsy?

According to some reports, PSP is estimated to affect as many as 5-17 in 100,000 people, but recent autopsy studies found PSP pathology in 2-6% of elderly people that had no diagnosis of PSP before death. The onset of this disorder occurs between 45 and 75 years of age, with the average age of onset at about 63 years.
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Why do PSP patients fall?

Nocturia in PSP relates to bladder instability and can also contribute to falls, especially if patients are trying to reach the bathroom or commode at night in low light, unattended, and without time to adjust to postural and thermal shifts on getting out of bed.
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Is PSP worse than Parkinson's?

People with PSP tend to stand straight or tilt their heads backwards (resulting in backwards falls), while people with Parkinson's usually bend forwards. Problems with speech and swallowing tend to be more common and severe in PSP than in Parkinson's and are often more apparent earlier.
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Do people with PSP sleep?

Sleep can be challenging for people who have been diagnosed with PSP with both insomnia and impaired sleep being common. Prior studies have shown that sleep/waking regulation and REM sleep regulation are disrupted in PSP, leading to profound sleep deprivation without any recuperation the following day.
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What are the traits of PSP?

As originally described, PSP was characterized by progressive supranuclear ophthalmoplegia, gait disorder and postural instability, dysarthria, dysphagia, rigidity, and frontal cognitive disturbance [1].
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Do PSP patients hallucinate?

Finally, 11% had hallucinations and 5% delusions. These behaviors pose a particular challenge in regards to patient management for caregivers of patients with PSP. Overall, there is significant neuropsychiatric morbidity in these patients who are primarily seen by movement disorder specialists and neurologists.
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Is PSP caused by stress?

Stress is associated with the development of neurofibrillary tangles via glucocorticoids. Hypertension is associated with an increased risk for PSP by inducing the aggravation of tau pathology and neuroinflammation. Inflammation may be associated with pathological tau accumulation and neurodegeneration.
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How rare is progressive supranuclear palsy?

Progressive supranuclear palsy (PSP) is a rare brain disorder that causes dementia and problems with walking and balance. About 20,000 Americans — or one in every 100,000 people over age 60 — have PSP.
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Is supranuclear palsy painful?

Pain was significantly more common and more severe in PD and MSA compared to PSP (P < 0.01). Pain locations were similar with limb pain being the most common followed by neck and back pain.
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