What is post-polio syndrome?
Post-polio syndrome (PPS) is a condition that affects polio
survivors 10 to 40 years after they had polio. PPS causes loss of
muscle function, tiredness, weakness, and trouble swallowing.
About 25% of polio survivors develop PPS.
Polio was a terrible viral disease in the 1900s up through the
1950s. Since then polio vaccination has almost eliminated polio
worldwide. The last US outbreak was in 1954. However, many people
who survived the disease and are still alive today are suffering
the aftereffects of polio and disability--a medical problem now
recognized as post-polio syndrome.
How does it occur?
The cause of PPS is not completely understood. The original
poliovirus infection attacked nerve cells responsible for muscle
movement, hurting or even killing the cells. Surviving nerve cells
grew extra branches. These branches attached to muscles that had
lost their original nerve supply during the polio infection. After
the new nerves attached, the muscles were able to work again. Some
researchers think that post-polio syndrome develops because these
extra nerve branches weaken over time. The muscle then loses its
ability to move properly.
What are the symptoms?
Symptoms of PPS are:
- tiredness
- increasing muscle weakness
- trouble swallowing
- wasting away of muscles (atrophy)
- joint pain
- skeletal problems, such as scoliosis (curvature of the spine).
How is it diagnosed?
Your healthcare provider will test how well your muscles work,
checking for a pattern of weakness that is typical of PPS. You may
also have other tests such as:
- imaging tests, or scans, such as MRI, CT, and PET
- tests of samples of muscle tissue (biopsies)
- tests of spinal fluid.
How is it treated?
No treatments have been found yet that can cure or prevent PPS.
Many unproven treatments are being tried in the hope that they
will have some effect. Small studies suggest that some drugs don't
work or have very little effect. Some case studies report benefits
of the medicine selegiline in 1 or 2 people, but larger studies
have not been reported. Other treatments show small positive
effects but not much overall benefit, such as immunoglobulin given
intravenously.
Electronic nerve stimulation devices (TENS) may help relieve pain.
Heavy use of muscles and massage may have been harmful for you
during the active poliovirus infection, but it may be helpful for
post-polio syndrome.
If you used a ventilator during your original polio infection, you
may need to use a ventilator again to help you breathe.
The future in PPS treatment may focus on helping the nerves grow
new branches.
How long will the effects last?
PPS worsens very slowly. There may be long periods of time when it
does not worsen. Unless you have severe lung problems, PPS is not
usually life threatening.
How can I take care of myself?
- Manage new weakness with strengthening, stretching, and
aerobic exercise. Avoid exercise that makes your joints hurt.
Stop exercising if your muscles start hurting or get tired.
- Don't let yourself get too tired. Have regular rest periods or
daytime naps. Early afternoon can be a good time to take a
nap.
- Take pain relievers such as acetaminophen or ibuprofen.
- Put ice or heat on your muscles to help relieve pain.
- Consider using devices that can help you be mobile, such as
canes, crutches, wheelchairs, and motorized scooters.
- Manage swallowing problems by:
- eating smaller and more frequent meals during the day
- avoiding eating when you are tired
- turning your head to one side or tucking down your chin
while swallowing.
For more information, contact:
International Polio Network/Gazette International
Phone: 1-314-534-0475
Web site: http://www.post-polio.org
The following journal article provides a summary of current
knowledge and recommendations for treatment of PPS: The guidelines
developed by the European Federation of Neurological Societies
emphasize regular exercise and getting helpful assistance from
braces or other adaptive devices if you need them: Farbu E, NE
Gilhus, MP Barnes, et al. EFNS guideline on diagnosis and
management of post-polio syndrome. Report of an EFNS task force.
Eur J Neurol 13 (2006): 795-801.
This content is reviewed periodically and is subject to
change as new health information becomes available. The
information is intended to inform and educate and is not a
replacement for medical evaluation, advice, diagnosis or
treatment by a healthcare professional.
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