- pain, breathing and/or swallowing difficulties, sleep disorders, muscle twitching (fasciculations), and gastrointestinal problems. The muscle problems in PPS can occur in previously-affected muscles, or in muscles that were thought not to be affected at the onset of polio. The onset of PPS is usually gradual, but it is sometimes abrupt, with major loss of function suffered over several months or a couple of years. This process often seems to start after a physical or emotional trauma, an illness, or accident. Complications of PPS may include neuropathies, nerve entrapments, arthritis, scoliosis, osteoporosis and, sometimes, post- polio muscular atrophy (PPMA). Diagnosis is made by history, by clinical findings, and by ruling out other diseases that may mimic PPS. There are no specific tests to provide unquestionable confirmation of the diagnosis of PPS. The general rule is that those who were most seriously affected by the virus at initial onset and made the best recovery come to suffer the worst PPS symptoms years later. No clearcut cause for PPS has been found. There is known to be a failure at the neuromuscular junction. One idea is that nerves and muscles that have had to overwork prematurely fail, but this is unproven. There is also known to be impairment in the production of certain hormones and neurotransmitters, but whether these changes are the cause of PPS or the effect of it is unknown. Polio survivors tend to be hard-driving, type-A personalities, as compared to nondisabled control subjects—and the more driven polio survivors tend to have more PPS symptoms. Treatment may include slowing down to conserve strength and energy. Musculoskeletal problems can sometimes be helped by antiinflammatory or pain medications, with or without surgical procedures.
Medical dictionary. 2011.
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