Key result
Postpolio syndrome is a sequela of acute poliomyelitis occurring decades after initial recovery, characterized by fatigue, muscle weakness, myalgia, and joint pain, requiring exclusion of other conditions for diagnosis.
This review highlights the clinical manifestations, risk factors, and management strategies for postpolio syndrome, emphasizing the need for diagnosis by exclusion and symptomatic care.
Supports diagnosis by exclusion and symptomatic care in polio survivors; leaves open prospective trials on prevention.
Postpolio syndrome (PPS) refers to a group of conditions that are present in patients, years after recovery from initial acute paralytic poliomyelitis. About 15%-80% of 20 million polio survivors worldwide will experience exacerbation of symptoms which typically appear 15-30 years after the resolution of initial poliomyelitis. Symptoms include new muscle weakness, fatigue, myalgia, joint pain, dysphagia, and difficulty breathing. Other reported symptoms include cold intolerance, sleep disorder, dysphonia, loss of stamina, musculoskeletal deformities, cardiovascular disorders, psychosocial problems, and restless legs syndrome. These symptoms are attributed to the superimposed neuronal loss of aging with inflammatory mechanisms, but without any convincing evidence of viral reactivation. Risk factors include female gender, respiratory symptoms, normal aging, permanent disability caused by motor neuron damage, muscle overuse and disuse, aging, and immunologic mechanisms. Hypothyroidism-induced myopathy and fibromyalgia are a differential diagnosis for PPS, and exclusion diagnosis is required as confirmatory criteria for PPS. The symptoms of PPS presented determine the course of management.
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Olunu et al. (2019) conducted a review in Postpolio syndrome. Postpolio syndrome is a sequela of acute poliomyelitis occurring decades after initial recovery, characterized by fatigue, muscle weakness, myalgia, and joint pain, requiring exclusion of other conditions for diagnosis.
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