Poliomyelitis

Polio is a viral neurological disease that vaccination has nearly eliminated, but survivors may develop post-polio syndrome and need ongoing rehabilitation.

Reviewed by
Hussein Imran Mousa, consultant neurosurgeon
Reading time
3 min read
Last reviewed
December 2020

At a glance

What it is

A neurological disease caused by the poliovirus. Systematic vaccination has all but eliminated new cases; almost all patients seen today are survivors living with late complications.

Late complications

Scoliosis, tendon problems, peripheral nerve entrapment, walking or wheelchair difficulties, respiratory insufficiency, osteoporotic fractures, and progressive loss of function.

Best approach

Long-term follow-up with a specialist, well-timed surgery where indicated, and sustained rehabilitation — aimed at preventing functional decline rather than curing the original infection.

Illustration of a child affected by poliomyelitis

Where the disease stands today

Poliomyelitis is a neurological disease caused by the poliovirus. Thanks to the systematic vaccination campaigns that began in 1963, the disease has been effectively eliminated locally since the late 1960s, and the last domestic case was recorded in 1988. In recent years, new cases have appeared only among immigrant populations or after travel to countries where polio is still endemic.

Most patients seen in the clinic today are not new infections — they are survivors of childhood polio who are now dealing with the long-term consequences of the disease.

Long-term effects and post-polio syndrome

Over the years, people who had polio in childhood may develop a range of movement disorders on a neurological basis: scoliosis, tendon problems in the back, peripheral nerve entrapments, difficulty walking or dependence on a wheelchair, respiratory insufficiency, osteoporotic fractures, and gradual loss of function and independence.

A smaller subset go on to develop what is called **post-polio syndrome** — new muscle weakness added to the pre-existing deficit, with no other cause to explain it. This new weakness may or may not be accompanied by fatigue, muscle pain, muscle atrophy, and further loss of function. Electromyography (EMG) can confirm the diagnosis according to the Halstead criteria.

At present, the best treatment is prevention of functional decline — through close follow-up with an experienced clinician, well-indicated surgical interventions, and consistent maintenance rehabilitation.

A multidisciplinary approach

Management focuses on preventing or minimising deformities and maximising the patient's capacity at home and in the community. The child (and later the adult) is best cared for by a multidisciplinary team, which may include:

- Nursing coordinator - Neurosurgeon — a surgeon specialising in operations on the brain and spinal cord - Neurologist — a physician specialising in conditions of the brain, spinal cord, and nerves - Physical and occupational therapists - Orthopaedic surgeon — a surgeon specialising in conditions of the muscles, ligaments, tendons, and bones - Orthotist — a specialist who designs and fits braces and splints

Treatment options at Alimran Center

The programme is built around the patient's specific deficits and combines physical rehabilitation, interventional pain and spasticity management, and — where indicated — neuromodulation.

Surgical interventions

When conservative and interventional care cannot correct a specific problem, surgery is considered:

- **Orthopaedic surgery** — for hip dislocations, ankle and foot deformities, and contracted muscles. - **Neurosurgery for spasticity** — including botulinum toxin (Botox) injection, selective dorsal rhizotomy, and intrathecal baclofen pumps.

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This article provides general information and is not a substitute for professional medical advice. If you have specific health concerns, please consult with a healthcare provider.