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Complex Regional Pain Syndrome

Complex regional pain syndrome, also known as reflex sympathetic dystrophy, is a condition that usu­ally involves one limb and more commonly the lower extremity in children.

Clinical Characteristics.

Complex regional pain syndrome is characterized by pain, hyperesthesia, edema, cold or warm extremity, cyanosis, mottling of skin, limited range of motion, and patchy bone demineralization.

Diagnostics. Unlike adults, who usually have an inciting event such as a fracture, surgery, prolonged immobilization, or vascular insult, children usually do not have a clear event that precipitates the condi­tion (366). There appears to be a sympathetic nervous system reflex arc mechanism of action. The major­ity of children with this condition are teenage girls around 12-13 years of age. Radiographs are useful to rule out a fracture or osteomyelitis (367). Regional nerve blocks may be both diagnostic and therapeu­tic. The diagnosis should be considered with trauma and pain that is out of proportion to the stimulus and worsened with use.

Treatment. A multidisciplinary approach is useful. The earlier the recognition and treatment, the more rap­idly recovery is possible. Once contractures and atro­phy set in, this is a much more difficult entity to treat. Some advocate medications such as calcium channel blockers, beta blockers (propranolol), and tricyclic antidepressants such as amitriptyline.

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Source: Alexander M.A., Matthews D.J.. Pediatric Rehabilitation: Principles and Practice. 4 th. åd. — New York: Demos Medical Publishing,2010. — 540 ð.. 2010
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