Sensorimotor Disorder
Restless legs syndrome, also known as Ekbom syndrome, is the most commonly experienced sensorimotor disorder among the general population (Bassetti et al., 2011). The disorder afflicts approximately 2 to 10% of the general population and it is experienced as periodic limb movements in 80% of individuals with restless legs syndrome (Bassetti et al., 2011). The most prominent symptoms of the disorder are urges to move the legs as well as unpleasant sensations in the legs (Lee et al., 2011). The symptoms generally commence or become worse during inactivity and individuals with the disorder generally feel relief from symptoms after movement (Lee et al., 2011). Also, symptoms of the disorder are generally worse during the evening hours in comparison to the daytime. Furthermore, restless leg syndrome often results in sleep disturbances such as delayed sleep onset, multiple awakenings, and reduced sleep efficiency (Lee et al., 2011). The disorder is generally defined as primary, stemming from genetic or idiopathic causes, or secondary, resulting from other medical occurrences or neurological disorders (Mitchell, 2011). There are a few different treatment options available for the treatment of the disorder, including pharmacologic and non-pharmacologic interventions. The following discussion outlines treatment options for restless legs syndrome and their effectiveness in alleviating symptoms of the disorder.
Pharmacologic interventions
The most commonly prescribed treatments for the symptoms associated with restless legs syndrome are dopaminergic medications (Bassetti et al., 2011). One of these dopaminergic agents commonly used for treatment is levodopa, a dopamine precursor, which has been demonstrated as effective in the reduction of restless legs syndrome symptoms when administered at bedtime (Bassetti et al., 2011). The effectiveness of another dopaminergic agent called pramipexole was investigated in a study conducted by Bassetti et al. (2011). This study sought to compare the effectiveness and safety of pramipexole, a dopamine agonist, with that of levodopa. The effectiveness of the treatments was assessed through measures of how frequent leg movements occurred while the subjects spent time in bed, rating scales for severity of restless legs syndrome in the day and night, as well as the SF-36 scale, Hospital Anxiety and Depression Scale, Epworth Sleepiness Scale, and Clinical Global Impression for measures of quality of life, mood, and daytime sleepiness (Bassetti et al., 2011).
Results of the study by Bassetti et al. (2011) indicated that levodopa and pramipexole are comparable in their effectiveness for the treatment of symptoms associated with restless legs syndrome, and both treatments were demonstrated to be well tolerated among participants in the study. Adverse drug reactions were observed among a large proportion of participants of the study, at rates of 59% and 61% respectively for pramipexole and levodopa (Bassetti et al., 2011). The adverse drug reactions included restless legs symptoms, dizziness, and nausea (Bassetti et al., 2011).
Another pharmacologic intervention used for the treatment of restless legs syndrome is gabapentin enacarbil, which is a non-dopaminergic agent (Lee et al., 2011). Researchers sought to investigate the effectiveness of this treatment in light of the fact that many dopaminergic medications used for the treatment of restless legs syndrome result in adverse side effects such as impulse control disorders and compulsive behaviors (Lee et al., 2011; Voon et al., 2011). A 12-week study investigating this agent yielded findings that indicated the medication was significantly effective in improving symptoms associated with restless legs syndrome and also reduced the occurrence of sleep disturbances (Lee et al., 2011). The dosages of gabapentin enacarbil used in the study were 600 mg and 1200 mg, both tolerated well by the participants (Lee et al., 2011). The negative aspects of this agent are that it may not be clinically effective with all individuals. This is due to the fact that plasma exposure to gabapectin differs between patients and its bioavailability decreases with increasing dose, necessitating frequent dosing (Lee et al., 2011).
Patients suffering from restless legs syndrome may also exhibit symptoms of depression (Bayard et al., 2011; Scholz et al., 2011). Patients experiencing severe symptoms are more likely to suffer from depression, and this comorbidity...
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