Pharmacotherapy of Restless Legs Syndrome with Pramipexole
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Merlino, Giovanni
[1
,2
]
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Lorenzut, Simone
[1
]
Sommaro, Martina
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机构:
Santa Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, ItalySanta Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
Sommaro, Martina
[1
]
Gigli, Gian Luigi
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Santa Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
Univ Udine, DPMSC, Udine, ItalySanta Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
Gigli, Gian Luigi
[1
,2
]
Valente, Mariarosaria
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Santa Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
Univ Udine, DPMSC, Udine, ItalySanta Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
Valente, Mariarosaria
[1
,2
]
机构:
[1] Santa Maria della Misericordia Univ Hosp, Dept Neurosci, Sleep Disorders Ctr, Udine, Italy
[2] Univ Udine, DPMSC, Udine, Italy
来源:
CLINICAL MEDICINE INSIGHTS-THERAPEUTICS
|
2010年
/
2卷
关键词:
restless legs syndrome;
pramipexole;
dopamine-agonists;
augmentation;
compulsive behaviors;
D O I:
暂无
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Restless Legs Syndrome (RLS) is one of the most common neurological diseases characterized by an urge to move the legs, often associated with unpleasant sensations relieved by movement. It is engendered by rest, and is worse in the evening or at night. Patients affected by severe RLS should be treated pharmacologically. Dopamine-agonists represent the first-line treatment for RLS symptoms. Pramipexole is a non-ergot derived dopamine agonist with a high selectivity for D-2 and D-3 receptors. At doses comprised between 0.125 and 0.75 mg, pramipexole improves subjective symptoms and objective signs of primary RLS even after the first administration. In addition, pramipexole seems to be safe and well tolerated. However, physicians should be aware that augmentation and compulsive behaviours might occur in their RLS patients treated with pramipexole. Further studies are needed to confirm the efficacy of pramipexole in uremic RLS and in children affected by the sleep disorder.
机构:
Japan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Tokyo Med Univ, Dept Somnol, Tokyo, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Inoue, Yuichi
Kuroda, Kenji
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Hannan Hosp, Osaka, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Kuroda, Kenji
Hirata, Koichi
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Dokkyo Med Univ, Dept Neurol, Tokyo, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Hirata, Koichi
Uchimura, Naohisa
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Kurume Univ, Dept Neuropsychiat, Fukuoka, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Uchimura, Naohisa
Kagimura, Tatsuo
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Nippon Boehringer Ingelheim Co Ltd, Med Data Serv Dept, Tokyo, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
Kagimura, Tatsuo
Shimizu, Tetsuo
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Akita Univ, Dept Neuropsychiat, Akita 010, JapanJapan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan