Becker P M, Jamieson A O, Brown W D
Sleep/Wake Disorders Center, Presbyterian Hospital of Dallas, Texas 75231.
Sleep. 1993 Dec;16(8):713-6. doi: 10.1093/sleep/16.8.713.
Restless legs syndrome (RLS) is a common neurosensorimotor disorder that presents with paresthesias, sleep disturbances and, in most cases, periodic limb movements of sleep (PLMS). Although many treatments have been described, interest has recently been focused on dopaminergic mechanisms of etiology and treatment. The dopamine agonists L-dopa/carbidopa, bromocriptine mesylate or both were initiated in 49 patients with RLS/PLMS who sought consultation at a sleep disorders center. This retrospective study describes the symptoms, time course of response and complications in 36 men and 13 women with a mean age of 53.9 years. Only 47 of the patients were available for extended follow-up. The most common presenting complaints were the sensation of restless legs and sleep maintenance insomnia lasting over 20 years. In the extended follow-up group of 47, four failed to respond to L-dopa or bromocriptine, five discontinued treatment because of side effects and two reported loss of therapeutic effect within the first month. Between month one and six, only three additional subjects discontinued treatment. At a mean follow-up of 283 days (SD 316), 33 patients continued on L-dopa/carbidopa at a mean bedtime dose of 160 mg L-dopa (SD 300). Treatment-emergent morning leg restlessness developed in eight patients, seven of whom required daytime medication for relief. Other side effects, generally nausea, occurred in only eight of 43 patients. Psychiatric side effects of dyskinesia were not seen. The > 70% long-term response is comparable to other studies in the literature.
不安腿综合征(RLS)是一种常见的神经感觉运动障碍,表现为感觉异常、睡眠障碍,且在大多数情况下伴有睡眠期周期性肢体运动(PLMS)。尽管已有多种治疗方法被描述,但近来人们的兴趣集中在病因和治疗的多巴胺能机制上。对49例到睡眠障碍中心咨询的RLS/PLMS患者开始使用多巴胺激动剂左旋多巴/卡比多巴、甲磺酸溴隐亭或两者联用。这项回顾性研究描述了36名男性和13名女性(平均年龄53.9岁)的症状、反应的时间过程及并发症。仅有47例患者可进行延长随访。最常见的主诉是不安腿的感觉和持续超过20年的维持睡眠性失眠。在47例的延长随访组中,4例对左旋多巴或溴隐亭无反应,5例因副作用停药,2例在第一个月内报告治疗效果丧失。在第1个月至第6个月期间,仅另外3名受试者停药。平均随访283天(标准差316)时,33例患者继续服用左旋多巴/卡比多巴,平均睡前剂量为左旋多巴160mg(标准差300)。8例患者出现治疗引发的晨起腿部不安,其中7例需要日间用药缓解。其他副作用,通常为恶心,仅在43例患者中的8例出现。未观察到运动障碍的精神副作用。超过70%的长期反应与文献中的其他研究相当。