Durif F
Fédération de Neurologie, CHRU Clermont-Ferrand, France.
Drugs Aging. 1999 May;14(5):337-45. doi: 10.2165/00002512-199914050-00002.
Prevention of levodopa-induced dyskinesias is a therapeutic challenge for physicians. At present, it seems only possible to delay dyskinesias and motor fluctuations. In younger patients (aged <50 years), the strategy is to use a dopamine D2 agonist as monotherapy and then to add levodopa treatment when the parkinsonian symptoms progress. In older patients, (aged >50 years to <70 years), the therapeutic approach is to use early combination therapy of levodopa and a D2 agonist. The treatment of levodopa-induced dyskinesias must be considered in regard to the subtype and the severity of dyskinesias, and the patient. The general approach to the treatment of peak dose dyskinesias is to maintain dopamine brain stimulation at as stable a level as possible by keeping plasma and brain levodopa concentrations in the therapeutic range (above the therapeutic threshold but below the dyskinesia threshold). An appropriate strategy is to reduce the individual dose of levodopa, to spread out the daily levodopa dose and/or to try treatment with the sustained-release form of the drug. Combination treatment with the standard and sustained-release levodopa formulations is also possible. Stopping selegiline (deprenyl) therapy may reduce dyskinesias; reducing the dose of, or stopping treatment with, a dopamine agonist may also be beneficial. Anti-dyskinetic drugs such as amantadine, buspirone, fluoxetine, propanolol and principally clozapine may be used. In severe dyskinesias, apomorphine infusion may be tried. In refractory dyskinesia, surgical procedures such as pallidotomy and chronic deep brain stimulation (globus pallidus/subthalamic nucleus) may be proposed. Theoretically, treatment of diphasic dyskinesias requires the maintenance of plasma levodopa concentrations above the dyskinesia threshold. However, this approach leads to constant and severe dyskinesia after only a few weeks of treatment. Thus, the strategy used to treat diphasic dyskinesia is close to the treatment of peak-dose dyskinesias. Apomorphine (or the liquid form of levodopa) may be helpful to prevent diphasic dyskinesias. In selected patients, a midday rest in the 'off' phase may decrease the duration of dyskinesia. Treatment of early morning dystonia is based on the addition to the regimen of the sustained release formulation of levodopa before bedtime. Liquid levodopa and apomorphine injection may be used just before the appearance of the dystonic posture. Botulinum toxin may be helpful in severe dystonia.
预防左旋多巴诱发的运动障碍是医生面临的一项治疗挑战。目前,似乎只能延缓运动障碍和运动波动的出现。对于较年轻的患者(年龄<50岁),策略是使用多巴胺D2激动剂作为单一疗法,然后在帕金森症状进展时添加左旋多巴治疗。对于老年患者(年龄>50岁至<70岁),治疗方法是早期使用左旋多巴和D2激动剂联合治疗。必须根据运动障碍的亚型、严重程度以及患者情况来考虑左旋多巴诱发运动障碍的治疗。治疗峰值剂量运动障碍的一般方法是通过将血浆和脑内左旋多巴浓度维持在治疗范围内(高于治疗阈值但低于运动障碍阈值),尽可能稳定地维持多巴胺脑刺激水平。一种合适的策略是减少左旋多巴的单次剂量,分散每日左旋多巴剂量和/或尝试使用药物的缓释剂型进行治疗。也可以将标准剂型和缓释剂型的左旋多巴联合使用。停用司来吉兰(丙炔苯丙胺)治疗可能会减少运动障碍;减少多巴胺激动剂的剂量或停用该药物治疗也可能有益。可以使用抗运动障碍药物,如金刚烷胺、丁螺环酮、氟西汀、普萘洛尔,主要是氯氮平。对于严重的运动障碍,可以尝试阿扑吗啡输注。对于难治性运动障碍,可以考虑手术治疗,如苍白球切开术和慢性脑深部电刺激(苍白球/丘脑底核)。从理论上讲,治疗双相性运动障碍需要将血浆左旋多巴浓度维持在运动障碍阈值以上。然而,这种方法在治疗几周后就会导致持续且严重的运动障碍。因此,用于治疗双相性运动障碍的策略与治疗峰值剂量运动障碍相近。阿扑吗啡(或左旋多巴的液体制剂)可能有助于预防双相性运动障碍。在部分患者中,在“关”期进行午间休息可能会缩短运动障碍的持续时间。治疗清晨肌张力障碍的方法是在睡前的治疗方案中添加左旋多巴缓释制剂。在肌张力障碍姿势出现前可使用左旋多巴液体制剂和阿扑吗啡注射。肉毒杆菌毒素可能对严重的肌张力障碍有帮助。