Krack P, Pollak P, Limousin P, Hoffmann D, Benazzouz A, Benabid A L
Department of Clinical and Biological Neurosciences and INSERM U318, Joseph Fourier University of Grenoble, France.
Mov Disord. 1998 Jul;13(4):648-52. doi: 10.1002/mds.870130407.
We report three patients with bilateral GPi stimulation for stage 4 Parkinson's disease (PD) with severe levodopa-induced dyskinesias (LID). In all three it was possible to completely inhibit LID using high-stimulation parameters. Parallel to complete inhibition of LID, an inhibition of the anti-akinetic effect of levodopa was observed, whereas, at the same time, rigidity was markedly improved. GPi stimulation is adaptable over time, and stimulation parameters have to be programmed according to off- and on-period motor symptoms. The main interest of stimulation is the possibility of finding a compromise between LID alleviation in on-phase without loss of the beneficial motor effects and improvement in parkinsonism in off-phase. In some patients, residual dyskinesias have to be accepted so as not to aggravate on-period motor symptoms by a presumed overinhibition of basal ganglia outflow.
我们报告了3例患有4期帕金森病(PD)且伴有严重左旋多巴诱导的异动症(LID)的患者接受双侧苍白球内侧核(GPi)刺激的情况。在所有3例患者中,使用高刺激参数能够完全抑制LID。在完全抑制LID的同时,观察到左旋多巴的抗运动不能作用受到抑制,而与此同时,强直明显改善。GPi刺激可随时间调整,刺激参数必须根据关期和开期的运动症状进行设定。刺激的主要意义在于有可能在不丧失有益运动效果的情况下减轻开期LID与改善关期帕金森症状之间找到折衷点。在一些患者中,必须接受残留的异动症,以免因推测的基底节输出过度抑制而加重开期运动症状。