Claveria L E, Teychenne P F, Calne D B, Haskayne L, Petrie A, Pallis C A, Lodge-Patch I C
J Neurol Sci. 1975 Apr;24(4):393-401. doi: 10.1016/0022-510x(75)90165-3.
We have investigated the action of pimozide in tardive dyskinesia induced by prolonged administration of phenothiazines. Improvement was recorded in a double blind study of 18 patients treated with maximum tolerated dosage (mean 18.8 mg/day) for 6 weeks. There was no deterioration in the therapeutic action of pimozide over this time. Parkinsonism and sedation were the main adverse effects. They were corrected by reduction of the dose of pimozide, but often recurred so that further adjustments of dosage were necessary. Our findings support the view that tardive dyskinesia is produced by a disturbance in the balance of central transmitters such that dopaminergic transmission is increased.
我们研究了匹莫齐特对长期服用吩噻嗪类药物所致迟发性运动障碍的作用。在一项双盲研究中,18例患者接受最大耐受剂量(平均18.8毫克/天)治疗6周,结果显示病情有所改善。在此期间,匹莫齐特的治疗作用没有恶化。帕金森综合征和镇静是主要的不良反应。通过减少匹莫齐特的剂量可纠正这些不良反应,但它们常常复发,因此需要进一步调整剂量。我们的研究结果支持这样一种观点,即迟发性运动障碍是由中枢递质平衡紊乱导致多巴胺能传递增加所致。