Sachdev P, Loneragan C
Neuropsychiatric Institute, Prince Henry Hospital, Sydney, Australia.
Psychopharmacology (Berl). 1993;113(1):119-22. doi: 10.1007/BF02244343.
We challenged five patients suffering from tardive akathisia (TA) with intravenous benztropine (2 mg), propranolol (1 mg) and placebo (saline) using a random, double-blind cross-over design to examine the effects of the drugs on the subjective, objective and global manifestations of neuroleptic-induced akathisia. Benztropine produced a marginally significant, and propranolol a significant improvement in the overall manifestations of the disorder. The patients demonstrated a considerable placebo effect and marked variation in their responses to the drugs. The implications of these findings for the pathophysiology of TA in relation to acute akathisia and tardive dyskinesia are discussed.
我们采用随机、双盲交叉设计,对5例迟发性静坐不能(TA)患者静脉注射苯海索(2毫克)、普萘洛尔(1毫克)和安慰剂(生理盐水),以研究这些药物对抗精神病药所致静坐不能的主观、客观及整体表现的影响。苯海索使该病症的整体表现有轻微显著改善,普萘洛尔则使其有显著改善。患者表现出相当大的安慰剂效应,且对药物的反应存在明显差异。本文讨论了这些发现对于TA与急性静坐不能和迟发性运动障碍相关的病理生理学的意义。