Gerken A, Wetzel H, Benkert O
Department of Psychiatry, University of Mainz, Germany.
Pharmacopsychiatry. 1991 Jul;24(4):132-7. doi: 10.1055/s-2007-1014456.
In order to verify the hypothesis of a strict relationship between clinical improvement and extrapyramidal side-effects, especially micrographia, twenty-two acutely ill schizophrenics were treated with perphenazine in a controlled prospective 28-day trial. During the study period, psychopathometric data, prolactin plasma levels, and handwriting samples were collected. According to the remission criteria fixed before the study began (both BPRS less than or equal to 25 and GAS greater than or equal to 80 points), 45.5% (10/22) of the total patient sample were classified as treatment responders. Handwriting tests were quantified in 21 patients. "Positive" handwriting results, i.e., a reduction of at least 13% in the overall area of 50% or more of the handwriting samples collected during the trial, were demonstrable in three of nine responders (33%) and nine of twelve nonresponders (75%). These results show that there is no positive correlation between clinical response and reduction in handwriting area. Consequently, the handwriting test is unable to predict clinical response. It is only one of a number of parameters with which to monitor the neurological side-effects of neuroleptic treatment. Outcome parameters show that psychopathological remission can be achieved with low neuroleptic dosages and few or virtually no extrapyramidal side-effects.
为了验证临床改善与锥体外系副作用尤其是小写症之间存在严格关联的假设,在一项为期28天的前瞻性对照试验中,对22例急性发病的精神分裂症患者使用奋乃静进行治疗。在研究期间,收集了心理测量数据、催乳素血浆水平和笔迹样本。根据研究开始前确定的缓解标准(简明精神病评定量表(BPRS)小于或等于25分且大体评定量表(GAS)大于或等于80分),将全部患者样本的45.5%(10/22)归类为治疗反应者。对21例患者的笔迹测试进行了量化。在9例反应者中有3例(33%)以及12例无反应者中有9例(75%)呈现出“阳性”笔迹结果,即在试验期间收集的50%或更多笔迹样本的总面积中至少减少13%。这些结果表明临床反应与笔迹面积减少之间不存在正相关。因此,笔迹测试无法预测临床反应。它只是用于监测抗精神病药物治疗神经学副作用的众多参数之一。结果参数表明,使用低剂量抗精神病药物且几乎没有或仅有极少锥体外系副作用的情况下,可实现精神病理学缓解。