Masui Takuya, Honma Hiroshi, Kondo Chihiro, Osawa Tatsuya, Iwasaki Syunji, Matsubara Shigehiro
Tokachi National Mental Hospital.
Seishin Shinkeigaku Zasshi. 2003;105(10):1247-53.
Perospirone is a novel serotonin-2 and dopamine-2 receptor antagonist (SDA) developed in Japan. Premarketing trials suggested that this agent was effective in reducing positive and negative symptoms of schizophrenia and had a favorable side-effect profile. However, these trials included only a few elderly patients, so the usefulness of perospirone in this population remains unknown. In this report we describe the treatment of 2 elderly patients with schizophrenia for whom perospirone therapy was efficacious. Case 1 was a patient with acute exacerbation of schizophrenic symptoms after discontinuance of medication. He was treated with 12 mg of perospirone daily and his symptoms reduced markedly from the 4th day of perospirone therapy. Efficacy was assessed by the positive and negative symptom scale (PANSS); all subscales of PANSS (positive symptom, negative symptom, and general psychopathology) reduced and the total score reduced from 78 to 38 by the end of the 6th week of treatment. No side effects such as extrapyramidal symptoms were noted. Thus, perospirone may be a useful antipsychotic for elderly patients with acute schizophrenia. Case 2 was a patient who had severe negative symptoms and extrapyramidal symptoms such as tardive dyskinesia, tardive dystonia, and sialorrhea. She had been hospitalized for more than 7 years. In this patient 12 mg of perospirone was administered daily after 3 mg of risperidone had been tapered off. The negative symptom subscale and general psychopathology subscale in PANSS were gradually reduced after perospirone therapy was started. Extrapyramidal symptoms were assessed by the drug-induced extrapyramidal symptoms scale (DIEPSS), which consists of eight individual parameters and one global assessment, and each parameter is graded on a 5-point (0 = none to 4 = severe) scale. Sialorrhea, muscle rigidity, tremor, dystonia and overall sererity were improved more than 2 points by the end of the 6th week. The clinical course of this patient suggests that the clinical characteristics of perospirone and risperidone may be different, even though these agents are categorized into the same class of antipsychotics, SDA. Because this is a case report, evaluations are limited the clinical properties of perospirone. Further examination is necessary to evaluate the efficacy and safety of perospirone for elderly patients with schizophrenia, who are more vulnerable to the side effect of antipsychotics than the younger population.
哌罗匹隆是一种在日本研发的新型5-羟色胺-2和多巴胺-2受体拮抗剂(SDA)。上市前试验表明,该药物在减轻精神分裂症的阳性和阴性症状方面有效,且副作用较小。然而,这些试验仅纳入了少数老年患者,因此哌罗匹隆在该人群中的有效性仍不明确。在本报告中,我们描述了2例接受哌罗匹隆治疗有效的老年精神分裂症患者。病例1是一名在停药后精神分裂症症状急性加重的患者。他接受了每日12毫克哌罗匹隆的治疗,从哌罗匹隆治疗的第4天起,他的症状明显减轻。通过阳性和阴性症状量表(PANSS)评估疗效;治疗第6周结束时,PANSS的所有子量表(阳性症状、阴性症状和一般精神病理学)均有所降低,总分从78分降至38分。未发现锥体外系症状等副作用。因此,哌罗匹隆可能是治疗老年急性精神分裂症患者的一种有效抗精神病药物。病例2是一名有严重阴性症状以及迟发性运动障碍、迟发性肌张力障碍和流涎等锥体外系症状的患者。她已住院7年多。在该患者中,在逐渐减少3毫克利培酮用量后,开始每日服用12毫克哌罗匹隆。开始哌罗匹隆治疗后,PANSS中的阴性症状子量表和一般精神病理学子量表逐渐降低。通过药物性锥体外系症状量表(DIEPSS)评估锥体外系症状,该量表由8个个体参数和1个整体评估组成,每个参数按5分制(0 = 无至4 = 严重)评分。到第6周结束时,流涎、肌肉僵硬、震颤、肌张力障碍和整体严重程度改善超过2分。该患者的临床病程表明,尽管哌罗匹隆和利培酮属于同一类抗精神病药物SDA,但它们的临床特征可能不同。由于这是一篇病例报告,对哌罗匹隆临床特性的评估有限。有必要进一步研究以评估哌罗匹隆对老年精神分裂症患者的疗效和安全性,因为老年患者比年轻人群更容易受到抗精神病药物副作用的影响。