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奥氮平肌内注射、氟哌啶醇肌内注射和左美丙嗪肌内注射治疗急性激越型精神分裂症患者疗效与安全性的自然对照研究

A naturalistic comparison study of the efficacy and safety of intramuscular olanzapine, intramuscular haloperidol, and intramuscular levomepromazine in acute agitated patients with schizophrenia.

作者信息

Suzuki Hidenobu, Gen Keishi, Takahashi Yuki

机构信息

Department of Psychiatry, Suzuki Clinic, Tokyo, Japan.

出版信息

Hum Psychopharmacol. 2014 Jan;29(1):83-8. doi: 10.1002/hup.2376.

DOI:10.1002/hup.2376
PMID:24424709
Abstract

OBJECTIVE

This study was a comparative investigation of the clinical efficacy and safety of intramuscular (IM) olanzapine, IM haloperidol, and IM levomepromazine in acute agitated patients with schizophrenia.

METHODS

The subjects were 122 inpatients. Their clinical symptoms were assessed using Positive and Negative Syndrome Scale Excited Component (PANSS-EC), PANSS, and Agitation-Calmness Evaluation Scale, and their safety were assessed using the Abnormal Involuntary Movement Scale, Barnes Akathisia Rating Scale (BARS), and Drug-induced Extrapyramidal Symptoms Scale (DIEPSS).

RESULTS

The mean changes from baseline on the PANSS-EC, Agitation-Calmness Evaluation Scale, Abnormal Involuntary Movement Scale, BARS, and DIEPSS scores were significantly better in both IM olanzapine and IM levomepromazine than in IM haloperidol. Of these, the mean changes from baseline on the BARS and DIEPSS scores were significantly better in IM olanzapine than in IM levomepromazine. The mean change from baseline on the PANSS positive score was significantly better in both IM olanzapine and IM haloperidol than in IM levomepromazine.

CONCLUSIONS

The results of this study suggest the possibility that the anti-agitation effects of IM olanzapine and IM levomepromazine are more rapid than those of IM haloperidol. No worsening of EPS was observed. Our results also suggest that compared with IM levomepromazine, IM olanzapine is safer and affords greater improvement in symptoms.

摘要

目的

本研究是对奥氮平肌内注射、氟哌啶醇肌内注射和左美丙嗪肌内注射治疗急性激越型精神分裂症患者的临床疗效和安全性进行的比较研究。

方法

研究对象为122名住院患者。使用阳性与阴性症状量表兴奋分量表(PANSS-EC)、PANSS和激越-平静评定量表评估其临床症状,使用异常不自主运动量表、巴恩斯静坐不能评定量表(BARS)和药物所致锥体外系症状量表(DIEPSS)评估其安全性。

结果

奥氮平肌内注射组和左美丙嗪肌内注射组在PANSS-EC、激越-平静评定量表、异常不自主运动量表、BARS和DIEPSS评分上较基线的平均变化均显著优于氟哌啶醇肌内注射组。其中,奥氮平肌内注射组在BARS和DIEPSS评分上较基线的平均变化显著优于左美丙嗪肌内注射组。奥氮平肌内注射组和氟哌啶醇肌内注射组在PANSS阳性评分上较基线的平均变化均显著优于左美丙嗪肌内注射组。

结论

本研究结果提示,奥氮平肌内注射和左美丙嗪肌内注射的抗激越作用可能比氟哌啶醇肌内注射更快。未观察到锥体外系症状加重。我们的结果还提示,与左美丙嗪肌内注射相比,奥氮平肌内注射更安全,症状改善更明显。

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