Tardy Magdolna, Dold Markus, Engel Rolf R, Leucht Stefan
Klinik und Poliklinik für Psychiatrie und Psychotherapie, Technische Universität München Klinikum rechts der Isar, Möhlstr. 26, München, Germany, 81675.
Cochrane Database Syst Rev. 2014 Sep 1;2014(9):CD009227. doi: 10.1002/14651858.CD009227.pub2.
Antipsychotic drugs are the core treatment for schizophrenia. Treatment guidelines state that there is no difference in efficacy between antipsychotic drugs, however, low-potency antipsychotic drugs are sometimes perceived as less efficacious than high-potency compounds by clinicians, and they also seem to differ in their side effects.
To review the effects in clinical response of flupenthixol and low-potency antipsychotics for people with schizophrenia.
We searched the Cochrane Schizophrenia Group Trials Register (July 2010).
Randomised controlled trials that compared flupenthixol with first-generation low-potency antipsychotic drugs for people with schizophrenia or schizophrenia-like psychosis.
We extracted data independently. For continuous data, we calculated mean differences (MD) based on a random-effects model.
The review currently includes one randomised trial from mainland China with 153 participants that lasted two months and compared flupenthixol with chlorpromazine. The exact methods of sequence generation and allocation concealment were not reported, and medication was provided in an open manner. There were no data on the outcomes that we had a priori selected for a 'Summary of findings' table.There was no significant difference between flupenthixol and chlorpromazine in the participants' general mental state at endpoint as measured by the Brief Psychiatric Rating Scale (BPRS) total score (1 randomised controlled trial (RCT), n = 153, MD 2.20 95% confidence interval (CI) -1.25 to 5.65). Chlorpromazine was associated with significantly less dizziness (1 RCT, n = 153, MD 0.12 95% CI 0.01 to 0.23); dystonia (1 RCT, n = 153, MD 0.29 95% CI 0.13 to 0.45); unsteady gait (1 RCT, n = 153, MD 0.46 95% CI 0.28 to 0.64); reduced facial expression (1 RCT, n = 153, MD 0.27 95% CI 0.09 to 0.45); restlessness (1 RCT, n = 153, MD 0.69 95% CI 0.45 to 0.93); rigidity (elbow) (1 RCT, n = 153, MD 0.48 95% CI 0.28 to 0.68); and tremor (1 RCT, n = 153, MD 0.56 95% CI 0.34 to 0.78). Chlorpromazine produced more dryness of mouth than flupenthixol (1 RCT, n = 153, MD -0.14 95% CI -0.25 to -0.03).
AUTHORS' CONCLUSIONS: The evidence base of flupenthixol versus low-potency first-generation antipsychotics is currently restricted to one randomised comparison with chlorpromazine. The few reported data do not suggest a difference in efficacy, but flupenthixol appeared to produce more movement disorders and dizziness, while chlorpromazine was associated with the anticholinergic side effect - dryness of mouth. More trials are needed to make conclusions about the relative effects of flupenthixol and low-potency antipsychotics.
抗精神病药物是精神分裂症的核心治疗药物。治疗指南指出,抗精神病药物在疗效上并无差异,然而,临床医生有时认为低效价抗精神病药物的疗效不如高效价药物,而且它们在副作用方面似乎也有所不同。
综述氟哌噻吨与低效价抗精神病药物对精神分裂症患者临床反应的影响。
我们检索了Cochrane精神分裂症研究组试验注册库(2010年7月)。
比较氟哌噻吨与第一代低效价抗精神病药物治疗精神分裂症或精神分裂症样精神病患者的随机对照试验。
我们独立提取数据。对于连续性数据,我们基于随机效应模型计算平均差(MD)。
本综述目前纳入了一项来自中国大陆的随机试验,共153名参与者,试验持续两个月,比较了氟哌噻吨与氯丙嗪。未报告序列产生和分配隐藏的确切方法,且药物是以开放方式提供的。对于我们事先选定列入“结果总结”表的结局,没有相关数据。根据简明精神病评定量表(BPRS)总分衡量,在终点时参与者的总体精神状态方面,氟哌噻吨与氯丙嗪之间无显著差异(1项随机对照试验(RCT),n = 153,MD 2.20,95%置信区间(CI)-1.25至5.65)。氯丙嗪导致的头晕显著较少(1项RCT,n = 153,MD 0.12,95% CI 0.01至0.23);肌张力障碍(1项RCT,n = 153,MD 0.29,95% CI 0.13至0.45);步态不稳(1项RCT,n = 153,MD 0.46,95% CI 0.28至0.64);面部表情减少(1项RCT,n = 153,MD 0.27,95% CI 0.09至0.45);坐立不安(1项RCT,n = 153,MD 0.69,95% CI 0.45至0.93);(肘部)僵硬(1项RCT,n = 153,MD 0.48,95% CI 0.28至0.68);以及震颤(1项RCT,n = 153,MD 0.56,95% CI 0.34至0.78)。氯丙嗪比氟哌噻吨导致更多口干(1项RCT,n = 153,MD -0.14,95% CI -0.25至-0.03)。
氟哌噻吨与第一代低效价抗精神病药物对比的证据基础目前仅限于与氯丙嗪的一项随机对照比较。少数报告的数据未显示疗效有差异,但氟哌噻吨似乎产生更多运动障碍和头晕,而氯丙嗪与抗胆碱能副作用——口干有关。需要更多试验才能得出关于氟哌噻吨和低效价抗精神病药物相对效果的结论。