Byerly Matthew J, Nakonezny Paul A, Bettcher Brianne Magouirk, Carmody Thomas, Fisher Robert, Rush A John
The University of Texas Southwestern Medical Center, Department of Psychiatry, Dallas, TX 75235-8828, USA.
Schizophr Res. 2006 Sep;86(1-3):244-50. doi: 10.1016/j.schres.2006.04.005. Epub 2006 May 30.
Evaluate sexual dysfunction, as measured by the Arizona Sexual Experience Scale (ASEX), in olanzapine-, quetiapine-, and risperidone-treated outpatients with schizophrenia or schizoaffective disorder.
The sexual functioning of 238 outpatients (age> or =18 years) with diagnoses of schizophrenia or schizoaffective disorder who took quetiapine (n=57), olanzapine (n=94), or risperidone (n=87) was evaluated with a one-time rating of the ASEX. The dose range for each treatment group was 5 to 40 mg/day (M=16.6 mg/day, SD=7.4) for olanzapine; 1 to 8 mg/day (M=3.9 mg/day, SD=1.6) for risperidone; and 50 to 900 mg/day (M=376.8 mg/day, SD=213.4) for quetiapine. Antipsychotic group designation was based on medication treatment at study entry (i.e., non-random assignment). Participant characteristics were collected to test for treatment group differences and for potential associations with severity of sexual dysfunction. The primary data analysis was a mixed linear model analysis of covariance with age, gender, and presence/absence of antidepressant known to cause sexual dysfunction included as covariates.
There was a significant treatment effect on severity of sexual dysfunction, as measured by ASEX total scores (p=.04). The adjusted average ASEX total scores were lower in the quetiapine (M=17.80) than in the risperidone (M=19.69) or olanzapine (M=20.34) groups. Individual comparisons of the treatments on adjusted average ASEX total scores indicated a significant difference between olanzapine and quetiapine (p=.04), but no difference between risperidone and quetiapine (p=.17) or olanzapine and risperidone (p=.76).
Quetiapine was associated with less severe sexual dysfunction than olanzapine and risperidone (albeit the effect between risperidone and quetiapine was not statistically significant). Olanzapine and risperidone were associated with a comparable degree of sexual dysfunction. Patients in all three treatment groups, nonetheless, experienced a moderately high degree of sexual dysfunction. Because the patients were not randomized, conclusions must be interpreted within the context of the quasi-experimental design.
采用亚利桑那性体验量表(ASEX)评估接受奥氮平、喹硫平及利培酮治疗的精神分裂症或分裂情感性障碍门诊患者的性功能障碍情况。
对238例年龄≥18岁、诊断为精神分裂症或分裂情感性障碍的门诊患者进行性功能评估,这些患者分别服用喹硫平(n = 57)、奥氮平(n = 94)或利培酮(n = 87),采用ASEX进行一次性评分。各治疗组的剂量范围为:奥氮平5至40毫克/天(M = 16.6毫克/天,SD = 7.4);利培酮1至8毫克/天(M = 3.9毫克/天,SD = 1.6);喹硫平50至900毫克/天(M = 376.8毫克/天,SD = 213.4)。抗精神病药物组的指定基于研究开始时的药物治疗情况(即非随机分配)。收集参与者特征以检测治疗组差异以及与性功能障碍严重程度的潜在关联。主要数据分析为协方差混合线性模型分析,将年龄、性别以及是否使用已知会导致性功能障碍的抗抑郁药物作为协变量纳入。
以ASEX总分衡量,治疗对性功能障碍严重程度有显著影响(p = 0.04)。喹硫平组调整后的ASEX平均总分(M = 17.80)低于利培酮组(M = 19.69)和奥氮平组(M = 20.34)。对调整后的ASEX平均总分进行各治疗组间的个体比较显示,奥氮平和喹硫平之间存在显著差异(p = 0.04),但利培酮和喹硫平之间(p = 0.17)以及奥氮平和利培酮之间(p = 0.76)无差异。
与奥氮平和利培酮相比,喹硫平所致性功能障碍的严重程度较低(尽管利培酮和喹硫平之间的差异无统计学意义)。奥氮平和利培酮所致性功能障碍的程度相当。然而,所有三个治疗组的患者均经历了中度较高程度的性功能障碍。由于患者未进行随机分组,结论必须在准实验设计的背景下进行解读。