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Olanzapine–valproate combination versus olanzapine or valproate monotherapy in the treatment of bipolar I mania: a randomized controlled study in a Chinese population group

机译:奥氮平-丙戊酸盐联合奥氮平或丙戊酸盐单药治疗双相性I型躁狂症:在中国人群中的一项随机对照研究

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Background: Bipolar disorder (BP) is a mental illness that has a high social burden estimated by disability-adjusted life years. In the present study, we investigated the efficacy of olanzapine–valproate combination therapy versus olanzapine or valproate monotherapy in the treatment of bipolar I mania in a Chinese population group.Subjects and methods: Patients aged 19–58 years who had had an acute manic episode of BP were enrolled in the present study and randomly assigned to receive 600 mg sodium valproate daily (group A), 10 mg olanzapine daily (group B), or a combination of 600 mg olanzapine and 10 mg sodium valproate daily (group C) for 4 weeks. The primary outcome was reduction in Young Mania Rating Scale (YMRS) scores. The secondary outcome was assessed with the Clinical Global Impression – Bipolar (CGI-BP) scale. Adverse reactions, such as weight gain, sleepy, and dizziness were also evaluated. Statistical analysis was carried out on a per-protocol basis.Results: Patients in groups B and C showed significant improvement in YMRS scores compared with those in group A (P<0.01) during weeks 1–4 of treatment. Patients in group C showed significant improvement in YMRS scores compared with those in group B (P<0.01) only after 4 weeks of treatment. Furthermore, after 3–4 weeks of treatment, patients in groups B and C showed significantly greater improvement in CGI-BP scale scores compared with group A?P<0.05), while Group C demonstrated significantly greater improvement in CGI-BP scale scores than group B (P<0.01). No significant difference existed in extrapyramidal reactions among these groups. Adverse reactions, including weight gain, drowsiness, dizziness, and constipation, were stronger in groups B and C than in group A (P<0.05). Conclusion: The combination therapy with olanzapine and sodium valproate had higher efficacy than monotherapy in patients with bipolar mania, which provides a crucial insight of the treatment regimen during clinical practice.
机译:背景:双相情感障碍(BP)是一种精神疾病,根据残疾调整生命年估算,其社会负担较高。在本研究中,我们研究了奥氮平-丙戊酸盐联合治疗与奥氮平或丙戊酸盐单药治疗在中国人群中双相性I型躁狂症的疗效。研究对象和方法:19-58岁的急性躁狂发作患者的BP纳入本研究,随机分配接受每天600毫克丙戊酸钠(A组),每天10毫克奥氮平(B组)或每天600毫克奥氮平和10毫克丙戊酸钠(C组)的组合4个星期主要结果是减少了青年躁狂症评分量表(YMRS)分数。次要结果通过临床总体印象-双相(CGI-BP)量表进行评估。还评估了不良反应,例如体重增加,困倦和头晕。结果:在治疗的第1至4周,B组和C组的患者的YMRS得分显着高于A组(P <0.01)。仅在治疗4周后,C组患者的YMRS评分才显着高于B组(P <0.01)。此外,在治疗3至4周后,与A?P <0.05组相比,B组和C组患者的CGI-BP量表评分改善显着更大,而C组的CGI-BP量表评分显着高于对照组。 B组(P <0.01)。这些组之间的锥体束外反应没有显着差异。 B组和C组的不良反应,包括体重增加,嗜睡,头昏眼花和便秘,比A组更强(P <0.05)。结论:奥氮平与丙戊酸钠联合治疗双相躁狂症的疗效优于单药治疗,这为临床实践中的治疗方案提供了重要的认识。

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