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Efficacy and Tolerability of Aripiprazole in a Nigerian Cohort with First-episode Psychosis: A Post-marketing Survey

机译:阿立哌唑在尼日利亚首发精神病人群中的疗效和耐受性:上市后调查

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Background: Individuals with first episode psychoses often discontinue pharmacotherapy due to poor symptom remission and/or intolerable side effects. Aripiprazole has been reported to show good efficacy with low side effect profiles in Caucasians. No studies have been conducted to assess its effectiveness and tolerability in a Nigerian population hence the need for this study. Methods: A post marketing surveillance was conducted involving patients with first episode psychosis presenting to a regional tertiary psychiatric facility in Nigeria. Participants were titrated through a dose range of 10-30 mg of aripiprazole depending on response or tolerability and followed up over a 12 week period. Assessments at baseline, at 2, 6, and 12-weeks post recruitment were done to rate severity of psychopathology (CGI, PANSS), side effects (MSAS), functioning (GAF), and medication adherence (MARS). Results: Of fifty patients completing the study (49.5% drop-out rate), we observed significant improvements at 12 weeks compared to baseline in symptom remission (p Conclusion: Aripiprazole may be effective and tolerable among individuals with first episode non-affective psychoses presenting at a tertiary psychiatric facility in Nigeria.
机译:背景:患有首发性精神病的个体通常因症状缓解和/或无法忍受的副作用而中止药物治疗。据报道,阿立哌唑在高加索人中显示出良好的疗效,且副作用低。尚未进行评估其在尼日利亚人群中的有效性和耐受性的研究,因此需要进行这项研究。方法:对上市后精神病患者进行了售后监测,该患者出现在尼日利亚的区域三级精神病学机构。根据反应或耐受性,在10-30 mg阿立哌唑的剂量范围内对参与者进行滴定,并在12周内进行随访。在基线时,募集后第2、6和12周进行评估,以评估心理病理学的严重程度(CGI,PANSS),副作用(MSAS),功能(GAF)和药物依从性(MARS)。结果:在完成研究的50例患者中(辍学率49.5%),我们观察到与基线相比,在12周时症状缓解显着改善(p结论:阿立哌唑在首发非情感性精神病患者中可能是有效和可耐受的在尼日利亚的第三级精神病院。

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