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作 者:王群芬
机构地区:[1]慈溪市第七人民医院精神科,浙江省慈溪315336
出 处:《中国基层医药》2018年第5期566-569,共4页Chinese Journal of Primary Medicine and Pharmacy
基 金:浙江省慈溪市科技计划项目(CN2010028)
摘 要:目的探讨帕利哌酮缓释片治疗精神分裂症的临床效果及安全性。方法选取80例精神分裂症患者为研究对象,遵循单盲随机分配原则分为两组,每组40例,对照组采用利培酮治疗,观察组采用帕利哌酮缓释片治疗,比较两组总有效率、阳性和阴性症状评分(PANSS评分)、精神残疾评分(WHO-DAS11评分)以及不良反应发生率。结果观察组的临床总有效率(95.00%)明显高于对照组(80.00%)(χ^2=4.114,P〈0.05);治疗后,观察组的PANSS评分、WHO.DASII评分相对于治疗前均明显降低(t=8.002、7.761,均P〈0.05),且其均低于对照组治疗后(t=4.114、3.702,均P〈0.05);两组不良反应发生率差异无统计学意义(7.50%比10.00%,χ^2==0.157,P〉0.05)。结论采用帕利哌酮缓释片治疗精神分裂症的临床疗效显著,可有效缓解患者的精神障碍,且安全性可靠。Objective To study the clinical effect and safety of paliperidone extended -release tablets in the treatment of schizophrenia. Methods 80 patients with schizophrenia were selected as the research subjects. Accord- ing to randomized single blind, the patients were divided into two groups ,40 cases in each group. The control group was given risperidone treatment, the observation group used paliperidone extended - release tablets treatment. The total effective rate, positive and negative symptoms score ( PANSS score), mental disability score ( WHO - DAS score II) and the incidence of adverse reactions were compared between the two groups. Results The clinical total effective rate (95.00%) in the observation group was significantly higher than the control group (80.00% , χ^2= = 4.114, P 〈 0.05 ). After treatment, the PANSS score and WHO - DAS II score in the observation group were significantly decreased compared with before treatment ( t = 8. 002,7. 761, all P 〈 0.05 ), which were lower than those in the control group after treatment ( t = 4.114,3. 702, all P 〈 0.05 ). The incidence rate of adverse reaction between the two groups had no statistically significant difference (7.50% vs. 10.00%, χ^2== 0. 157, P 〉 0. 05 ). Conclusion The clinical efficacy of paliperidone extended - release tablets in the treatment of schizophrenia is significant, which can effectively relieve patients with mental disorders, and it is safe and reliable.
分 类 号:R749.3[医药卫生—神经病学与精神病学]
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