临床心身疾病杂志
臨床心身疾病雜誌
림상심신질병잡지
JOURNAL OF CLINICAL PSYCHOSOMATIC DISEASES
2015年
4期
45-47
,共3页
蒋健昌%祁富生%刘益亮%黎建容%谢文
蔣健昌%祁富生%劉益亮%黎建容%謝文
장건창%기부생%류익량%려건용%사문
精神分裂症%帕利哌酮缓释片%利培酮%阳性与阴性症状量表%个人和社会功能量表%副反应量表
精神分裂癥%帕利哌酮緩釋片%利培酮%暘性與陰性癥狀量錶%箇人和社會功能量錶%副反應量錶
정신분렬증%파리고동완석편%리배동%양성여음성증상량표%개인화사회공능량표%부반응량표
Schizophrenia%paliperidone extended release tablets%risperidone%PANSS%PSP%TESS
目的:探讨帕利哌酮缓释片与利培酮治疗男性急性精神分裂症患者的临床疗效和安全性,以及对社会功能影响。方法将80例男性急性精神分裂患者随机分为两组,每组40例,研究组口服帕利哌酮缓释片治疗,对照组口服利培酮治疗,观察12周。治疗前后采用阳性与阴性症状量表评定临床疗效,个人和社会功能量表评定社会功能,副反应量表评定不良反应。结果治疗12周末两组阳性与阴性症状量表总分及各因子分均较治疗前显著下降( P<0.01),研究组较对照组下降更显著(P<0.01);两组个人和社会功能量表总分较治疗前显著升高(P<0.01),研究组较对照组升高更显著( P<0.01);研究组总有效率为85.0%,对照组为75.0%,两组比较差异无显著性(χ2=2.54,P>0.05);研究组不良反应发生率为20.0%,对照组为42.5%,研究组不良反应发生率显著低于对照组(χ2=4.71,P<0.05)。结论帕利哌酮缓释片与利培酮均能有效改善男性急性精神分裂症患者的各种精神症状和社会功能,但帕利哌酮缓释片改善社会功能方面优于利培酮,安全性更高。
目的:探討帕利哌酮緩釋片與利培酮治療男性急性精神分裂癥患者的臨床療效和安全性,以及對社會功能影響。方法將80例男性急性精神分裂患者隨機分為兩組,每組40例,研究組口服帕利哌酮緩釋片治療,對照組口服利培酮治療,觀察12週。治療前後採用暘性與陰性癥狀量錶評定臨床療效,箇人和社會功能量錶評定社會功能,副反應量錶評定不良反應。結果治療12週末兩組暘性與陰性癥狀量錶總分及各因子分均較治療前顯著下降( P<0.01),研究組較對照組下降更顯著(P<0.01);兩組箇人和社會功能量錶總分較治療前顯著升高(P<0.01),研究組較對照組升高更顯著( P<0.01);研究組總有效率為85.0%,對照組為75.0%,兩組比較差異無顯著性(χ2=2.54,P>0.05);研究組不良反應髮生率為20.0%,對照組為42.5%,研究組不良反應髮生率顯著低于對照組(χ2=4.71,P<0.05)。結論帕利哌酮緩釋片與利培酮均能有效改善男性急性精神分裂癥患者的各種精神癥狀和社會功能,但帕利哌酮緩釋片改善社會功能方麵優于利培酮,安全性更高。
목적:탐토파리고동완석편여리배동치료남성급성정신분렬증환자적림상료효화안전성,이급대사회공능영향。방법장80례남성급성정신분렬환자수궤분위량조,매조40례,연구조구복파리고동완석편치료,대조조구복리배동치료,관찰12주。치료전후채용양성여음성증상량표평정림상료효,개인화사회공능량표평정사회공능,부반응량표평정불량반응。결과치료12주말량조양성여음성증상량표총분급각인자분균교치료전현저하강( P<0.01),연구조교대조조하강경현저(P<0.01);량조개인화사회공능량표총분교치료전현저승고(P<0.01),연구조교대조조승고경현저( P<0.01);연구조총유효솔위85.0%,대조조위75.0%,량조비교차이무현저성(χ2=2.54,P>0.05);연구조불량반응발생솔위20.0%,대조조위42.5%,연구조불량반응발생솔현저저우대조조(χ2=4.71,P<0.05)。결론파리고동완석편여리배동균능유효개선남성급성정신분렬증환자적각충정신증상화사회공능,단파리고동완석편개선사회공능방면우우리배동,안전성경고。
Objective Objective To explore the efficacy and safety of paliperidone extended‐release (pali‐peridone ER) tablets and risperidone in male acute schizophrenic and their influence on social function . Methods Eighty male acute schizophrenics were randomly divided into two groups of 40 ones each ,re‐search group took orally paliperidone ER and control group did risperidone for 12 weeks .Before and after treatment efficacies were assessed with the Positive and Negative Syndrome Scale (PANSS ) ,social per‐formances with the Personal and Social Performance Scale (PSP) ,and adverse reactions with the Treatment Emergent Symptom Scale (TESS) .Results At the end of the 12th week the total and each factor scores of the PANSS of both groups lowered more significantly compared with pretreatment (P< 0 .01) ,so did those in research than in control group (P<0 .01);the total scores of the PSP of both groups heightened more significantly (P<0 .01) ,so did that in research than in control group (P<0 .01);total effective rate was respectively 85 .0% in research and 75 .0% in control group ,which showed no significant difference (χ2 =2 .54 ,P>0 .05);the incidence was respectively 20 .0% in research and 42 .5% in control group ,the former significantly lower than the latter (χ2 =4 .71 ,P<0 .05) .Conclusion Both paliperidone ER and risperidone could effectively improve various kinds of mental symptoms and social performances ,but the former has an advantage in improving social performances and higher safety over the latter .