首页|期刊导航|中国临床药理学杂志|艾司西酞普兰联合奥拉西坦治疗脑卒中后认知功能障碍的临床研究

艾司西酞普兰联合奥拉西坦治疗脑卒中后认知功能障碍的临床研究OA

Clinical trial of escitalopram combined with oxiracetam in treating post-stroke cognitive impairment

中文摘要英文摘要

目的 探究艾司西酞普兰片和奥拉西坦胶囊治疗脑卒中后认知功能障碍(PSCI)患者的临床疗效和安全性.方法 用随机数表法将本院收治的PSCI患者分为试验组和对照组,对照组给予奥拉西坦胶囊治疗(0.8 g bid),试验组在对照组基础上加用艾司西酞普兰片(初始5 mg qd,1周后增至10 mg qd),连续治疗4周并随访3个月.比较2组的临床疗效、简易精神状态检查量表(MMSE)、日常生活能力量表(ADL)、神经精神量表(NPI)评分、脑血流量、血清指标及安全性.结果 最终2组各纳入60例.治疗后,对照组和试验组的MMSE分别为(20.85±4.38)和(23.67±4.81)分,ADL 分别为(58.92±6.87)和(67.53±7.72)分,NPI 分别为(59.85±6.93)和(48.88±5.73)分,大脑前动脉血流速度分别为(48.97±5.77)和(53.81±6.45)cm·s-1,中动脉血流速度分别为(63.97±7.45)和(75.23±8.63)cm·s-1,后动脉血流速度分别为(35.28±4.24)和(41.25±5.06)cm·s-1,C 反应蛋白(CRP)分别为(4.89±1.03)和(3.13±0.84)mg·L-1,神经元特异性烯醇化酶(NSE)分别为(20.64±3.21)和(16.28±2.45)ng·mL-1,同型半胱氨酸(Hcy)为(22.31±3.42)和(16.84±2.82)μmol·L-1,试验组的上述指标与对照组比较,在统计学上差异均有统计学意义(均P<0.05).试验和对照组的临床总有效率分别为90.00%(54例/60例)和71.67%(43例/60例),在统计学上差异有统计学意义(P<0.05).对照组药物不良反应有恶心呕吐、便秘、失眠,试验组药物不良反应有恶心呕吐、头晕、便秘、失眠,对照和试验组药物不良反应总发生率分别为5.00%(3例/60例)和8.33%(5例/60例),在统计学上差异无统计学意义(P>0.05).结论 艾司西酞普兰片联合奥拉西坦胶囊应用于PSCI患者的临床治疗,可以显著提高患者的临床有效率、生活质量和精神状态,改善患者大脑血流,降低患者血清CRP、Hcy、NSE水平,同时其治疗过程中安全性较高.

Objective To investigate the clinical efficacy and safety of escitalopram tablets and oxiracetam capsules in treating post-stroke cognitive impairment(PSCI)patients.Methods Patients with PSCI were divided into treatment group and control group using a random number table.The control group received oxiracetam capsules(0.8 g each time,twice daily),and the treatment group additionally received escitalopram tablets(initially 5 mg once daily,increased to 10 mg once daily after 1 week).The efficacy,scale score,cerebral blood flow,serum indicators and safety of the two groups were compared and analyzed.Results Finally,60 cases were included in each group.After treatment,the mini-mental state examination(MMSE)scores in control and treatment groups were(20.85±4.38)and(23.67±4.81)points,respectively;activities of daily living(ADL)scores were(58.92±6.87)and(67.53±7.72)points,respectively;neuropsychiatric inventory(NPI)scores were(59.85±6.93)and(48.88±5.73)points,respectively;anterior cerebral artery blood flow velocity was(48.97±5.77)and(53.81±6.45)cm·s-1,respectively;middle cerebral artery blood flow velocity was(63.97±7.45)and(75.23±8.63)cm·s-1,respectively;posterior cerebral artery blood flow velocity was(35.28±4.24)and(41.25±5.06)cm·s-1,respectively;C-reactive protein(CRP)levels were(4.89±1.03)and(3.13±0.84)mg·L-1,respectively;neuron-specific enolase(NSE)levels were(20.64±3.21)and(16.28±2.45)ng·mL-1,respectively;homocysteine(Hcy)levels were(22.31±3.42)and(16.84±2.82)μmol·L-1,respectively.The above indicators all had statistically significant difference compared between the two groups(all P<0.05).The total effective rates of the treatment group and the control group were 90.00%(54 cases/60 cases)and 71.67%(43 cases/60 cases),with a statistically significant difference(P<0.05).The adverse drug reactions of control group were nausea and vomiting,constipation and insomnia,while the adverse drug reactions of treatment group were nausea and vomiting,dizziness,constipation and insomnia.The total incidences of adverse drug reactions were 8.33%(5 cases/60 cases)and 5.00%(3 cases/60 cases),respectively,with no statistically significant difference(P>0.05).Conclusion The combination of escitalopram tablets and oxiracetam capsules in the clinical treatment of PSCI patients can obviously improve the clinical efficacy,quality of life and mental state of patients,improve cerebral blood flow,reduce serum CRP,Hcy and NSE levels,and have high safety during the treatment process.

刘丛;高雅博;齐玉凤;卢丽君;马振兴

中国中医科学院 广安门医院 保定医院脑病科,河北保定 071000中国中医科学院 广安门医院 保定医院脑病科,河北保定 071000中国中医科学院 广安门医院 保定医院脑病科,河北保定 071000中国中医科学院 广安门医院 保定医院脑病科,河北保定 071000中国中医科学院 广安门医院 保定医院脑病科,河北保定 071000

医药卫生

艾司西酞普兰片奥拉西坦胶囊脑卒中认知障碍生活质量

escitalopram tabletoxiracetam capsulestrokecognitive impairmentquality of life

《中国临床药理学杂志》 2026 (13)

1820-1824,5

保定市科技计划项目基金资助项目(NO.2341ZF297)

10.13699/j.cnki.1001-6821.2026.13.004

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