尤瑞克林联合胞磷胆碱钠治疗卒中后认知障碍患者的临床研究OA
Clinical trial on the treatment of post-stroke cognitive impairment patients using ureklin combined with cytidine diphosphate choline sodium
目的 探讨注射用尤瑞克林联合胞磷胆碱钠胶囊治疗卒中后认知障碍(PSCI)患者的临床疗效和安全性.方法 将我院收治的PSCI患者,按照治疗方法分为对照组和试验组.对照组患者在基础治疗基础上口服胞磷胆碱钠胶囊,每次0.2 g,tid;试验组在对照组基础上加用注射用尤瑞克林,每次0.15 PNA单位+生理盐水100 mL静脉滴注30 min,qd,2组均连续治疗8周.比较2组临床疗效、脑血流灌注情况及血液流变学、神经损伤标志物水平、脑电生理参数、临床评分,并进行安全性评价.结果 入组96例患者,试验组49例、对照组47例.试验组和对照组的临床总有效率分别为89.80%(44例/49例)和72.34%(34例/47例),在统计学上差异有统计学意义(P<0.05).治疗后,试验组和对照组的大脑中动脉舒张期最小血流速度(Vmin)分别为(10.05±1.86)和(9.17±1.65)cm·s-1,平均血流量(Qmean)分别为(12.67±2.08)和(11.51±1.92)cm·s-1,血清脑源性神经营养因子(BDNF)水平分别为(15.24±2.59)和(13.76±2.24)μg·L-1,P300 波幅分别为(7.86±0.94)和(7.43±0.87)μV,阻力指数(RI)分别为(0.51±0.07)和(0.55±0.09),全血高切黏度(HBV)分别为(5.24±0.83)和(5.69±1.01)m·Pa·s,纤维蛋白原(FIB)分别为(3.14±0.52)和(3.40±0.64)g·L-1,血清神经元特异性烯醇化酶(NSE)分别为(7.35±1.23)和(8.07±1.44)μg·L-1,视锥蛋白样蛋白-1(VILIP-1)分别为(321.72±53.18)和(348.64±60.86)ng·L-1,P300 潜伏期分别为(334.59±21.57)和(346.25±23.63)ms,蒙特利尔认知评估量表(MoCA)评分分别为(26.13±3.71)和(23.73±3.24)分,简易精神状态检查量表(MMSE)评分分别为(27.19±3.85)和(25.06±3.42)分,卒中专用生活质量量表(SS-QOL)评分分别为(79.65±9.83)和(74.52±10.34)分,上述指标2组比较,在统计学上差异均有统计学意义(P<0.05,P<0.01,P<0.001).试验组发生血压下降1例、输注部位红肿2例、恶心2例,对照组出现恶心2例.试验组和对照组的不良反应总发生率分别为10.20%(5例/49例)和4.26%(2例/47例),在统计学上差异无统计学意义(P>0.05).结论 注射用尤瑞克林联合胞磷胆碱钠胶囊治疗PSCI患者疗效确切,可有效改善脑血流灌注与血液流变学状态,缓解神经损伤,促进脑电生理活动正常化,显著提升患者认知功能与日常生活能力,且安全性较高.
Objective To investigate the clinical efficacy and safety of urinary kallidinogenase for injection combined with citicoline sodium capsules in the treatment of patients with post-stroke cognitive impairment(PSCI).Methods PSCI patients admitted to our hospital were divided into control group and treatment group according to the treatment method.Patients in the control group were orally administered citicoline sodium capsules,0.2 g each time,tid;patients in the treatment group were additionally given urinary kallidinogenase for injection,0.15 PNA Unit+normal saline 100 mL intravenous drip for 30 min,qd,on the basis of the control group,and both groups were continuously treated for 8 weeks.The clinical efficacy,cerebral blood flow perfusion,hemorheology,levels of nerve injury markers,electrophysiological parameters,clinical scores,and safety evaluation were compared between the two groups.Results A total of 96 cases were enrolled,with 49 cases in the treatment group and 47 cases in the control group.The total clinical effective rates of the treatment group and the control group were 89.80%(44 cases/49 cases)and 72.34%(34 cases/47 cases),respectively,and the difference was statistically significant(P<0.05).After treatment,the middle cerebral artery end-diastolic minimum blood flow velocity(Vmin)of the treatment group and the control group was(10.05±1.86)and(9.17±1.65)cm·s-1,respectively;the mean blood flow volume(Qmean)was(12.67±2.08)and(11.51±1.92)cm·s-1,respectively;the serum brain-derived neurotrophic factor(BDNF)level was(15.24±2.59)and(13.76±2.24)μg·L-1,respectively;the P300 amplitude was(7.86±0.94)and(7.43±0.87)μV,respectively;the resistance index(RI)was(0.51±0.07)and(0.55±0.09),respectively;the whole blood high-shear viscosity(HBV)was(5.24±0.83)and(5.69±1.01)m·Pa·s,respectively;the fibrinogen(FIB)was(3.14±0.52)and(3.40±0.64)g·L-1,respectively;the serum neuron-specific enolase(NSE)was(7.35±1.23)and(8.07±1.44)μg·L-1,respectively;the visinin-like protein-1(VILIP-1)was(321.72±53.18)and(348.64±60.86)ng·L-1,respectively;the P300 latency was(334.59±21.57)and(346.25±23.63)ms,respectively;the Montreal Cognitive Assessment(MoCA)score was(26.13±3.71)and(23.73±3.24)points,respectively;the Mini-Mental State Examination(MMSE)score was(27.19±3.85)and(25.06±3.42)points,respectively;and the Stroke-Specific Quality of Life(SS-QOL)score was(79.65±9.83)and(74.52±10.34)points,respectively.The differences between the two groups in the above indicators were all statistically significant(P<0.05,P<0.01,P<0.001).In the treatment group,1 case of hypotension,2 cases of infusion site redness and swelling,and 2 cases of nausea were observed;only 2 cases of nausea occurred in the control group.The total incidence of adverse reactions in the treatment group and the control group was 10.20%(5 cases/49 cases)and 4.26%(2 cases/47 cases),respectively,and the difference was not statistically significant(P>0.05).Conclusion Urinary kallidinogenase for injection combined with citicoline sodium capsules in the treatment of PSCI patients has definite efficacy,can effectively improve cerebral blood flow perfusion and hemorheological status,alleviate nerve injury,promote the normalization of electrophysiological activity,significantly improve patients' cognitive function and daily living ability,and has high safety.
王潇慧;杨蕾;迟群;韩雪梅
青岛大学附属青岛市中医医院/海慈医院 神经内科三病区/神经内监护室,山东青岛 266033青岛大学附属青岛市中医医院/海慈医院 神经内科三病区/神经内监护室,山东青岛 266033青岛大学附属青岛市中医医院/海慈医院 神经内科三病区/神经内监护室,山东青岛 266033青岛大学附属青岛市中医医院/海慈医院 针灸推拿科,山东青岛 266033
医药卫生
注射用尤瑞克林胞磷胆碱钠胶囊卒中后认知障碍脑血流灌注神经损伤蒙特利尔认知评估量表评分视锥蛋白样蛋白-1
urinary kallidinogenase for injectioncytidine diphosphate choline sodium capsulespost-stroke cognitive impairmentcerebral perfusionneuronal injuryMontreal cognitive assessment scorevisinin-like protein-1
《中国临床药理学杂志》 2026 (14)
1964-1970,7
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