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Clinical Effect of Ilaprazole Enteric-Coated Tablets in Patients with Peptic Ulcer
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作者 Fanghui Chen 《Journal of Biosciences and Medicines》 2024年第9期155-160,共6页
Objective: To discuss the actual effect of ilaprazole enteric-coated tablets in the treatment of peptic ulcer patients. Methods: 200 peptic ulcer patients who received treatment from January to December 2023 were sele... Objective: To discuss the actual effect of ilaprazole enteric-coated tablets in the treatment of peptic ulcer patients. Methods: 200 peptic ulcer patients who received treatment from January to December 2023 were selected as the study sample, and all patients were randomly and evenly divided into the study group (n = 100) and the control group (n = 100), and the serum inflammatory factors and the disappearance time of symptoms were compared. Results: After treatment, the serum inflammatory factors in the observation group were better than those in the control group, and the time of belching and burning sensation in the observation group was shorter than that in the control group, all of which were statistically significant (P Conclusion: Ilaprazole enteric-coated tablets in the treatment of peptic ulcer have a good effect and can effectively improve the symptoms of patients with clinical signs, with reference significance. 展开更多
关键词 Ilaprazole enteric-coated Tablets Peptic Ulcer SYMPTOMS
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Analysis of the Therapeutic Effect of Clopidogrel Bisulfate Tablets + Aspirin Enteric-Coated Tablets on Acute Myocardial Infarction
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作者 Yiru Chen 《Journal of Clinical and Nursing Research》 2024年第6期290-294,共5页
Objective:To investigate and analyze the clinical effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on acute myocardial infarction(AMI)patients.Methods:The study period was from Janu... Objective:To investigate and analyze the clinical effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on acute myocardial infarction(AMI)patients.Methods:The study period was from January 2020 to December 2023,the sample source was 82 AMI patients admitted to our hospital,grouped into an observation group(n=41)and a control group(n=41)by the numerical table method.The patients in the control group were treated with aspirin enteric-coated tablets,and the patients in the observation group were treated with aspirin enteric-coated tablets combined with clopidogrel bisulfate.The clinical efficacy,coagulation indexes,and the incidence of cardiovascular adverse events between the two groups were compared.Results:The clinical efficacy of the observation group was higher than that of the control group(P<0.05);the platelet aggregation rate(PAR)of the observation group was lower than that of the con-trol group after treatment(P<0.05),and there was no significant difference in the prothrombin time(PT)and activated partial thromboplastin time(APTT)between the two groups(P>0.05).The incidence of cardiovascular adverse events in the observation group was lower than that of the control group(P<0.05).Conclusion:The treatment effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on AMI patients is remarkable.It reduces the PAR and the incidence of cardiovascular adverse events,so this treatment method should be popularized. 展开更多
关键词 Clopidogrel bisulfate Aspirin enteric-coated tablets Acute myocardial infarction
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Chemotherapy with enteric-coated tegafur/uracil for advanced hepatocellular carcinoma 被引量:1
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作者 Toru Ishikawa 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第18期2797-2801,共5页
Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, including Japan. Although the development of imaging modalities has made the early diagnosis of HCC possible, surgically resectable case... Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, including Japan. Although the development of imaging modalities has made the early diagnosis of HCC possible, surgically resectable cases are relatively uncommon because of hepatic function reserve and/or an advanced stage at presentation. Several modalities, such as transcatheter arterial chemoembolization, percutaneous ethanol injection, microwave coagulation therapy and radiofrequency ablation are reportedly useful in treating patients with non-resectable disease. However, unfortunately, many HCC patients have tumor recurrence. The overall prognosis of patients with HCC is very poor, and treatment of the advanced form is still problematic. In this article, we review the clinical efficacy and toxicity of enteric-coated tegafur/uracil in the treatment of patients with advanced non-resectable HCC. 展开更多
关键词 Advanced hepatocellular carcinoma Tumor dormancy enteric-coated tegafur/uracil CHEMOTHERAPY Portal vein tumor thrombus Lung metastasis
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Formulation Optimization Utilizing D-Optimal Experimental Design of Oral Capsules Containing Enteric-Coated Pellets of Lansoprazole and<i>in vivo </i>Bioequivalence
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作者 Anh Quang Luong Thang Ngoc Vu +3 位作者 Dang Hoa Nguyen Sultan M. Alshahrani John Mark Christensen Chien Ngoc Nguyen 《Pharmacology & Pharmacy》 2017年第5期153-171,共19页
An optimized formulation of capsules containing Lansoprazole enteric-coated pellets using D-Optimal design with a polynomial statistical model were prepared by using Eudragit?L100 as an enteric coated polymer to provi... An optimized formulation of capsules containing Lansoprazole enteric-coated pellets using D-Optimal design with a polynomial statistical model were prepared by using Eudragit?L100 as an enteric coated polymer to provide resistance to simulated gastric acid dissolution in buffer media. D-Optimal experimental design was used to determine the optimal level for three coating layers that were applied to formulate the enteric-coated pellets including a drug loading layer, a sub-coating, and an outer enteric coating. Dissolution studies were performed on the prepared Lansoprazole capsules. Less than 5 percent of Lansoprazole was released in 60 minutes in an acidic dissolution medium (pH 1.2) and greater than 90 percent of active ingredient was released in the next 60 minutes in a buffer dissolution medium (pH 6.8). The Lansoprazole capsules were stable with no observable change in physico-chemical properties in accelerated and normal storage conditions for 6 and 18 months, respectively. The pharmacokinetic parameters Cmax, Tmax, AUC0-t, and AUC0-∞ were determined after administration of the D-Optimal design optimized capsules of LPZ to healthy beagle dogs and were statistically compared to Gastevin? capsules as a reference (KRKA, Slovenia) using the non-compartmental method with the aid of WinNonlin 5.2 software. The analysis of variance showed that the two formulations did not demonstrate bioequivalence using a 90% confidence interval range (80% - 120%) of Cmax, AUC0-t, and AUC0-∞. No significant difference in Tmax was found at the 0.95 significance level using the Wilcoxon signed-rank test. D-Optimal Experimental Design provided definitive direction for an optimal formulation of capsules containing enteric-coated pellets of lansoprazole loaded within the coating of pellets that provided similar bioequivalence to Gastevin. 展开更多
关键词 LANSOPRAZOLE D-Optimal Pellets enteric-coating PHARMACOKINETIC Parameters
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Pharmacokinetic Evaluation of Chitosan-Succinyl-Prednisolone Conjugate Microparticles as a Colonic Delivery System: Comparison with Enteric-Coated Conjugate Microparticles
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作者 Hiraku Onishi 《Health》 2014年第11期1286-1295,共10页
In the previous study, chitosan-succinyl-prednisolone conjugate microparticles (MP) were found to exhibit good efficacy and reduced toxicity nearly as well as their Eudragit L-coated microparticles (MP/EuL). This prop... In the previous study, chitosan-succinyl-prednisolone conjugate microparticles (MP) were found to exhibit good efficacy and reduced toxicity nearly as well as their Eudragit L-coated microparticles (MP/EuL). This proposes a question whether enteric-coating of MP is necessary or not. Although MP/EuL were already examined for their pharmacokinetic and gastrointestinal behaviors, MP have not been done yet. Therefore, in this study, MP were evaluated by investigating pharmacokinetic features in detail. MP with the in vitro features equivalent to those of the previous conjugate microparticles could be produced more readily in the modified preparative method. Pharmacokinetic and gastrointestinal behaviors of MP were investigated by intragastric dosing (5 mg PD eq./kg) to rats with 2,4,6-trinitrobenzenesulfonic acid-induced ulcerative colitis. The plasma concentration was suppressed extensively in MP as well as MP/EuL, supporting the reduction of PD systemic toxic side effects. However, the plasma level increased gradually up to 7 h in MP, but not in MP/EuL. At 8 h after dosing, MP were detected in the stomach to a fair extent, and free PD was found there, indicating that MP were subjected to trapping in the stomach probably due to positive charge of chitosan molecules. For MP, such prolonged localization and slow release of PD in the stomach were probably associated with the gradual increase in plasma concentration. Therefore, MP/EuL were evaluated to be superior to MP for effective targeting to ulcerative colitis. It is concluded that enteric-coating is very important for the targeting system using MP. 展开更多
关键词 Chitosan-Succinyl-Prednisolone CONJUGATE Microparticle enteric-coating Pharmacokinetic Feature Gastrointestinal Behavior 2 4 6-Trinitrobenzenesulfonic Acid-Induced Ulcerative Colitis
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Influence of Xiaoshuan enteric-coated capsules + aniracetam therapy on cerebral blood perfusion and nerve function in patients with convalescent cerebral infarction
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作者 Bo Wu 《Journal of Hainan Medical University》 2017年第24期134-137,共4页
Objective: To investigate the influence of Xiaoshuan enteric-coated capsules + aniracetam therapy on cerebral blood perfusion and nerve function in patients with convalescent cerebral infarction. Methods: A total of 1... Objective: To investigate the influence of Xiaoshuan enteric-coated capsules + aniracetam therapy on cerebral blood perfusion and nerve function in patients with convalescent cerebral infarction. Methods: A total of 177 cases of patients with convalescent cerebral infarction were retrospectively reviewed and then divided into the control group (n=109) and the Xiaoshuan enteric-coated capsules group (n=68). Control group received aniracetam therapy on the basis of routine treatment, and Xiaoshuan enteric-coated capsules group received Xiaoshuan enteric-coated capsules + aniracetam therapy on the basis of routine treatment. The differences in ultrasound cerebral blood perfusion parameter levels as well as serum neurotrophy index and nerve injury index contents were compared between the two groups. Results: Before treatment, there was no statistically significant difference in ultrasound cerebral blood perfusion parameter levels as well as serum neurotrophy index and nerve injury index contents between the two groups. After treatment, ultrasound cerebral blood perfusion parameters PSV and TMV levels in Xiaoshuan enteric-coated capsules group were higher than those in control group whereas RI level was lower than that in control group;serum neurotrophy indexes bFGF, BDNF and VEGF contents were higher than those of control group;serum nerve injury indexes GFAP, NSE, UCH-L1 and S100B contents were lower than those of control group. Conclusion: Xiaoshuan enteric-coated capsules + aniracetam therapy can significantly increase cerebral blood perfusion and optimize nerve function in patients with convalescent cerebral infarction. 展开更多
关键词 Convalescent CEREBRAL infarction Xiaoshuan enteric-coated CAPSULES ANIRACETAM CEREBRAL blood perfusion NERVE FUNCTION
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Efficacy and mechanism of Xiaoshuan enteric-coated capsule as an adjunctive treatment for ischemic stroke:A randomized clinical trial
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作者 Chunli Wen Zhixia Su +4 位作者 Zhibin Ding Cungen Ma Fengyun Hu Lijuan Song Lingqun Zhu 《Journal of Traditional Chinese Medical Sciences》 CAS 2024年第4期405-414,共10页
Objective:To explore the clinical efficacy of Xiaoshuan enteric-coated capsule(XSECC)in treating ce-rebral infarction and its potential mechanism of action.Methods:Patients with acute ischemic stroke(AIS)of the qi def... Objective:To explore the clinical efficacy of Xiaoshuan enteric-coated capsule(XSECC)in treating ce-rebral infarction and its potential mechanism of action.Methods:Patients with acute ischemic stroke(AIS)of the qi deficiency and blood stasis type were randomly assigned to the control and observation groups.They were evaluated using the National In-stitutes of Health Stroke Scale(NIHSS),Activities of Daily Living(ADL),Hachinskilnchemic Scale(HIS),Barthel Index(BI),clinical efficacy scores,and TCM syndrome scores on days 0,14,30,and 90.Furthermore,VEGF and BDNF levels were measured on days 30 and 90.Finally,we analyzed the changes in each scale score and vascular neurological factor in both groups.Results:After 14 days of treatment,the difference values in NIHSS,ADL,and BI were higher,and TCM syndrome and clinical efficacy scores were increased in the observation group compared with those of the control group(all P<0.05).After 30 days,the NIHSS,ADL,HIS,and TCM syndrome scores were decreased compared with those of the control group,while BI and clinical efficacy scores were increased(all P<0.05).After 90 days,the difference value in ADL was higher,and TCM syndrome score was increased in the observation group compared with that of the control group(P=0.047,P=0.005,respectively).The levels of VEGF and BDNF were higher in the observation group than in the control group on days 14,30,and 90(all P<0.05).VEGF and BDNF levels on day 0 were associated with prognosis of patients with AIS;therefore,they have a predictive value for the prognosis of acute cerebral infarction.Conclusions:XSECC therapy can improve clinical outcomes in patients with acute and recurrent cerebral infarctions.Its mechanism of action may be associated with the secretion of VEGF and BDNF. 展开更多
关键词 Cerebral infarction Xiaoshuan enteric-coated capsule Qi deficiency and blood stasis Vascular endothelial growth factor Brain-derived neurotrophic factor
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拜阿司匹林联合氯比格雷治疗PCI术后患者1年再入院风险预测模型构建
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作者 吕远 陈佩佩 +1 位作者 吴琼碧 张伟 《药学前沿》 CAS 2024年第9期41-48,共8页
目的探究拜阿司匹林联合氯比格雷治疗经皮冠状动脉介入术(PCI)术后患者1年再入院危险因素,并构建风险预测模型。方法回顾性分析2020年1月至2023年6月丽水市人民医院心内科初次行PCI的心肌梗死(MI)患者的临床资料。根据1年内是否因心肌... 目的探究拜阿司匹林联合氯比格雷治疗经皮冠状动脉介入术(PCI)术后患者1年再入院危险因素,并构建风险预测模型。方法回顾性分析2020年1月至2023年6月丽水市人民医院心内科初次行PCI的心肌梗死(MI)患者的临床资料。根据1年内是否因心肌再梗死或MI并发症再次入院分为再入院组(RG)和非再入院组(NRG)。采用单因素分析探究RG和NRG组间差异变量。采用(逐步)多因素Logistic回归探究PCI术后患者1年再入院的危险因素及“最优模型”,使用R software对“最优模型”进行可视化,转化为Nomogram风险预测模型。采用受试者工作特征曲线(ROC)评估Nomogram风险预测模型的预测能力;采用校准曲线(重取样,Bootstrap n=1000)评估Nomogram风险预测模型的校准度;采用决策曲线评估Nomogram风险预测模型的净获益大小。结果研究共纳入患者100例,1年内再入院率为34.00%。年龄(≥63岁)、糖尿病、病变血管数(≥2支)、单核细胞计数-高密度脂蛋白比值(≥0.36)和预后营养指数(<39.39)是PCI术后MI患者再入院的独立危险因素(P<0.05)。ROC分析表明,再入院风险预测模型预测PCI后MI患者再入院效能较好,其ROC曲线下面积为0.903[95%CI(0.836,0.970)]。校准曲线表明预测再入院概率和实际再入院概率大致符合;决策曲线表明再入院风险预测模型Nomogram净获益高于全部临床净获益。结论本研究所构建的PCI术后MI患者再入院预测模型,能较为准确地识别再入院的高危人群,可有利于临床对PCI术后患者进行规范化管理,提高患者的长期预后。 展开更多
关键词 心肌梗死 经皮冠状动脉介入术 再入院 预测模型 拜阿司匹林 氯比格雷
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拜阿司匹林联合气压仪治疗对剖宫产产妇产后足甲襞微循环及下肢血流的影响研究
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作者 蔡紫微 夏萍 《中外医学研究》 2024年第36期28-31,共4页
目的:探究拜阿司匹林联合气压仪治疗对剖宫产产妇产后足甲襞微循环及下肢血流的影响。方法:选取2022年1月—2023年6月孝感市孝南区妇幼保健院收治的180例剖宫产产妇作为研究对象,依据随机数表法分为A组、B组和C组,每组各60例。A组采用... 目的:探究拜阿司匹林联合气压仪治疗对剖宫产产妇产后足甲襞微循环及下肢血流的影响。方法:选取2022年1月—2023年6月孝感市孝南区妇幼保健院收治的180例剖宫产产妇作为研究对象,依据随机数表法分为A组、B组和C组,每组各60例。A组采用拜阿司匹林治疗,B组采用气压仪治疗,C组采用拜阿司匹林联合气压仪治疗。比较三组的下肢深静脉血栓发生率、治疗前后的下肢肿胀情况(细胞外水分比率)、足甲襞微循环(足甲襞微循环加权积分)及下肢血流速度。结果:C组的下肢深静脉血栓发生率低于A组及B组,差异有统计学意义(P<0.05);治疗前三组的细胞外水分比率、足甲襞微循环加权积分及下肢血流速度比较,差异无统计学意义(P>0.05);治疗5 d后C组的细胞外水分比率及足甲襞微循环加权积分低于A组及B组,下肢血流速度高于A组及B组,差异有统计学意义(P<0.05);A组与B组的下肢深静脉血栓发生率、细胞外水分比率、足甲襞微循环加权积分及下肢血流速度比较,差异无统计学意义(P>0.05)。结论:拜阿司匹林联合气压仪治疗可显著改善剖宫产产妇的产后足甲襞微循环及下肢血流,有助于下肢深静脉血栓的防控。 展开更多
关键词 拜阿司匹林 气压仪 剖宫产 产妇 足甲襞微循环 下肢血流
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缺血性卒中二级预防服用拜阿司匹林的依从性随访研究 被引量:22
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作者 居克举 杨梅 +1 位作者 郭建一 曹化 《中国全科医学》 CAS CSCD 北大核心 2010年第2期153-154,共2页
目的分析缺血性卒中患者出院后1年内使用拜阿司匹林的依从性及其影响因素,探讨解决办法。方法对我科连续出院的157例缺血性卒中患者进行随访,按其是否停药分为依从性好组和依从性差组,对其停用拜阿司匹林的原因及影响因素进行统计分析... 目的分析缺血性卒中患者出院后1年内使用拜阿司匹林的依从性及其影响因素,探讨解决办法。方法对我科连续出院的157例缺血性卒中患者进行随访,按其是否停药分为依从性好组和依从性差组,对其停用拜阿司匹林的原因及影响因素进行统计分析。结果157例患者中依从性差组39例(24.8%),依从性好组118例(75.2%),两组在文化水平、发病次数方面差异有统计学意义(P<0.05),在停药时间上66.67%的患者在1~2个月内停药,56.41%的患者是因为症状好转停药。结论患者中断服药的根本原因是因为对疾病的认识不够,开展广泛的科普教育是提高服药依从性的关键,对首次发病的患者在1~2月之间随访,进行跟踪指导可能是提高服药依从性的有效措施。 展开更多
关键词 缺血性卒中 拜阿司匹林 抗血小板治疗 依从性
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阿司匹林联合阿托伐他汀对缺血性脑血管病患者血清ox-LDL、炎性因子和颈动脉斑块的影响 被引量:30
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作者 王跃慧 田跃雷 +2 位作者 梁文华 白莹 吴玲玲 《河北医药》 CAS 2016年第11期1628-1631,共4页
目的观察缺血性脑血管病患者血清氧化型低密度脂蛋白(ox-LDL)、脂蛋白相关磷脂酶A2(LpPLA2)、超敏C-反应蛋白(hs-CRP)与颈动脉粥样硬化斑块的关系,并观察阿司匹林联合阿托伐他汀的治疗效果。方法缺血性脑血管病患者103例(病例组)包括IM... 目的观察缺血性脑血管病患者血清氧化型低密度脂蛋白(ox-LDL)、脂蛋白相关磷脂酶A2(LpPLA2)、超敏C-反应蛋白(hs-CRP)与颈动脉粥样硬化斑块的关系,并观察阿司匹林联合阿托伐他汀的治疗效果。方法缺血性脑血管病患者103例(病例组)包括IMT正常组20例,IMT增厚组15例,颈动脉斑块组68例(稳定斑块36例,不稳定斑块32例),同期体检的健康人80例为正常组。病例组随机分为对照组51例和观察组52例,均给予抗血小板聚集等常规治疗,观察组加用阿司匹林100 mg联合阿托伐他汀20 mg口服,疗程12个月。比较2组治疗前后血清ox-LDL、Lp-PLA2、hs-CRP及颈动脉IMT、斑块面积变化。结果 (1)血清ox-LDL、Lp-PLA2、hs-CRP水平病例组高于正常组(P<0.05);颈动脉斑块组高于IMT增厚组,IMT增厚组高于IMT正常组(P<0.05);颈动脉斑块组中不稳定斑块组高于稳定斑块组(P<0.05)。颈动脉斑块形成与血清ox-LDL、Lp-PLA2、hs-CRP水平呈正相关(P<0.05)。(2)治疗后对照组和观察组血清ox-LDL、Lp-PLA2、hs-CRP水平均较治疗前降低(P<0.05),同时颈动脉IMT、斑块面积缩小(P<0.05),且观察组均小于对照组(P<0.05)。结论缺血性脑血管病患者血清ox-LDL、LpPLA2、hs-CRP水平与动脉粥样硬化形成及发展有关,并可反映动脉粥样硬化程度。阿司匹林联合阿托伐他汀治疗缺血性脑血管病能降低患者血清ox-LDL、Lp-PLA2、hs-CRP水平,对延缓或逆转动脉粥样硬化斑块进展有积极意义。 展开更多
关键词 阿司匹林 阿托伐他汀 缺血性脑血管病
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阿司匹林联合阿托伐他汀治疗缺血性脑血管病疗效观察 被引量:10
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作者 王跃慧 田跃雷 +2 位作者 梁文华 白莹 吴玲玲 《河北医药》 CAS 2016年第12期1796-1799,共4页
目的观察阿司匹林联合阿托伐他汀治疗缺血性脑血管病的临床疗效。方法选取2013年6月至2015年6月诊治的缺血性脑血管病患者103例,随机分为对照组(n=51)和观察组(n=52)。2组均给予抗血小板聚集等常规治疗,观察组在常规治疗基础上给予阿司... 目的观察阿司匹林联合阿托伐他汀治疗缺血性脑血管病的临床疗效。方法选取2013年6月至2015年6月诊治的缺血性脑血管病患者103例,随机分为对照组(n=51)和观察组(n=52)。2组均给予抗血小板聚集等常规治疗,观察组在常规治疗基础上给予阿司匹林100 mg联合阿托伐他汀20 mg口服治疗,疗程12个月。比较2组临床疗效、症状消失时间、总治疗时间、血脂(TC、TG、LDL-C、HDL-C)、血液流变学指标(血浆黏度比、纤维蛋白原、血沉)、脑血管储备能力、屏气指数、不良反应、复发情况及SF-36生活质量评分。结果对照组和观察组总有效率分别为62.75%、90.38%,差异有统计学意义(P<0.05)。与对照组比较,观察组症状消失时间、总治疗时间明显缩短,TC、TG、LDL-C、血浆黏度比、纤维蛋白原、血沉及复发率明显降低,HDL-C、脑血管储备能力、屏气指数及SF-36生活质量评分明显提高(P<0.05)。2组不良反应比较差异无统计学意义(P>0.05)。结论阿司匹林联合阿托伐他汀治疗缺血性脑血管病疗效良好,能够明显改善患者血脂、血液流变学及脑血管储备能力,且无明显不良反应。 展开更多
关键词 阿司匹林 阿托伐他汀 缺血性脑血管病 疗效
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氢氯吡格雷联合拜阿司匹林治疗急性脑梗死的效果评估与分析 被引量:11
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作者 焦俊杰 孙亚红 马凤仪 《中国现代药物应用》 2017年第6期41-43,共3页
目的探究氢氯吡格雷联合拜阿司匹林治疗急性脑梗死的效果。方法 150例急性脑梗死患者,随机分为单一组和双联组,各75例。单一组采用拜阿司匹林治疗;双联组采用氢氯吡格雷联合拜阿司匹林治疗。比较两组患者急性脑梗死干预效果;治疗前后患... 目的探究氢氯吡格雷联合拜阿司匹林治疗急性脑梗死的效果。方法 150例急性脑梗死患者,随机分为单一组和双联组,各75例。单一组采用拜阿司匹林治疗;双联组采用氢氯吡格雷联合拜阿司匹林治疗。比较两组患者急性脑梗死干预效果;治疗前后患者神经功能缺损评分、溶酶体颗粒膜糖蛋白水平、二磷酸腺苷;不良反应发生率。结果双联组患者急性脑梗死干预总有效率为97.33%高于单一组的82.67%,差异有统计学意义(P<0.05)。双联组治疗后患者神经功能缺损评分、溶酶体颗粒膜糖蛋白水平、二磷酸腺苷优于单一组,差异有统计学意义(P<0.05)。两组患者不良反应发生率比较,差异无统计学意义(P>0.05)。结论氢氯吡格雷联合拜阿司匹林治疗急性脑梗死的效果确切,可有效改善患者临床症状,减轻神经功能缺损程度,改善生化指标,且无明显不良反应,安全可靠,值得推广。 展开更多
关键词 氢氯吡格雷 拜阿司匹林 急性脑梗死 效果
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通心络联合瑞舒伐他汀钙片、拜阿司匹林治疗高脂血症伴颈动脉粥样硬化的临床疗效观察 被引量:17
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作者 倪正仙 高怀林 +1 位作者 谢传星 裴如弟 《世界中医药》 CAS 2017年第4期807-810,共4页
目的:观察并分析通心络联合瑞舒伐他汀钙片、拜阿司匹林对高脂血症伴颈动脉粥样硬化的治疗效果。方法:选择门诊治疗伴有颈动脉粥样硬化的高脂血症患者64例,采用随机数字表法将患者分为2组,对照组32例患者给予瑞舒伐他汀钙片联合拜阿司... 目的:观察并分析通心络联合瑞舒伐他汀钙片、拜阿司匹林对高脂血症伴颈动脉粥样硬化的治疗效果。方法:选择门诊治疗伴有颈动脉粥样硬化的高脂血症患者64例,采用随机数字表法将患者分为2组,对照组32例患者给予瑞舒伐他汀钙片联合拜阿司匹林治疗,治疗组32例患者给予"金三角"方案(通心络联合瑞舒伐他汀钙片、拜阿司匹林)联合治疗。测定患者晨起空腹血脂及血浆同型半胱氨酸(Hcy)、高敏C-反应蛋白(hs-CRP)水平,并采用颈动脉彩色多普勒超声检测患者颈动脉内-中膜厚度(c IMT)及斑块数量、面积。治疗6个月后,对2组患者治疗前后的血脂、血浆Hcy、hs-CRP水平及颈动脉粥样硬化斑块治疗情况进行分析比较。结果:2组患者经治疗后空腹血浆三酰甘油(TG)、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、Hcy、hs-CRP水平及颈动脉斑块数量、面积、c IMT等均较治疗前有明显改善,且治疗组效果优于对照组(P<0.05,P<0.01)。结论:"金三角"方案对伴有颈动脉粥样硬化的高脂血症患者血脂、血浆Hcy、hs-CRP水平及颈动脉斑块情况均有明显的改善作用,其效果优于单纯应用西药治疗。 展开更多
关键词 高脂血症 颈动脉粥样硬化 通心络 瑞舒伐他汀钙片 拜阿司匹林
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依达拉奉联合双抗治疗进展性缺血性卒中炎性因子及生活能力的影响 被引量:4
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作者 李孟修 王艳竹 +1 位作者 任志军 文晓燕 《中国医学创新》 CAS 2017年第25期43-46,共4页
目的:观察依达拉奉联合双抗治疗进展性缺血性卒中患者血清炎性因子和生活能力的改善效果。方法:选取2015年1月-2016年12月在本院诊治的进展性卒中患者60例作为研究对象,根据抗凝方案将其分为双抗组29例接受常规双抗抗凝治疗(拜阿司匹林... 目的:观察依达拉奉联合双抗治疗进展性缺血性卒中患者血清炎性因子和生活能力的改善效果。方法:选取2015年1月-2016年12月在本院诊治的进展性卒中患者60例作为研究对象,根据抗凝方案将其分为双抗组29例接受常规双抗抗凝治疗(拜阿司匹林联合氯吡格雷),联合组31例使用依达拉奉联合双抗治疗,分别检测比较治疗前后血清炎性因子和评价生活能力。结果:治疗后,联合组血清IL-6(216.94±24.87)pg/mL、TNF-α(1.01±0.24)pg/mL、hs-CRP(3.29±0.97)mg/mL、CSS评分(10.67±1.96)分均显著低于双抗组,Barthel评分(84.26±10.98)分显著高于双抗组,两组比较差异均有统计学意义(P<0.05)。结论:依达拉奉联合双抗抗凝方案能够抑制进展性卒中患者血清炎性因子表达,提升患者的生活能力,对进展性卒中预后有明显改善效果。 展开更多
关键词 进展性卒中 依达拉奉 拜阿司匹林 氯吡格雷 炎性因子 生活能力
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三联抗凝治疗患者低分子肝素脐周皮下注射部位的研究 被引量:20
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作者 朱敏 史作霞 +2 位作者 张文彦 李馨 王莹 《护理学杂志》 2011年第23期39-40,共2页
目的探讨三联抗凝治疗患者低分子肝素脐周注射的最佳部位,降低皮下出血发生率。方法将389例脐周皮下注射低分子肝素同时口服拜阿司匹林、硫酸氢氯吡格雷片患者采用自身对照法,分别于脐至外侧缘连线,将左侧连线分为3等份,选择外1/3处上下... 目的探讨三联抗凝治疗患者低分子肝素脐周注射的最佳部位,降低皮下出血发生率。方法将389例脐周皮下注射低分子肝素同时口服拜阿司匹林、硫酸氢氯吡格雷片患者采用自身对照法,分别于脐至外侧缘连线,将左侧连线分为3等份,选择外1/3处上下5cm范围进行注射;将右侧连线分为2等份,选择1/2处上下5cm范围进行注射。两处各注射2 080例次,观察皮下出血的发生率。结果 1/3处皮下出血发生率显著低于1/2处(P<0.01)。结论三联抗凝治疗患者行低分子肝素脐周皮下注射时选择在腹部外侧部位进针,可减少皮下出血。 展开更多
关键词 低分子肝素 拜阿司匹林 硫酸氢氯吡格雷片 抗凝治疗 皮下注射 注射部位 脐周 皮下出血
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阿托伐他汀联合阿司匹林在预防老年脑梗死再发中的临床意义 被引量:10
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作者 梁力晖 《中国医药导刊》 2012年第12期2152-2153,共2页
目的:探讨阿托伐他汀联合拜阿司匹林在脑梗死再发预防方面的作用。方法:将首发脑梗死的老年患者256例随机分为研究组和对照组两组,所有患者均常规进行基础疾病的相应治疗,研究组给予拜阿司匹林联合阿托伐他汀治疗;对照组给予拜阿司匹林... 目的:探讨阿托伐他汀联合拜阿司匹林在脑梗死再发预防方面的作用。方法:将首发脑梗死的老年患者256例随机分为研究组和对照组两组,所有患者均常规进行基础疾病的相应治疗,研究组给予拜阿司匹林联合阿托伐他汀治疗;对照组给予拜阿司匹林治疗,血脂控制方面使用非他汀类药物治疗。并分别于入院时及治疗后第3、6、12个月动态监测患者血液流变学、血脂水平等变化,并对患者颈动脉粥样斑块的积分变化行评估,以及1年内患者脑梗死的再发生率进行比较。结果:在脑梗死的再发率方面,研究组为3.8%,较对照组的10.1%明显降低(P<0.01)。两组患者在血液流变学变化、血脂水平变化方面,在治疗前后比较差异具有统计学意义(P<0.05),组间比较差异无统计学意义(P>0.05)。研究组患者在颈动脉斑块积分变化方面,治疗前后比较差异具有统计学意义(P>0.05),而对照组治疗前后比较差异无统计学意义(P>0.05),治疗后的两组之间比较差异具有统计学意义(P>0.05)。结论:在预防脑梗死的再发生治疗方面,阿托伐他汀联合拜阿司匹林可以达到很好的治疗效果,明显优于单用拜阿司匹林治疗。 展开更多
关键词 阿托伐他汀 拜阿司匹林 老年人 脑梗死再发预防
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氟伐他汀与拜阿司匹灵对高血压血栓前状态分子标志物的影响 被引量:1
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作者 马宏 张七一 《青岛大学医学院学报》 CAS 2007年第3期215-216,219,共3页
目的观察氟伐他汀与拜阿司匹灵对原发性高血压血栓前状态分子标志物的影响。方法选取80例原发性高血压血栓前状态分子标志物异常病人,随机分成两组。在药物基础降压前提下,治疗组加用氟伐他汀(来适可)40 mg和拜阿斯匹灵0.1 g,每日1次... 目的观察氟伐他汀与拜阿司匹灵对原发性高血压血栓前状态分子标志物的影响。方法选取80例原发性高血压血栓前状态分子标志物异常病人,随机分成两组。在药物基础降压前提下,治疗组加用氟伐他汀(来适可)40 mg和拜阿斯匹灵0.1 g,每日1次口服;对照组加用拜阿斯匹灵0.1 g,每日1次口服。治疗4周后检测两组病人血浆血栓调节蛋白(TM)、血管性血友病因子(VWF)、纤溶酶原激活剂抑制物-1(PAI-1)的水平,并进行比较。结果两组病人治疗后血浆TM、VWF、PAI-1水平显著下降(t=2.21-3.57,P〈0.05、0.01),但治疗组下降较对照组更显著(t=3.27-8.47,P〈0.01)。结论氟伐他汀与拜阿司匹灵联合应用能显著降低原发性高血压血栓前状态分子标志物的水平。 展开更多
关键词 拜阿斯匹灵 氟伐他汀 高血压 血栓前状态
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拜阿司匹灵对脑梗死患者血浆血小板4因子的影响 被引量:1
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作者 罗永杰 刘洁 《国际神经病学神经外科学杂志》 2006年第4期303-304,共2页
目的观察脑梗死患者用拜阿司匹灵治疗前、后血浆血小板4因子(PF4)的变化。方法70例脑梗死患者被随机分为不用拜阿司匹灵组(n=40)和服用拜阿司匹灵组(100mg/次,睡前服用,n=30),其他治疗两组间无差异。用酶标免疫测定法测定二组治疗前、... 目的观察脑梗死患者用拜阿司匹灵治疗前、后血浆血小板4因子(PF4)的变化。方法70例脑梗死患者被随机分为不用拜阿司匹灵组(n=40)和服用拜阿司匹灵组(100mg/次,睡前服用,n=30),其他治疗两组间无差异。用酶标免疫测定法测定二组治疗前、治疗后7d及30例正常对照组血浆PF4的含量。结果急性脑梗死不用拜阿司匹灵组的患者血浆PF4治疗前为15.12±6.32ng/ml,治疗后为9.83±4.93ng/ml,治疗后PF4的明显下降(P<0.01),但显著高于正常对照组(6.50±2.70ng/ml,P<0.01);服用拜阿司匹灵组的患者血浆PF4治疗前为15.48±3.16ng/ml,治疗7d后为7.66±1.47ng/ml,较治疗前明显下降(P<0.01),也明显低于不用拜阿司匹灵组的患者(P<0.01),但仍高于正常对照组(6.50±2.70ng/ml,P<0.05)。结论拜阿司匹灵能降低脑梗死患者血浆PF4含量水平,抑制血小板活性。 展开更多
关键词 脑梗死 血小板4因子 阿司匹林 拜阿司匹灵
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前列地尔注射液静滴联合拜阿司匹林、瑞舒伐他汀、复方丹参滴丸口服对颈动脉斑块的影响 被引量:3
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作者 王庆军 刘骁 《泰山医学院学报》 CAS 2015年第9期995-997,共3页
目的探讨前列地尔注射液静滴联合拜阿司匹林、瑞舒伐他汀、复方丹参滴丸口服治疗颈动脉斑块的临床疗效。方法选取2011年5月-2014年5月我院保健科住院患者及健康查体中心的门诊患者140例,随机分为对照组和治疗组各70例。两组患者均给予... 目的探讨前列地尔注射液静滴联合拜阿司匹林、瑞舒伐他汀、复方丹参滴丸口服治疗颈动脉斑块的临床疗效。方法选取2011年5月-2014年5月我院保健科住院患者及健康查体中心的门诊患者140例,随机分为对照组和治疗组各70例。两组患者均给予低盐、低脂、低蛋白饮食,对照组患者均予以口服拜阿司匹林100 mg,每早1次;瑞舒伐他汀10 mg,每晚1次,共服2个月。治疗组在对照组基础上以前列地尔注射液10μg加入0.9%氯化钠溶液100 ml静脉滴注每天1次,治疗14 d,并加服复方丹参滴丸10丸/次,一日3次,共服2个月。治疗结束后评价两组临床疗效、比较两组患者治疗前后颈动脉内膜中层厚度(IMT)、斑块面积、斑块数量的变化及斑块性质。结果 1临床疗效:治疗组总有效率(97.14%)优于对照组总有效率(74.29%)。2检测指标:治疗后,治疗组在IMT、斑块面积、斑块数量方面与治疗前比较均有明显改善(P<0.05);且各项指标均明显优于对照组(P<0.05);治疗后治疗组不稳定斑块数量(41,38.68%)少于对照组(110,69.18%),差异具有统计学意义(P<0.05)。结论前列地尔注射液静滴,联合拜阿司匹林、瑞舒伐他汀、复方丹参滴丸口服可明显减少颈动脉斑块数量并逆转颈动脉斑块状态,安全可靠,值得临床推广。 展开更多
关键词 颈动脉粥样硬化斑块 瑞书伐他汀 拜阿司匹林 复方丹参滴丸
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