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基于真实世界的银杏酮酯滴丸用药安全性研究 被引量:7
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作者 迟航 刘凯 +4 位作者 赵英强 邢永发 路美娟 何晓清 张栋蔚 《中草药》 CAS CSCD 北大核心 2022年第9期2768-2775,共8页
目的研究真实世界银杏酮酯滴丸用药的安全性,为银杏酮酯滴丸临床大规模推广应用提供依据。方法采用前瞻性、非干预、多中心、开放性、大样本真实世界研究的方法,收集银杏酮酯滴丸适用人群药物不良事件(adverse event,AE)和药物不良反应(... 目的研究真实世界银杏酮酯滴丸用药的安全性,为银杏酮酯滴丸临床大规模推广应用提供依据。方法采用前瞻性、非干预、多中心、开放性、大样本真实世界研究的方法,收集银杏酮酯滴丸适用人群药物不良事件(adverse event,AE)和药物不良反应(adverse drug reaction,ADR)发生情况及相关因素、发生与转归特点。结果纳入天津中医药大学第二附属医院等29家机构的1084患者。其中99例患者发生139例次AE,发生率为9.1%,发生率最高的AE为感染及侵染类疾病(3.3%);相关因素分析发现女性、60~70岁患者、冠心病心绞痛(血瘀证)、社区医院、合并代谢及营养类疾病的患者银杏酮酯滴丸AE发生率较高。共有7例患者发生11例次ADR,总发生率为1.0%,胃肠系统疾病为ADR发生率最高,女性、70岁以上患者、冠心病心绞痛(血瘀证)、社区医院和合并高血压的患者银杏酮酯滴丸ADR发生率最高。针对AE采取相对措施,其中保持剂量不变131例次,导致降低剂量的AE 2例次、暂停用药的AE 3例次、永久停药的AE 3例次;105例次AE转归为已恢复且不伴后遗症,22例次AE未恢复,未知的12例次。针对ADR采取相对措施,其中保持剂量不变7例次,剂量降低的ADR 2例次,暂停用药的ADR 2例次,所有ADR转归为已恢复并不伴后遗症。结论真实世界患者服用银杏酮酯滴丸安全性良好,临床应加强银杏酮酯滴丸AE和ADR的监测,保障用药安全。 展开更多
关键词 银杏酮酯滴丸 不良事件 药物不良反应 转归 安全性
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Shexiang Tongxin Dropping Pill Improves Stable Angina Patients with Phlegm-Heat and Blood-Stasis Syndrome:A Multicenter,Randomized,Double-Blind,Placebo-Controlled Trial
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作者 ZHAO Ying-qiang xing yong-fa +20 位作者 ZOU Ke-yong JIANG Wei-dong DU Ting-hai CHEN Bo YANG Bao-ping QU Bai-ming WANG Li-yue GONG Gui-hong SUN Yan-ling WANGLi-qi ZHOU Gao-feng DONG Yu-gang CHEN Min ZHANG Xue-juan YANG Tian-lun ZHANG Min-zhou ZHAO Mingjun DENG Yue XIAO Chang-jiang WANG Lina WANG Bao-he 《Chinese Journal of Integrative Medicine》 2025年第8期685-693,共9页
Objective To evaluate the efficacy and safety of Shexiang Tongxin Dropping Pill(STDP)in treating stable angina patients with phlegm-heat and blood-stasis syndrome by exercise duration and metabolic equivalents.Methods... Objective To evaluate the efficacy and safety of Shexiang Tongxin Dropping Pill(STDP)in treating stable angina patients with phlegm-heat and blood-stasis syndrome by exercise duration and metabolic equivalents.Methods This multicenter,randomized,double-blind,placebo-controlled clinical trial enrolled stable angina patients with phlegm-heat and blood-stasis syndrome from 22 hospitals.They were randomized 1:1 to STDP(35 mg/pill,6 pills per day)or placebo for 56 days.The primary outcome was the exercise duration and metabolic equivalents(METs)assessed by the standard Bruce exercise treadmill test after 56 days of treatment.The secondary outcomes included the total angina symptom score,Chinese medicine(CM)symptom scores,Seattle Angina Questionnaire(SAQ)scores,changes in ST-T on electrocardiogram and adverse events(AEs).Results This trial enrolled 309 patients,including 155 and 154 in the STDP and placebo groups,respectively.STDP significantly prolonged exercise duration with an increase of 51.0 s,compared to a decrease of 12.0 s with placebo(change rate:−11.1%vs.3.2%,P<0.01).The increase in METs was significantly greater in the STDP group than in the placebo group(change:−0.4 vs.0.0,change rate:−5.0%vs.0.0%,P<0.01).The improvement of total angina symptom scores(25.0%vs.0.0%),CM symptom scores(38.7%vs.11.8%),reduction of nitroglycerin consumption(100.0%vs.11.3%),and all domains of SAQ,were significantly greater with STDP than placebo(all P<0.01).The changes in Q-T intervals at 28 and 56 days from baseline were similar between the two groups(both P>0.05).Twenty-five participants(16.3%)with STDP and 16(10.5%)with placebo experienced AEs(P=0.131),with no serious AEs observed.Conclusion STDP could improve exercise tolerance in patients with stable angina and phlegm-heat and blood stasis syndrome,with a favorable safety profile. 展开更多
关键词 Shexiang Tongxin Dropping Pill Chinese medicine coronary artery disease stable angina phlegm-heat and blood stasis syndrome excercise tolerance randomized controlled trial
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