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A multicenter randomized, double-blind, placebo-controlled trial to evaluate the safety and efficacy of rhubarb in treating acute exacerbation of chronic obstructive pulmonary disease of the syndrome type phlegm-heat obstructing the lungs 被引量:1
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作者 Fengjie Zheng Yan Sun +6 位作者 Xianggen Zhong Yueqi Wang Ruohan Wu Miao Liu Yuchao Liu Kuo Gao Yuhang Li 《Journal of Traditional Chinese Medical Sciences》 2016年第2期71-80,共10页
Objective:To observe the clinical efficacy and safety of oral administration of the traditional Chinese herb rhubarb to treat acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Method:This was a multi... Objective:To observe the clinical efficacy and safety of oral administration of the traditional Chinese herb rhubarb to treat acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Method:This was a multicenter randomized double-blinded placebo controlled study that took place in 7 provinces of China that enrolled 244 patients(aged 18e80 years)who had acute exacerbation of COPD with the traditional Chinese syndrome pattern of phlegm-heat obstructing lung.Participants were divided into experimental and control groups.The experimental group received 4.5 g of rhubarb granules twice daily and the control group received placebo granules.Both groups also received conventional Western therapy consisting of oxygen therapy,an antibiotic,expectorant,and a bronchodilator.Treatment lasted 10 days.Symptom scores for cough,sputum volume and color,wheezing and chest tightness before treatment and on days 3,5,7,and 10 during the treatment were recorded.Lung function,arterial blood gas and levels of serum inflammatory factors,interleukin-4(IL-4),interleukin-8(IL-8),and interleukin-10(IL-10)and tumor necrosis factor-alpha(TNF-a),before and after treatment were measured.Results:The sample size of the full analysis set(FAS)was 244 participants,and the sample size of per protocol set(PPS)was 235.Following 10 days’treatment,symptom scores of the experimental group were markedly lower than those of the placebo group(FAS:mean difference1.67,95%CI:e2.66 to0.69,P Z 0.001;PPS:mean difference1.55,95%CI:2.56 to0.54,P Z 0.003).Lung function in the experimental group was significantly higher than in the placebo group(FEV1,FAS:mean difference 0.12,95%CI:0.06 to 0.18;P<0.001;PPS:mean difference 0.12,95%CI 0.05 to 0.18;P<0.001.FVC:FAS:mean difference 0.16,95%CI:0.06 to 0.26;P Z 0.002;PPS:mean difference 0.16,95%CI 0.05 to 0.26;P Z 0.003.FEV1%,FAS:mean difference 5.95,95%CI:3.36 to 8.53;P<0.001;PPS:mean difference 5.92,95%CI 3.28 to 8.56;P<0.001.).PaO2,PaCO2,as well as serum inflammatory factors were also improved when compared to the placebo group.There were no significant differences in the incidence rate of adverse reaction between the two groups.Conclusions:Compared with placebo,rhubarb granules significantly reduced symptom scores,improved blood oxygen level,controlled systemic inflammatory response,without significant adverse effects.Thus,rhubarb may be a beneficial adjuvant method for treating the phlegm-heat obstructing the lung syndrome pattern of AECOPD. 展开更多
关键词 Traditional Chinese medicine COPD phlegm-heat obstructing the lung syndrome RHUBARB Randomized controlled trial
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清金止咳解痉汤治疗老年慢性支气管炎急性发作痰湿蕴肺证
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作者 张树红 陈华 +2 位作者 付秀丽 聂鑫鑫 梁军 《长春中医药大学学报》 2024年第8期874-878,共5页
目的探讨清金止咳解痉汤治疗老年慢性支气管炎急性发作痰湿蕴肺证的临床疗效。方法将老年慢性支气管炎急性发作患者102例随机分为对照组和观察组,各51例。对照组予常规西药治疗,观察组在对照组基础上联合清金止咳解痉汤治疗,2组疗程均为... 目的探讨清金止咳解痉汤治疗老年慢性支气管炎急性发作痰湿蕴肺证的临床疗效。方法将老年慢性支气管炎急性发作患者102例随机分为对照组和观察组,各51例。对照组予常规西药治疗,观察组在对照组基础上联合清金止咳解痉汤治疗,2组疗程均为7 d,对比2组中医证候积分,炎症指标C反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)、白细胞介素6(IL-6),血气分析指标血氧饱和度(SaO_(2))、动脉血氧分压(PaO_(2))、二氧化碳分压(PCO_(2)),肺功能指标最大肺活量(FVC)、第1秒用力呼气容积(FEV_(1))、FEV_(1)/FVC,SF-36评分及临床疗效,记录2组不良反应发生情况。结果治疗后观察组中医证候积分、CRP、TNF-α、IL-6、PCO_(2)指标水平均低于对照组(P<0.05),SaO_(2)、PaO_(2)、FVC、FEV_(1)、FEV_(1)/FVC指标水平及生活质量各维度评分均高于对照组(P<0.05);观察组总有效率(92.16%,47/51)高于对照组(76.47%,39/51)(P<0.05);2组均未发生严重不良反应,不良反应发生率组间比较差异无统计学意义(P>0.05)。结论清金止咳解痉汤结合常规西药治疗老年慢性支气管炎急性发作疗效良好,能够调节患者血气指标,抑制炎症反应,改善肺功能。 展开更多
关键词 老年慢性支气管炎 急性发作 痰湿蕴肺证 清金止咳解痉汤 炎症指标 血气指标 肺功能
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黄英咳喘糖浆辅助治疗儿童肺炎支原体肺炎的临床效果分析
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作者 孟斌 刘政欣 李卓 《中国社区医师》 2024年第32期92-94,共3页
目的:分析黄英咳喘糖浆辅助治疗儿童肺炎支原体肺炎(MPP)的临床效果。方法:选取2023年12月—2024年2月于本溪满族自治县中医院儿科住院的MPP患儿110例作为研究对象,根据随机数字表法分为对照组和观察组,每组55例。对照组给予注射用乳糖... 目的:分析黄英咳喘糖浆辅助治疗儿童肺炎支原体肺炎(MPP)的临床效果。方法:选取2023年12月—2024年2月于本溪满族自治县中医院儿科住院的MPP患儿110例作为研究对象,根据随机数字表法分为对照组和观察组,每组55例。对照组给予注射用乳糖酸红霉素治疗,观察组在对照组基础上联合黄英咳喘糖浆治疗。比较两组患儿治疗效果、症状缓解时间、肺部啰音消失时间、住院时间及不良反应发生情况。结果:观察组治疗总有效率高于对照组(P=0.034)。观察组发热、咳嗽、咯痰、喘息缓解时间均短于对照组(P<0.05)。观察组肺部啰音消失时间、住院时间均短于对照组(P<0.05)。两组不良反应总发生率比较,差异无统计学意义(P>0.05)。结论:黄英止咳糖浆辅助治疗儿童MPP的临床效果显著,能够缩短患儿症状缓解时间、肺部啰音消失时间及住院时间,且安全性较高。 展开更多
关键词 肺炎 支原体肺炎 黄英咳喘糖浆 儿童 痰热蕴肺证
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桂龙咳喘宁片联合西药治疗慢性支气管炎急性发作期痰湿蕴肺证临床疗效分析 被引量:8
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作者 吴仁凯 王杰 徐清喜 《新中医》 CAS 2018年第5期69-72,共4页
目的:观察桂龙咳喘宁片联合西药治疗慢性支气管炎急性发作期痰湿蕴肺证的临床疗效。方法:将纳入的慢性支气管炎急性发作期痰湿蕴肺证患者随机分为对照组和观察组。对照组59例服用盐酸氨溴索片,合并感染者加用阿莫西林胶囊,喘息严重者加... 目的:观察桂龙咳喘宁片联合西药治疗慢性支气管炎急性发作期痰湿蕴肺证的临床疗效。方法:将纳入的慢性支气管炎急性发作期痰湿蕴肺证患者随机分为对照组和观察组。对照组59例服用盐酸氨溴索片,合并感染者加用阿莫西林胶囊,喘息严重者加用氨茶碱口服溶液。观察组58例在对照组治疗的基础上加用桂龙咳喘宁片。2组疗程均为10天。治疗前后评价咳嗽症状积分、痰湿蕴肺证积分、咳嗽视觉模拟评分法(VAS)评分,记录咳嗽缓解时间,评价2组的临床疗效。采用莱塞斯特咳嗽生命质量问卷(LCQ)评定生活质量。结果:愈显率观察组为82.76%,对照组为66.10%,组间比较,差异有统计学意义(P<0.05)。2组白天咳嗽积分、夜间咳嗽积分、总分和咳嗽VAS评分均较治疗前降低(P<0.01),观察组咳嗽积分、总分和咳嗽VAS评分均低于对照组(P<0.01);观察组咳嗽缓解时间短于对照组(P<0.01)。2组LCQ(生理、心理、社会)3个维度评分和总分均较治疗前升高(P<0.01),痰湿蕴肺证积分均较治疗前下降(P<0.01);观察组LCQ各维度评分和总分均高于对照组(P<0.01),痰湿蕴肺证积分低于对照组(P<0.01)。结论:在常规西药基础上加用桂龙咳喘宁片治疗慢性支气管炎急性发作期痰湿蕴肺证患者,可进一步控制咳嗽等症状,提高患者的生活质量,临床疗效优于单纯西药治疗。 展开更多
关键词 慢性支气管炎(CB) 急性发作期 痰湿蕴肺证 中西医结合疗法 桂龙咳喘宁片 生活质量
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Efficacy and safety of Qingfei Huatan formula in the treatment of acute exacerbation of chronic obstructive pulmonary disease:A multi-centre,randomised,double-blind,placebo-controlled trial
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作者 Hui-zhi Zhu Cheng-yi Li +9 位作者 Liang-ji Liu Jia-bing Tong Zhi-hui Lan Shu-guang Tian Qiao Li Xiang-li Tong Ji-feng Wu Zhen-gang Zhu Su-yun Li Jian-sheng Li 《Journal of Integrative Medicine》 SCIE CAS CSCD 2024年第5期561-569,共9页
Background Chronic obstructive pulmonary disease(COPD),a common respiratory disease,can be effectively treated by traditional Chinese medicine(TCM).Qingfei Huatan,a TCM formula,has been reported to effectively allevia... Background Chronic obstructive pulmonary disease(COPD),a common respiratory disease,can be effectively treated by traditional Chinese medicine(TCM).Qingfei Huatan,a TCM formula,has been reported to effectively alleviate the clinical symptoms of COPD patients.However,there is a lack of multi-centre,randomised,double-blind,controlled clinical trials documenting the clinical efficacy and safety of this formula in the treatment of acute exacerbation of COPD(AECOPD).Objective This study evaluated the efficacy and safety of Qingfei Huatan formula in the treatment of AECOPD,thereby providing high-quality clinical evidence.Design,setting,participants and interventions A total of 276 patients with AECOPD were included in this multi-centre,randomised,double-blind,placebo-controlled trial and were randomised into treatment and control groups at a ratio of 1:1.Patients in the treatment and control groups took Qingfei Huatan granules or simulated Qingfei Huatan granules twice a day,for 14 days,in addition to Western medicine treatment.All patients were followed up for 3 months.Main outcome measures The primary outcome was time taken to symptom stabilisation.The secondary outcomes included duration of antibiotic use,clinical symptom and sign score,TCM syndrome score,dyspnoea score,and quality of life(QOL)score.Meanwhile,the safety of the formula was assessed through routine urine and stool tests,electrocardiograms,liver and kidney function tests,and the observation of adverse events throughout the trial.Results The time taken for effective stabilisation(P<0.05)and obvious stabilisation(P<0.01),and the duration of antibiotic use(P<0.05)were significantly shorter in the treatment group than in the control group.On days 6,9,12 and 14 of treatment,clinical symptom and sign score decreased in both groups,particularly in the treatment group(P<0.01).On days 9,12 and 14 of treatment,the TCM syndrome scores of both groups were reduced(P<0.01),with more significant reductions in the treatment group.At 3 months after the end of treatment,the treatment group continued to have lower clinical symptom and sign score and TCM syndrome score than the control group(P<0.01).On days 6,9,12 and 14 of treatment,dyspnoea and QOL scores were markedly reduced in the two groups(P<0.05 and P<0.01,respectively),especially in the treatment group.At 3 months after the end of treatment,dyspnoea and QOL scores were lower in the treatment group than those in the control group(P<0.01).No serious adverse events were observed in either group.Conclusion The Qingfei Huatan formula can effectively shorten the duration of AECOPD and antibiotic use,significantly relieve clinical symptoms,and increase QOL for AECOPD patients,with a favourable safety profile.These results suggest that this formula can be used as a complementary treatment for AECOPD patients. 展开更多
关键词 Acute exacerbation of chronic obstructive pulmonary disease Clinical trial syndrome of phlegm-heat congesting lung Qingfei Huatan formula Traditional Chinese medicine
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