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Efficacy and safety of Suhuang Zhike capsule(苏黄止咳颗粒)forcough variant asthma:a multicenter,single-arm,open-label phaseⅣreal-world clinical trial
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作者 ZHANG Hongchun LIU Jian +12 位作者 CHEN Sheng ZHANG Wei LU Xuechao LI Ying YU Xueqing HUANG Yan SU Lianhua WEI Baolin LI Zhuyin PEI Shuai LEI Xiang YANG Daowen GUO Jianning 《Journal of Traditional Chinese Medicine》 2025年第4期817-828,共12页
OBJECTIVE:To summarize the clinical efficacy characteristics of Suhuang Zhike capsule(苏黄止咳颗粒)and evaluate the incidence of adverse reactions in its broad clinical application.METHODS:This was a multicenter,prosp... OBJECTIVE:To summarize the clinical efficacy characteristics of Suhuang Zhike capsule(苏黄止咳颗粒)and evaluate the incidence of adverse reactions in its broad clinical application.METHODS:This was a multicenter,prospective,singlearm,open-label phase IV clinical trial.A total of 1100 patients diagnosed with cough variant asthma(CVA)and the Traditional Chinese Medicine(TCM)syndrome of wind evil invading the lung and lung Qi failing to propagate were planned for recruitment.Participants received Suhuang Zhike capsule orally,three capsules per dose,taken three times daily,for a treatment duration of 14 d.The primary outcome was the change in cough symptom scores from baseline to week 2.Cough severity was assessed twice daily.Additional evaluations included the rate and time of cough disappearance or basic disappearance rate,as well as the time of cough relief.TCM symptom scores were recorded at baseline and on days 7 and 14 of treatment.Safety assessments included monitoring for adverse events and conducting laboratory tests.RESULTS:A total of 1033 patients with CVA from 40 hospitals across China were enrolled in the study.Of these,1026 patients received the study medication and were included in the safety analysis.Fifty-four patients withdrew from the study,resulting in a drop-out rate of 5.23%.Treatment with Suhuang Zhike capsules significantly reduced cough symptom scores and improved cough-related symptoms in patients with CVA.The overall rate of cough disappearance or basic disappearance increased over the course of treatment,reaching 67.21%after 14 d.The median time of cough relief was 3 d,while the median time to cough disappearance or basic disappearance was 11 d.Additionally,the treatment led to reductions in TCM symptom scores and improvements in accompanying symptoms such as throat itching,expectoration,and shortness of breath.In terms of safety,no serious adverse events were reported.The incidence of related adverse events(AEs)was 2.24%(23 cases,30 events).The incidence of adverse reactions listed in the drug's instructions was 2.14%.Other related AEs not listed in the drug's instructions occurred in 0.39%of patients and included dizziness(0.19%),headache(0.10%),pruritus(0.10%),and palpitation(0.10%).CONCLUSION:Suhuang Zhike capsules demonstrated good efficacy and safety for the treatment of CVA.These findings offer valuable clinical evidence to support their broader application in routine clinical practice. 展开更多
关键词 cough-variant asthma treatment outcome safety Suhuang zhike capsule
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Simultaneous determination of five major components of Glycyrrhizae Radix et Rhizoma in Xiaoer Zhike Tangjiang with standardized reference extract 被引量:2
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作者 孟兰兰 李铮 +3 位作者 陈有根 傅欣彤 张英涛 郭洪祝 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2015年第7期449-457,共9页
In this study, we developed a novel and simple HPLC-DAD method for simultaneous qualitative and quantitative determination of five major components of Glycyrrhizae Radix et Rhizoma (GRR) in Xiaoer Zhike Tangjiang (... In this study, we developed a novel and simple HPLC-DAD method for simultaneous qualitative and quantitative determination of five major components of Glycyrrhizae Radix et Rhizoma (GRR) in Xiaoer Zhike Tangjiang (XEZKTJ) with standardized reference extract (SRE). The five analytes (liquiritin apioside, liquiritin, isoliquiritin apioside, liquirigenin and glycyrrhizic acid) were well separated with good linearity, precision, stability and repeatability. The recovery rates ranged from 95.69% to 100.80%. The content of the five compounds in 34 batches of commercial XEZKTJ products was determined using standardized GRR extract (SRE method) and individual chemical reference standards (CRS method). Highly similar results were obtained from the two methods, demonstrating the feasibility of the proposed SRE method. Taken together, we proposed an efficient and low-cost way to perform multi-component quality control of XEZKTJ in this study. 展开更多
关键词 Standardized reference extract HPLC Quantitative determination Xiaoer zhike Tangjiang Glycyrrhizae Radix et Rhizoma
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Effectiveness and safety of Suhuang Zhike capsule(苏黄止咳胶囊)as adjuvant treatment for acute exacerbation of chronic obstructive pulmonary disease:a systematic review and Meta-analysis 被引量:10
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作者 DAI Linfeng ZHUANG Yan +2 位作者 LüHai CHEN Mingqi WANG Xing 《Journal of Traditional Chinese Medicine》 SCIE CSCD 2023年第2期231-238,共8页
OBJECTIVE:To evaluate the efficacy and safety of Suhuang Zhike capsule(苏黄止咳胶囊)in the adjuvant treatment of acute exacerbation of chronic obstructive pulmonary disease(AECOPD).METHODS:The database including PubMe... OBJECTIVE:To evaluate the efficacy and safety of Suhuang Zhike capsule(苏黄止咳胶囊)in the adjuvant treatment of acute exacerbation of chronic obstructive pulmonary disease(AECOPD).METHODS:The database including PubMed,Embase,Cochrane Library,China National Knowledge Infrastructure Database,China Science and Technology Journal Database,Chinese Biomedical Literature Database and Wanfang Data was searched.The retrieval time was from database establishment to May 2021.Randomized controlled trial(RCT)of Suhuang zhike capsule adjuvant treatment for AECOPD was included.The quality of the studies was independently evaluated and cross-checked by two reviewers,and Meta-analysis was performed by using RevMan5.3 software.RESULTS:Thirteen RCT results were included with a total sample number of 1195 cases,including 597 in the experimental group and 598 in the control group.The results showed that Suhuang zhike capsule adjuvant treatment of AECOPD could improve the total clinical effect rate compared with conventional treatment.Suhuang zhike capsule adjuvant treatment could improve forced vital capacity(FVC),forced expiratory volume in one second(FEV1),FEV1/FVC,peak expiratory flow(PEF)and other pulmonary function indexes;decrease Creactive protein(CRP),white blood cells,neutrophils and other infectious indicators;besides,the 1-year recurrence rate of the disease was decreased(all P<0.05).CONCLUSIONS:Suhuang Zhike capsule can improve the lung function and clinical efficacy of AECOPD,thus increasing the exercise endurance,and reducing the infection and recurrence rate in AECOPD patients. 展开更多
关键词 pulmonary disease chronic obstructive META-ANALYSIS acute exacerbation Suhuang zhike capsule
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Proteomic analysis of a chronic obstructive pulmonary disease mouse model to determine the efficacy of treatment using Guben Zhike decoction 被引量:2
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作者 Mingzhe Wang Guoxing Liu +6 位作者 Yao Xiao Zhe Cai Chang Liu Lin Pan Ying Liu Mengchao Liu Hongchun Zhang 《Journal of Traditional Chinese Medical Sciences》 2021年第1期34-42,共9页
Background:Guben Zhike decoction(GBZKD)is derived from the experience of Professor Enxiang Chao,an esteemed master of Chinese medicine,while treating chronic obstructive pulmonary disease(COPD).GBZKD reinforces the he... Background:Guben Zhike decoction(GBZKD)is derived from the experience of Professor Enxiang Chao,an esteemed master of Chinese medicine,while treating chronic obstructive pulmonary disease(COPD).GBZKD reinforces the healthy qi and consolidates defensive qi.This study explored the efficacy and potential mechanism of action of GBZKD in a COPD mouse model using proteomics.Methods:A COPD mouse model was established through cigarette smoke exposure and intranasal lipopolysaccharide administration.The model was verified through lung function test and lung histopathological observation.Label-free quantitative proteomics was used to detect the lung tissue proteins of mice from the GBZKD,COPD,and control groups.Results:GBZKD markedly improved the lung function and associated pathological conditions in the COPD mouse model.Proteomic analysis identified 4316 proteins,of which 3696 were quantitative proteins.We highlighted 287 and 184 proteins with significant regulatory roles in the lung tissues of COPD mice and GBZKD-treated mice,respectively.These proteins participated in multiple functions,including complement/coagulation cascade,immune response,and metabolic pathways.Conclusion:GBZKD exhibits multitarget and multipathway therapeutic effects in a COPD mouse model. 展开更多
关键词 Guben zhike decoction Chronic obstructive pulmonary disease Proteomic analysis Mouse model
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Effects of Suhuang Zhike Capsule on Pulmonary Function, Blood Gas Analysis Index, Serum PCT and CRP Expression in Patients with Acute Exacerbation of Chronic Obstructive Pulmonary Disease 被引量:4
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作者 Ren Junqing 《World Journal of Integrated Traditional and Western Medicine》 2019年第2期32-38,共7页
OBJECTIVE: To observe the effects of Suhuang Zhike Capsule on pulmonary function, blood gas analysis index, serum PCT and CRP expression in patients with acute exacerbation of chronic obstructive pulmonary disease. ME... OBJECTIVE: To observe the effects of Suhuang Zhike Capsule on pulmonary function, blood gas analysis index, serum PCT and CRP expression in patients with acute exacerbation of chronic obstructive pulmonary disease. METHODS: A total of 88 patients with acute exacerbation of chronic obstructive pulmonary disease admitted to the Department of Respiratory Medicine, Xuancheng People's Hospital of Anhui Province from December 2014 to December 2016 were randomly divided into the observation group and the control group, with 44 cases in each group. The control group was given routine clinical treatment, and the observation group was given Suhuang Zhike Capsule on the basis of the treatment method of the control group. After 7 days' treatment, the improvement of lung function indexes were observed and evaluated before and after treatment(forced expiratory volume in one second(FEV_1), forced expiratory volume occupancy in the 1^(st) second percentage of vital capacity(FEVl/FVC), peak expiatory flow(PEF)), blood gas analysis index(Arterial oxygen partial pressure(PaO_2) and arterial blood carbon dioxide partial pressure(PaCO_2), oxygenation index(OI)) and serum cytokine levels(procalcitonin(PCT) and C reactive protein(CRP). RESULTS: The total effective rate of the observation group was significantly higher than that of the control group(P < 0.05). The FEV_1, FEV_1/FVC and PEF in 2 groups were significantly increased after the treatment(P < 0.05), and the above lung function indexes in the observation group were significantly higher than the control group(P < 0.05). PaO_2 and OI were significantly increased after the treatment(P < 0.05), PaCO_2 was significantly decreased after the treatment(P < 0.05), and the improvement of above blood gas analysis indexes were significantly superior of the observation group than the control group(P < 0.05). The serum PCT and CRP levels in 2 groups were significantly decreased after the treatment(P < 0.05), and the improvement in the observation group were more significant than that in the control group(P < 0.05). CONCLUSION: Suhuang Zhike Capsule can inhibit serum inflammatory cytokine levels in patients with acute exacerbation of chronic obstructive pulmonary disease, improve blood gas analysis indicators, and improve lung functions. 展开更多
关键词 Chronic OBSTRUCTIVE PULMONARY disease Acute EXACERBATION Suhuang zhike CAPSULE Lung function BLOOD gas analysis index PROCALCITONIN C-reactive protein
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Anti-inflammatory Effect of Wumen Zhike Gancao Decoction on Rats with Lumbar Disc Herniation Associated with Lipid Metabolic Disorder
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作者 Xiaofeng SHEN Yuwei LI Guoqiang LIANG 《Medicinal Plant》 CAS 2019年第4期24-33,共10页
[Objectives] To study the anti-inflammatory effect of Wumen Zhike Gancao Decoction (ZKGC) on rats with lumbar disc herniation (LDH) associated with lipid metabolic disorder.[Methods] A rat model of LDH was established... [Objectives] To study the anti-inflammatory effect of Wumen Zhike Gancao Decoction (ZKGC) on rats with lumbar disc herniation (LDH) associated with lipid metabolic disorder.[Methods] A rat model of LDH was established by implantation of the autologous nucleus pulposus from the coccygeal vertebra of each rat tail, and histopathology, immunohistochemistry and biochemistry assays were employed to evaluate the treatment effects of ZKGC. In addition, the metabolic characteristics of LDH and ZKGC treatment were investigated with a liquid-chromatography with time-of-flight mass spectrometer (LC/Q-TOF-MS)-based metabolomics study. Nucleus pulpous tissues from rat models were collected and analyzed by metabolomics.[Results] By metabolism network analysis, lipid metabolism was up-regulated in LDH rat models and the treatment with ZKGC significantly reversed the abnormal up-regulated lipid metabolism. Meanwhile, the treatment of ZKGC also regulated the markers of neuron autophagy and inflammatory response in serum.[Conclusions] These results indicated that a complex mechanism, including abnormal lipid metabolism, associates with the progress of LDH, and multiple pathways might be involved in ZKGC s therapeutic effects on LDH. 展开更多
关键词 zhike GANCAO DECOCTION LUMBAR disc HERNIATION NUCLEUS pulpous Metabolic profiles Traditional Chinese medicine LC/Q-TOF-MS
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Long-term Toxicity of Maxing Erchen Zhike Granules
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作者 Jiabao MA Zhenyuan WEI +4 位作者 Shuang WU Jiahuan WEI Shengbin CHEN Jinhua LIU Zhengteng YANG 《Medicinal Plant》 CAS 2020年第5期27-31,共5页
[Objectives]To study the long-term toxicity of Maxing Erchen Zhike granules to rats after intragastric administration,so as to provide reference for its preclinical safety evaluation.[Methods]Total 80 rats were random... [Objectives]To study the long-term toxicity of Maxing Erchen Zhike granules to rats after intragastric administration,so as to provide reference for its preclinical safety evaluation.[Methods]Total 80 rats were randomly and evenly divided into high-dose group(1.2 mL/100 g,120 g/kg),middle-dose group(96.0 g/kg),low-dose group(72.0 g/kg)and blank control group.The rats in the treatment groups were administered with corresponding doses of Maxing Erchen Zhike granules,and those in the blank control group were given with equal-amount normal saline.The administration lasted for 30 consecutive days.During the experiment,the rats'feed intake,activity,feces and other conditions and toxicity reactions were observed every day.After 24 h of the last administration,12 rats(half male and half female)were randomly selected from each group.Each of the rats was anesthetized with 10%chloral hydrate solution(0.3 mL/100 g)through intraperitoneal injection and subjected to abdominal aorta blood collection(two tubes)for hematological examination and blood biochemical examination(serum).Then,the main organs of the rats were weighed,and pathological examinations were performed.After that,the main organs were weighed and pathological examination was performed.The remaining rats in each group were discontinued and observed for 14 d.On the 15th d,they were subjected to the same treatment,and the body weight,organ coefficients,hematological indices,blood biochemical indices and pathological indices were examined.[Results]After 30 d of administration,there was no abnormality in the appearance and behavior of the animals.There was no significant difference in the daily consumption of feed among the groups,and there was no special case of weight gain.Among the blood biochemical indices,the ALB and ALT levels of each administration group were significantly different from those of the blank control group(P<0.05).The results of histopathological examination show that there was one case of interstitial pneumonia in each of the high-dose group,middle-dose group and blank control group.After 14 d that the administration was stopped,one case of focal myocarditis appeared in the high-dose group,and one case of interstitial pneumonia appeared in the middle-dose group.[Conclusions]Maxing Erchen Zhike granules are safe to be administered to rats at 100 times the clinical dose.and there should be no safety hazards clinically when used at conventional doses. 展开更多
关键词 Maxing Erchen zhike granules Long-term toxicity Blood examination Pathological section
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Effects of Suhuang Zhike Capsules on Pulmonary Function and Peripheral Blood Eosinophil Count and Exhaled Nitric Oxide in Patients with Acute Attack of Bronchial Asthma
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作者 Geng Xinpu Liu Rong +1 位作者 Le Zhaoxi Liu Shoulin 《World Journal of Integrated Traditional and Western Medicine》 2019年第4期16-20,共5页
OBJECTIVE: To observe the effects of Suhuang Zhike Capsules on lung function and peripheral blood eosinophil count (EOS) and exhaled nitric oxide (eNO) in patients with acute asthma attack.METHODS: A total of 80 patie... OBJECTIVE: To observe the effects of Suhuang Zhike Capsules on lung function and peripheral blood eosinophil count (EOS) and exhaled nitric oxide (eNO) in patients with acute asthma attack.METHODS: A total of 80 patients with acute exacerbation of bronchial asthma admitted to Huai'an Cancer Hospital from January 2017 to January 2018 were randomly divided into an observation group and a control group,with 40 cases in each group.The control group was given conventional treatment with western medicine,and the observation group was given Suhuang Zhike Capsules on the basis of the treatment method of the control group.After 1 week of treatment,the improvement of individual symptoms (cough,wheezing,wheezing rale),lung function [1 second forced expiratory volume (FEV1),forced expiratory volume occupational capacity of vital capacity (FVC) in 1 second and peak expiratory flow (PEF)] and peripheral blood EOS and eNO levels and efficacy before and after the treatment were observed and assessed.RESULTS: The total effective rate of the observation group was 92.5%,which was significantly higher than the total effective rate of the control group (75.0%)(P < 0.05).The cough,wheezing and wheezing scores of the 2 groups were significantly decreased after treatment (P < 0.05).The scores of the above symptoms were significantly lower in the observation group than in the control group (P < 0.05).The FEV1,FVC and PEF were significantly increased after treatment (P < 0.05),and the above lung functions in the observation group were significantly higher than the control group (all P < 0.05).The EOS and eNO levels in the peripheral blood of the 2 groups were significantly decreased after treatment (P < 0.05),and the EOS and eNO levels in the peripheral blood in the observation group were significantly lower than those in the control group (P < 0.05).CONCLUSION: Suhuang Zhike Capsules can reduce the levels of EOS and eNO in peripheral blood of patients with acute asthma attack,improve the lung function of patients,relieve the clinical symptoms and improve the prognosis. 展开更多
关键词 Suhuang zhike CAPSULES Acute attack of BRONCHIAL asthma Lung function AIRWAY HYPERRESPONSIVENESS EOS ENO
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Effect of inhalant combined with Dingchuan Zhike decoction therapy on the airway remodeling, inflammation and PARC/CCL-18 pathways in patients with cough variant asthma
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作者 Ben Han Zi-Yan Huang 《Journal of Hainan Medical University》 2017年第8期52-56,共5页
Objective:To study the effect of inhalant combined with Dingchuan Zhike decoction therapy on the airway remodeling, inflammation and PARC/CCL-18 pathways in patients with cough variant asthma.Methods: A total of 60 pa... Objective:To study the effect of inhalant combined with Dingchuan Zhike decoction therapy on the airway remodeling, inflammation and PARC/CCL-18 pathways in patients with cough variant asthma.Methods: A total of 60 patients with cough variant asthma who were treated in our hospital between January 2014 and May 2016 were collected and divided into the control group (n=30) who received conventional inhalant treatment and the observation group (n=30) who received inhalant combined with Dingchuan Zhike decoction treatment according to single-blind randomized controlled method, and the treatment lasted for 6 months. Before treatment and after 6 months of treatment, high-resolution CT was used to determine the airway remodeling index levels, RIA method was used to detect the peripheral blood airway remodeling index contents, and enzyme-linked immunosorbent assay (ELISA) was used to detect the contents of inflammatory mediators in induced sputum and the PARC/CCL-18 in serum.Results: Before treatment, the differences in the airway remodeling degree as well as the contents of inflammatory mediators and PARC/CCL-18 were not statistically significant between the two groups. After 6 months of treatment, CT airway remodeling indexes LA and TA levels of observation group were higher than those of control group while WA level was lower than that of control group, and peripheral blood airway remodeling indexes CTGF, YKL-39, MMP-9 and TIMP-1 contents were lower tha=n those of control group;inflammatory mediators IL-5, IL-6 and IL-8 contents in induced sputum of observation group were lower than those of control group, and serum PARC/CCL-18 content was lower than that of control group.Conclusion:Inhalant combined with Dingchuan Zhike decoction can inhibit the airway remodeling and reduce the airway inflammation in patients with cough variant asthma. 展开更多
关键词 COUGH variant asthma Dingchuan zhike DECOCTION Airway remodeling INFLAMMATION PARC/CCL-18 PATHWAYS
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苏黄止咳胶囊治疗老年上呼吸道感染的临床效果
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作者 胡文倩 《首都食品与医药》 2026年第1期148-150,共3页
目的探讨苏黄止咳胶囊治疗老年上呼吸道感染(URTI)的临床效果。方法在2023年1月-2025年1月期间选择本院收治的共计120例老年URTI患者,以入院先后顺序分组,对照组(n=60)采用复方甲氧那明胶囊治疗,观察组(n=60)基于对照组采用苏黄止咳胶... 目的探讨苏黄止咳胶囊治疗老年上呼吸道感染(URTI)的临床效果。方法在2023年1月-2025年1月期间选择本院收治的共计120例老年URTI患者,以入院先后顺序分组,对照组(n=60)采用复方甲氧那明胶囊治疗,观察组(n=60)基于对照组采用苏黄止咳胶囊治疗,比较两组中医证候积分、炎性因子、不良反应发生率。结果两组治疗后中医证候积分均下降(P<0.05),且观察组较对照组更低(P<0.05);两组治疗后炎性因子水平均下降(P<0.05),且观察组较对照组更低(P<0.05);两组不良反应发生率(头晕、腹泻、皮疹)比较,无显著差异(P>0.05)。结论苏黄止咳胶囊治疗老年URTI,可提升临床疗效,改善中医证候,降低其炎性因子水平,安全性较高。 展开更多
关键词 苏黄止咳胶囊 老年上呼吸道感染 炎性因子
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芩暴红止咳口服液治疗急性支气管炎及慢性支气管炎急性发作临床应用专家共识 被引量:2
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作者 刘剑 张洪春 +26 位作者 王成祥 崔红生 崔霞 张纾难 杨道文 冯淬灵 郭宇博 孙增涛 张惠勇 李光熙 苗青 王素梅 史利卿 杨洪军 刘婷 张方博 陈生 陈薇 王海 林琳 曲妮妮 武蕾 吴登山 刘亚峰 张文艳 张越英 范永芬 《中国实验方剂学杂志》 北大核心 2025年第4期182-188,共7页
中华中医药学会于2023年12月13日批准发布《芩暴红止咳口服液治疗急性支气管炎及慢性支气管炎急性发作临床应用专家共识》(GS/CACM 337-2023)。本共识严格按照研制要求,结合最新的循证医学证据及国内呼吸科(肺系病)、儿科领域知名专家... 中华中医药学会于2023年12月13日批准发布《芩暴红止咳口服液治疗急性支气管炎及慢性支气管炎急性发作临床应用专家共识》(GS/CACM 337-2023)。本共识严格按照研制要求,结合最新的循证医学证据及国内呼吸科(肺系病)、儿科领域知名专家的用药经验,联合方法学专家、药学和中药学专家,从适用人群、疗效评价、用法用量、联合用药、安全性等方面明确了芩暴红止咳口服液在痰热壅肺所致咳嗽、痰多;急性支气管炎及慢性支气管炎急发性发作中的应用。旨在指导医疗卫生机构规范合理用药,充分发挥芩暴红止咳口服液的独特价值,大力促进中成药的传承创新。 展开更多
关键词 芩暴红止咳口服液 急性支气管炎 慢性支气管炎急性发作 专家共识
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小儿荆杏止咳颗粒联合特布他林治疗小儿急性支气管炎疗效观察及对肺通气功能的影响 被引量:1
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作者 杨静 朱萍 王书举 《新中医》 2025年第2期86-90,共5页
目的:观察小儿荆杏止咳颗粒联合特布他林治疗急性支气管炎患儿的临床疗效及对肺通气功能的影响。方法:选择2021年6月—2023年6月南阳市中心医院收治的急性支气管炎患儿126例,按照随机数字表法分为治疗组与对照组各63例。对照组给予硫酸... 目的:观察小儿荆杏止咳颗粒联合特布他林治疗急性支气管炎患儿的临床疗效及对肺通气功能的影响。方法:选择2021年6月—2023年6月南阳市中心医院收治的急性支气管炎患儿126例,按照随机数字表法分为治疗组与对照组各63例。对照组给予硫酸特布他林雾化吸入用溶液治疗,治疗组在对照组基础上联合小儿荆杏止咳颗粒治疗。比较2组总有效率、中医证候评分、肺通气功能指标[潮气量(TV)、达峰时间比(TPTEF/TE)、呼吸频率(RR)]、炎症因子[C-反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)]水平及不良反应发生情况。结果:治疗后,治疗组总有效率为96.83%(61/63),对照组为80.95%(51/63),2组比较,差异有统计学意义(P<0.05)。治疗后,2组中医证候评分均较治疗前下降(P<0.05),且治疗组评分低于对照组(P<0.05)。治疗后,2组TV、TPTEF/TE水平较治疗前升高(P<0.05),RR水平较治疗前下降(P<0.05);且治疗组TV、TPTEF/TE水平高于对照组(P<0.05),RR水平低于对照组(P<0.05)。治疗后,2组CRP、TNF-α水平均较治疗前降低(P<0.05),且治疗组CRP、TNF-α水平低于对照组(P<0.05)。治疗组不良反应发生率为4.76%(3/63),对照组为12.70%(8/63),2组比较,差异无统计学意义(P>0.05)。结论:小儿荆杏止咳颗粒联合特布他林治疗急性支气管炎患儿可提高临床疗效,下调炎症因子水平,有效改善患儿中医证候及肺功能,且不良反应相对较少。 展开更多
关键词 小儿急性支气管炎 小儿荆杏止咳颗粒 特布他林 肺功能 炎症因子
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止咳平喘十二味合剂治疗痰热型哮喘-慢阻肺重叠临床研究 被引量:1
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作者 洪儿 陶伟 +2 位作者 鲍翊君 陈希尔 俞亚丽 《新中医》 2025年第4期31-35,共5页
目的:观察止咳平喘十二味合剂治疗痰热型哮喘-慢阻肺重叠(ACO)的临床疗效。方法:将2020年9月—2023年10月于浙江中医药大学附属宁波市中医院就诊的88例ACO患者,按随机数字表法分为对照组和治疗组各44例。对照组采用布地奈德福莫特罗吸... 目的:观察止咳平喘十二味合剂治疗痰热型哮喘-慢阻肺重叠(ACO)的临床疗效。方法:将2020年9月—2023年10月于浙江中医药大学附属宁波市中医院就诊的88例ACO患者,按随机数字表法分为对照组和治疗组各44例。对照组采用布地奈德福莫特罗吸入粉雾剂(Ⅱ)治疗,治疗组在对照组基础上联合止咳平喘十二味合剂治疗,疗程均为4周。比较2组治疗前后慢性阻塞性肺疾病评估测试(CAT)和哮喘控制测试(ACT)、6 min步行距离(6MWT)、呼出气一氧化氮(Fe NO)、肺功能指标[第1秒用力呼气量(FEV_(1))、呼气峰值流速(PEF)、用力呼气中期流速(MMEF_(75/25))]及外周血嗜酸性粒细胞计数(EOS)、免疫球蛋白E(Ig E)、白细胞介素-5(IL-5)水平变化。结果:治疗后,2组CAT评分均较治疗前降低(P<0.05),ACT评分均较治疗前上升(P<0.05);且治疗组CAT评分低于对照组(P<0.05),ACT评分高于对照组(P<0.05)。治疗后,2组6MWT均较治疗前增加(P<0.05),且治疗组6MWT大于对照组(P<0.05)。治疗后,2组FEV_(1)、PEF及MMEF_(75/25)水平均较前增加(P<0.05),且治疗组FEV_(1)、PEF及MMEF_(75/25)水平均高于对照组(P<0.05)。治疗后,2组Fe NO水平均较治疗前降低(P<0.05),且治疗组Fe NO水平低于对照组(P<0.05)。治疗后,2组外周血EOS、Ig E、IL-5水平均较治疗前降低(P<0.05),且治疗组外周血EOS、Ig E、IL-5水平低于对照组(P<0.05)。结论:止咳平喘十二味合剂可抑制气道炎症反应,降低外周血炎症介质水平,减轻ACO患者的临床症状,提高活动耐力,改善生活质量和肺通气功能。 展开更多
关键词 哮喘-慢阻肺重叠 止咳平喘十二味合剂 白细胞介素-5 免疫球蛋白E
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麻甘止咳合剂治疗痰热闭肺证儿童肺炎支原体肺炎的临床观察
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作者 龚晓薇 蔡建新 徐和祥 《时珍国医国药》 北大核心 2025年第21期4109-4112,共4页
目的探讨麻甘止咳合剂治疗痰热闭肺证儿童肺炎支原体肺炎的临床疗效。方法纳入72例确诊为痰热闭肺证的肺炎支原体肺炎患儿,随机分为两组,对照组36例予阿奇霉素抗感染等基础治疗,观察组36例在此基础上加用麻甘止咳合剂口服,疗程14d,统计... 目的探讨麻甘止咳合剂治疗痰热闭肺证儿童肺炎支原体肺炎的临床疗效。方法纳入72例确诊为痰热闭肺证的肺炎支原体肺炎患儿,随机分为两组,对照组36例予阿奇霉素抗感染等基础治疗,观察组36例在此基础上加用麻甘止咳合剂口服,疗程14d,统计两组临床表现及炎症、免疫指标以评估疗效。结果在临床疗效方面,观察组的退热时间、咳嗽缓解时间以及肺部啰音消退时间均显著优于对照组(P<0.01);经过治疗,观察组IL-6、IL-10、TNF-α指标均低于对照组;观察组CD4^(+)、CD4^(+)/CD8^(+)指标高于对照组(P<0.05),CD8^(+)低于对照组(P<0.05)。结论麻甘止咳合剂治疗痰热闭肺证儿童肺炎支原体肺炎安全有效,调整机体免疫功能、缓解炎症反应是其发挥作用的机制。 展开更多
关键词 麻甘止咳合剂 儿童肺炎支原体肺炎 免疫功能 炎症因子
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苏黄止咳胶囊联合多索茶碱治疗慢性阻塞性肺疾病急性期的临床效果
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作者 罗慧玲 张容轩 +5 位作者 张瑜 杨洋 吕科娟 李莉 沈雪云 郭嘉琳 《临床合理用药》 2025年第36期9-12,共4页
目的观察苏黄止咳胶囊联合多索茶碱治疗慢性阻塞性肺疾病(COPD)急性期的临床效果。方法选取2023年3月—2025年5月兰州市第二人民医院收治的COPD急性期患者80例,按照随机数字表法分为试验组和对照组,各40例。试验组予苏黄止咳胶囊联合多... 目的观察苏黄止咳胶囊联合多索茶碱治疗慢性阻塞性肺疾病(COPD)急性期的临床效果。方法选取2023年3月—2025年5月兰州市第二人民医院收治的COPD急性期患者80例,按照随机数字表法分为试验组和对照组,各40例。试验组予苏黄止咳胶囊联合多索茶碱治疗,对照组予多索茶碱治疗,2组均治疗2周。比较2组临床疗效,治疗前后肺功能指标[第1秒用力呼气容积(FEV_(1))、用力肺活量(FVC)、FEV_(1)/FVC]、炎性因子[肿瘤坏死因子(TNF-α)、白介素-8(IL-8)、白介素-17(IL-17)]水平、改良呼吸困难量表(mMRC)评分、6 min步行距离。结果试验组总有效率(97.50%)高于对照组(80.00%)(χ^(2)=6.135,P=0.013)。治疗2周后,2组FEV_(1)、FVC、FEV_(1)/FVC高于治疗前,TNF-α、IL-8、IL-17水平低于治疗前,且试验组高/低于对照组(P<0.01);2组mMRC评分低于治疗前,6 min步行距离长于治疗前,且试验组低/长于对照组(P<0.01)。结论苏黄止咳胶囊联合多索茶碱应用于COPD急性期患者效果较好,可有效减轻患者呼吸困难症状,改善肺功能,降低机体炎性反应。 展开更多
关键词 慢性阻塞性肺疾病 急性期 苏黄止咳胶囊 多索茶碱 肺功能指标 炎性因子
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止咳合剂治疗成人病毒性肺炎患者的临床疗效及对其肺功能、气道反应性的影响
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作者 王磊 任翔 +4 位作者 周伟 张志良 彭妍 陈晓勤 陈道鹏 《世界中西医结合杂志》 2025年第9期1853-1858,共6页
目的观察止咳合剂治疗成人病毒性肺炎患者的临床疗效及对其肺功能、气道反应性的影响。方法选取2023年3月-2024年3月在太仓市中医医院就诊的成人病毒性肺炎患者86例,按随机数字表法分为对照组和观察组,每组各43例。对照组采用西医治疗,... 目的观察止咳合剂治疗成人病毒性肺炎患者的临床疗效及对其肺功能、气道反应性的影响。方法选取2023年3月-2024年3月在太仓市中医医院就诊的成人病毒性肺炎患者86例,按随机数字表法分为对照组和观察组,每组各43例。对照组采用西医治疗,观察组在对照组治疗的基础上联合止咳合剂治疗。治疗2周后,观察比较两组患者临床疗效、主要症状消退时间及安全性、治疗前后中医证候积分变化,并检测用力肺活量(Forced vital capacity,FVC)、第1秒用力呼气量(Forced expiratory volume in one second,FEV1)与FVC比值(FEV1/FVC)、最大呼气中段流量(Maximal mid-expiratory flow curve,MMEF)和峰值呼气流速(Peak expiratory flow,PEF)。结果治疗后两组患者中医各项评分及总积分均较治疗前降低,差异有统计学意义(P<0.05);且观察组各项评分及总积分均低于对照组,差异有统计学意义(P<0.05)。观察组各症状(发热、咳嗽、咳痰、憋喘、肺音)消失时间及肺部病灶吸收时间均较对照组明显缩短,差异有统计学意义(P<0.05)。治疗后两组患者FVC、FEV1/FVC、MMEF和PEF均较治疗前升高,差异有统计学意义(P<0.05);且观察组FVC、FEV1/FVC、MMEF和PEF均高于对照组,差异有统计学意义(P<0.05)。治疗后观察组临床总有效率97.67%(42/43)与对照组90.70%(39/43)比较,差异无统计学意义(χ^(2)=3.254,P>0.05);观察组愈显率90.70%(39/43)明显高于对照组74.42%(32/43),差异有统计学意义(χ^(2)=8.108,P<0.05)。治疗期间,两组患者安全性指标均未见明显异常变化。结论止咳合剂治疗成人病毒性肺炎能够促进病情缓解,提高治疗效果,保护肺功能,减轻气道高反应性。 展开更多
关键词 病毒性肺炎 止咳合剂 肺功能 气道高反应性
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益肺止咳胶囊临床应用专家共识 被引量:3
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作者 崔鑫 张洪春 +6 位作者 郭伟伟 班承钧 王志飞 黎元元 支英杰 于雪峰 谢雁鸣 《中国实验方剂学杂志》 北大核心 2025年第11期218-224,共7页
益肺止咳胶囊是红云制药(贵州)有限公司的独家苗族药,为处方药与非处方药(OTC)双跨品种。其主要成分包括猫爪草、三七等,具有养阴润肺、止咳祛痰的功效,常用于急慢性支气管炎、肺结核等疾病的治疗,但临床对其疗效、适用证候及安全性认... 益肺止咳胶囊是红云制药(贵州)有限公司的独家苗族药,为处方药与非处方药(OTC)双跨品种。其主要成分包括猫爪草、三七等,具有养阴润肺、止咳祛痰的功效,常用于急慢性支气管炎、肺结核等疾病的治疗,但临床对其疗效、适用证候及安全性认识不足,且缺乏相关临床应用专家共识。为规范其临床应用,该研究邀请30名来自呼吸科、药学、循证医学专业的专家,运用循证医学方法制定了《益肺止咳胶囊临床应用专家共识》(以下简称《共识》)。该《共识》明确了其在治疗急/慢性支气管炎、肺结核时的证候特点、疾病分期、剂量、疗程、联合用药等规范,适用于各级医疗卫生机构的临床医师和药师。在疾病诊断方面,提供了中医和西医的诊断标准,明确其适宜的中医证候为气阴两虚兼痰瘀互结证。临床研究证实,益肺止咳胶囊联合标准抗结核疗法可有效改善肺结核患者的症状,提高痰菌转阴率,促进病灶吸收;治疗呼吸道感染致急性咳嗽,能提高咳嗽症状疗效愈显率及7 d消失率。同时,针对不同疾病给出了具体的用法用量和疗程建议,并指出长疗程用药需重点监测不良反应。安全性方面,益肺止咳胶囊的不良反应涉及消化系统、过敏反应等多个方面,孕妇及月经期妇女禁用。此外,现代研究表明其对结核性胸膜炎有辅助治疗作用,对炎性和良性肺结节可能有效,但长疗程使用的毒理安全性有待进一步研究。该《共识》的制定,为益肺止咳胶囊的临床合理应用提供了科学依据,有助于提高临床疗效,减少用药风险。 展开更多
关键词 专家共识 益肺止咳胶囊 呼吸 临床应用 苗族药
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苏黄止咳胶囊治疗呼吸系统疾病临床应用专家共识 被引量:3
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作者 明雨 黄常芮 +4 位作者 俞邦 常文婧 孙增涛 陈薇 张洪春 《中国中药杂志》 北大核心 2025年第3期817-823,共7页
临床上苏黄止咳胶囊广泛用于呼吸系统疾病的治疗,已纳入《国家基本医疗保险、工伤保险和生育保险药品目录》《国家基本药物目录》,但在实际应用中仍存在疗程界定不清、禁忌人群不明等问题。因此,该共识由中医肺系病、呼吸及危重症医学... 临床上苏黄止咳胶囊广泛用于呼吸系统疾病的治疗,已纳入《国家基本医疗保险、工伤保险和生育保险药品目录》《国家基本药物目录》,但在实际应用中仍存在疗程界定不清、禁忌人群不明等问题。因此,该共识由中医肺系病、呼吸及危重症医学领域的临床、方法学和药学专家共同制订,严格遵循中华中医药学会中成药临床应用专家共识步骤进行研制,以期指导临床正确使用苏黄止咳胶囊治疗咳嗽变异性哮喘、感冒后咳嗽和其他呼吸系统疾病。共识采用问卷调查、专家访谈的形式,根据PICOS原则确定临床关注问题,并进行证据评价和GRADE系统分级,采用名义组法和GRADE网格化方法产生推荐意见和共识建议,最终形成17条推荐意见和共识建议。该共识进一步明确了苏黄止咳胶囊治疗咳嗽变异性哮喘和感冒后咳嗽的适应证、中医证候、用法用量等,说明其临床安全性,旨在推进规范用药,促进苏黄止咳胶囊的临床合理应用。 展开更多
关键词 苏黄止咳胶囊 咳嗽变异性哮喘 感冒后咳嗽 专家共识 GRADE
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苏黄止咳胶囊联合硫酸沙丁胺醇对COPD急性加重期肺功能及中医证候积分的影响
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作者 沙莉 房磊号 谢晴晴 《中国急救复苏与灾害医学杂志》 2025年第1期61-65,共5页
目的 探究苏黄止咳胶囊联合硫酸沙丁胺醇治疗COPD急性加重期肺功能及中医证候积分的影响。方法 选取2020年3月-2023年3月南京医科大学附属明基医院纳入的100例慢性阻塞性肺病(COPD)急性加重期患者作为研究对象,根据随机抽签结果分为单... 目的 探究苏黄止咳胶囊联合硫酸沙丁胺醇治疗COPD急性加重期肺功能及中医证候积分的影响。方法 选取2020年3月-2023年3月南京医科大学附属明基医院纳入的100例慢性阻塞性肺病(COPD)急性加重期患者作为研究对象,根据随机抽签结果分为单一组和联合组,各50例。单一组给予硫酸沙丁胺醇治疗,联合组给予苏黄止咳胶囊和硫酸沙丁胺醇治疗。比较两组治疗后的临床疗效、肺功能[第1秒用力呼气量(FEV1)、用力肺活量(FVC)、FEV1/FVC]、免疫功能[分化群3(CD3^(+))、分化群4(CD4^(+))、白细胞(WBC)、中性白细胞计数(NBC)]、炎症因子[C-反应蛋白(CRP)、白细胞介素17(IL-17)、白细胞介素8(IL-8)]、中医证候积分(咳嗽、咯痰、喘息、胸部胀满、口渴、发热、大便干)及圣乔治呼吸问卷(SGRQ)评分、改良呼吸困难指数(mMRC)、临床COPD问卷(CCQ)、COPD评估测试(CAT)评分。结果 治疗后,联合组患者的临床疗效高于单一组(χ^(2)=5.983,P<0.05);联合组FEV_1、FVC、FEV_1/FVC高于单一组(t=3.889、5.669、2.495,P<0.05);联合组的WBC、NBC低于单一组,CD3^(+)、CD4^(+)高于单一组(t=3.938、11.301、11.110、6.402,P<0.05);联合组的CRP、IL-17、IL-8低于单一组(t=4.958、4.200、5.952,P<0.05);联合组中医证候各项积分均低于单一组(t=10.386、5.392、9.024、8.413,P<0.05);联合组SGRQ、mMRC、CCQ、CAT评分低于单一组(t=10.578、10.571、9.501、13.193,P<0.05)。结论 苏黄止咳胶囊联合硫酸沙丁胺醇治疗对COPD急性加重期的肺功能和中医证候积分影响显著。 展开更多
关键词 苏黄止咳胶囊 硫酸沙丁胺醇 慢性阻塞性肺病 临床疗效 肺功能
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