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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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Molecular Mechanism of Prescription for the Syndrome of Cold-Dampness Obstructing the Lung in the Treatment of COVID-19 Based on Network Pharmacology
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作者 ZHAO Wenyu SI Fuchun 《Chinese Medicine and Natural Products》 2021年第2期21-30,共10页
Objective:To explore the molecular mechanism of the prescription for the syndrome of cold-damp-ness obstructing the lung in the treatment of corona virus disease 2019(COVID-19).Methods:The medicinals for the treatment... Objective:To explore the molecular mechanism of the prescription for the syndrome of cold-damp-ness obstructing the lung in the treatment of corona virus disease 2019(COVID-19).Methods:The medicinals for the treatment of the syndrome of cold-dampness obstructing the lung,such as Cangzhu(Rhizoma Atractylo-dis),Chenpi(Pericarpium Gitri Reticulatae),Houpo(Cortex Magnoliae Officinalis),Huoxiang(Herba Agastachis),Caoguo(Fructus Tsaoko),Mahuang(Herba Ephedrae),Qianghuo(Rhizoma et Radix Notoptery-gi),Shengjiang(Rhizoma Zingiberis Recens),Binlang(Semen Arecae)in the Diagnosis and Treatment Pro-gram of COVID-19(Trial Version 6)were taken as research subjects,and the combination of these nine me-dicinals can be called Hanshi Zufei Fang(寒湿阻肺方,HSZFF).The active components and targets of each single Chinese materia medica was screened and obtained through the Traditional Chinese Medicine Systems Pharmacology(TCMSP)database.The target information related to COVID-19 was retrieved through the Gene-Cards disease-related target database.The medicinal prediction targets were mapped to the disease target to ob-tain the intersection targets.The DAVID database was applied to perform gene ontology(GO)enrichment anal-ysis and kyoto encyclopedia of genes and genomes(KEGG)pathway analysis on the targets;GraphPad Prism 5.0 software was applied to plot the biological process(BP)of GO enrichment analysis,cellular component(CC),molecular function(MF)histograms;OmicShare online software was applied to make KEGG advanced bubble chart;Cytoscape software was applied to visualize the interaction with the targets and Chinese materia medica-components-targets results.Results:Totally 56 key active components of 9 Chinese materia medica for cold-dampness obstructing lung syndrome were screened,and 55 targets were obtained.The results of GO and KEGG enrichment analysis showed that the compound prescription mainly regulated the body's immune re-sponse and reduced inflammation by regulating such signaling pathways of inflammatory response and immune regulation as TNF signaling pathway,HIF-1 signaling pathway,Toll-like receptor signaling pathway,infuenza A signaling pathway,T cell receptor signaling pathway.Conclusion:HSZFF can eliminate infl ammation and inhibit virus by regulating immune inflammatory factors closely related to the occurrence and development of diseases through multi-component and multi-target. 展开更多
关键词 network pharmacology COVID-19 cold-dampness obstructing lung syndrome molecular mechanism
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The Effect of Sanzi Yangqin Decoction Combined with Maxing Ganshi Decoction on Syndrome Differentiation and Treatment of Chronic Obstructive Pulmonary Disease with Phlegm and Heat Blocking the Lung
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作者 SHA Sha 《外文科技期刊数据库(文摘版)医药卫生》 2021年第7期062-064,共5页
Objective: to explore how to apply traditional Chinese medicine therapy to improve the related clinical symptoms of patients with chronic obstructive pulmonary disease (phlegm-heat obstructing lung syndrome). Methods:... Objective: to explore how to apply traditional Chinese medicine therapy to improve the related clinical symptoms of patients with chronic obstructive pulmonary disease (phlegm-heat obstructing lung syndrome). Methods: within one year after January 2019, patients admitted to our hospital for chronic obstructive pulmonary disease (COPD) were selected to meet the inclusion criteria of this study, and were treated in groups. One group of patients was treated with western medicine only, and the other group was treated with western medicine. Another group of patients were treated with western medicine while taking traditional Chinese medicine decoction. The patients in this group were treated with combination of traditional Chinese medicine and western medicine. Then list the relevant indicators, and then compare and analyze the effect of the two groups of patients after treatment. The improvement of pulmonary function and various symptoms in the two groups were compared and analyzed. Results: compared with the western medicine group, the total effective rate of the western medicine group was higher, the lung function related indicators were better, and the TCM syndrome score was lower (P < 0.05). Conclusion: Sanzi Yangqin Decoction combined with Maxing Ganshi Decoction can effectively improve various clinical symptoms of COPD patients with phlegm-heat blocking lung syndrome, and can also improve the lung function of patients to a certain extent. 展开更多
关键词 chronic obstructive pulmonary disease syndrome of phlegm-heat obstructing the lung Sanzi Yangqin a
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Stem/progenitor cells and obstructive sleep apnea syndrome - new insights for clinical applications 被引量:1
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作者 Miruna Mihaela Micheu Ana-Maria Rosca Oana-Claudia Deleanu 《World Journal of Stem Cells》 SCIE CAS 2016年第10期332-341,共10页
Obstructive sleep apnea syndrome(OSAS) is a widespread disorder, characterized by recurrent upper airway obstruction during sleep, mostly as a result of complete or partial pharyngeal obstruction. Due to the occurrenc... Obstructive sleep apnea syndrome(OSAS) is a widespread disorder, characterized by recurrent upper airway obstruction during sleep, mostly as a result of complete or partial pharyngeal obstruction. Due to the occurrence of frequent and regular hypoxic events, patients with OSAS are at increased risk of cardiovascular disease, stroke, metabolic disorders, occupational errors, motor vehicle accidents and even death. Thus, OSAS has severe consequences and represents a significant economic burden. However, some of the consequences, as well as their costs can be reduced with appropriate detection and treatment. In this context, the recent advances that were made in stem cell biology knowledge and stem cell- based technologies hold a great promise for various medical conditions, including respiratory diseases. However, the investigation of the role of stem cells in OSAS is still recent and rather limited, requiring further studies, both in animal models and humans. The goal of this review is to summarize the current state of knowledge regarding both lung resident as well as circulating stem/progenitor cells and discuss existing controversies in the field in order to identify future research directions for clinical applications in OSAS. Also, the paper highlights the requisite for inter-institutional, multi-disciplinary research collaborations in order to achieve breakthrough results in the field. 展开更多
关键词 obstructIVE sleep APNEA syndrome Continuous positive airway pressure therapy lung resident stem/progenitor CELLS Circulating stem/progenitor CELLS lung homeostasis
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基于因子分析和聚类分析探讨病毒性急性肺损伤的中医证候规律
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作者 谢林 宋栋 +3 位作者 陈余姗 黄海阳 王凯 连乐燊 《广州中医药大学学报》 2026年第1期1-7,共7页
【目的】研究病毒性急性肺损伤(VALI)患者的中医证候分布规律,为该病的临床规范化、精准辨证论治提供客观的参考依据。【方法】回顾性收集2021年7月至2024年8月期间在广州中医药大学东莞医院(东莞市中医院)呼吸与危重症医学科住院诊治的... 【目的】研究病毒性急性肺损伤(VALI)患者的中医证候分布规律,为该病的临床规范化、精准辨证论治提供客观的参考依据。【方法】回顾性收集2021年7月至2024年8月期间在广州中医药大学东莞医院(东莞市中医院)呼吸与危重症医学科住院诊治的222例VALI患者的一般资料及中医四诊信息,提取、整理后将数据录入Excel表,运用因子分析和聚类分析方法对数据进行统计分析,归纳出VALI患者的中医证型分布规律。【结果】对222例VALI患者的中医四诊信息进行频数分析,共得到36个与VALI密切相关的症状或体征,其中出现频率排前10位的分别为喘息气促、咳嗽、黄脓痰、胸中烦闷、苔黄腻、口渴欲饮、脉滑、舌红、胸痛、黄白痰。通过因子和聚类分析,最终得出4类中医证型,分别是痰热壅肺证(43.24%)、热毒袭肺证(27.93%)、气阴两虚证(19.82%)、正虚喘脱证(9.01%)。【结论】VALI患者的中医证候分布,实证方面以痰热壅肺证、热毒袭肺证为主,虚证方面主要表现为气阴两虚证和正虚喘脱证。病位主要在肺脏,涉及脾、肾、心,病理因素主要为“热”“毒”“痰”“虚”,尤以“热”“痰”为重。 展开更多
关键词 病毒性急性肺损伤 中医证候 痰热壅肺证 热毒袭肺证 气阴两虚证 正虚喘脱证 因子分析 聚类分析
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补肺汤联合布地格福治疗稳定期慢性阻塞性肺疾病研究
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作者 王保芹 杨敏 +2 位作者 华文山 刘宗伟 石岫岩 《辽宁中医杂志》 北大核心 2026年第2期103-107,共5页
目的观察补肺汤联合布地格福吸入气雾剂治疗稳定期慢性阻塞性肺疾病肺气虚证临床效果及安全性。方法合计纳入98例稳定期慢性阻塞性肺疾病肺气虚证患者(2021年1月—2024年3月收集)以随机数字表法进行分组,将患者平均分为布地格福组及联... 目的观察补肺汤联合布地格福吸入气雾剂治疗稳定期慢性阻塞性肺疾病肺气虚证临床效果及安全性。方法合计纳入98例稳定期慢性阻塞性肺疾病肺气虚证患者(2021年1月—2024年3月收集)以随机数字表法进行分组,将患者平均分为布地格福组及联合汤剂组,各49例,布地格福组患者均采取布地格福吸入气雾剂治疗,联合汤剂组患者在采取布地格福吸入气雾剂治疗基础上联合补肺汤治疗,比较各组数据:临床疗效及治疗前后咳喘无力、畏风、咳痰、自汗、痰清稀等中医证候积分变化、肺功能以及炎症因子相关指标变化、T淋巴细胞变化、圣乔治呼吸调查问卷(SGRQ)变化、观察不良反应。结果联合汤剂组患者治疗总有效率比布地格福组更高(P<0.05);治疗前两组患者咳喘无力、畏风、咳痰、自汗、痰清稀等中医证候积分、第一秒用力呼气容积(FEV_(1))、用力肺活量(FVC)、第1秒用力呼气容积占肺活量比值(FEV_(1)/FVC)等肺功能指标、白介素-4(IL-4)及白介素-8(IL-8)以及肿瘤坏死因子-α(TNF-α)等炎症因子、CD_(4)^(+)、CD_(8)^(+)、CD_(4)^(+)/CD_(8)^(+)等T淋巴细胞指标、SGRQ评分比较,差异无统计学意义(P>0.05),治疗后两组患者咳喘无力、畏风、咳痰、自汗、痰清稀等中医证候积分、肺功能指标(FEV_(1)、FVC、FEV_(1)/FVC)、炎症因子水平(IL-4、IL-8及TNF-α)、CD_(4)^(+)、CD_(8)^(+)、CD_(4)^(+)/CD_(8)^(+)等T淋巴细胞指标、SGRQ评分均明显改善,联合汤剂组患者治疗后咳喘无力、畏风、咳痰、自汗、痰清稀等中医证候积分、肺功能指标(FEV_(1)、FVC、FEV_(1)/FVC)、炎症因子水平(IL-4、IL-8及TNF-α)、CD_(4)^(+)、CD_(8)^(+)、CD_(4)^(+)/CD_(8)^(+)等T淋巴细胞指标、SGRQ评分均优于布地格福组,P<0.05;布地格福组出现1例恶心,联合汤剂组未见治疗不良反应,差异无统计学意义(P>0.05)。结论补肺汤联合布地格福吸入气雾剂治疗稳定期慢性阻塞性肺疾病肺气虚证临床效果良好,患者炎症得以控制,临床症状及肺功能改善,耐力及生活质量、免疫功能提升,未见不良反应,治疗较为安全可靠。 展开更多
关键词 慢性阻塞性肺疾病 肺气虚证 布地格福吸入气雾剂 补肺汤 肺功能 免疫功能 不良反应
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儿童肺炎中医证型分布及相关危险因素探析
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作者 徐萍 周陶成 《河南中医》 2026年第3期437-443,共7页
目的:分析儿童肺炎的中医证型分布和病情分级情况,并探讨其与临床资料等相关危险因素的相关性。方法:收集安徽省儿童医院收治的430例肺炎患儿的临床资料,包括性别、年龄、既往呼吸道疾病病史、中医证型、肺炎病情分级、咳嗽时长、发热... 目的:分析儿童肺炎的中医证型分布和病情分级情况,并探讨其与临床资料等相关危险因素的相关性。方法:收集安徽省儿童医院收治的430例肺炎患儿的临床资料,包括性别、年龄、既往呼吸道疾病病史、中医证型、肺炎病情分级、咳嗽时长、发热时长、发热峰值、病原体感染情况、呼吸道症状评估、胃肠道症状评估、实验室指标[白细胞计数(white blood cell,WBC)、中性粒细胞计数、血小板计数(platelet,PLT)、C反应蛋白(C reactive protein,CPR)和降钙素原(procalcitonin,PCT)、全身免疫炎症指数(systemic immune-inflammation index,SII)]等,统计肺炎患儿的证型分布和病情分级情况,并分析其与临床资料之间的相关性。结果:430例肺炎患儿中风热闭肺证192例、痰热闭肺证170例、毒热闭肺证33例、湿热闭肺证13例、肺脾气虚证12例;轻症361例、重症69例;单一感染335例、混合感染95例。各证型患儿单一感染率均高于混合感染率,仅风热闭肺证、痰热闭肺证、肺脾气虚证比较,差异具有统计学意义(P<0.05)。风热闭肺证、痰热闭肺证患儿轻症比例高于重症,毒热闭肺证、湿热闭肺证患儿重症比例高于轻症,差异均有统计学意义(P<0.05);肺脾气虚证患儿肺炎病情分级比较,差异无统计学意义(P>0.05)。不同肺炎病情分级患儿在性别、年龄段和既往呼吸道病史方面比较,差异无统计学意义(P>0.05)。不同肺炎病情分级患儿在病原体感染方面比较,差异有统计学意义(P<0.05)。不同中医证型患儿WBC、SII、CRP、PCT及呼吸道症状积分、胃肠道症状积分、发热峰值及发热、咳嗽时长比较,差异均有统计学意义(P<0.05)。不同肺炎病情分级患儿WBC、CRP、LDH比较,差异均无统计学意义(P>0.05);SII、PCT及呼吸道症状积分≥34分、胃肠道症状积分≥8分、咳嗽≥11 d、发热≥7 d、咳嗽≥11 d、热峰≥39.1℃比较,差异均有统计学意义(P<0.05)。Logistic回归分析显示,发热≥7 d、SII>1000×10^(9)·L^(-1)、胃肠道症状积分≥8分、混合感染、湿热闭肺证及毒热闭肺证是重症肺炎的独立危险因素(P<0.05)。结论:430肺炎患儿中,轻症和风热闭肺证最多,毒热闭肺证和湿热闭肺证与重症肺炎密切相关,混合感染、发热时长、SII升高和胃肠道症状是重症肺炎的重要危险因素。 展开更多
关键词 儿童肺炎 风热闭肺证 痰热闭肺证 毒热闭肺证 湿热闭肺证 中医证型 病原体
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穴位贴敷联合清肺蠲饮汤治疗热饮阻肺型肺炎49例
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作者 张彦芳 丁梦圆 《河南中医》 2026年第2期300-306,共7页
目的:观察穴位贴敷联合清肺蠲饮汤治疗热饮阻肺型肺炎的临床疗效。方法:选取南阳市第一人民医院2024年1月至2025年1月收治的98例热饮阻肺型肺炎患儿为研究对象,按照随机数字表法分为对照组和观察组,每组各49例。对照组给予常规西医治疗... 目的:观察穴位贴敷联合清肺蠲饮汤治疗热饮阻肺型肺炎的临床疗效。方法:选取南阳市第一人民医院2024年1月至2025年1月收治的98例热饮阻肺型肺炎患儿为研究对象,按照随机数字表法分为对照组和观察组,每组各49例。对照组给予常规西医治疗,观察组给予穴位贴敷联合清肺蠲饮汤治疗。比较两组患儿的临床疗效、症状缓解时间、不良反应发生率及治疗前后淋巴细胞亚群、免疫水平[免疫球蛋白A(immunoglobulin A,Ig A)与免疫球蛋白M(immunoglobulin M,Ig M)]、血清指标[白细胞介素-6(interleukin-6,IL-6)、C反应蛋白(C-reactive protein,CRP)、中性粒细胞比例(neutrophil Percentage,NEU%)、淋巴细胞比例(lymphocyte percentage,LYM%)]。结果:观察组有效率为97.96%,高于对照组的79.59%,差异具有统计学意义(P<0.05)。两组患儿治疗后CD3+、CD4+、CD4+/CD8+指标均高于本组治疗前,CD8+低于本组治疗前,且治疗后组间比较,差异具有统计学意义(P<0.05)。两组患儿治疗后Ig A、Ig M水平高于本组治疗前,且治疗后观察组高于对照组,差异具有统计学意义(P<0.05)。两组患儿治疗后IL-6、CRP、NEU%低于本组治疗前,LYM%高于本组治疗前,且治疗后组间比较,差异具有统计学意义(P<0.05)。观察组发热、咳嗽、咳痰、肺部啰音消退时间短于对照组,差异具有统计学意义(P<0.05)。观察组不良反应发生率为6.12%,低于对照组的24.49%,差异具有统计学意义(P<0.05)。结论:清肺蠲饮汤联合穴位贴敷治疗热饮阻肺型肺炎,临床疗效确切,能显著改善肺炎患儿免疫功能及炎症状态,缩短症状缓解时间。 展开更多
关键词 肺炎 热饮阻肺证 清肺蠲饮汤 穴位贴敷
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解炎汤辅助西药治疗慢性阻塞性肺疾病急性加重期的效果观察
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作者 王涛 王娜 +1 位作者 代慧敏 房颖 《成都医学院学报》 2026年第1期73-77,共5页
目的探究解炎汤辅助西药在慢性阻塞性肺疾病急性加重期(AECOPD)治疗中的应用价值。方法选取2023年3月至2024年10月在北京市大兴区中西医结合医院就诊的190例AECOPD患者为研究对象,根据随机数字表法将其分为西药组和试验组,每组95例。西... 目的探究解炎汤辅助西药在慢性阻塞性肺疾病急性加重期(AECOPD)治疗中的应用价值。方法选取2023年3月至2024年10月在北京市大兴区中西医结合医院就诊的190例AECOPD患者为研究对象,根据随机数字表法将其分为西药组和试验组,每组95例。西药组采用常规西药疗法,试验组在西药组基础上联合解炎汤治疗,两组均治疗2周。比较两组疗效、血清相关指标[白细胞介素-6(IL-6)、IL-21、IL-33]、中医证候积分、呼吸困难程度[改良版英国医学研究委员会呼吸困难问卷(mMRC)评分]、病情严重程度[慢性阻塞性肺疾病评估测试问卷(CAT)评分]、血气指标[血氧分压(PaO_(2))、二氧化碳分压(PaCO_(2))]、肠道菌群计数及不良反应发生率。结果试验组总有效率高于西药组,且试验组病情严重程度II级患者总有效率高于西药组同级别患者(P<0.05)。治疗2周后,试验组血清IL-6、IL-21、IL-33水平低于西药组(P<0.05);试验组喘息气急、咯痰不爽、痰多色黄、口渴喜冷饮、大便干结等中医证候积分低于西药组(P<0.05);试验组CAT评分、mMRC评分、PaCO_(2)水平及肠球菌、肠杆菌计数低于西药组,PaO_(2)水平、乳酸杆菌和双歧杆菌计数高于西药组(P<0.05)。两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论解炎汤辅助西药治疗AECOPD能抑制炎症反应,改善血气指标和菌群环境,有助于缓解临床症状、提升临床疗效,且对病情严重程度II级患者疗效更优,同时可确保用药安全。 展开更多
关键词 慢性阻塞性肺疾病 急性加重期 痰热壅肺证 解炎汤 中医证候积分 肠道菌群
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宣肺败毒汤治疗痰热壅肺型慢性阻塞性肺疾病急性加重期疗效观察
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作者 渠展 徐红艳 卢奎斌 《河南中医》 2026年第1期127-132,共6页
目的:探讨宣肺败毒汤治疗痰热壅肺型慢性阻塞性肺疾病急性加重期(acute exacerbation chronic obstructive pulmonary disease,AECOPD)的临床疗效。方法:将108例AECOPD患者采用随机数字表法分为对照组和观察组,每组各54例。对照组给予... 目的:探讨宣肺败毒汤治疗痰热壅肺型慢性阻塞性肺疾病急性加重期(acute exacerbation chronic obstructive pulmonary disease,AECOPD)的临床疗效。方法:将108例AECOPD患者采用随机数字表法分为对照组和观察组,每组各54例。对照组给予噻托溴铵吸入粉雾剂治疗,观察组在对照组治疗的基础上联合宣肺败毒汤治疗。比较两组患者的临床疗效、症状缓解时间、不良反应发生率及治疗前后中医证候积分、急性发作次数、炎症因子水平[甲壳质酶蛋白40(human chitinase-3 like protein 1,YKL-40)、C-反应蛋白(C-reactive protein,CRP)、降钙素原(procalcitonin,PCT)、干扰素-γ(interferon-γ,IFN-γ)、白细胞介素-8(interleukin-8,IL-8)]、血气指标[动脉血氧分压(arterial partial pressure of oxygen,PaO_(2))、动脉血氧饱和度(arterial blood oxygen saturation,SaO_(2))、动脉血二氧化碳分压(partial pressure of carbon dioxide,PaCO_(2))]变化情况。结果:观察组有效率为90.74%,高于对照组的74.07%,差异具有统计学意义(P<0.05)。两组患者治疗后咯血、浓痰腥臭、痰量多、心烦、口渴等中医证候积分低于本组治疗前(P<0.05),且治疗后观察组低于对照组(P<0.05)。观察组咯血、浓痰腥臭、痰量多、心烦、口渴等症状缓解时间均短于对照组(P<0.05)。两组患者治疗后YKL-40、CRP、PCT和痰液IL-8含量低于本组治疗前,痰液IFN-γ水平高于本组治疗前,且治疗后组间比较,差异具有统计学意义(P<0.05)。两组患者治疗后PaO_(2)、SaO_(2)均高于本组治疗前,PaCO_(2)低于本组治疗前,且治疗后组间比较,差异具有统计学意义(P<0.05)。两组患者治疗后急性发作次数低于本组治疗前,且治疗后观察组低于对照组(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:宣肺败毒汤治疗痰热壅肺型AECOPD,可加速临床症状的缓解,降低中医证候积分和炎症因子水平,调节血气指标,减少急性发作次数。 展开更多
关键词 慢性阻塞性肺疾病 宣肺败毒汤 痰热壅肺证 噻托溴铵吸入粉雾剂 中西医结合疗法
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推拿联合桑杏前桔汤治疗急性支气管炎(痰热郁肺证)的临床研究
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作者 许璿 袁洋 +4 位作者 齐心 周海霞 沙寰 郑洲 高屹文 《中国医学创新》 2026年第5期40-43,共4页
目的:探究推拿联合桑杏前桔汤治疗急性支气管炎(痰热郁肺证)的临床效果。方法:回顾性选取2023年6月—2025年6月盐城市中医院收治的120例急性支气管炎(痰热郁肺证)患儿作为研究对象,按治疗方法分为对照组(n=40)和联合组(n=80)。对照组给... 目的:探究推拿联合桑杏前桔汤治疗急性支气管炎(痰热郁肺证)的临床效果。方法:回顾性选取2023年6月—2025年6月盐城市中医院收治的120例急性支气管炎(痰热郁肺证)患儿作为研究对象,按治疗方法分为对照组(n=40)和联合组(n=80)。对照组给予小儿肺热咳喘口服液治疗,联合组给予推拿联合桑杏前桔汤治疗,两组均持续治疗2周。比较两组临床疗效、不良反应发生率和治疗前后的中医证候积分、WBC、hs-CRP。结果:联合组临床总有效率高于对照组(P<0.05);治疗后,联合组咳嗽、咯痰、发热积分低于对照组(P<0.05);治疗后,联合组WBC、hs-CRP均低于对照组(P<0.05)。两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:推拿联合桑杏前桔汤治疗急性支气管炎(痰热郁肺证)的临床效果较为显著。 展开更多
关键词 推拿 桑杏前桔汤 急性支气管炎 痰热郁肺证 中医证候积分
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麻石清肺合剂治疗社区获得性肺炎(痰热壅肺证)的临床观察
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作者 龚雪 郑邦本 +3 位作者 吕超 王磊 魏大荣 牟方政 《中国中医急症》 2026年第2期173-176,共4页
目的观察麻石清肺合剂治疗社区获得性肺炎(痰热壅肺证)的临床疗效。方法选取我院社区获得性肺炎(痰热壅肺证)患者60例,随机分为两组,对照组予西医常规治疗,观察组加用联合麻石清肺合剂,观察两组治疗前后临床疗效、中医证候积分、血清炎... 目的观察麻石清肺合剂治疗社区获得性肺炎(痰热壅肺证)的临床疗效。方法选取我院社区获得性肺炎(痰热壅肺证)患者60例,随机分为两组,对照组予西医常规治疗,观察组加用联合麻石清肺合剂,观察两组治疗前后临床疗效、中医证候积分、血清炎症因子等指标,并进行统计学分析。结果观察组总有效率为93.33%,高于对照组的76.67%(P<0.05);两组治疗后,观察组在缓解咳嗽、咯黄痰、咳嗽甚则胸痛、发热、口渴、尿黄、腹胀便结临床症状方面均明显优于对照组(P<0.05);观察组发热、咳嗽、咯黄痰、咳嗽甚则胸痛、肺部啰音症状缓解时间均短于对照组(P<0.05);观察组血清炎症因子降钙素原、超敏C反应蛋白(hs-CRP)、血沉(ESR)、白细胞介素-6(IL-6)下降趋势较对照组明显(P<0.05)。结论麻石清肺合剂可提高社区获得性肺炎(痰热壅肺证)患者临床疗效,改善血清炎症因子,安全性良好,且在治疗病毒性肺炎患者方面可能具有潜在优势,其原因可能与通过多靶点抗病毒作用有关。 展开更多
关键词 社区获得性肺炎 麻石清肺合剂 痰热壅肺证 中医药 临床疗效
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清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎痰热壅肺证患者的效果
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作者 李宗富 《中国民康医学》 2026年第1期103-105,109,共4页
目的:观察清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎(CB)痰热壅肺证患者的效果。方法:选取2022—2023年该院收治的86例CB痰热壅肺证患者进行前瞻性研究,采用随机数字表法将其分为对照组和观察组各43例。对照组予以头孢哌酮钠... 目的:观察清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎(CB)痰热壅肺证患者的效果。方法:选取2022—2023年该院收治的86例CB痰热壅肺证患者进行前瞻性研究,采用随机数字表法将其分为对照组和观察组各43例。对照组予以头孢哌酮钠舒巴坦钠治疗,观察组在对照组基础上联合清金化痰汤治疗。比较两组临床疗效,治疗前后中医证候积分(咳嗽气促、痰多黄稠、口干烦躁、小便短赤、大便秘结)、血气分析指标[动脉血氧分压(PaO_(2))、动脉血二氧化碳分压(PaCO_(2))]水平,以及不良反应发生率。结果:观察组治疗总有效率为95.35%(41/43),高于对照组的81.40%(35/43),差异有统计学意义(P<0.05);治疗后,两组咳嗽气促、痰多黄稠、口干烦躁、小便短赤、大便秘结等中医证候积分均低于治疗前,且观察组低于对照组,差异有统计学意义(P<0.05);治疗后,两组PaO_(2)水平均高于治疗前,且观察组高于对照组,两组PaCO_(2)水平均低于治疗前,且观察组低于对照组,差异有统计学意义(P<0.05);两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:清金化痰汤联合头孢哌酮钠舒巴坦钠治疗CB痰热壅肺证患者可提高治疗总有效率,改善血气分析指标水平,降低中医证候积分,效果优于单纯头孢哌酮钠舒巴坦钠治疗。 展开更多
关键词 清金化痰汤 头孢哌酮钠舒巴坦钠 慢性支气管炎 痰热壅肺证 中医证候积分 血气分析 不良反应
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自拟清热化痰宣肺汤辅助治疗儿童肺炎支原体肺炎痰热闭肺证54例临床观察
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作者 应洁 潘锦辉 陈媛媛 《中医儿科杂志》 2026年第1期59-63,共5页
目的观察自拟清热化痰宣肺汤辅助治疗儿童肺炎支原体肺炎(MPP)痰热闭肺证的临床疗效。方法选取2021年6月至2024年6月在仙居县中医院内科收治的MPP痰热闭肺证患儿108例,采用随机数字表法分为对照组和治疗组,各54例。对照组给予阿奇霉素... 目的观察自拟清热化痰宣肺汤辅助治疗儿童肺炎支原体肺炎(MPP)痰热闭肺证的临床疗效。方法选取2021年6月至2024年6月在仙居县中医院内科收治的MPP痰热闭肺证患儿108例,采用随机数字表法分为对照组和治疗组,各54例。对照组给予阿奇霉素序贯疗法治疗,治疗组在对照组治疗方法的基础上予自拟清热化痰汤治疗,2组均治疗10 d后统计临床疗效。结果治疗组发热、咳嗽、气喘及肺部湿啰音消失时间较对照组明显提前,2组比较,差异有统计学意义(P<0.05)。治疗前2组血清C反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)水平比较,差异无统计学意义(P>0.05),具有可比性;治疗后2组血清CRP、TNF-α、IL-6水平均显著降低,与同组治疗前比较,差异有统计学意义(P<0.05),且治疗组降低更显著(P<0.05)。治疗前2组血清免疫球蛋白A(IgA)、免疫球蛋白M(IgM)、免疫球蛋白G(IgG)水平比较,差异无统计学意义(P>0.05),具有可比性;治疗后2组血清IgA、IgM、IgG水平均明显上升,与同组治疗前比较,差异有统计学意义(P<0.05),且治疗组上升更显著(P<0.05)。对照组总有效率为81.48%(44/54),治疗组为94.44%(51/54),2组比较,差异有统计学意义(P<0.05)。治疗期间,对照组、治疗组不良反应总发生率分别为7.40%(4/54),5.55%(3/54),2组比较,差异无统计学意义(P>0.05)。结论自拟清热化痰宣肺汤辅助治疗小儿MPP痰热闭肺证疗效显著,不仅能明显缓解症状和体征、减轻炎症反应、提高机体免疫力,而且不良反应少,值得临床推广应用。 展开更多
关键词 儿童 肺炎支原体肺炎 痰热闭肺证 自拟清热化痰宣肺汤 临床观察
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Relationship between Occurrence and Progression of Lung Cancer and Nocturnal Intermittent Hypoxia, Apnea and Daytime Sleepiness 被引量:3
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作者 Wei LIU Miao LUO +3 位作者 Yuan-yuan FANG Shuang WEI Ling ZHOU Kui LIU 《Current Medical Science》 SCIE CAS 2019年第4期568-575,共8页
The possible relationship between lung cancer and nocturnal intermittent hypoxia,apnea and daytime sleepiness,especially the possible relationship between the occurrence and progression of lung cancer and obstructive ... The possible relationship between lung cancer and nocturnal intermittent hypoxia,apnea and daytime sleepiness,especially the possible relationship between the occurrence and progression of lung cancer and obstructive sleep apnea syndrome (OSAS) was explored.Forty-five cases of primary lung cancer suitable for surgical resection at the Third Affiliated Hospital of Kunming Medical University between January 2017 and December 2017 were recruited (lung cancer group),and there were 45 patients in the control group who had no significant differences in age,sex and other general data from lung cancer group.The analyzed covariates included general situation,snore score,the Epworth Sleeping Scale (ESS),Pittsburgh Sleep Quality Index (PSQI),apnea and hypopneas index (AHI),oxygen desaturation index 4 (ODk),lowest arterial oxygen saturation [LSpCh (%)],oxygen below 90% of the time [T90%(min)],the percentage of the total recorded time spend below 90% oxygen saturation (TS90%),to explore the possible relationship between lung cancer and above indicators.The participants were followed up for one year.The results showed that:(1) There was significant difference in body mass index (BMI),ESS,AHI,T90%(min),TS90%,ODh,snore score and LSpCh (%) between lung cancer group and control group (P<0.05).There was no statistically significant difference in age,gender,PSQI score,incidence of concurrent hypertension,diabetes and coronary heart disease (CHD),and smoking history between the two groups (P>0.05);(2) Patients in the lung cancer group were divided into OSAS subgroup and non- OSAS subgroup according to the international standard for the diagnosis of OSAS.There was significant difference in BMI,age,staging,incidence of concurrent hypertension and concurrent CHD,snore score,ESS score,T90%(min),TS90%,ODh and LSpCh (%) between OSAS subgroup and non-OSAS subgroup (P<0.05).There was no statistically significant difference in gender,PSQI score,incidence of concurrent diabetes,smoking history and lung cancer type between the two groups (P>0.05);(3) AHI was strongly negatively correlated with the LSpCh (%) and positively with ESS,staging,snoring score,T90%(min),TS90%,ODh and BMI (P<0.05);(4) There were 3 deaths,5 cases of recurrence,and 4 cases of metastasis in OSAS subgroup;and there was 1 death,4 cases of recurrence and 2 cases of metastasis in non-OSAS subgroup during the follow-up period of one year,respectively.There was no significant difference in mortality,recurrence rate and metastasis rate between the two subgroups,and the total rate of deterioration in OSAS subgroup was significantly increased compared to the non-OSAS subgroup (P<0.05).It was concluded that the patients with lung cancer are prone to nocturnal hypoxemia,apnea,snoring and daytime sleepiness compared to control group.The incidence of OSAS in patients with lung cancer was higher,and the difference in the hypoxemia-related indicators was statistically significant.The mortality,recurrence rate,and metastasis rate increases in lung cancer patients with OSAS during the one-year follow-up period,suggesting that OSAS may be a contributing factor to the occurrence and progression of lung cancer. 展开更多
关键词 lung cancer NOCTURNAL INTERMITTENT hypoxia APNEA DAYTIME SLEEPINESS obstructIVE sleep APNEA syndrome
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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 被引量:2
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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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清肺化痰祛瘀法合穴位贴敷治疗痰热郁肺证慢性阻塞性肺疾病急性加重期的疗效研究 被引量:1
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作者 沈爱娟 张峰 +1 位作者 胡健 孙雪渊 《辽宁中医杂志》 北大核心 2025年第6期91-95,共5页
目的观察慢性阻塞性肺疾病急性加重期(acute exacerbation of chronic obstructive pulmonary disease,AECOPD)痰热郁肺证患者,通过清肺化痰祛瘀法联合穴位贴敷治疗后的临床缓解效果以及对肺功能和相关炎症因子的作用。方法选择了符合AE... 目的观察慢性阻塞性肺疾病急性加重期(acute exacerbation of chronic obstructive pulmonary disease,AECOPD)痰热郁肺证患者,通过清肺化痰祛瘀法联合穴位贴敷治疗后的临床缓解效果以及对肺功能和相关炎症因子的作用。方法选择了符合AECOPD痰热郁肺证的92例住院患者,随机分为45例试验组和47例对照组。试验组在西医治疗基础上增加了口服清肺化痰祛瘀汤药联合外用穴位贴敷,对照组进行单纯西医治疗。治疗14 d后评估两组中医证候积分、肺功能指标[第1秒用力呼气的容积占预计值的百分比(FEV1/pred)、FEV1/用力肺活量(forced vital capacity,FVC)、最大呼气中段流量(maximal mid-expiratory flow curve,MMEF)75%~25%pred、最大呼气流量(maximum expiratory flow,MEF)50%pred、MEF75%pred),比较两组血清肿瘤坏死因子-α(tumor necorsis factor-α,TNF-α)、白细胞介素-6(interleukin-6,IL-6)和降钙素原(procalcitonin,PCT)水平的变化。结果①中医证候积分:治疗后试验组与对照组比较降低[(13.28±2.75)分vs(16.16±2.18)分,P<0.01]。②肺功能:治疗后试验组与对照组比较,FEV1/pred有明显改善[(45.70±16.63)分vs(52.59±13.67)分,P<0.05],而对于FEV1/FVC、MMEF75%~25%/pred、EF50%/pred、MEF25%/pred,较对照组无明显改善。③血清炎症因子IL-6水平:治疗后试验组与对照组比较下降明显[(11.04±8.53)pg/mL vs(16.29±14.68)pg/mL,P<0.05]、TNF-α[(3.34±2.20)pg/mL vs(4.95±2.11)pg/mL,P<0.01];而血清PCT降低水平两组治疗后统计结果差异无统计学意义。结论该研究提示痰热郁肺证AECOPD患者采用清肺化痰祛瘀法+穴位贴敷的方法治疗可使其临床治疗效果增加,炎症反应水平降低,比单纯西医治疗效果更好,临床安全有保障。 展开更多
关键词 清肺化痰祛瘀法 穴位贴敷 AECOPD 痰热郁肺证
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参芩龙清肺培元颗粒对HIV/AIDS合并肺部感染痰热壅肺证患者外周血巨噬细胞自噬的作用机制研究 被引量:1
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作者 宋夕元 郭润泽 +6 位作者 雷丽亚 孟鹏飞 桑锋 刘真 徐立然 郝明玲 杨柳 《中国中医基础医学杂志》 2025年第7期1248-1253,共6页
目的 基于巨噬细胞自噬探讨参芩龙清肺培元颗粒的作用机制。方法 选择人类免疫缺陷病毒(HIV)/艾滋病(AIDS)合并肺部感染痰热壅肺证患者36例,应用流式细胞术检测治疗前后患者外周血T淋巴细胞亚群中CD4^(+)及CD8^(+)T淋巴细胞计数,巨噬细... 目的 基于巨噬细胞自噬探讨参芩龙清肺培元颗粒的作用机制。方法 选择人类免疫缺陷病毒(HIV)/艾滋病(AIDS)合并肺部感染痰热壅肺证患者36例,应用流式细胞术检测治疗前后患者外周血T淋巴细胞亚群中CD4^(+)及CD8^(+)T淋巴细胞计数,巨噬细胞亚群CD11b、CD86、CD206的表达及巨噬细胞自噬探针CD11b+DALGreen、CD86+DALGreen、CD206+DALGreen的表达。ELISA法检测治疗前后血清肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、IL-10、转化生长因子(TGF)-β1等炎性因子的表达。采用荧光定量PCR法检测治疗前后患者外周血中组蛋白去乙酰化酶(HDAC)2 m RNA、Unc-51样激酶1(ULK1)m RNA的表达。结果 治疗后,患者CD11b、CD206、CD11b+DALGreen、CD206+DALGreen、ULK1 m RNA表达明显升高(P<0.05);CD86、TNF-α、IL-1β、HDAC2 m RNA的表达明显下降(P<0.05);CD4^(+)T淋巴细胞计数、IL-10、TGF-β1表达呈上升趋势(P>0.05)。结论 参芩龙清肺培元颗粒可能通过调节HDAC2/ULK1信号轴,促进巨噬细胞自噬,调节M1/M2的平衡,抑制炎症反应,从而发挥治疗HIV/AIDS患者合并肺部感染的作用。 展开更多
关键词 参芩龙清肺培元颗粒 HIV/AIDS合并肺部感染 痰热壅肺证 巨细胞自噬
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肺炎宁药贴贴敷治疗小儿肺炎喘嗽痰热闭肺证的临床疗效 被引量:1
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作者 庄玲伶 王增玲 《延边大学医学学报》 2025年第7期112-114,共3页
目的:探讨小儿肺炎喘嗽痰热闭肺证治疗中应用肺炎宁药贴贴敷的临床疗效。方法:选取2023年10月—2024年10月某医院收治的130例小儿肺炎喘嗽痰热闭肺证患儿,采用随机数表法分组,分为常规组和试验组。常规组予西医常规治疗,试验组在西医常... 目的:探讨小儿肺炎喘嗽痰热闭肺证治疗中应用肺炎宁药贴贴敷的临床疗效。方法:选取2023年10月—2024年10月某医院收治的130例小儿肺炎喘嗽痰热闭肺证患儿,采用随机数表法分组,分为常规组和试验组。常规组予西医常规治疗,试验组在西医常规治疗的基础上联合肺炎宁药贴贴敷治疗。对比两组疗效差异。结果:试验组治疗后中医证候积分低于常规组,治疗总有效率高于常规组,差异显著(P<0.05)。试验组不良反应总发生率与常规组之间比较差异不显著(P>0.05)。结论:小儿肺炎喘嗽痰热闭肺证应用肺炎宁药贴贴敷治疗可以提升疗效,具有较高的临床借鉴意义。 展开更多
关键词 小儿肺炎 喘嗽 痰热闭肺证 肺炎宁药贴贴敷
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