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慢性荨麻疹发作时辰与中医病机病证的研究
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作者 陈丽嫦 黄冬梅 +1 位作者 邹珊 潘林平 《深圳中西医结合杂志》 2021年第23期62-65,共4页
目的:探索慢性荨麻疹发作时辰与中医病机病证的关系。方法:选取广州市越秀区中医医院2019年1月至2019年12月皮肤科门诊就诊的慢性荨麻疹患者83例为研究对象,把每日24 h分为十二时辰,对83例具有皮损发作时辰节律特点的慢性荨麻疹患者进... 目的:探索慢性荨麻疹发作时辰与中医病机病证的关系。方法:选取广州市越秀区中医医院2019年1月至2019年12月皮肤科门诊就诊的慢性荨麻疹患者83例为研究对象,把每日24 h分为十二时辰,对83例具有皮损发作时辰节律特点的慢性荨麻疹患者进行问卷调查,收集皮损发作时辰、临床症状并记录舌脉体征等,使用常见症状计量辨证表得出患者的病位、病性,分别与皮损发作时辰所提示的循行经脉及六经病证相比较,以Spearman进行相关性分析。结果:皮损发作时辰与病位、病性均不存在相关性,差异无统计学意义(P>0.05)。结论:切忌生硬套用慢性荨麻疹发作时辰进行中医辨证。 展开更多
关键词 慢性荨麻疹 发作时辰 病机病证
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支气管哮喘“辨病、辨期、辨证、辨体”防治体系探讨
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作者 郭安 王汝佳 +5 位作者 魏媛 贺梦雪 吴清原 李娟 封继宏 孙增涛 《中国中医急症》 2024年第6期986-989,共4页
本文梳理辨证论治及辨病论证的源流脉络,结合现代医学的研究成果,提出基于病证结合的支气管哮喘“辨病、辨期、辨证、辨体”防治体系,以哮喘核心病机为着眼点,以不同临床分期的阶段病机为落脚点,以达到缓解急性发作、改善疾病控制、调... 本文梳理辨证论治及辨病论证的源流脉络,结合现代医学的研究成果,提出基于病证结合的支气管哮喘“辨病、辨期、辨证、辨体”防治体系,以哮喘核心病机为着眼点,以不同临床分期的阶段病机为落脚点,以达到缓解急性发作、改善疾病控制、调节禀赋体质、延缓疾病进展的目的,为相关现代中西医结合疾病防治体系的构建提供思路与启示。 展开更多
关键词 支气管哮喘结合核心 辨期 辨体
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以虚实二纲统领病机辨证体系探讨 被引量:3
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作者 舒长兴 《光明中医》 2008年第5期555-556,共2页
体系,包括要素及要素间的联系方式两方面。病机辨证体系即以病机为要素建立的辨证体系。病机十九条以病性和病位充实虚实二纲,奠定了病机辨证的先河。我们将这种以中医理论为指导,以病性为经、以病位为纬建立起来的辨证体系,称为病机辨... 体系,包括要素及要素间的联系方式两方面。病机辨证体系即以病机为要素建立的辨证体系。病机十九条以病性和病位充实虚实二纲,奠定了病机辨证的先河。我们将这种以中医理论为指导,以病性为经、以病位为纬建立起来的辨证体系,称为病机辨证体系。以虚实二纲来统领病机辨证体系可以起到执简驭繁的作用。 展开更多
关键词 --关系 虚实 体系
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浅议燥邪的发病季节 被引量:6
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作者 林旭红 《时珍国医国药》 CAS CSCD 北大核心 2006年第9期1804-1804,共1页
关键词 燥邪 季节 病机病证
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基于“体-病-证”的组方模式解析气虚体质相关方剂 被引量:3
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作者 王雪可 李天星 李玲孺 《北京中医药大学学报》 CAS CSCD 北大核心 2023年第1期87-92,共6页
本文首先基于“辨体-辨病-辨证”诊疗思想,系统剖析了气虚体质的生理病理特点、常见病机及证候,指出气具有运化、防御、气化、升举、推动、营养等系列作用,气虚体质若调理不当,常出现脾胃运化失常、肌表不固、清阳不升、气机下陷、大肠... 本文首先基于“辨体-辨病-辨证”诊疗思想,系统剖析了气虚体质的生理病理特点、常见病机及证候,指出气具有运化、防御、气化、升举、推动、营养等系列作用,气虚体质若调理不当,常出现脾胃运化失常、肌表不固、清阳不升、气机下陷、大肠传导失司、心脾亏损等六大病机,并可见湿浊内生、痰阻气滞、湿盛濡泄、饮食积滞、表虚自汗、表虚血痹、风湿、湿热遏阳、阴火上炎、气津两伤、中气下陷、脾虚下陷、大气下陷、气虚便秘、气血两虚等诸多证候。进一步基于以体统病(证)、以体统方(药)的思想,以气虚体质常见病机为纲,以“体-病-证”的组方模式解析相关方剂14首,系统地阐述了气虚体质相关方剂组方的共性与个性规律,总结气虚体质常用调体药物及针对病证的常用加减,以期更好地把握气虚体质相关病证选方用药整体图景,更加灵活地遣方用药。 展开更多
关键词 气虚体质 体(体质)-()-(候) 组方模式 方剂
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Inflammatory bowel disease: An evaluation of health information on the internet 被引量:4
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作者 Samy A Azer Thekra I AlOlayan +1 位作者 Malak A AlGhamdi Malak A AlSanea 《World Journal of Gastroenterology》 SCIE CAS 2017年第9期1676-1696,共21页
To evaluate the quality and accuracy of websites written to the public on inflammatory bowel disease (IBD) (Crohn’s disease and ulcerative colitis) and assess their readability level.METHODSGoogle™, Bing™, and Yahoo™... To evaluate the quality and accuracy of websites written to the public on inflammatory bowel disease (IBD) (Crohn’s disease and ulcerative colitis) and assess their readability level.METHODSGoogle™, Bing™, and Yahoo™ search engines were searched independently by three researchers in December 2014. Only English-language websites were selected on the basis of predetermined inclusion and exclusion criteria. Researchers independently evaluated the quality of each website by using the DISCERN and the HONcode instruments. The readability levels were calculated using two formulas; the Flesch-Kincaid Grade Level Index, and the Coleman-Liau Readability Index. The agreement between the evaluators was calculated using Cohen kappa coefficient.RESULTSEighty-four websites were finally identified. Scores varied from a minimum DISCERN score of 18 to a maximum of 68 [mean ± SD, 42.2 ± 10.7; median = 41.5, interquartile range, interquartile range (IQR) = 15.8] and a minimum score of HONcode of 0.14 and a maximum of 0.95 (mean ± SD, 0.16 ± 0.19; median = 0.45, IQR = 0.29). Most of these websites were reviewed in 2014 and 2015 (n = 51). The creators of these websites were: universities and research centers (n = 25, 30%), foundations and associations (n = 15, 18%), commercial and pharmaceutical companies (n = 25, 30%), charities and volunteer work (n = 9, 10%), and non-university educational bodies (n = 10, 12%). The Flesch-Kincaid Grade Level readability score (mean ± SD) was 11.9 ± 2.4 and the Coleman-Liau Readability Index score was 12.6 ± 1.5. Significant correlation was found between the two readability scores (R<sup>2</sup> = 0.509, P = 0.001). The overall agreement between evaluators measured by Cohen kappa coefficient was in the range of 0.804-0.876; rated as 'Good'.CONCLUSIONThe DISCERN and the HONcode scores of websites varied and the readability levels of most websites were above the public readability level. The study highlights the areas that need further improvement and development in patient education online materials about IBD. 展开更多
关键词 Inflammatory bowel disease The internet Patients’ information EVIDENCE Patients’ education online resources
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Crohn’s disease:Evidence for involvement of unregulated transcytosis in disease etio-pathogenesis
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作者 Jay Pravda 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第11期1416-1426,共11页
Crohn’s disease(CD)is a chronic inflammatory bowel disease.Research has identified genetic predisposition and environmental factors as key elements in the development of the disease.However,the precise mechanism that... Crohn’s disease(CD)is a chronic inflammatory bowel disease.Research has identified genetic predisposition and environmental factors as key elements in the development of the disease.However,the precise mechanism that initiates immune activation remains undefined.One pathway for luminal antigenic molecules to enter the sterile lamina propria and activate an immune response is via transcytosis.Transcytosis,although tightly regulated by the cell,has the potential for transepithelial transport of bacteria and highly antigenic luminal molecules whose uncontrolled translocation into the lamina propria can be the source of immune activation.Viewed as a whole,the evidence suggests that unregulated intestinal epithelial transcytosis is involved in the inappropriate presentation of immunogenic luminal macromolecules to the intestinal lamina propria.Thus fulfilling the role of an early pre-morbid mechanism that can result in antigenic overload of the lamina propria and initiate an immune response culminating in chronic inflammation characteristic of this disease.It is the aim of this paper to present evidence implicating enterocyte transcytosis in the early etio-pathogenesis of CD. 展开更多
关键词 Crohn’s TRANSCYTOSIS ENDOCYTOSIS
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