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特发性肺纤维化是一种临床难治疾病,历来医家多从肺痹或肺痿进行单独论述。文章结合肺脏生理病理特点和特发性肺纤维化的现代研究,提出肺虚为特发性肺纤维化发病之本,为病机的启动因素。以虚瘀毒为核心病机思想,经四诊合参、辨证论治,将特发性肺纤维化发病的全过程总结为初起于肺虚,继而肺络痹阻,终致肺痿,应用经验方肺维康方、间质肺纤饮治疗特发性肺纤维化具有显著的临床疗效。
Abstract:Idiopathic pulmonary fibrosis(IPF) is a clinical refractory disease. Traditionally,medical practitioners have mostly discussed it separately from pulmonary arthralgia or pulmonary impotence. This article,in combination with the physiological and pathological characteristics of the lungs and modern research on IPF,puts forward that pulmonary deficiency is the root cause of IPF and the initiating factor of the pathogenesis.Based on the core pathogenesis idea of “deficiency,stasis and toxicity”,through the combination of the four diagnostic methods and syndrome differentiation and treatment,the entire process of IPF onset is summarized as initial pulmonary deficiency,which is followed by obstruction of the lung meridians and eventually leading to pulmonary impotence. The application of empirical formulas such as Feiweikang Formula(肺维康方) and Jianzhi Feixian Decoction(间质肺纤饮) has achieved remarkable clinical efficacy in treating IPF.
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基本信息:
DOI:10.16295/j.cnki.0257-358x.2025.07.002
中图分类号:R259
引用信息:
[1]景传庆,孔慧,张伟,等.基于“虚瘀毒”探析特发性肺纤维化[J].山东中医杂志,2025,44(07):729-733.DOI:10.16295/j.cnki.0257-358x.2025.07.002.
基金信息:
国家自然科学基金面上项目(编号:81874442); 山东省自然科学基金面上项目(编号:ZR2021LZY031); 泰山学者工程专项经费资助项目(编号:tsqn202306393)
2025-07-05
2025-07-05