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Chinese traditional medicine composition for treating IPF(Idiopathic Pulmonary Fibrosis) and preparation method thereof

A technology for pulmonary interstitial fibrosis and a composition is applied in the field of traditional Chinese medicine compositions for treating idiopathic pulmonary interstitial fibrosis and the preparation thereof, which can solve the problems of poor effect and the like, and achieves remarkable effect, convenient use, and matching ratio. simple effect

Inactive Publication Date: 2014-11-19
QINGDAO MUNICIPAL HOSPITAL
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Traditional Chinese medicine is a treasure in the traditional culture of the Chinese nation. It has a good curative effect on many miscellaneous diseases. For the disease of idiopathic pulmonary interstitial fibrosis, although traditional glucocorticoid or oxygen therapy can play a certain role , but the effect is not good, but traditional Chinese medicine has a significant effect on the recovery of the disease. According to the theory of traditional Chinese medicine: idiopathic pulmonary interstitial fibrosis is mostly classified in the category of "lung impotence" in traditional Chinese medicine.

Method used

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  • Chinese traditional medicine composition for treating IPF(Idiopathic Pulmonary Fibrosis) and preparation method thereof

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Embodiment 1

[0019] Liu, male, 46 years old. Dry cough, dyspnea after exertion, clubbing, wet rales at the bottom of the lungs, limited lung function: VC-60 diffusing capacity ~ 40%, partial pressure of oxygen decreased after exertion, chest X-ray, high-definition CT (HRCT), lung Basal honeycombing, uneven reticular cell fibrosis, taking the following prescriptions:

[0020] 20g Pseudostellariae Radix, 20g Nanshashen, 20g Ophiopogon japonicus, 20g Scrophulariae Radix, 20g Astragalus, 20g Codonopsis Codonopsis, 15g Atractylodes Rhizoma Atractylodes Rhizome, 15g Atractylodes Rhizoma, 15g Scutellaria baicalensis, 12g peach kernel, 10g platycodon, 12g Citrus aurantii, 12g turmeric, Danshen 12g, raw licorice 10g.

[0021] Shuijianbi, 2 times a day, 5 days a course of treatment, after taking 5 courses of treatment, no cough, chest X-ray, showing the reduction of honeycomb changes in the base of the lung, uneven reticular cell fibrosis disappeared, continue to take 5 courses of treatment , The ...

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Abstract

The invention discloses a Chinese traditional medicine composition for treating IPF(Idiopathic Pulmonary Fibrosis). The Chinese traditional medicine composition is composed of following ingredients in unit of weight: 10-20 g of radix pseudostellariae, 10-20 g of adenophora tetraphylla, 10-20 g of radix ophiopogonis, 10-20 g of radix scrophulariae, 10-20 g of astragalus membranaceus, 10-20 g of codonopsis pilosula, 10-15 g of rhizoma atractylodis, 10-15 g of rhizoma atractylodis macrocephalae, 10-15 g of the root bark of white mulberry, 10-15 g of scutellaria baicalensis, 10-12 g of peach kernel, 5-10 g of radix platycodi, 10-12 g of fructus aurantii, 10-12 g of radix curcumae, 10-12 g of the root of red-rooted salvia and 5-10 g of radix glycyrrhizae. The Chinese traditional medicine composition provided by the invention has the advantages of simple proportioning and great convenience in use, has the effects of reinforcing Qi and nourishing Yin, promoting blood circulation to remove blood stasis, regulating vital energy and allowing Qi and blood to circulate, and has a remarkable effect on treating IPF.

Description

technical field [0001] The invention relates to a medical preparation containing raw materials derived from plants, in particular to a traditional Chinese medicine composition for treating idiopathic pulmonary interstitial fibrosis and a preparation method thereof. Background technique [0002] Idiopathic pulmonary fibrosis (IPF) refers to a diffuse inflammatory disease of the lower airways of unknown etiology. Inflammation invades the alveolar walls and adjacent alveolar spaces, causing thickening of the alveolar septa and pulmonary fibrosis. Alveolar epithelial cells and capillary endothelial cells, as well as small airways and small blood vessels, may also be affected. Its clinical features include progressive dyspnea, Velcro rales, and progressive hypoxemia. Impaired lung function is mainly restricted ventilatory dysfunction and diffusion dysfunction. IPF is less common and difficult to diagnose. The prevalence rate is about 2-5 / 100,000, and the age of onset is mostly...

Claims

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Application Information

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IPC IPC(8): A61K36/9066A61P11/00
Inventor 郝月琴唐华平杨玲孙岩
Owner QINGDAO MUNICIPAL HOSPITAL
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