纤结散治疗痰瘀热结型中低危肺结节临床研究
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R259

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河南省中医药科学研究专项(2023ZY2204);第七批全国老中医药专家学术经验继承项目(国中医药人教函〔2022〕76号);河南省 中医药传承与创新人才工程(仲景工程) 中医药学科拔尖人才培养项目(豫卫中医函〔2021〕15号)


Clinical Study on Treatment of Low-Medium Risk Pulmonary Phlegm Stasis and Heat Junction Type with Xianjie Powder
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    摘要:

    目的:观察纤结散治疗痰瘀热结型中低危肺结节的临床疗效。方法:选取2023年11月—2024年 11月就诊于河南省职工医院及河南中医药大学第一附属医院的痰瘀热结型中低危肺结节患者144例,按照随机 数字表法分为观察组和对照组各72例。治疗期间,观察组剔除12例,对照组剔除8例。观察组口服中药纤结 散(颗粒剂),对照组服用纤结散模拟剂(颗粒剂)。治疗3个月后,复查胸部CT,比较2组临床疗效和不良反 应发生情况,评估肺结节分级,以及治疗前后胸部CT中肺结节最大径面的结节面积、结节数量及密度变化。 结果:治疗3个月,观察组总有效率为55.0%(33/60),对照组为12.5%(8/64),组间比较,差异有统计学意 义(P<0.05)。治疗后,观察组最大径面的结节面积较治疗前缩小(P<0.05);与对照组治疗后比较亦有所缩 小,但差异无统计学意义(P>0.05)。治疗后,观察组肺结节数量较治疗前减少(P<0.05);与对照组比较亦 有所减少,但差异无统计学意义(P>0.05)。对照组治疗前后最大径面积的结节面积、肺结节数量比较,差异 无统计学意义(P>0.05)。2组治疗前后肺结节密度分级比较,差异无统计学意义(P>0.05)。2组治疗过程中 均未出现不良反应。结论:纤结散治疗痰瘀热结型中低危肺结节疗效肯定,能减少肺结节最大径面的结节面 积、结节数量,且安全性良好。

    Abstract:

    Abstract:Objective:To observe the clinical efficacy of Xianjie Powder in treating low-medium risk pulmonary nodules of phlegm stasis and heat junction type. Methods: A total of 144 patients with low-medium risk pulmonary nodules of phlegm stasis and heat junction type who visited the Henan General Hospital and the First Affiliated Hospital of Henan University of Chinese Medicine from November 2023 to November 2024 were selected and divided into an observation group and a control group,with 72 cases in each group,using a random number table method. During the treatment,12 cases in the observation group and 8 cases in the control group were excluded. The observation group took the Chinese medicine Xianjie Powder (Granules) orally, while the control group took a placebo of Xianjie Powder (Granules). After three months of treatment, a follow-up chest CT was performed; the clinical efficacy and incidence of adverse reactions were compared between the two groups;the grading of pulmonary nodules was assessed; the changes in the maximum diameter of the nodules,the number of nodules,and their density in the chest CT before and after treatment were compared. Results:After three months of treatment,the total effective rate was 55.0% (33/ 60) in the observation group and 12.5% (8/64) in the control group,with a statistically significant difference between the two groups (P<0.05) . After treatment, the pulmonary nodule area on the maximum diameter section in the observation group was reduced compared with that before treatment (P<0.05);with superior reduction compared with the control group, while the difference was not statistically significant (P>0.05). After treatment, the number of pulmonary nodules in the observation group significantly decreased compared with that before treatment (P<0.05); with greater reduction compared with the control group,while the difference was not statistically significant (P>0.05). No statistically significant difference was observed in the pulmonary nodule area on the maximum diameter and pulmonary nodule number in the control group before and after treatment (P>0.05). Both groups showed no statistically significant differences in pulmonary nodule density grading before and after treatment (P>0.05). No adverse reactions occurred in either group during the treatment period. Conclusion:Xianjie Powder has good clinical efficacy in treating low-medium risk pulmonary nodules of phlegm stasis and heat junction type. It can reduce the nodule area at the maximum diameter section,the number,and has good safety.

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张恒,杨秦梅,邬欣怡,曹梦霞,徐立然.纤结散治疗痰瘀热结型中低危肺结节临床研究[J].新中医,2025,57(14):59-64

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  • 在线发布日期: 2025-07-26
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