清气化痰散结汤治疗肺郁痰瘀型中危肺结节临床研究
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R256.1;R563

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2022年衢州市科技攻关项目(2022K123)


Clinical Study on Qingqi Huatan Sanjie Decoction in the Treatment of Intermediate- Risk Pulmonary Nodules of Lung Stagnation and Phlegm Stasis Type
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    摘要:

    目的:观察清气化痰散结汤治疗肺郁痰瘀型中危肺结节的临床疗效。方法:选择2025 年1—9 月衢州市中医医院收治的104例肺郁痰瘀型中危肺结节患者,按随机数字表法分为观察组和对照组各52例。观察组给予清气化痰散结汤治疗,对照组不予以药物治疗。3个月后,比较2组临床疗效、中医证候评分、最大结节直径和面积变化、炎症因子[肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-17A(IL-17A)]及T淋巴细胞亚群水平。结果:治疗后,观察组总有效率为44.23%(23/52),对照组为9.62%(5/52),2组比较,差异有统计学意义(P<0.05)。治疗后,观察组中医证候评分较治疗前及对照组降低(P<0.05);而对照组治疗前后中医证候评分比较,差异无统计学意义(P>0.05)。治疗后,观察组最大结节直径、最大结节面积均较治疗前及对照组缩小(P<0.05);而对照组治疗前后最大结节直径、最大结节面积比较,差异无统计学意义(P>0.05)。治疗后,观察组TNF-α、IL-6、IL-17A水平均较治疗前及对照组降低(P<0.05);而对照组治疗前后TNF-α、IL-6、IL-17A水平比较,差异无统计学意义(P>0.05)。治疗后,观察组CD4+、CD4+/CD8+水平均较治疗前及对照组升高(P<0.05),CD8+水平较治疗前及对照组降低(P<0.05);对照组治疗前后CD4+、CD8+、CD4+/CD8+水平比较,差异无统计学意义(P>0.05)。研究期间,2组患者均未出现明显不良反应。结论:清气化痰散结汤治疗肺郁痰瘀型中危肺结节效果良好,可改善中医证候,缩小结节,减轻机体炎症反应,改善患者免疫功能,且安全性良好。

    Abstract:

    Abstract: Objective: To observe the clinical efficacy of Qingqi Huatan Sanjie Decoction in the treatment of intermediate-risk pulmonary nodules of lung stagnation and phlegm stasis type. Methods:A total of 104 patients with intermediate-risk pulmonary nodules of lung stagnation and phlegm stasis type admitted to Quzhou Hospital of Traditional Chinese Medicine from January to September 2025 were enrolled. They were randomly divided into the observation group and the control group using the random number table method, with 52 cases in each group. The observation group received Qingqi Huatan Sanjie Decoction, while the control group received no intervention. After three months, the two groups were compared in terms of clinical efficacy, changes in traditional Chinese medicine syndrome score,maximum nodule diameter and area,levels of inflammatory factors [tumor necrosis factor-α( TNF-α), interleukin-6 (IL-6),interleukin-17A (IL-17A)],and T lymphocyte subsets. Results:After treatment,the total effective rate was 44.23% (23/52) in the observation group and 9.62% (5/52) in the control group,and the difference between the two groups was statistically significant (P<0.05). After treatment, the traditional Chinese medicine syndrome score in the observation group decreased compared with that before treatment,and it was also lower than that in the control group (P<0.05);whereas no statistically significant difference was found in the control group before and after treatment (P>0.05). After treatment,the maximum nodule diameter and maximum nodule area in the observation group were reduced compared with those before treatment and with the control group (P<0.05); no significant differences were observed in the control group before and after treatment (P>0.05). After treatment, the levels of TNF-α,IL-6,and IL-17A in the observation group decreased compared with those before treatment,and the levels were also lower than those in the control group (P<0.05);no significant differences were found in the control group before and after treatment (P>0.05). After treatment, CD4+ levels and CD4+/CD8+ ratio in the observation group increased,and CD8+ levels decreased,compared with those before treatment and with the control group (P<0.05); no significant changes in levels of CD4+ and CD8+,or CD4+/CD8+ ratio were observed in the control group before and after treatment (P>0.05). During the study, no obvious adverse reactions occurred in either group. Conclusion: Qingqi Huatan Sanjie Decoction is effective in the treatment of intermediate-risk pulmonary nodules of lung stagnation and phlegm stasis type. It can improve traditional Chinese medicine syndrome manifestations, reduce nodule size, alleviate systemic inflammatory response,enhance immune functory,and has a good safety profile.

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陈柏竹,王水有,胡玲红.清气化痰散结汤治疗肺郁痰瘀型中危肺结节临床研究[J].新中医,2026,58(18):27-31

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  • 在线发布日期: 2026-09-29
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