国际医药卫生导报 ›› 2025, Vol. 31 ›› Issue (21): 3587-3591.DOI: 10.3760/cma.j.cn441417-20250731-21013

• 论著 • 上一篇    下一篇

痰热清胶囊辅治热毒袭肺证流行性感冒临床观察

陈烁文1  谢琳娜1  李佳遥1  程耀慷1  李乔2,3   

  1. 1安徽中医药大学研究生院,合肥 230012;2安徽中医药大学附属太和县中医院呼吸与危重症医学科,阜阳 236600;3界首市中医院呼吸与危重症医学科,界首 236500
  • 收稿日期:2025-07-31 出版日期:2025-11-01 发布日期:2025-11-18
  • 通讯作者: 李乔,Email:liqiao5354@163.com
  • 基金资助:
    安徽省中医药传承创新科研项目(2024ZYYXH079)

Clinical observation of phlegm-heat-clearing capsules in the adjuvant treatment of influenza with heat-toxin attacking lung syndrome

Chen Shuowen1, Xie Linna1, Li Jiayao1, Cheng Yaokang1, Li Qiao2,3   

  1. 1 Graduate School, Anhui University of Chinese Medicine, Hefei 230012, China; 2 Department of Respiratory and Critical Care Medicine, Taihe County Hospital of Traditional Chinese Medicine, Anhui University of Chinese Medicine, Fuyang 236600, China; 3 Department of Respiratory and Critical Care Medicine, Jieshou Hospital of Traditional Chinese Medicine, Jieshou 236500, China
  • Received:2025-07-31 Online:2025-11-01 Published:2025-11-18
  • Contact: Li Qiao, Email: liqiao5354@163.com
  • Supported by:
    Anhui Provincial Traditional Chinese Medicine Inheritance and Innovation Research Project (2024ZYYXH079)

摘要: 目的 观察痰热清胶囊辅治热毒袭肺证流行性感冒的临床疗效。方法 选择2023年9月至2024年9月界首市中医院呼吸与危重症学科热毒袭肺证流行性感冒患者72例,采用随机数字表法分为对照组(36例)和试验组(36例)。试验组男19例,女17例,年龄53.50(42.50,58.75)岁;对照组男20例,女16例,年龄50.00(35.00,55.75)岁。对照组给予磷酸奥司他韦胶囊口服,每次75 mg,每日2次。试验组在对照组基础上加用痰热清胶囊,每次0.8 g,每日3次。疗程5 d,随访至病情痊愈。观察完全退热时间、中医症状积分、临床疗效、C反应蛋白(CRP)、白细胞计数异常比例、中性粒细胞百分比异常比例及不良反应。采用配对样本t检验、独立样本t检验、Welch校正t检验、Mann-Whitney U检验、χ2检验、校正χ2检验、Fisher确切概率法进行统计学分析。结果 试验组的完全退热时间为(34.06±12.25)h,短于对照组的(40.72±13.77)h,差异有统计学意义(t=-2.170,P=0.033)。治疗后第4天,试验组中医症状积分低于对照组[(3.06±1.84)分比(5.75±2.75)分],差异有统计学意义(t=-4.889,P<0.001);试验组总愈显率高于对照组[80.56%(29/36)比50.00%(18/36)],差异有统计学意义(χ2=7.414,P=0.006);试验组CRP水平、白细胞计数异常比例、中性粒细胞百分比异常比例均低于对照组[(7.44±2.24)mg/L比(10.05±3.16)mg/L、2.78%(1/36)比22.22%(8/36)、11.11%(4/36)比30.56%(11/36)](均P<0.05)。治疗过程中,试验组出现1例不良反应(轻度腹泻),对照组0例,采用Fisher确切概率法检验两组不良反应发生率,差异无统计学意义(P=1.000)。结论 痰热清胶囊联合磷酸奥司他韦胶囊治疗热毒袭肺证流行性感冒,在退热时间、症状缓解、炎症改善方面优于单用磷酸奥司他韦胶囊。

关键词: 流行性感冒, 热毒袭肺证, 痰热清胶囊, 中医药, 临床观察

Abstract: Objective To observe the clinical efficacy of phlegm-heat-clearing capsules in the adjuvant treatment of influenza with heat-toxin attacking lung syndrome. Methods From September 2023 to September 2024, 72 patients with influenza of heat-toxin attacking lung syndrome in the Department of Respiratory and Critical Care Medicine, Jieshou Hospital of Traditional Chinese Medicine were selected, and were divided into a control group (36 cases) and an experimental group (36 cases) using the random number table method. In the experimental group, there were 19 males and 17 females, with a median age of 53.50 (42.50, 58.75) years old; in the control group, there were 20 males and 16 females, with a median age of 50.00 (35.00, 55.75) years old. The control group was given oral oseltamivir phosphate capsules, 75 mg each time, twice a day; the experimental group was additionally treated with phlegm-heat-clearing capsules, 0.8 g each time, three times a day. The treatment course was 5 days, with follow-up until complete recovery. The complete fever reduction time, total score of traditional Chinese medicine symptoms, clinical efficacy, C-reactive protein (CRP) level, abnormal rate of white blood cell count, abnormal rate of neutrophil percentage, and adverse reactions were observed. Statistical analysis was conducted using paired sample t test, independent sample t test, Welch-corrected t test, Mann-Whitney U test, χ2 test, corrected χ2 test, and Fisher's exact probability method. Results The complete fever reduction time of the experimental group was (34.06±12.25) hours, which was shorter than that of the control group [(40.72±13.77) hours], with a statistically significant difference (t=-2.170, P=0.033). On the 4th day after treatment, the total score of traditional Chinese medicine symptoms of the experimental group was lower than that of the control group [(3.06±1.84) points vs. (5.75±2.75) points], with a statistically significant difference (t=-4.889, P<0.001); the total recovery rate of the experimental group was higher than that of the control group [80.56% (29/36) vs. 50.00% (18/36)], with a statistically significant difference (χ2=7.414, P=0.006); the CRP level, abnormal rate of white blood cell count, and abnormal rate of neutrophil percentage in the experimental group were all lower than those in the control group [(7.44±2.24) mg/L vs. (10.05±3.16) mg/L, 2.78% (1/36) vs. 22.22% (8/36), 11.11% (4/36) vs. 30.56% (11/36)] (all P<0.05). During the treatment process, one adverse reaction occurred in the experimental group (mild diarrhea), while there were no such cases in the control group. The incidences of adverse reactions in the two groups were compared using the Fisher's exact probability method, and the difference was not statistically significant (P=1.000). Conclusion The combination of phlegm-heat-clearing capsules and oseltamivir phosphate capsules in the treatment of influenza with heat-toxin attacking lung syndrome outperforms the use of oseltamivir phosphate capsules alone in terms of fever reduction time, symptom relief, and improvement of inflammation.

Key words: Influenza, Heat-toxin attacking lung syndrome, Phlegm-heat-clearing capsules, Traditional Chinese medicine, Clinical observation