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疏風清肺止咳方治療感染后咳嗽風熱郁肺證的臨床研究

發(fā)布時間:2018-07-04 18:13

  本文選題:感染后咳嗽 + 風熱郁肺證。 參考:《湖南中醫(yī)藥大學》2016年碩士論文


【摘要】:目的:觀察疏風清肺止咳方治療感染后咳嗽風熱郁肺證的臨床療效,并對其安全性及有效性進行評估。方法:將符合納入標準的60例感染后咳嗽患者隨機分為治療組(30例)和對照組(30例),治療組給予疏風清肺止咳方湯劑治療,對照組給予復方甲氧那明膠囊聯合維生素C片口服治療,觀察療程均為7天。通過觀察治療前后兩組視覺模擬評分(VAS),中醫(yī)證候分級量化評分,咳嗽起效時間,疾病總療程等指標以評估臨床療效。結果:(1)兩組總體療效比較,治療組總有效率93.33%與對照組(70%)比較,差異有統(tǒng)計學意義(P0.05),說明治療組總有效率高于對照組。(2)兩組視覺模擬評分比較,治療后治療組視覺模擬評分2.57?1.89,對照組3.76?2.07,差異有統(tǒng)計學意義(P0.05),說明治療組在緩解咳嗽癥狀方面優(yōu)于對照組。(3)兩組主癥積分比較,治療后治療組主癥積分為3.20?2.07,對照組為5.91?3.18,差異具有統(tǒng)計學意義(P0.05),說明在改善主癥上,治療組較對照組優(yōu)。(4)兩組次癥積分比較,兩組療后咽干,便干癥狀積分比較,治療組優(yōu)于對照組(P0.05),說明治療組在緩解咽干、便干癥狀方面效果更佳;兩組療后在咳痰、口干癥狀積分方面比較,兩組差異均無統(tǒng)計學意義(P0.05),說明兩組在緩解咳痰、口干癥狀效果相當;(5)兩組中醫(yī)證候總積分比較,療后治療組中醫(yī)證候總積分為3.77?1.76,與對照組為7.09?1.92比較,差異有統(tǒng)計學意義(P0.05),說明治療組在緩解感染后咳嗽中醫(yī)癥狀方面優(yōu)于對照組。(6)兩組咳嗽起效時間比較,治療組咳嗽平均起效時間為30.40?9.20h,對照組為32.80?10.42h,差異無統(tǒng)計學意義(P0.05),說明兩組咳嗽起效時間相當。(7)兩組疾病療程比較,治療組疾病平均療程為4.95?0.92天,對照組為5.57?1.05天,差異有統(tǒng)計學意義(P0.05),說明在疾病療程上,治療組短于對照組。結論:疏風清熱止咳方在治療感染后咳嗽風熱郁肺證具有良好臨床療效,且可縮短疾病療程,未見明顯不良反應。
[Abstract]:Objective: to observe the clinical effect of Shufeng Qingfei Zhike recipe in treating cough wind heat depression lung syndrome after infection, and to evaluate its safety and effectiveness. Methods: sixty patients with post-infection cough were randomly divided into treatment group (n = 30) and control group (n = 30). The treatment group was treated with Shufeng Qingfei Zhike decoction. The control group was treated with compound methoxylamine capsule combined with vitamin C tablet orally for 7 days. The clinical efficacy was evaluated by observing the visual analogue score (VAS), the quantitative score of TCM syndromes, the onset time of cough and the total course of treatment before and after treatment. Results: (1) the total effective rate of the treatment group was 93.33% compared with the control group (70%), the difference was statistically significant (P0.05), which indicated that the total effective rate of the treatment group was higher than that of the control group. (2) the visual analogue score of the two groups was higher than that of the control group. After treatment, the visual analogue score of the treatment group was 2.57 ~ 1.89, while that of the control group was 3.76 ~ 2.07, the difference was statistically significant (P0.05), which indicated that the treatment group was superior to the control group in relieving cough symptoms. (3) the main symptom scores of the two groups were compared. After treatment, the score of main symptom in the treatment group was 3.20 鹵2.07, and that in the control group was 5.91 鹵3.18, the difference was statistically significant (P0.05), which indicated that the treatment group was superior to the control group in improving the main symptom. (4) the score of the two groups was higher than that of the control group. The treatment group was superior to the control group (P0.05), indicating that the treatment group was more effective in relieving the symptoms of dry pharynx and dry stool; after treatment, there was no significant difference between the two groups in the score of expectoration and dry oral symptoms (P0.05), which indicated that the two groups had no significant difference in relieving expectoration. (5) the total score of TCM syndromes in the treatment group was 3.77 ~ 1.76, and that in the control group was 7.09 ~ 1.92, compared with that in the control group, (5) the total score of TCM syndromes in the treatment group was 3.77 ~ 1.76 and 7.09 ~ 1.92 respectively. The difference was statistically significant (P0.05), indicating that the treatment group was superior to the control group in relieving the symptoms of cough after infection. (6) the time of onset of cough in the two groups was higher than that in the control group. The average onset time of cough in the treatment group was 30.40 鹵9.20 h, and that in the control group was 32.80 鹵10.42 h. The difference was not statistically significant (P0.05), which indicated that the onset time of cough was the same between the two groups. (7) the average course of treatment was 4.95 鹵0.92 days in the treatment group and 5.57 鹵1.05 days in the control group. The difference was statistically significant (P0.05), indicating that the treatment group was shorter than the control group in the course of treatment. Conclusion: Shufeng Qingre Zhike prescription has good clinical effect in treating cough with wind-heat depression and lung syndrome after infection and can shorten the course of disease without obvious adverse reactions.
【學位授予單位】:湖南中醫(yī)藥大學
【學位級別】:碩士
【學位授予年份】:2016
【分類號】:R256.11

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