Observation Of Clinical Efficacy Of Ginger Moxibustion Combined With Wenfei Zhike Decoction In The Treatment Of Laryngeal Cough Caused By Lung Cold And Insufficient Body Resistance

Objective: This study evaluated the clinical efficacy of Ginger Moxibustion Combined with Wenfei Zhike Decoction in the Treatment of Laryngeal Cough Caused by Lung Cold and Insufficient Body,and compared it with that of Suhuang Zhike Capsules.The purpose of this study is to explore a feasible and effective clinical treatment for laryngeal cough.Methods: Sixty patients who attended the Otolaryngology Clinic of Shandong Provincial Hospital of Traditional Chinese Medicine who met the inclusion criteria and volunteered to participate in the study were selected.According to the randomization scheme,they were divided into a treatment group and a control group with 30 cases each.Patients in the treatment group were given oral Wenfei Zhike Decoction,1 dose per day,12 doses as a course of treatment.Ginger moxibustion was performed during the medication period.Moxibustion was performed once every 3 days and 4 times as a course of treatment.The control group was given oral Suhuang Zhike Capsules,3 capsules/time,3times/day,for 12 consecutive days as a course of treatment.Both the treatment group and the control group were treated for a course of treatment.Before and after treatment,observe and fill in the TCM Syndrome Score Scale and Cough Visual Simulation Scale(VAS Scale),record the adverse reactions,and analyze the data obtained to compare the clinical efficacy.Results:According to statistical analysis,both the treatment group and the control group are effective in treating laryngeal cough caused by lung cold and insufficient body resistance.The total effective rate in the treatment group is 96.67% and the total effective rate in the control group is 90%.After the two groups were treated,the curative effects at all levels were quantitatively compared.The rank sum test proved that there were extremely significant differences(P<0.01),and the rank average and rank sum of the treatment group were lower than those of the control group.This shows that the treatment group has better efficacy than the control group.The score analysis of various syndromes before and after treatment in the treatment group showed that,except for the pulse condition,there was no statistical difference,the other symptoms were all improved.P<0.01,there is a significant statistical difference,and the median score after treatment is less than the median score before treatment.The comparison between the two groups of symptoms before and after treatment d group shows that,except for the tongue picture,there is no statistical difference,in terms of other symptoms,the therapeutic effect of the treatment group is better than the control group.Pharyngeal mucosa,posterior pharyngeal lymphatic follicles,cold tolerance,irritating cough,dry throat,pharyngeal itching,fatigue,P<0.01,there is a significant statistical difference,shortness of breath P<0.05,the difference is statistically significant,and treatment The rank average and rank sum of the group are higher than those of the control group.The intra-group comparison of VAS scores before and after treatment between the treatment group and the control group showed significant statistical differences.P<0.01,and the median and quartile of the score after treatment are lower than those before treatment,indicating that both groups can reduce the VAS score.After the end of the treatment course,the comparison between the two groups before and after treatment showed significant statistical difference(P<0.01),and the rank average and rank sum of the treatment group were higher than those of the control group,indicating that the treatment group had better efficacy than the control group group.