肝气虚失眠症机探讨及大补肝汤临床疗效观察.pdfVIP

L iv er q i d eficien cy in som n ia M ech an ism an d C lin ical R esearch on th e T reatm en t of In som n ia W ith D a-B u-G an T an g D ecoction Sp eciality : N euro logical m edicine ofT C M  ? A u th o r : G a o Y an Tutor : Prof.W ang Zhonglin A b str a ct O bjective : D eficiency the pathogenesis of D a-B u-G an Tang clin ical ob servation, that its clinical app licab ility of th e treatm ent of insom n ia. M eth od s: C h oose from a clin ical study m et th e in clu sion criteria of th e L iv er Q i D eficiency 60 patients w ere random ly divided into tw o group s, nam ely the treatm ent group 30 patients in th e control group 30 cases, resp ectiv ely, given th e appropriate drug for clin ical treatm en t course of 3 w eek s. B efore and after treatm ent P SQ I scale, clin ical sym ptom s score ch an ges. R esu lts: A fter statistical analysis, before treatm ent in th e general inform ation including age, gender, P SQ I points and so no sign ificant difference, com parab le. A fter treatm ent has im proved than before, but the treatm ent group in im proving sym ptom s in traditional C h inese m edicin e than th e control group . 1 .A ccording to C h in ese h erb al m edicine clinical research gu iding princip le of th e clin ical curative effect of standard evaluation com parison, the total effective rate of the treatm ent group and control group total effectiv eness is 93.33% 、73.33% , b etw een tw o group s of clin ical curativ e effect w as sign ificant difference (p 0.0 1). 2 . C om pare P SQ I p eriod in accordance w ith , and th e th erap eutic evaluation and greater 63.33% , w ith th e total effective rate of 90% ; T h e control group , the total effective rate of exp licit 20.00% 、76.67% ; Tw o group s w as statistically sign