參麻顆粒治療小兒風(fēng)寒感冒的臨床研究
本文關(guān)鍵詞: 小兒風(fēng)寒感冒 中醫(yī)治療 臨床研究 急性毒性實(shí)驗(yàn) 出處:《云南中醫(yī)學(xué)院》2014年碩士論文 論文類型:學(xué)位論文
【摘要】:目的:本文通過(guò)對(duì)參麻顆粒治療小兒風(fēng)寒感冒的療效進(jìn)行系統(tǒng)觀察和研究,探討該方的作用機(jī)制,,并通過(guò)急性毒性實(shí)驗(yàn)對(duì)參麻顆粒的安全性進(jìn)行初步評(píng)價(jià),以尋求中醫(yī)藥治療小兒風(fēng)寒感冒的新思路。 方法:(1)本研究采用隨機(jī)單盲法將符合診斷標(biāo)準(zhǔn)的60例風(fēng)寒感冒患兒用數(shù)字隨機(jī)分組法分為參麻顆粒組(觀察組)和風(fēng)寒感冒顆粒組(對(duì)照組),觀察組與對(duì)照組各30例,治療1-2個(gè)療程(3~6天),觀察并對(duì)比兩組患兒服藥后癥狀、體征的量化評(píng)分的改變情況,進(jìn)行綜合療效評(píng)定。(2)急性毒性實(shí)驗(yàn)在不能求得半數(shù)致死量的情況下,采用最大耐受量法求得小鼠1日的最大耐受量。 結(jié)果:(1)在總的療效比較方面,觀察組與對(duì)照組療效相當(dāng),差異無(wú)統(tǒng)計(jì)學(xué)意義(P0.05)。在改善臨床癥狀方面,觀察組對(duì)咳嗽等癥狀的改善優(yōu)于對(duì)照組。(2)急性毒性實(shí)驗(yàn)求得小鼠1日最大耐受量為生藥8.932g/kg,相當(dāng)于成人全日臨床推薦量的32.48倍,提示參麻顆粒臨床用藥安全。 結(jié)論:通過(guò)對(duì)參麻顆粒的臨床研究及急性毒性實(shí)驗(yàn),證明參麻顆粒治療小兒風(fēng)寒感冒療效肯定,且該藥物無(wú)明顯毒副作用,值得推廣和應(yīng)用。
[Abstract]:Objective: to observe and study the therapeutic effect of Shenma granule on children with wind-cold colds, to explore the mechanism of its action, and to evaluate the safety of Shenma granule through acute toxicity experiment. In order to seek traditional Chinese medicine to treat children with cold cold new ideas. Methods in this study, 60 children with wind-cold cold were randomly divided into Shenma granule group (observation group) and wind cold cold granule group (control group) by random single blind method. There were 30 cases in the observation group and 30 cases in the control group, who were treated with 1-2 courses of treatment for 3 days or 6 days. The changes of the quantitative scores of symptoms and signs of the two groups were observed and compared. In the acute toxicity test, the maximum tolerance dose of mice in 1st was obtained by using the method of maximum tolerance dose under the condition that half lethal dose could not be obtained. Results compared with the control group, the curative effect of the observation group was similar to that of the control group, but the difference was not statistically significant (P 0.05). The improvement of cough and other symptoms in the observation group was better than that in the control group. (2) Acute toxicity test showed that the maximum tolerance dose in 1st was 8.932 g / kg crude drug. It is 32. 48 times that of adult clinical recommendation, suggesting that Shenma granule is safe in clinical use. Conclusion: through the clinical study and acute toxicity experiment of Shenma granule, it is proved that Shenma granule is effective in treating cold in children, and it has no obvious side effects, so it is worth popularizing and applying.
【學(xué)位授予單位】:云南中醫(yī)學(xué)院
【學(xué)位級(jí)別】:碩士
【學(xué)位授予年份】:2014
【分類號(hào)】:R272
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