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1. 成都中医药大学附属医院感染科
2. 山西省中医药研究院和平分院
纸质出版日期:2011
移动端阅览
[1]扈晓宇,张扬,张德雄.经方本源剂量治疗流行性感冒风寒证[J].中国实验方剂学杂志,2011,17(13):230-234.
HU Xiao-yu1, ZHANG Yang1, ZHANG De-xiong2. Original Dosage of Classical Prescription in Treating Influenza with Cold Syndrome[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(13): 230-234.
[1]扈晓宇,张扬,张德雄.经方本源剂量治疗流行性感冒风寒证[J].中国实验方剂学杂志,2011,17(13):230-234. DOI: 10.13422/j.cnki.syfjx.2011.13.009.
HU Xiao-yu1, ZHANG Yang1, ZHANG De-xiong2. Original Dosage of Classical Prescription in Treating Influenza with Cold Syndrome[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(13): 230-234. DOI: 10.13422/j.cnki.syfjx.2011.13.009.
目的:评价麻黄汤《伤寒论》本源剂量(下称经方本源剂量)治疗流行性感冒(下称流感)风寒证的临床疗效及安全性。方法:采用随机、阳性药平行对照研究的方法
入选年龄18~65岁的患者
并同时符合流行性感冒的诊断标准及中医风寒证的辨证标准
体温≥38.0℃、病程在48 h之内。所有患者随机分为A组(32例
给予麻黄汤
采用经考证后的《伤寒论》本源剂量
每日1剂
水煎分3次口服)、B组[31例
给予麻黄汤
采用现行中医药高等院校《方剂学》教材所推荐的常用剂量(下称常用剂量)
每日1剂
水煎分3次口服]、C组(30例
给予泰诺酚麻美敏片
每6 h 1次
每次1~2片)
疗程均为3 d。结果:①24 h体温疗效评价:A组的总显效率为93.75%(30/32)
B组为67.74%(21/31)
C组为36.67%(11/30)
3组两两比较(P<α’=0.017)
差异均有统计学意义;②中医证候疗效评价:A组总显效率为90.63%(29/32)、B组为61.29%(19/31)
C组为30.00%(9/30)
3组两两比较(P<0.017)
差异均有统计学意义;③发热缓解时间及症状全部缓解时间的比较:A组与B组、C组两两比较(P<0.05)
差异均有统计学意义。④并发症发生率及抗生素使用率比较:A组低于C组
P<0.017
差异有统计学意义。不良反应发生率:除C组有1例嗜睡、1例头昏、1例胃部不适外
其余2组均未发现明显的不良反应。结论:口服麻黄汤经方本源剂量可有效缩短流感病程
缓解流感临床症状、缩短发热时间
降低流感并发症的发生率
其临床疗效显著优于麻黄汤常用剂量及泰诺酚麻美敏片
麻黄汤经方本源剂量治疗流感早期安全、有效。
Objective:To evaluate the efficacy and safety of Ephedra decoction of original dosage of treatise on febrile disease in the treatment of influenza with cold syndrome.Method: A randomized
positive drug-led trial was conducted on patients(aged 18 to 65 years)with cold syndrome in influenza
which presented influenza symptoms and elevated body temperature(38.0 ℃ or higher) within 48 hours.These patients were randomly divided into 3 groups:group A(32 patients
Ephedra decoction of original dosage
oral decoction 3 times a day
for 3 days)
group B(31 patients
Ephedra decoction of conventional dosage recommended by the textbook of the current Chinese medicine colleges and universities
oral decoction 3 times a day
for 3 days)
group C(30 patients
compound dextromethorphan hydrobromide granules
1-2 granules once
3 times a day
for 3 days).Result: ninty three patients with cold syndrome of influenza were defined as effective analysis cases(32 cases in group A
31 cases in group B and 30 cases in group C.①The total significant efficiency rate of 24 h temperature effect test in group A was 93.75%(30/32)
which was significantly higher than that in group B(67.74%
21/31)and in group C(36.67%
11/30)(P<α′=0.017).②The effective rate of TCM symptoms test in group A was(90.63%
29/32)
which was significantly higher than that in group B(61.29%
19/31))and in group C(30.00%
9/30)
there was a significant difference between group A
group B and group C(P<0.017).③The effect of remission fever and symptoms:The course of fever and symptoms in group A was(23.91±12.87) h and(38.45±20.53) h
which was significantly shorter than that in group B(35.78±16) h
(51.34±29.71) h and that in group C(85.45±22.16) h
(106.34±35.45)h
through binary comparison of the 3 groups(P<0.05).④The ratio of complications incidence and antibiotic utilization:3.13%(1/32)and 3.13%(1/32)in group A
which was significantly lower than that in group C(30.00%
9/30)
30.00%(9/30)(P<0.017).For safety analysis
adverse reaction was found in neither group A nor group B
except for 1 case of somnolence
1 case of dizziness
1 case of stomach discomfort in group C.Conclusion: Ephedra decoction of original dosage can effectively shorten the course of influenza
alleviate influenza symptoms
shorten fever time and reduce the incidence of influenza complications.The clinical curative effect was significantly better than Ephedra decoction of conventional dosage or dextromethorphan hydrobromide granules.Ephedra decoction of original dosage is effective and quite safe in treating early influenza.
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