“先心1号汤”治疗小儿先天性心脏房、室间隔缺损的疗效观察

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目的:探讨中药“先心1号汤”治疗小儿单纯性先天性房、室间隔缺损的疗效。方法:将小儿单纯性先天性房、室间隔缺损患儿随机分为2组。治疗组133例中男66例,女67例;年龄6个月~10岁(平均4.3岁);房间隔缺损(房缺)75例,室间隔缺损(室缺)58例。对照组105例中男49例,女56例;年龄4个月~9岁(平均4.1岁);房缺61例,室缺44例。2组患儿年龄,房、室间隔缺损分型均具可比性。治疗组用“先心1号汤”治疗;对照组不用药,观察缺损自然闭合情况。结果:治疗组患儿服药2个疗程后房缺痊愈54例(40.6%),好转15例(11.3%);室缺痊愈40例(30.1%),好转13例(9.8%),总有效率91.7%。对照组房缺痊愈4例(3.8%),好转6例(5.7%);室缺痊愈5例(4.8%),好转4例(3.8%),总有效率18.1%。2组疗效比较,治疗组疗效显著优于对照组,差异显著(P<0.01)。结论:“先心1号汤”治疗小儿单纯性先天性房、室间隔缺损疗效肯定,安全可靠,无毒副作用,值得临床推广。确切机制尚待探讨。 Objective: To investigate the curative effect of traditional Chinese medicine “Xian Xin Yi Tang” in the treatment of simple congenital atria and ventricular septal defect in children. Methods: Children with simple congenital atrial septal defect were randomly divided into two groups. In the treatment group, there were 66 males and 67 females in 133 cases, ranging in age from 6 months to 10 years (mean, 4.3 years). There were 75 cases of atrial septal defect (atrial septal defect) and 58 cases of ventricular septal defect (atrial septal defect). The control group of 105 patients, 49 males and 56 females; aged 4 months to 9 years (mean 4.1 years); atrial septal defect in 61 cases, 44 cases of ventricular septal defect. Two groups of children age, room, ventricular septal defect type were comparable. Treatment group with “heart No. 1 soup” treatment; control group without medication to observe the natural closure of defects. Results: In the treatment group, 54 cases (40.6%) were ameliorated in 15 cases (11.3%), 40 cases (30.1%) were cured, 13 cases improved (9 .8%), the total effective rate of 91.7%. In the control group, 4 cases (3.8%) were cured and 6 cases (5.7%) were cured, 5 cases (4.8%) were cured, 4 cases (3.8%) were improved, and the total effective rate was 18 .1%. The curative effect of the two groups was significantly better than that of the control group, the difference was significant (P <0.01). Conclusion: “Xian Xin Yi Tang” treatment of children with congenital simplex room, ventricular septal defect sure, safe, reliable, non-toxic side effects, is worthy of clinical promotion. The exact mechanism remains to be explored.
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