Clinical efficacy and mechanism of Banxia Houpu Decoction in the treatment of refractory gastroesophageal reflux disease
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摘要:
目的观察半夏厚朴汤加减治疗难治性胃食管反流病的疗效并探讨其机制。 方法选择符合诊断标准的80例患者通过随机分配方案隐匿的方法(按顺序编码、不透光、密封的信封)分为实验组和对照组,对照组给予雷贝拉唑及莫沙必利治疗,实验组在上述西药基础上配合半夏厚朴汤加减煎服,观察8周,治疗前后分别进行胃食管反流病诊断问卷症状积分(Gerd Q),评分及高分辨率食管测压检查。 结果治疗后实验组Gerd Q积分与对照组相比有明显改善,实验组总有效率为94.74%,对照组总有效率为77.14%,且实验组食管食管下括约肌静息压力治疗后(15.01±7.79 mmHg)较治疗前(14.35±7.83 mmHg)有明显升高,差异均有统计学意义(P < 0.05)。 结论半夏厚朴汤治疗难治性胃食管反流病临床疗效显著,可改善食管食管下括约肌静息压力。 Abstract:ObjectiveTo observe the clinical effect and mechanisms of Banxia Houpu decoction for refractory gastroesophageal reflux disease (rGERD). MethodsA total of 80 patients were randomly divided into two groups. The control group was given rabeprazole and mosapride. The experimental group was administered with Pinelliae and Magnoliae Officinalis Decoction besides the western medicine. Gerd Q and high resolution manometry were performed before and after 8 week treatment. ResultsAfter treatment, the Gerd Q score of the experimental group was significantly improved compared with the control group. The total effective rate of experimental group was 94.74% while the control group was 77.14%. And the resting pressure of esophageal LES (15.01±7.79 mmHg) was significantly higher than that before treatment (14.35±7.83 mmHg) in the experimental group. The difference was statistically significant (P < 0.05). ConclusionBanxia Houpu decoction has significant effect in treatment of rGERD. It can improve the resting pressure of the esophageal LES. -
表 1 两组研究对象的基本资料
组别 年龄(岁) 男性[n(%)] 病程(月) 对照组(n=35) 47.62±9.74 24(68.57) 28.62±12.56 实验组(n=38) 48.71±10.18 28(73.68) 30.13±12.22 P 0.338 0.630 0.476 表 2 两组研究对象Gerd Q积分比较(x±s,分)
组别 治疗前 治疗后 治疗前后积分差值 对照组(n=35) 18.27±1.34 8.24±1.43* 9.67±1.44 实验组(n=38) 17.98±1.41 6.38±1.46* 11.78±1.48** *P<0.05 vs 治疗前; **P<0.05 vs 对照组. 表 3 两组研究对象临床疗效比较[n%)]
组别 痊愈 显效 有效 无效 总有效率(%) 对照组(n=35) 4(11.43) 17(48.57) 6(17.14) 8(22.9) 77.14 实验组(n=38) 6(15.79) 21(55.26) 9(23.68) 2(5.26) 94.74* *P<0.05 vs 对照组. 表 4 两组研究对象食管LES静息压的比较(x±s,mmHg)
组别 治疗前 治疗后 对照组(n=35) 14.32±7.92 14.35±7.84 实验组(n=38) 14.35±7.83 15.01±7.79* *P<0.05 vs 治疗前. -
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