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作 者:江舒曼[1] 贾林[1] 李伟冬[1] 邓聪[2] JIANG Shu-man;JIA Lin;LI Wei-dong;DENG Cong(Department of Gastroenterology,Guangzhou First People's Hospital,Guangzhou 510180,Guangdong,China)
机构地区:[1]广州市第一人民医院消化内科,广东广州510180 [2]广州市第一人民医院中医科,广东广州510180
出 处:《广东医学》2018年第20期3119-3122,共4页Guangdong Medical Journal
基 金:广州市卫计委医药卫生科技项目(编号:20172A011003)
摘 要:目的探讨半夏厚朴清心汤联合经皮穴位电刺激(TEAS)治疗癔球症的临床疗效。方法选取广州市第一人民医院南沙医院消化专科门诊癔球症患者75例,经知情同意后随机分为常规对照组(泮托拉唑,40 mg/d)、半夏厚朴汤组、半夏厚朴清心汤组、联合治疗组(半夏厚朴清心汤+TEAS),各组15例,疗程均为4周。在治疗前后及过程中,采用高分辨率食管测压(HRM)进行食管上括约肌(UES)及食管下括约肌(LES)检测,结合癔球症症状评分(GETS)、汉密尔顿抑郁/焦虑量表(HAMD/HAMA)及匹兹堡睡眠质量指数(PSQI)进行疗效评估。结果治疗4周后,联合治疗组UES、GETS评分、HAMD/HAMA评分及PSQI评分均较治疗前明显改善,且优于其余各组,差异有统计学意义(P <0. 05)。结论联用半夏厚朴清心汤及TEAS治疗癔球症具有良好的临床疗效,为进一步临床推广提供有力证据。Objective To investigate the clinical therapeutic effect of the combination of modified Banxia Houpu decoction and transcutaneous electrical acupoint stimulation( TEAS) on globus pharyngeus. Methods After informed consent,75 out-patients with globus pharyngeus from Department of Gastroenterology in Guangzhou First People's Hospital Nansha Hospital were randomly divided into normal control group( pantoprazole,40 mg/d),Banxia Houpu decoction group,modified Banxia Houpu decoction group,TEAS group,and combinative treatment group( modified Banxia Houpu decoction + TEAS),with 15 cases in each group and a 4-weeks treatment course. Before and after the treatment,high-resolution manometry( HRM) was used to measure the pressure of upper oesophageal sphincter( UES) and lower esophageal sphincter( LES),meanwhile Glasgow-Edinburgh Throat Scale( GETS),Hamilton Rating Scale Anxiety/Depression( HAMD/HAMA) and Pittsburgh Sleep Quality Index( PSQI) were used to assess the therapeutic effects.Results After 4 weeks of treatment,UES,GETS,HAMD/HAMA and PSQI were obviously improved in combinative treatment group,and superior to other groups,with significant difference( all P〈0. 05). Conclusion The combination of modified Banxia Houpu decoction and TEAS exhibited a good clinical therapeutic effect on globus pharyngeus,and it provides strong evidence for further clinical promotion.
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