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1.
目的 评价通腑泻肺方对痰热遏肺型慢性阻塞性肺疾病急性加重(acute exacerbation of chronic obstructive pulmonary disease,AECOPD)患者的疗效.方法 将符合入选标准的78例AECOPD患者采用随机数字表法分为2组,每组39例.对照组采用西医常规疗法并给予安慰剂治疗,治疗组在西医常规疗法基础上配合口服通腑泻肺方颗粒剂.2组均治疗2周,随访4周.观察2组治疗前后及随访期间症状、体征积分,圣乔治呼吸问卷(St George's breath questionnaire,SGRQ)评分及血气分析变化,评价临床疗效,记录不良反应.结果 治疗后,治疗组咳嗽[(2.34±1.11)分比(2.67±1.05)分,t=2.277]、咳痰[(1.91±1.41)分比(2.35±1.83)分,t=2.106]、喘憋[(1.73±1.15)分比(2.04±1.53)分,t=2.214]评分低于对照组(P<0.05),SGRQ评分[(42.47±17.24)分比(59.95±17.58)分,t=2.112]低于对照组(P<0.05).治疗组总有效率为91.9%(34/37)、对照组为84.4%(27/32),2组比较差异有统计学意义(χ2=4.578,P=0.040).结论 通腹泻肺方可有效缓解痰热壅肺型AECOPD患者的症状、体征,改善血气分析指标.  相似文献   

2.
目的 评价丹红注射液联合针刺治疗血管性帕金森综合征(vascular parkinsonism,VP)的疗效.方法 将符合入选标准的98例VP患者按随机数字表法分为2组,每组49例.对照组采用西医常规疗法治疗,观察组在对照组基础上加用丹红注射液及针刺治疗.2组均治疗8周.采用帕金森病综合评价量表进行运动功能评分,采用中医症状量表进行非运动功能评分;采用超声经颅多普勒血流分析仪检测脑血流动力学指标,采用全自动血液流变仪检测血浆黏度和纤维蛋白原含量,评价临床疗效.结果 观察组总有效率为87.8%(43/49)、对照组为71.4%(35/49),2组比较差异有统计学意义(χ2=4.021,P<0.05).治疗后,观察组运动功能评分[(27.4±10.5)分比(32.8±8.2)分,t=2.865]、非运动功能评分[(4.1±2.2)分比(9.8±4.0)分,t=8.785]均低于对照组(P<0.05);血浆黏度[(1.49±0.21)mPa?s比(1.64±0.28)mPa?s,t=3.000]、纤维蛋白原[(3.18±0.77)g/L比(3.86±0.70)g/L,t=4.574]、阻力指数[(0.49±0.12)比(0.62±0.16),t=4.550]均低于对照组(P<0.05);收缩期最大血流速度[(81.97±12.65)cm/s比(74.39±9.48)cm/s,t=3.357]、平均血流速度[(61.54±7.10)cm/s比(55.87±6.24)cm/s,t=4.199]高于对照组(P<0.05).观察组不良反应发生率为14.3%(7/49)、对照组为16.3%(8/49),2组比较差异有统计学意义(χ2=0.079,P>0.05).结论 丹红注射液结合针刺可改善VP患者临床症状及血液循环,提高疗效.  相似文献   

3.
目的 观察自拟疏木运土止咳方结合西医常规疗法治疗胃食管反流性咳嗽(gastroesophageal reflux cough,GERC)的疗效.方法 将符合入选标准的64例GERC患者按随机数字表法分为2组,每组32例.对照组口服莫沙必利片与雷贝拉唑肠溶胶囊,治疗组在对照组基础上加服自拟疏木运土止咳方,2组均治疗8周.分别于治疗前后采用VAS评分法评价咳嗽强度,采用反流性疾病问卷(Reflux Diagnostic Questionnaire,RDQ)评价胃反流症状的变化,采用慢性咳嗽影响量表(Chronic Cough Impact Questionnaire,CCIQ)评价患者近2周咳嗽严重程度及对生活质量的影响.结果 治疗后4周,治疗组VAS评分[(4.47±1.32)分比(6.22±1.34)分,t=-5.859]、CCIQ评分[(32.60±5.83)分比(47.32±5.56)分,t=-11.548]较对照组降低(P<0.01),RDQ评分[(13.62±2.89)分比(13.67±2.77)分,t=-0.079]与对照组比较,差异无统计学意义(P>0.05).治疗后8周,治疗组VAS评分[(2.57±1.69)分比(4.55±2.06)分,t=-4.676]、CCIQ评分[(12.47±3.41)分比(23.47±3.55)分,t=-14.126]较对照组降低(P<0.01),RDQ评分[(9.18±2.77)分比(9.30±2.43)分,t=-0.202]与对照组比较,差异无统计学意义(P>0.05).治疗后,治疗组总有效率为90.6%(29/32)、对照组为68.8%(22/32),2组比较差异有统计学意义(χ2=4.730,P=0.030).结论 自拟疏木运土止咳方结合西医常规疗法可较好改善GERC患者的反酸、咳嗽症状.  相似文献   

4.
目的 评价玉屏风散加味结合西医常规疗法治疗慢性支气管炎急性发作的疗效.方法 将符合入选标准的慢性支气管炎急性发作患者80例,采用随机数字表法分为2组,每组40例.对照组采用西医常规疗法治疗,治疗组在对照组基础上结合玉屏风散加味治疗.2组均治疗2周.采用肺功能检测仪检测用力肺活量(forced vital capacity,FVC)、深吸气量(total lung capacity,TLC)、肺活量(vital capacity,VC)、最大通气量(maximal voluntary ventilation,MVV);采用全自动免疫发光分析仪和血液分析仪检测hs-CRP、WBC和中性粒细胞百分比;分别于治疗前后进行中医证候积分评估,评价临床疗效.结果 观察组总有效率为92.5%(37/40)、对照组为72.5%(29/40),2组比较差异有统计学意义(χ2=5.541,P=0.037).治疗后,观察组中医证候积分[(4.58±1.16)分比(7.74±2.35)分,t=3.256]低于对照组(P<0.05);FVC[(2.58±0.35)L比(2.15±0.32)L,t=5.664]、TLC[(2.68±0.49)L比(2.41±0.37)L,t=3.523]、VC[(2.43±0.38)L比(1.52±0.35)L,t=11.152]、MVV[(72.5±14.54)L比(51.2±12.47)L,t=7.305]高于对照组(P<0.01);血清hs-CRP[(12.55±4.55)mg/L比(24.72±5.70)mg/L,t=3.543]、WBC[(5.03±1.10)×109/L比(7.52±1.41)×109/L,t=2.347]、中性粒细胞[(60.32±4.49)%比(71.13±4.14)%,t=3.651]水平低于对照组(P<0.01).结论 玉屏风散加味结合西医常规疗法可改善慢性支气管炎急性发作患者的肺功能,降低炎性细胞因子水平,提高临床疗效.  相似文献   

5.
目的 观察真武汤合并苓桂术甘汤加减联合西医常规疗法治疗老年心功能衰竭患者的疗效.方法 将符合入选标准的123例心功能衰竭患者采用随机数字表法分为3组,每组41例.对照组采用西医常规疗法治疗,真武汤组在对照组基础上加用真武汤,合方组在对照组基础上加用真武汤合苓桂术甘汤.3组均治疗8周,随访1个月.分别于治疗前后采用放射免疫分析法检测脑钠肽(brain natriuretic peptide,BNP)、N端B型利钠肽原(nt-proBNP),采用ELISA法检测TGF-?1,采用心脏超声检测仪检测左心室射血分数(left ventricular ejection fraction,LVEF);比较3组治疗前后中医症状、体征积分,评价临床疗效.结果 治疗后8周,合方组心悸[(0.68±0.53)分比(0.79±0.64)分、(1.12±0.70)分,F=7.207]、胸闷[(0.66±0.52)分比(0.79±0.60)分、(1.36±0.70)分,F=6.367]、浮肿[(0.32±0.31)分比(0.43±0.41)分、(0.52±0.37)分,F=7.054]、喘息[(0.62±0.55)分比(0.82±0.69)分、(0.88±0.68)分,F=6.634]、乏力[(0.73±0.47)分比(0.94±0.62)分、(1.49±0.58)分,F=5.832]、自汗[(0.46±0.39)分比(0.89±0.62)分、(0.99±0.79)分,F=7.207]、眠差[(0.42±0.39)分比(0.74±0.50)分、(0.79±0.58)分,F=6.672]评分均低于真武汤组与对照组(P<0.05);血清TGF-?1[(102.75±15.79)ng/L比(121.57±19.25)ng/L、(184.35±23.74)ng/L,F=160.776]水平低于真武汤组与对照组(P<0.01).合方组总有效率为81.8%(27/33)、真武汤组为78.1%(25/32)、对照组为62.16%(23/37),3组比较差异有统计学意义(χ2=7.089,P=0.037).结论 真武汤合苓桂术甘汤联合西医常规疗法可改善老年心功能衰竭患者的症状、体征,降低血清TGF-?1水平.  相似文献   

6.
目的 评价针刺王氏五脏俞加膈俞治疗女性肝气郁结型更年期抑郁症(climacteric depression,CD)的疗效.方法 将符合入选标准的肝气郁结型CD患者82例采用随机数字表法分为2组,每组41例.对照组口服盐酸氟西汀(百忧解),观察组采用针刺五脏俞加膈俞治疗,2组均治疗6周.全部患者分别于治疗前后进行汉密顿抑郁量表(Hamilton Depression Scale,HAMD)评分,计算减分率,比较中医证候积分变化,评价临床疗效.结果 观察组总有效率为97.6%(40/41)、对照组为82.9%(34/41),2组比较差异有统计学意义(χ2=4.986,P=0.026).治疗后,观察组HAMD评分[(7.7±4.3)分比(10.2±4.4)分,t=2.551]低于对照组,HAMD减分率[(55.1±13.3)%比(41.5±15.2)%,t=4.327]高于对照组(P<0.01);观察组中医证候评分[(2.5±1.8)分比(3.7±2.3)分,t=2.692]低于对照组(P<0.01).结论 针刺五脏俞加膈俞可改善肝气郁结型女性CD患者的症状和情绪状态,提高临床疗效.  相似文献   

7.
目的 探讨乳癌康复汤对乳腺癌术后患者生命质量的影响.方法 将符合入选标准的107例乳腺癌术后患者,采用随机数字表法分为对照组54例和观察组53例.对照组给予常规放化疗及对症支持治疗,观察组在对照组基础上加服乳癌康复汤治疗.2组均治疗12个月,随访6个月.采用欧洲癌症研究与治疗组织生命质量量表(quality of life questionnaire-core 30,QLQ-C30)和乳腺癌生存质量量表(quality of life questionnaire-breast cancer module 23,QLQ-BR23)评价乳腺癌术后患者生命质量.结果 治疗后,观察组QLQ-C30量表功能维度中躯体功能[(76.4±16.6)分比(70.4±16.4)分,t=-2.087]、角色功能[(59.2±12.8)分比(54.6±12.8)分,t=-2.085]、情绪功能[(77.2±17.0)分比(71.2±16.7)分,t=-2.075]、认知功能[(38.5±14.7)分比(34.3±11.6)分,t=2.104]、社会功能[(59.3±12.4)分比(54.6±12.8)分,t=-2.105]评分及总体健康状况[(76.7±19.7)分比(65.5±18.6)分,t=-2.152]评分均高于对照组(P<0.05);症状维度中疲乏[(40.9±8.4)分比(45.3±9.6)分,t=2.149]、恶心呕吐[(42.9±8.8)分比(47.5±10.1)分,t=2.145]、疼痛[(36.9±7.6)分比(40.9±8.7)分,t=2.143]、呼吸困难[(44.8±9.2)分比(49.6±10.6)分,t=2.148]、失眠[(41.8±8.6)分比(46.3±9.9)分,t=2.152]、食欲丧失[(35.0±7.2)分比(38.7±8.2)分,t=2.113]、便秘[(15.9±3.3)分比(17.6±3.8)分,t=2.057]、腹泻[(15.2±3.1)分比(16.9±3.6)分,t=2.092]评分均低于对照组(P<0.05).观察组QLQ-BR23量表中体型[(74.7±18.5)分比(64.8±15.4)分,t=-2.153]、性功能[(36.3±9.0)分比(42.8±10.2)分,t=2.045]、性乐趣[(41.4±10.2)分比(48.9±11.6)分,t=2.046]、未来看法[(67.6±16.7)分比(58.6±14.0)分,t=-2.132]、系统疗法副作用[(48.2±10.4)分比(55.2±12.2)分,t=2.149]、乳房症状[(39.6±8.6)分比(45.5±10.2)分,t=2.127]、手臂症状[(30.3±6.6)分比(34.8±7.7)分,t=2.129],脱发引起的烦恼[(36.1±7.8)分比(41.4±9.1)分,t=2.113]评分均高于对照组(P<0.05).结论 乳癌康复汤可调整乳腺癌术后患者的精神状态,提高生命质量.  相似文献   

8.
目的 观察中药熏洗联合康复锻炼对肘关节恐怖三联征术后关节功能恢复的影响.方法 将符合纳入标准的60例肘关节恐怖三联征术后患者按随机数字表法分为2组,每组30例.治疗组采用中药熏洗联合康复锻炼治疗,对照组采用康复锻炼治疗.2组均治疗8周.观察患者治疗前后肘关节活动度及De Boer YA肘关节功能评分变化,评价临床疗效.结果 治疗组优良率为83.3%(25/30)、对照组为60.0%(18/30),2组比较差异有统计学意义(χ2=4.021,P=0.044).治疗后8周,治疗组肘关节屈曲[(126.98±10.46)°比(120.86±10.37)°,t=2.275]、过伸[(8.26±1.23)°比(6.79±1.29)°,t=4.517]、旋前[(80.46±8.60)°比(74.79±8.52)°,t=2.565]、旋后[(78.53±8.26)°比(73.42±8.20)°,t=2.404]角度均大于对照组(P<0.05或P<0.01);De Boer YA肘关节功能评分中,疼痛[(27.13±2.56)分比(24.86±2.42)分,t=3.529]、日常活动[(32.26±4.24)分比(29.48±4.36)分,t=2.503]、运动[(31.46±4.66)分比(28.74±4.59)分,t=2.277]评分及总分[(90.42±8.76)分比(83.82±8.42)分,t=2.975]均高于对照组(P值均<0.01).结论 中药熏洗联合康复锻炼可促进肘关节恐怖三联征术后关节功能的恢复.  相似文献   

9.
目的:评价桂枝茯苓丸加减结合西医常规疗法治疗T2DM合并DPN患者的疗效。方法将78例DPN患者按随机数字表法分为治疗组40例,对照组38例。对照组在常规治疗基础上口服甲钴胺片,治疗组在对照组基础上服用桂枝茯苓丸加减。2组均治疗2周。检测患者治疗前后血清同型半胱氨酸水平(homocysteine, Hcy)及运动神经传导速度(motor nerve conduction velocity, MNCV)和感觉神经传导速度(sensory nerve conduction velocity, SNCV),采用多伦多神经病变评分(Toronto clinical scoring system, TCSS)评价疗效。结果治疗组总有效率为95.0%(38/40)、对照组为76.3%(29/38),2组比较差异有统计学意义(χ2=5.616,P=0.018)。治疗后,治疗组MNCV中腓总神经[(46.1±6.3)m/s比(42.5±5.5)m/s,t=2.734]、正中神经[(49.8±5.2)m/s 比(46.3±5.9)m/s , t=2.607],以及 SNCV 中腓总神经[(38.5±4.6)m/s 比(35.4±4.3)m/s,t=3.105]、正中神经[(45.3±5.2)m/s 比(42.3±4.8)m/s,t=2.627]的传导速度均快于对照组(P<0.05);治疗组TCSS评分[(5.3±3.1)分比(7.2±2.9)分,t=2.823]及血清Hcy水平[(13.3±3.2)μmol/L比(17.1±3.4)μmol/L,t=5.178]低于对照组(P<0.05)。结论桂枝茯苓丸加减结合西医常规疗法可提高DPN患者神经传导速度,降低Hcy水平,提高临床疗效。  相似文献   

10.
目的 评价防旋髓内钉联合健步虎潜膏治疗高龄股骨转子间骨折伴骨质疏松症患者的疗效.方法 将符合入选标准的高龄骨质疏松症患者单侧股骨转子间骨折85例,采用随机数字表法分为对照组45例和观察组40例.2组患者均行股骨近端防旋髓内钉内固定治疗,观察组在此基础上联用健步虎潜膏治疗.2组均连续观察6个月.采用VAS量表评价患者疼痛程度,采用Harris髋关节评分表评价髋关节功能,比较治疗前后股骨粗隆及Ward区的骨密度差异,记录骨痂出现时间、下地行走时间、骨折愈合时间及并发症.结果 观察组VAS疼痛评分在治疗后1周[(6.2±1.6)分比(7.9±1.6)分,t=3.683]、3周[(3.1±1.1)分比(5.4±1.4)分,t=4.239]、7周[(2.3±0.9)分比(4.0±1.3)分,t=3.571]时低于对照组(P<0.05);骨痂出现时间[(42.4±5.9)d比(49.2±6.2)d,t=4.139]、下地行走时间[(6.9±1.1)周比(8.7±1.2)周,t=3.695]、骨折愈合时间[(13.6±2.2)周比(16.2±3.1)周,t=3.473]均较对照组缩短(P<0.05);Harris髋关节评分[(89.8±7.2)分比(81.4±5.9)分,t=3.728]高于对照组(P<0.05);股骨粗隆骨密度[(0.782±0.142)g/cm2比(0.691±0.135)g/cm2,t=3.759]、Ward三角区骨密度[(0.628±0.071)g/cm2比(0.513±0.059)g/cm2,t=4.386]高于对照组(P<0.05);观察组与治疗后并发症发生率为15.0%(6/40)、对照组为37.8%(17/45),2组比较差异有统计学意义(χ2=5.567,P<0.05).结论 健步虎潜膏联合防旋髓内钉可减轻高龄股骨转子间骨折伴骨质疏松症患者疼痛程度,促进骨折愈合,有效预防术后并发症.  相似文献   

11.
目的 探讨针灸联合中药保留灌肠对急性盆腔炎患者子宫血流动力学指标及血清高迁移率族蛋白1(high mobility group box-1 protein,HMGB1)、toll样受体4(toll-like Receptor 4,TLR4)水平的影响.方法 将符合入选标准的66例急性盆腔炎患者按随机数字表法分为2组,每组33例.常规治疗组采用西医常规治疗治疗,联合治疗组在常规治疗组基础上给予针灸联合中药保留灌肠治疗.2组均治疗10d.采用彩色多普勒超声诊断仪检测子宫血流动力学指标,包括最大血流速度(maximum velocity,Vmax)、搏动指数(pulsatility index,PI)、阻力指数(resistance index,RI).采用ELISA法检测血清HMGB1、TLR4水平,评价临床疗效.结果 联合治疗组总有效率为90.91%(30/33)、常规治疗组为69.70%(23/33),2组比较差异有统计学意义(χ2=8.246,P<0.05).治疗后,联合治疗组Vmax左侧[(39.16±0.73)cm/s比(35.47±0.83)cm/s]、右侧[(41.23±1.12)cm/s比(36.24±0.75)cm/s]高于常规治疗组(P<0.01),PI左侧[(2.23±0.25)cm/s比(3.11±0.45)cm/s]、右侧[(2.17±0.22)cm/s比(2.62±0.23)cm/s],RI左侧[(0.48±0.08)cm/s比(0.73±0.13)cm/s]、右侧[(0.43±0.11)cm/s比(0.71±0.16)cm/s]低于常规治疗组(P<0.01);血清HMGB1[(17.45±5.01)ng/ml比(21.32±6.15)ng/ml,t=2.803]、TLR4[(1.05±0.64)ng/ml比(1.75±0.91)ng/ml,t=3.614]水平低于常规治疗组(P<0.01).结论 针灸联合中药保留灌肠可较好改善急性盆腔炎患者子宫血流动力学状态,其机制可能与抑制HMGB1、TLR4释放及其诱发的炎症反应有关.  相似文献   

12.
针刺辨证治疗中风后抑郁症150例临床观察   总被引:2,自引:0,他引:2  
目的:观察针刺辨证治疗中风后抑郁症的临床疗效。方法:300例中风后抑郁症患者随机分为针刺组150例(以"四神针"为主穴,配合中医证候分型取穴,每日1次)及氟西汀组150例(口服氟西汀每日20mg),两组疗程均为2个月。分别在治疗前后用汉密尔顿抑郁量表(HAMD)对两组患者进行评定,统计两组疗效,并对疗效与证型的关系进行分析。结果:治疗后,两组的HAMD评分均较治疗前明显下降(P0.05);针刺组HAMD的评分优于氟西汀组(P0.05)。针刺组总有效率为89.3%(134/150),氟西汀组总有效率为76.0%(114/150),两组比较差异有统计学意义(P0.05)。针刺组各证型的疗效也均优于氟西汀组(均P0.05)。结论:针刺辨证治疗中风后抑郁症疗效较好。  相似文献   

13.
目的:观察针刺治疗脑卒中后抑郁及对患者神经功能康复的干预作用。方法:将200例PSD患者随机分为两组,针刺组给予醒脑安神通络针法,药物组口服盐酸氟西汀胶囊。治疗8周末采用汉密尔顿抑郁量表(HAMD)、美国国立卫生研究院卒中量表(NIHSS)、日常生活活动能力量表Barthel指数评定临床疗效,并观察两组不良反应。结果:针刺组总有效率为96%,药物组总有效率为87%,两组比较差异有统计学意义(P<0.05);针刺组在改善患者HAMD、NIHSS、Barthel指数、TESS评分方面显著优于药物组(P<0.01)。结论:针刺疗法可以有效改善脑卒中后抑郁症状,促进患者神经功能康复,明显提高患者生活质量,副作用少。  相似文献   

14.
张毅敏 《针刺研究》2006,31(3):166-168
目的:观察针刺配合口服真人益智宝对先天愚型儿童智商(IQ)及社会适应行为(ADQ)的影响。方法:将50例先天愚型儿童分为针药结合组与药物组。针刺以头三针为主,配合体针,药物采用口服香港宗歧氏药厂生产的真人益智宝。治疗前后均采用斯坦福-比奈智力量表、儿童社会适应能力量表对患儿进行IQ、ADQ测定。结果:针药结合及单纯口服药物均能提高先天愚型患儿的IQ及ADQ水平(均P<0·01);针药结合对IQ、ADQ的影响较单纯口服药物更为明显(P<0·01)。结论:针刺配合口服真人益智宝能提高先天愚型儿童智商及社会适应能力水平,其疗效优于单纯口服真人益智宝。  相似文献   

15.
目的 评价直流感应电定向透穴疗法治疗特发性面神经炎的疗效.方法 将符合入选标准的65例特发性面神经炎患者按随机数字表法分为治疗组33例和对照组32例,对照组采用西医常规疗法治疗,治疗组在对照组基础上配合地仓透颊车、阳白透太阳直流感应单向脉冲波定向透穴治疗.2组均治疗3周.分别于治疗前后行House-Brackmann面神经功能分级评估及肌电图瞬目反射检测,评价患者临床疗效及面神经功能的改善情况.结果 治疗组总有效率为66.7%(22/33)、对照组为43.8%(14/32),2组比较差异有统计学意义(U=2.175,P=0.013).治疗后,治疗组House-Brackmann面神经功能Ⅰ级15例、Ⅱ级4例、Ⅲ级3例,对照组Ⅰ级5例、Ⅱ级7例、Ⅲ级2例,2组比较差异有统计学意义(U=2.069,P=0.018);治疗组瞬目反射R1、R2波检出率为87.9%(29/33)、对照组为81.3%(26/32),2组比较差异有统计学意义(U=2.135,P=0.016).治疗后,治疗组瞬目反射R1波[(12.28±2.55)ms比(13.84±3.07)ms,t=2.227]、R2波[(32.28±7.08)ms比(35.95±5.11)ms,t=2.396]潜伏期低于对照组(P值分别为0.030、0.020).结论 直流感应电定向透穴疗法可缩短特发性面神经炎患者瞬目反射R1、R2波,提高临床疗效.  相似文献   

16.

Objective

To explore the therapeutic effects of scalp acupuncture on sleep disorder induced by pre-examination anxiety in the undergraduates.

Methods

A total of 60 undergraduates with sleep disorder induced by the final examination anxiety were randomized into three groups, named a control group (20 cases), a traditional acupuncture group (20 cases) and a scalp acupuncture group (20 cases). In the control group, no any treatment was given. In the traditional acupuncture group, acupuncture was given at Sìshéncōng (四神聪EX-HN1), bilateral Shénmén (神门HT 7) and bilateral Sānyīnjiāo (三阴交SP 6). The needles were manipulated with the even-needling technique and retained for 30?min. In the scalp acupuncture group, acupuncture was applied to upper-middle line of occiput (枕上正中线MS 12), middle line of vertex (顶中线MS 5) and middle line of forehead (额中线MS 1). The needles were manipulated with the even-needling technique and retained for 30?min. The treatment was given once a day and 5 treatments made one course. There were 2 days at interval among the courses. The therapeutic effects were analyzed statistically after 4 courses of treatment. Before and after treatment, the Hamilton anxiety scale (HAMA) and the Pittsburgh sleep quality index (PSQI) were adopted to evaluate the conditions of pre-examination anxiety and sleep in the patients.

Results

In comparison of PSQI score, compared with those before treatment, the score in the scalp acupuncture group (12.95?±?1.76?vs 15.95?±?1.82) and in the traditional acupuncture group (13.75?±?1.62?vs 15.75?±?1.86) after 1-week of treatment were reduced (both P?<?0.05). Compared with control group, the score in the scalp acupuncture group (12.95?±?1.76 vs15.78?±?2.02) and in the traditional acupuncture group (13.75?±?1.62?vs 15.78?±?2.02) were better (both P?<?0.05). The difference was not significant between the scalp acupuncture group and the traditional acupuncture group (P?>?0.05). In 2 and 4 weeks of treatment, as well as 1 week after treatment termination, compared with the control group at the same time point, the scores in the scalp acupuncture group (in 2-week treatment: 8.95?±?1.88?vs 15.94?±?1.89, in 4-week treatment: 5.95?±?1.05?vs 16.5?±?1.95, 1 week after treatment termination: 4.7?±?0.77?vs 9.78?±?2.10) and the traditional acupuncture group (in 2-week treatment: 11.15?±?1.31?vs 15.94?±?1.89, in 4-week treatment: 8.05?±?0.89?vs 16.5?±?1.95, 1 week after treatment termination: 6.25?±?0.85?vs 9.78?±?2.10) were all lower (all P?<?0.05) separately. The scores in the scalp acupuncture group were superior to the traditional acupuncture group (all P?<?0.05). In comparison of HAMD score, compared with those before treatment, the score in the scalp acupuncture group (22.4?±?5.31?vs 25.2?±?6.18) and in the traditional acupuncture group (22.4?±?5.31?vs 25?±?5.97) after 1-week of treatment were reduced (both P?<?0.05). Compared with control group, the score in the scalp acupuncture group (22.4?±?5.31?vs 23.28?±?5.53) and in the traditional acupuncture group (22.4?±?5.31?vs 23.28?±?5.53) were better (both P?<?0.05). The difference was not significant between the scalp acupuncture group and the traditional acupuncture group (P?>?0.05). In 2 and 4 weeks of treatment, as well as 1 week after treatment termination, compared with the control group at the same time point, the scores in the scalp acupuncture group (in 2-week treatment: 18.5?±?4.56?vs 24.22?±?5.22, in 4-week treatment: 5.8?±?3.52?vs 21.22?±?6.7,1 week after treatment termination: 4.55?±?2.72?vs 11.78?±?9.36) and the traditional acupuncture group (in 2-week treatment: 17.5?±?4.59?vs 24.22?±?5.22, in 4-week treatment: 6.95?±?3.33?vs 21.22?±?6.7, 1 week after treatment termination: 5.8?±?2.76?vs 11.78?±?9.36) were all lower (all P?<?0.05) separately. The scores in the scalp acupuncture group were superior to the traditional acupuncture group (all P?<?0.05). In 4-week treatment and 1 week after treatment termination, compared with control group, the total effective rates in the traditional acupuncture group (in 4-week treatment: 95% vs 11%, 1 week after treatment termination: 100% vs 83.33%, both P?<?0.05) and the scalp acupuncture group (in 4-week treatment: 95% vs 11%, 1 week after treatment termination: 100% vs 83.33%, both P?<?0.05) were better and the difference was not significant between the traditional acupuncture group and the scalp acupuncture group (both P?>?0.05).

Conclusion

Both scalp acupuncture and traditional acupuncture therapies are effective on sleep disorder induced by pre-examination anxiety in the undergraduates. The scalp acupuncture therapy achieves the better effects on the instant relief of symptoms.  相似文献   

17.
目的:通过随机对照的研究方法观察针药结合疗法治疗卒中后抑郁的综合疗效。方法:将150例卒中后抑郁患者随机分为药物治疗组、针刺治疗组与针药结合组,采用单盲的方法观察三组患者治疗前后HAMD、肢体功能、ADL及血清NE与5-HT含量的变化情况。结果:三组患者治疗前后HAMD、肢体功能、ADL及血清NE与5-HT含量均有显著改善,其中针药结合组在这些指标治疗前后差值方面显著优于药物治疗组与针刺治疗组。结论:针药结合疗法治疗卒中后抑郁较单纯针刺或药物治疗均显示出了明显的综合优势。  相似文献   

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