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ID:32851993
大小:2.57 MB
页数:40页
时间:2019-02-16
《补肾活血熄风方治疗血管性帕金森综合征的临床研究》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、目的:探讨补肾活血熄风方治疗血管性帕金森综合征(VPS)患者的临床有效性和安全性,从而拓宽中医药治疗VPS的新思路及方法。方法:选取符合标准的病例60例,随机分为治疗组和对照组各30例。治疗组予补肾活血熄风方,水煎服日一剂:对照组予美多芭125-250mg/天口服。两组均治疗8周后观察治疗前后临床症状与体征的变化情况,评定国际通用统一帕金森病评定量表(UPDRS)评分,以此来判定临床疗效,并观察其安全性。结果:治疗后的UPDRS评分均较治疗前有明显降低,经t检验,PC0.0L提示治疗组的临床疗效明显优于对
2、照组。结论:补肾活血熄风方治疗VPS的临床疗效显著,对改善VPS患者的症状、UPDRS评分及延缓疾病进展均有一定的作用。关键词血管性帕金森综合征:补肾活血熄风方:UPDRS评分;临床研究ClinicalResearchonTreatmentoftheVascularParkinsonSyndromebyBushenHuoxueXifengFangSpeciality:theclinicalstudyofneuro-medicaldiseaseofTCMAutlior:RenWenwenTutor:Prof
3、.SunLijunAbstractObjective:ThediscussioninvigoratesBushenHuoxueXifengFangtreatmentthevascularparkinsonsyndromepatient'sclinicalvalidityandthesecurity,forthedevelopmentChinesemedicinetreatmentvascularparkinsonsyndromenewmentalityandmethod.Methods:Theselect
4、ionofstandardcase60cases,wererandomlydividedintotreatmentgroupandcontrolgroupwith30casesineachgroup.ThetreatmentgroupwasgivenBushenHuoxueXifengFang.Shuijianbidayagent;thecontrolgroupwasgivenMadopar,adailxoraldoseof125-250mg.Bothgroupsweretreatedafter8week
5、sofobservationonclinicalsymptomsandsignsofchangesbeforeandaftertreatment,assessmentofinternationalunifiedParkinson'sDiseaseRatingScale(UPDRS)scores,inordertodeterminetheclinicalcurativeeffectandobservationonitssecurity.Results:Aftertreatmentofinternationa
6、lunifiedParkinson'sDiseaseRatingScalescorethanbeforetreatmentisobviouslydecreased,byStudent'sttest.P<0.01,promptingthecurativeeffectoftreatmentgroupwassuperiortocontrolgroup.Conclusion:;BushenHuoxueXifengFangTreatmentofvascularparkinsonismsignificantclini
7、caleffect,toimprovesthevascularparkinsonsyndromepatient'ssymptom,internationalgeneralunificationparkinsonsicknessevaluationmetergradingandpostponementdiseaseprogresseshascertainfunction.KeywordstheVascularParkinsonsyndrome(VPS);BushenHuoxueXifengFang;inte
8、mationalunifiedParkinson'sDiseaseRatingScale(UPDRS)score:clinicalresearch目录临床研究........一、研究对象(一)诊断标准2(二)纳入标准2(三)排除标准3(四)剔除标准3〔五)治疗方法3(六)疾病疗效判定标准3(七)统计学处理4三、临床资料及研究结果4(一)两组性别比较4(二)两组文化程度比较4('三)两组间年龄比较4(四)两组间Hoehn—Yah
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