苦参散联合LEEP刀治疗宫颈慢性炎症病变临床探究.doc

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1、苦参散联合LEEP刀治疗宫颈慢性炎症病变临床探究［摘要］目的：观察自主开发研制的苦参散的临床疗效及安全性。方法：选择符合入选标准的宫颈慢性炎症病变患者80例，随机分为试验组（50例）和对照组（30例），其中试验组在常规行宫颈LEEP术后，以苦参散喷敷宫颈表对照组单用LEEP术治疗。两组都连续观察随访5周，并于不同时期进行宫颈炎症评分，比较临床疗效。结果：试验组的临床疗效优于对照组，其创面愈合时间明显短于对照组（PV0.01）。结论：苦参散能明显减少LEEP术后异常带下及出血，促进宫颈创面愈合，缩短病程。［关键词］苦参散；局部治疗；宫颈炎症病变；创面愈［中图分类号］R7

2、11.32E文献标识码］A［文章编号］1673-7210(2009)05(b)-027-02CombinedtherapyofKushenPowderwithLEEPknifeminimallyinvasivemethodfortreatingchronicinflammatorydiseaseofcervixHELiyal,LILiqiang2,CHENHuilanl,LIUGuiyingl,CHENGuangfeng3,WANGYongxiaol,LIANGQifenl(1.DepartmentofObstetricsandGynecology,Hospitalo

3、fTraditionalChineseMedicineofZhaoqingCity,Zhaoqing526020,China；2.DepartmentofSecondBranchofInternalMedicine,HospitalofTraditionalChineseMedicineofZhaoqingCity,Zhaoqing526020,China；3.DepartmentofPathology,HospitalofTraditionalChineseMedicineofZhaoqingCity,Zhaoqing526020,China)[Abstract]O

4、bjective：ToobservetheclinicalefficacyandsafetyofKushenPowderdevelopedbyourselves・Methods：80patientswhowereaccordantwiththestandardsofchronicinflammatorydiseasesofcervixweredividedintotreatmentgroup(50cases)andcontrolgroup(30cases)・InadditiontoLEEPknifetreatmentofcervix,thetreatmentgroup

5、wasalsotreatedwithKushenPowderbysprayingonthesurfaceofcervix・ThepatientsincontrolgroupacceptedLEEPknifetreatmentonly.Thenscoresforthedegreeofinflammationatdifferentstagesintwogroupswereevaluated,andtheclinicalefficacywasalsocompared・ResuIts：Thetreatmentgrouphadbetterclinicalefficacy,and

6、timeofwoundhealingwasshorterthancontrolgroup(P1.7统计学方法数据以均数土标准差(x±s)表示，计量资料用t检验或秩和检验，计数资料采用？字2检验，P<0.05表示差异有统计学意义。2结果1.1两组治疗后宫颈炎症评分比较术前两组的宫颈炎症评分平均秩次无显著性差异(P>0.05)；术后第1、2、3、4、5周试验组的宫颈炎症评分平均秩次低于对照组(P<0.05),见表2。表2两组患者治疗前后不同时期宫颈炎症评分平均秩次的比较(分)与同期对照组比较，