河北医学
河北醫學
하북의학
HEBEI MEDICINE
2015年
7期
1142-1144
,共3页
刘学清%高风%李妍%李长荣%赵健新
劉學清%高風%李妍%李長榮%趙健新
류학청%고풍%리연%리장영%조건신
双嘧达莫%厄贝沙坦%IgA肾病
雙嘧達莫%阨貝沙坦%IgA腎病
쌍밀체막%액패사탄%IgA신병
Dipyridamole%Irbesartan%IgA nephropathy
目的:观察厄贝沙坦对IgA肾病的疗效及其安全性。方法:将IgA肾病患者62例随机分为治疗组32例和对照组30例。治疗组给予双嘧达莫150mg/d、厄贝沙坦150mg~300mg/d,共12周;对照组单纯给予双嘧达莫150mg/d,共12周;观察两组患者治疗前后收缩压、舒张压、24h尿蛋白定量、血尿素氮、肌酐和血K±等变化。结果:治疗12周后治疗组患者收缩压( SBP )、舒张压( DBP )、24h尿蛋白定量、血尿素氮(BUN)、肌酐均降低(P<0.05);对照组患者用药后收缩压(SBP)、舒张压(DBP)、24h尿蛋白定量、血尿素氮(BUN)、肌酐均无明显降低(P>0.05)。结论:厄贝沙坦治疗IgA肾病能明显降低血压、减少尿蛋白,改善肾功能,且无明显不良反应。
目的:觀察阨貝沙坦對IgA腎病的療效及其安全性。方法:將IgA腎病患者62例隨機分為治療組32例和對照組30例。治療組給予雙嘧達莫150mg/d、阨貝沙坦150mg~300mg/d,共12週;對照組單純給予雙嘧達莫150mg/d,共12週;觀察兩組患者治療前後收縮壓、舒張壓、24h尿蛋白定量、血尿素氮、肌酐和血K±等變化。結果:治療12週後治療組患者收縮壓( SBP )、舒張壓( DBP )、24h尿蛋白定量、血尿素氮(BUN)、肌酐均降低(P<0.05);對照組患者用藥後收縮壓(SBP)、舒張壓(DBP)、24h尿蛋白定量、血尿素氮(BUN)、肌酐均無明顯降低(P>0.05)。結論:阨貝沙坦治療IgA腎病能明顯降低血壓、減少尿蛋白,改善腎功能,且無明顯不良反應。
목적:관찰액패사탄대IgA신병적료효급기안전성。방법:장IgA신병환자62례수궤분위치료조32례화대조조30례。치료조급여쌍밀체막150mg/d、액패사탄150mg~300mg/d,공12주;대조조단순급여쌍밀체막150mg/d,공12주;관찰량조환자치료전후수축압、서장압、24h뇨단백정량、혈뇨소담、기항화혈K±등변화。결과:치료12주후치료조환자수축압( SBP )、서장압( DBP )、24h뇨단백정량、혈뇨소담(BUN)、기항균강저(P<0.05);대조조환자용약후수축압(SBP)、서장압(DBP)、24h뇨단백정량、혈뇨소담(BUN)、기항균무명현강저(P>0.05)。결론:액패사탄치료IgA신병능명현강저혈압、감소뇨단백,개선신공능,차무명현불량반응。
Objective:To investigate the effect and the safety of irbesartan on IgA nephropathy.Meth-od:Sixty-two cases of IgA nephropathy were randomly divided into treatment group and control group.Pa-tients of treatment group ( n=32) were given 150mg dipyridamole and 150~300mg irbesartan, and the pa-tients of control group ( n=30) were given 150mg dipyridamole per day for 12 weeks.Systolic blood pressure, diastolic blood pressure, proteinuria in 24 hours, blood urea nitrogen, creatinine and potassium were ob-served.Result:Systolic blood pressure, diastolic blood pressure, proteinuria in 24 hours, blood urea nitro-gen and creatinine in treatment group decreased obviously (P<0.05).There was no decrease(P>0.05) in control group after treatment.Conclusion: Irbesartan can obviously reduce blood pressure and proteinuria, improve renal function without severe side-effects in treating IgA nephropathy.