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氯沙坦治疗高血压病左室肥厚的临床疗效 被引量:1

Clinical efficacy of anti-hyperetnsive drug Iosartan in hypretensive patients with left ventricular hypertrophy
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摘要 目的 研究新型的降压药物——血管紧张素受体拮抗剂氯沙坦治疗高血压病左室肥厚的临床疗效.方法21例高血压病左室肥厚患者给予氯沙坦口服20wk.治疗前后行24h动态血压监测和心脏超声检查.结果 24 h SBP、24 h DBP、dSBP、dDBP、nSBP、nDBP由治疗前(151±15)、(93±9)、(155±15)、(96±10)、(146±16)、(88±11)mmHg分别降至(132±11)、(82±8)、(137±12)、(88±9)、(120±15)、(74±9)mmHg;IVST、PWT、LV-MI由治疗前(14.2±1.5)mm、(13.9±1.45)mm、(152.1±24.2)g·m^(2-1)分别降至(12.1±1.31)mm、(12.2±1.41)mm、(130.6±23.1)g·m^(2-1),以上参数用药后均较用药前有显著下降(P<0.0l).结论 氯沙坦能够明显降低高血压病左室肥厚患者24 h 血压,并能使其左室肥厚明显消退. Aim The study is to observe the clinical efficacy of losartan in hypertentive patientswith left ventricular hypertrophy. Methods 21 case were given losartan for 20 wk and 24h ambulatory blood pressure monitoring and color doppler echocardiography were per-formed in the patients before and after treatment.Results The 24 h SBP, 24 h DBP,dDBP, nSBP were from (151 ± 15) 、(93 ±9)、(155 ± 15)、(96 ± 10)、(146 ± 16)、(88 ± 11)mmHg before treatment to (132 ± 11)、(82 ± 8)、(137 ± 12)、(88 ± 9)、(120 ± 9)、(120 ± 15)、(74 ± 9) mmHg after treatment respectively and the IVST, PWT and LVMI were from(14.2 ± 1 .5) mm、(13. 9 ± 1. 45) mm、(152. 1 ± 24. 2) g· m2-1 BSA before treatment to(12. 1 ± 1. 31) mm、 (12. 2 ± 1. 41) mm、(130. 6 ± 23. 1) g· m2-1 BSA after treatment re-spectively. All the parameters after treatment in the patients were significantly decreased ascompared with those before treatment (P< 0. 01 ). Conclusion Losartan can significantlylower the blood pressure and the left ventricular hypertrophy in hypertensive patients withleft ventricular hypertrophy.
出处 《中国临床药理学与治疗学》 CAS CSCD 1999年第4期316-318,共3页 Chinese Journal of Clinical Pharmacology and Therapeutics
关键词 高血压 左室肥厚 药物疗法 氯沙坦 血压监测仪 hypertension left ventricular hypertrophy/drug therapy losartan/therapyuse ambulatory blood pressure monitoring color doppler echocardiography/methods
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  • 1胡艳茹.非肽类血管紧张素Ⅱ受体拮抗剂——洛沙坦[J].华北药学,1999,10(2):24-24.
  • 2刘健 李春江 张宏伟 等.缬沙坦对支架后新生内膜增生抑制作用的实验研究[J].药物与临床,1999,14(6):7-10.
  • 3Owens DR. Repaglinide--prandial glucose regulator,a new class of oral antidiabetic drugs [J]. Diabeted,1998,15(supp1 4) :28.
  • 4Timmermans PB. pharmacokinetics of antiotensin I(AT1) recept or antagonists [J]. Car J cardiol, 1999,15(suppl F) :26.
  • 5Israili ZH. Clinical pharmacokinetics of angiotensin I receptor blockers in hypertension [ J ]. J. Hum Hypertens, 2000,14 (suppl 1 ) : 73.
  • 6Oparil S. Newly emerging pharmacologic differences in angiotensin I receptor blockers [J]. Am J Hypertens, 2000,13 (2):18.
  • 7Shokei kim,Yumei zhan,Yasukatsu zsumi. Cardiovascular Effects of combination of perindopril,candesartan, and Amlodipine in Hypertensive Rats [J].Hypertension, 2000,2000 (4) : 769.
  • 8Hernandez Hernandez R, Velasco M, Armas Hernandez MJ,et al. Angiotensin I receptor antagonists in arterial hypertension [J]. J Hum Hypertens,2000,14(suppl 1 ) :69.
  • 9Qin-Gui Xia, Oliver chung, Thomas unger.significance of Timing of Angiotensin AT1 Receptor Blockade in Rats with Myocardial infarction-induced Heart Failure[J]. Cardiovascular Research, 2001,49(1):10.
  • 10Jain M ,Liao R,Ngoy s ,Anglotensin I receptor blockadl attenuates the deleterions effects of exercise training on post-MI ventricular remodelling in Rats [J].Cardiovasc Res, 2000,46(1):66.

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