• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

左心室肥厚

Left Ventricular Hypertrophy.

作者信息

Liebson PR

机构信息

Section of Cardiology, Rush-Presbyterian-St. Luke's Medical Center, 1653 W. Congress Parkway, Chicago, IL 60612, USA.

出版信息

Curr Treat Options Cardiovasc Med. 1999 Oct;1(3):219-230. doi: 10.1007/s11936-999-0038-0.

DOI:10.1007/s11936-999-0038-0
PMID:11096487
Abstract

The presence of left ventricular hypertrophy (LVH) as a treatable entity is of particular importance in patients with primary hypertension. Because LVH is associated with a strong risk of adverse clinical events (eg, heart failure, ischemic events, and cardiovascular death) and because evidence from retrospective studies suggests that regression of LVH, along with a decrease in blood pressure, may help modify these outcomes, the use of antihypertensive agents that have been shown to promote regression of LVH has been recommended. These include diuretics, beta-blockers (except those with intrinsic sympathomimetic activity ), angiotensin-converting enzyme (ACE) inhibitors, calcium channel blockers, peripheral alpha(1)-blockers, and central alpha(2)-stimulators. Agents to be avoided include direct arterial vasodilators (eg, hydralazine and minoxidil), which have strong sympathetic stimulating properties and tend to maintain LVH despite lowering blood pressure. The use of ACE inhibitors is increasing. Unfortunately, the cost of these agents is higher than that of some other classes of agents, such as diuretics, which show excellent evidence of regression of hypertrophy. African-American and elderly persons, in particular, may benefit from diuretics for treatment of hypertension as well as reduction of left ventricular (LV) mass. Beta-blockers should be considered in the elderly, especially those with greatly thickened LV walls and small chamber sizes, factors associated with hyperdynamic systolic performance, systolic midcavity obliteration, and diastolic relaxation abnormalities on echocardiography. Calcium channel blockers may also be useful in patients with LVH who have normal systolic performance and diastolic compliance abnormalities. The purpose of serial echocardiographic studies in patients already being treated for hypertension is to ensure that LV geometry has not worsened and that function is unchanged or improved (especially with respect to previously noted diastolic Doppler inflow abnormalities). Considerable changes in estimated LV mass (>60 g on serial intrapatient evaluation) are needed before the clinician can conclude with confidence that LV mass has decreased. More specific definitive recommendations based on the outcomes of current large-scale clinical trials are awaited.

摘要

左心室肥厚(LVH)作为一种可治疗的病症,在原发性高血压患者中具有特别重要的意义。由于LVH与不良临床事件(如心力衰竭、缺血性事件和心血管死亡)的高风险相关,且回顾性研究证据表明LVH的消退以及血压的降低可能有助于改善这些结局,因此推荐使用已被证明可促进LVH消退的抗高血压药物。这些药物包括利尿剂、β受体阻滞剂(除具有内在拟交感活性的药物外)、血管紧张素转换酶(ACE)抑制剂、钙通道阻滞剂、外周α1受体阻滞剂和中枢α2受体激动剂。应避免使用的药物包括直接动脉血管扩张剂(如肼屈嗪和米诺地尔),它们具有强烈的交感神经刺激特性,尽管能降低血压,但往往会维持LVH。ACE抑制剂的使用正在增加。不幸的是,这些药物的成本高于其他一些药物类别,如利尿剂,利尿剂在肥大消退方面有充分的证据。特别是非裔美国人和老年人,使用利尿剂治疗高血压以及减少左心室(LV)质量可能会受益。对于老年人,尤其是那些LV壁明显增厚且腔室较小的患者,应考虑使用β受体阻滞剂,这些因素与超声心动图上的高动力收缩性能、收缩期心腔中部闭塞和舒张期松弛异常有关。钙通道阻滞剂对于LVH且收缩功能正常但存在舒张顺应性异常的患者也可能有用。对已接受高血压治疗的患者进行系列超声心动图研究的目的是确保LV几何形状没有恶化,功能未改变或有所改善(特别是对于先前发现的舒张期多普勒血流异常)。在临床医生能够自信地得出LV质量已降低的结论之前,估计LV质量需要有相当大的变化(在患者内系列评估中>60 g)。目前正在等待基于当前大规模临床试验结果的更具体明确的建议。

相似文献

1
Left Ventricular Hypertrophy.左心室肥厚
Curr Treat Options Cardiovasc Med. 1999 Oct;1(3):219-230. doi: 10.1007/s11936-999-0038-0.
2
Serial echocardiographic-Doppler assessment of left ventricular geometry and function in rats with pressure-overload hypertrophy. Chronic angiotensin-converting enzyme inhibition attenuates the transition to heart failure.对压力超负荷肥大大鼠左心室几何形状和功能进行系列超声心动图-多普勒评估。慢性血管紧张素转换酶抑制可减轻向心力衰竭的转变。
Circulation. 1995 May 15;91(10):2642-54. doi: 10.1161/01.cir.91.10.2642.
3
Changes in left ventricular geometry during antihypertensive treatment.抗高血压治疗期间左心室几何形状的变化。
Pharmacol Res. 2018 Aug;134:193-199. doi: 10.1016/j.phrs.2018.06.026. Epub 2018 Jun 26.
4
Angiotensin converting enzyme inhibition and dihydropyridine calcium channel blockade in the treatment of left ventricular hypertrophy in arterial hypertension.血管紧张素转换酶抑制和二氢吡啶类钙通道阻滞在治疗动脉高血压左心室肥厚中的应用
Minerva Cardioangiol. 2002 Jun;50(3):169-74.
5
Treatment of left ventricular hypertrophy in hypertensive patients.高血压患者左心室肥厚的治疗
Eur Heart J. 1993 Nov;14 Suppl J:102-6.
6
[Regression of left ventricular hypertrophy with antihypertensive treatment].[抗高血压治疗使左心室肥厚消退]
Presse Med. 1990 Nov 10;19(37):1715-9.
7
Regression of increased left ventricular mass by antihypertensives.
Drugs. 1991 Dec;42(6):945-61. doi: 10.2165/00003495-199142060-00004.
8
Angiotensin-converting enzyme inhibition prolongs survival and modifies the transition to heart failure in rats with pressure overload hypertrophy due to ascending aortic stenosis.血管紧张素转换酶抑制可延长因升主动脉狭窄导致压力超负荷肥大的大鼠的生存期,并改变其向心力衰竭的转变。
Circulation. 1994 Sep;90(3):1410-22. doi: 10.1161/01.cir.90.3.1410.
9
Reversal of left ventricular hypertrophy in essential hypertension. A meta-analysis of randomized double-blind studies.原发性高血压患者左心室肥厚的逆转。随机双盲研究的荟萃分析。
JAMA. 1996 May 15;275(19):1507-13.
10
The importance of left ventricular hypertrophy in human hypertension.左心室肥厚在人类高血压中的重要性。
J Hypertens Suppl. 1998 Sep;16(7):S23-9.

引用本文的文献

1
Electrocardiographic Left Ventricular Hypertrophy Among Gambian Diabetes Mellitus Patients.冈比亚糖尿病患者的心电图左心室肥厚
Ghana Med J. 2015 Mar;49(1):19-24. doi: 10.4314/gmj.v49i1.4.

本文引用的文献

1
Influence of the angiotensin II antagonist valsartan on left ventricular hypertrophy in patients with essential hypertension.血管紧张素II拮抗剂缬沙坦对原发性高血压患者左心室肥厚的影响。
Circulation. 1998 Nov 10;98(19):2037-42. doi: 10.1161/01.cir.98.19.2037.
2
Regression of left ventricular hypertrophy in patients with hypertension: blockade of the renin-angiotensin-aldosterone system.
Circulation. 1998 Nov 10;98(19):1987-9. doi: 10.1161/01.cir.98.19.1987.
3
Influence of left ventricular geometric patterns on prognosis in patients with or without coronary artery disease.
J Am Coll Cardiol. 1998 Jun;31(7):1635-40. doi: 10.1016/s0735-1097(98)00131-4.
4
Effect of treatment of isolated systolic hypertension on left ventricular mass.单纯收缩期高血压治疗对左心室质量的影响。
JAMA. 1998 Mar 11;279(10):778-80. doi: 10.1001/jama.279.10.778.
5
Left ventricular hypertrophy in athletes.运动员的左心室肥厚
Am J Cardiol. 1997 Nov 15;80(10):1384-8. doi: 10.1016/s0002-9149(97)00693-0.
6
Hydrochlorothiazide is superior to isradipine for reduction of left ventricular mass: results of a multicenter trial. The Isradipine Study Group.氢氯噻嗪在减轻左心室质量方面优于伊拉地平:一项多中心试验的结果。伊拉地平研究组。
J Am Coll Cardiol. 1997 Dec;30(7):1802-8. doi: 10.1016/s0735-1097(97)00311-2.
7
The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure.全国高血压防治联合委员会第六次报告。
Arch Intern Med. 1997 Nov 24;157(21):2413-46. doi: 10.1001/archinte.157.21.2413.
8
Regression of left ventricular hypertrophy with captopril restores normal ventricular action potential duration, dispersion of refractoriness, and vulnerability to inducible ventricular fibrillation.
Circulation. 1997 Aug 19;96(4):1330-6. doi: 10.1161/01.cir.96.4.1330.
9
The Losartan Intervention For Endpoint reduction (LIFE) in Hypertension study: rationale, design, and methods. The LIFE Study Group.氯沙坦降低高血压终点事件(LIFE)研究:原理、设计与方法。LIFE研究组
Am J Hypertens. 1997 Jul;10(7 Pt 1):705-13.
10
Effect of single-drug therapy on reduction of left ventricular mass in mild to moderate hypertension: comparison of six antihypertensive agents. The Department of Veterans Affairs Cooperative Study Group on Antihypertensive Agents.单药治疗对轻至中度高血压患者左心室质量降低的影响:六种抗高血压药物的比较。退伍军人事务部抗高血压药物合作研究组。
Circulation. 1997 Apr 15;95(8):2007-14. doi: 10.1161/01.cir.95.8.2007.