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导致收缩期前三尖瓣反流的临床情况。

Clinical settings leading to presystolic tricuspid regurgitation.

作者信息

Szymański Piotr, Lipczyńska Magdalena, Klisiewicz Anna, Hoffman Piotr

机构信息

Echocardiographic Laboratory, Valvular Heart Disease Department, Warsaw, Poland.

出版信息

Echocardiography. 2015 Jan;32(1):19-27. doi: 10.1111/echo.12604. Epub 2014 Apr 4.

Abstract

PURPOSE

Few studies describe diastolic (presystolic) tricuspid regurgitation (DTR) mainly in the context of atrioventricular conduction abnormalities. Little is known about its occurrence in the other clinical settings.

METHODS

We identified patients with DTR recorded during routine echocardiographic examinations. DTR was defined as low velocity backward flow through the tricuspid valve orifice during end-diastole recorded with a continuous and/or pulsed-wave Doppler and/or color-coded M-mode Doppler echocardiography.

RESULTS

Diastolic tricuspid regurgitation was present in a wide variety of clinical entities. Of the 23 patients with DTR 6 patients had ischemic and 10 dilated cardiomyopathy. Others had clinical conditions including: inappropriate pacemaker settings, decompensated hypertrophic cardiomyopathy, biventricular dysfunction following orthotropic heart transplantation, torrential aortic regurgitation, low ejection fraction aortic stenosis, advanced endocardial fibroelastosis, and complex congenital heart disease. Twenty of 23 patients had significantly impaired right ventricle (RV) systolic function. Systolic tricuspid regurgitation was estimated as moderate or severe in 13 cases and mild in the remaining 10 cases. RV systolic pressure was significantly elevated in all but 2 cases. In all but 4 cases DTR was transient. The persistence of DTR was associated with severe pulmonary hypertension, severe biventricular failure, and persistent severe pulmonary regurgitation.

CONCLUSIONS

Diastolic tricuspid regurgitation may be encountered in a variety of clinical settings and should be sought for especially in patients with advanced RV systolic dysfunction, pulmonary hypertension, pulmonary regurgitation, or conduction abnormalities. Significant systolic regurgitation is not prerequisite for the development of DTR.

摘要

目的

很少有研究主要在房室传导异常的背景下描述舒张期(收缩前期)三尖瓣反流(DTR)。对于其在其他临床情况下的发生情况知之甚少。

方法

我们识别出在常规超声心动图检查中记录到DTR的患者。DTR被定义为在舒张末期通过三尖瓣口的低速逆向血流,通过连续和/或脉冲波多普勒和/或彩色编码M型多普勒超声心动图记录。

结果

舒张期三尖瓣反流存在于多种临床情况中。在23例DTR患者中,6例患有缺血性心肌病,10例患有扩张型心肌病。其他患者的临床情况包括:起搏器设置不当、失代偿性肥厚型心肌病、原位心脏移植后的双心室功能障碍、重度主动脉瓣反流、低射血分数主动脉瓣狭窄、晚期心内膜弹力纤维增生症以及复杂先天性心脏病。23例患者中有20例右心室(RV)收缩功能明显受损。13例患者的收缩期三尖瓣反流估计为中度或重度,其余10例为轻度。除2例患者外,所有患者的RV收缩压均显著升高。除4例患者外,DTR均为短暂性。DTR的持续存在与严重肺动脉高压、严重双心室衰竭和持续性严重肺动脉反流有关。

结论

舒张期三尖瓣反流可能在多种临床情况下出现,尤其应在晚期RV收缩功能障碍、肺动脉高压、肺动脉反流或传导异常的患者中寻找。显著的收缩期反流不是DTR发生的先决条件。

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