Abstract

Heart failure (HF) is a debilitating and life-threatening condition, with 5-year survival rate lower than breast or prostate cancer. It is the leading cause of hospital admission in over 65s, and these admissions are projected to rise by more than 50% over the next 25 years. Transthoracic echocardiography (TTE) is the first-line step in diagnosis in acute and chronic HF and provides immediate information on chamber volumes, ventricular systolic and diastolic function, wall thickness, valve function and the presence of pericardial effusion, while contributing to information on aetiology. Dilated cardiomyopathy (DCM) is the third most common cause of HF and is the most common cardiomyopathy. It is defined by the presence of left ventricular dilatation and left ventricular systolic dysfunction in the absence of abnormal loading conditions (hypertension and valve disease) or coronary artery disease sufficient to cause global systolic impairment. This document provides a practical approach to diagnosis and assessment of dilated cardiomyopathy that is aimed at the practising sonographer.

Highlights

  • The BSE Education Committee has previously published a minimum dataset for a standard adult transthoracic echocardiogram (TTE)

  • The views and measurements are focussed upon dilated cardiomyopathy and are supplementary to those outlined in the TTE minimum dataset

  • This document is a guideline for echocardiography in dilated cardiomyopathy and will be updated in accordance with changes directed by publications or changes in practice

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Summary

Introduction

The BSE Education Committee has previously published a minimum dataset for a standard adult transthoracic echocardiogram (TTE). These are published online in Echo Research and Practice (1). This document states that the minimum dataset is usually only sufficient when the echocardiographic study is entirely normal. The aim of the Education Committee is to publish a series of appendices to cover specific pathologies to support this minimum dataset. This final document completes the cardiomyopathy series (hypertrophic (2), restrictive (3), ARVC (4) and dilated cardiomyopathies)

The intended benefits of such supplementary recommendations are to:
Findings
Dilated cardiomyopathy
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