(Circulation. 2003;108:2191.)
© 2003 American Heart Association, Inc.
Clinician Update |
From the Cardiovascular Division, Brigham and Womens Hospital, Harvard Medical School, Boston, Mass.
Correspondence to Samuel Z. Goldhaber, MD, Cardiovascular Division, Brigham and Womens Hospital, Harvard Medical School, 75 Francis St, Boston, MA 02115. E-mail sgoldhaber@partners.org
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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Severe dyspnea, cyanosis, and syncope indicate life-threatening PE. The clinical examination may reveal signs of acute right ventricular dysfunction, including tachycardia, a low arterial blood pressure, distended neck veins, an accentuated P 2, or a tricuspid regurgitation murmur. On the ECG, T-wave inversion or a pseudoinfarction pattern (Qr) in the anterior precordial leads indicates right ventricular dilation and dysfunction.3 Chest computed tomography or magnetic resonance imaging may not only confirm PE but also demonstrate right ventricular dilation.
Echocardiography has emerged as the principal tool for risk stratification in acute PE. From a prognostic point of view, echocardiography helps to classify patients with PE into 3 groups: Low-risk PE (no right ventricular dysfunction), with a hospital mortality of <4%, submassive PE (right ventricular dysfunction and a preserved arterial pressure), with a hospital mortality of 5% to 10%, and massive PE (right ventricular dysfunction and cardiogenic shock), with a hospital mortality of approximately 30%.4 Right ventricular dysfunction on the echocardiogram is an
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