Ecocardiografia ed ipertensione arteriosa polmonare

Translated title of the contribution: Echocardiography and pulmonary arterial hypertension

Eduardo Bossone, Rodolfo Citro, Alberto Ruggiero, Bettina Kuersten, Giovanni Gregorio, Francesco Blasi, Luigi Allegra

Research output: Contribution to journalArticlepeer-review


Echocardiography and Pulmonary Arterial Hypertension. E. Bossone, R. Citro, A. Ruggiero, B. Kuersten, G. Gregorio, F. Blasi, L. Allegra. Pulmonary Arterial Hypertension (PAH) is an heterogeneous condition brought on by a wide range of causes. It is characterized by structural changes in small pulmonary arteries, that produce a progressive increase in pulmonary artery pressure and pulmonary vascular resistance, ultimately leading to right ventricle failure and death. Given the non-specific nature of its early symptoms and signs, PAH is often diagnosed in its advanced stages. Along with a careful clinical assessment and an accurate electrocardiogram/Chest X-ray interpretation, echocardiography is an essential test in the evaluation of patient with PAH. In fact it not only provides an accurate estimate of pulmonary pressure at rest and during exercise, but may also help to exclude any secondary causes, predict the prognosis, monitor the efficacy of specific therapeutic interventions and detect the preclinical stage of the disease.

Translated title of the contributionEchocardiography and pulmonary arterial hypertension
Original languageItalian
Pages (from-to)219-226
Number of pages8
JournalMonaldi Archives for Chest Disease - Cardiac Series
Issue number4
Publication statusPublished - Dec 2007

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Cardiology and Cardiovascular Medicine


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