Related Experiment Video
Updated: May 17, 2026

Increasing Pulmonary Artery Pulsatile Flow Improves Hypoxic Pulmonary Hypertension in Piglets
Published on: May 11, 2015
Prognostic factors in pulmonary hypertension
Flavia Catalina Corciova1, Catalina Arsenescu-Georgescu
1"Gr. T. Popa" University of Medicine and Pharmacy, Iasi, Romania ; "Prof. Dr. George Georgescu" Institute of Cardiovascular Diseases, Iasi, Romania.
Background And Objectives:
Pulmonary hypertension is a hemodynamic and pathophysiological condition defined as an increase in mean pulmonary pressure more than or equal to 25 mm Hg. Evaluation of pulmonary hypertension severity and prognosis plays a central role in the management of these patients, between diagnosis and therapeutic decision making. The aim of our study was to identify the adverse prognostic factors in patients with pulmonary hypertension and their impact on mortality, quality of life, need for hospitalization and complications during hospitalization.
Material And Methods:
We performed a prospective study that included 553 patients diagnosed with pulmonary hypertension in the Institute of Cardiovascular Diseases of Iasi between 1st November 2008 and 1st July 2011. We analyzed a series of demographic and clinical data, echocardiographic and hemodynamic parameters, which correlated with mortality, WHO functional class, complications and need for hospitalization.
Outcomes:
We identified as main negative prognostic factors: WHO functional class III and IV, the pulmonary artery systolic pressure value, right chambers dilation, TAPSE, pericardial effusion, cardiac index and right atrial pressure.
Conclusions:
Pulmonary hypertension, despite the development of treatment methods, remains a serious disease, with progressive and inexorable evolution, but the prognosis of patients with pulmonary hypertension is very variable, depending on the etiology, functional class, clinical, echocardiographic and hemodynamic parameters.
Related Concept Videos
Pulmonary Hypertension: Classification and Pathogenesis
There are various classifications for PH, each relating to different underlying causes and also...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Pulmonary Embolism I: Introduction
Pulmonary Embolism I: Introduction
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme (ECE). Of...

