Pulmonary Hypertension - StatPearls - NCBI Bookshelf
May 1, 2024 · Besides the above clinical distinctions, pulmonary hypertension has a hemodynamic classification scheme that can aid diagnosis. A mean pulmonary artery pressure (mPAP) greater than 20 mm Hg is above the upper normal limit.
Clinical features and diagnosis of pulmonary hypertension of ... - UpToDate
Dec 11, 2024 · Patients suspected of having pulmonary hypertension (PH) undergo extensive diagnostic testing. The purpose of diagnostic testing is to confirm that PH exists and identify the underlying cause so that appropriate treatment can be administered. The clinical features, diagnostic evaluation, and diagnostic criteria for PH are reviewed here.
Pulmonary Hypertension - AAFP
The differential diagnosis for pulmonary hypertension is broad and includes HF, coronary artery disease, pulmonary fibrosis, chronic obstructive pulmonary disease, valvular heart disease ...
Pulmonary Idiopathic Hypertension - StatPearls - NCBI Bookshelf
Apr 27, 2023 · Therefore, the differential diagnosis of idiopathic pulmonary hypertension includes congenital or acquired heart disease, veno-occlusive disease, pulmonary diseases, chronic hypoventilation secondary to sleep apnea, chronic exposure to high altitude, liver disease, ingestion of anorectic medications or pharmaceutical agents, and fibrosing ...
Pulmonary Arterial Hypertension Differential Diagnoses - Medscape
Pulmonary hypertension (PH), defined as a mean pulmonary arterial pressure greater than 25 mm Hg at rest or greater than 30 mm Hg during exercise, is often characterized by a progressive and...
PAH Differential Diagnosis | Rare Disease Advisor
Pulmonary hypertension (PH) is classified into 5 types, one of which is pulmonary arterial hypertension (PAH) or Group 1 PH, characterized by symptoms such as dyspnea, fatigue, chest pain, syncope, or edema. However, PH is more commonly caused by other cardiopulmonary diseases as compared to PAH.
Pulmonary Hypertension: Diagnosis and Management - PMC
The current article provides an overview of the pathobiologic mechanisms of pulmonary arterial hypertension, including genetic substrates and molecular and cellular mechanisms, and describes the clinical manifestations and classification of pulmonary arterial hypertension.
Group 4 Pulmonary Hypertension Differential Diagnoses - Medscape
These include pulmonary arterial hypertension (PAH) (WHO group 1), pulmonary hypertension (WHO groups 2, 3, and 5), and other pulmonary arterial obstruction (eg, tumors of the pulmonary...
Echocardiography is recommended as the initial step in the evaluation of patients with suspected pulmonary hypertension. A definitive diagnosis cannot be made on echocardiographic abnormalities...
Diagnosis and differential assessment of pulmonary arterial ...
Jun 16, 2004 · Most patients are diagnosed as the result of an evaluation of symptoms, whereas others are diagnosed during screening of asymptomatic populations at risk. Right heart catheterization (RHC) must be performed in patients with suspected PH to establish the diagnosis and document pulmonary hemodynamics.
- Some results have been removed