Pulmonary Hypertension is defined as raised pulmonary pressures and is associated with significant morbidity and mortality
Presentation: reduced exercise tolerance, sob, peripheral oedema; BG systemic inflammatory condition
Diagnosis: ECHO, right heart catheterisation or implantable sensor
Management: endothelin receptor antagonists
Primary pulmonary hypertension
Due to LHF
Due to lung disease, e.g. COPD
Due to chronic venous thrombotic disease
Everything else: e.g. inflammatory, metabolic, blood and kidney disorders
Secondary pulmonary HTN: types 2-5.
Presentation
Syncope
Progressive reduced exercise tolerance
Tricuspid or pulmonary regurgitation (secondary to pulmonary HTN increased pressure
Hepatomegaly
Investigations
ECHO: RVH
CXR: may be normal
HRCT ?primary lung disease ?ILD
ECHO: raised pulmonary pressures
Management
Endothelin A receptor antagonists: bosentan
Pregnancy with pulmonary hypertension comes with a significant risk to the mother and baby.
Management
Prostacyclin analogues
Anticoagulation considered
Educated on worsening cardiac function and risk to mother & foetus
Core Pulmonale is simply right sided heart failure from pulmonary hypertension.
Signs
Right sided heart failure: peripheral oedema- pretibial, sacral; ascites/ pleural effusions/ raised JVP
Pulmonary hypertension: raised JVP, loud P2, right parasternal heave (RVH)
Pulmonary hypertension - victor chang cardiac research institute (no date) The Victor Chang Cardiac Research Institute. Available at: https://www.victorchang.edu.au/heart-disease/pulmonary-hypertension (Accessed: 07 October 2024).
Written in 2022