Pulmonary Hypertension Disorders

Advanced Evaluation of Pulmonary Hypertension, Complex Blood Pressure Disorders, and Haemodynamic Disease

Specialist assessment and management of pulmonary hypertension, resistant systemic hypertension, and complex haemodynamic conditions using invasive pressure studies and catheterisation-based evaluation. The focus is on accurately defining the mechanism and severity of abnormal pressure disorders and guiding targeted, evidence-based treatment rather than empirical blood pressure management.

Understanding Pulmonary and Resistant Hypertension

Blood pressure disorders are not uniform conditions with a single cause or a single treatment pathway. Their correct management depends entirely on accurate classification of the underlying haemodynamic mechanism, and this cannot be achieved from a blood pressure reading or a standard echocardiogram alone.

Pulmonary hypertension refers to elevated pressure within the pulmonary arteries, the vessels that carry blood from the right side of the heart to the lungs. Elevated pulmonary pressures impose a progressive overload on the right ventricle, leading over time to right heart failure. The condition presents insidiously with progressive breathlessness, reduced exercise capacity, fatigue, and, in advanced cases, peripheral oedema and syncope. The underlying cause may be intrinsic pulmonary arterial disease, left heart disease, chronic lung disease, chronic thromboembolic disease, or a combination of mechanisms. Each requires a different treatment strategy, and the distinction between them cannot be made without invasive haemodynamic measurement.

Resistant systemic hypertension refers to blood pressure that remains elevated despite three or more antihypertensive medications at optimal doses. In these patients, the persistence of hypertension reflects a specific underlying mechanism that standard medication is not addressing. Effective management requires identification and targeted treatment of that underlying cause.

Hypertension Management
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Conditions Treated

Pulmonary Arterial Hypertension (PAH)

Primary disease of the small pulmonary arteries causing progressive elevation of pulmonary vascular resistance and right ventricular failure. Requires haemodynamic confirmation by right heart catheterisation and is managed with targeted pulmonary vasodilator therapy.

Chronic Thromboembolic Pulmonary Hypertension (CTEPH)

Persistent elevation of pulmonary artery pressure following pulmonary embolism, caused by incomplete resolution of embolic material. A potentially surgically or catheter-based treatable condition that requires pulmonary angiography and right heart catheterisation to confirm.

Renal Artery Stenosis Causing Renovascular Hypertension

Significant narrowing of one or both renal arteries reducing kidney perfusion pressure and driving hypertension that is difficult to control with medication. Identified by renal angiography and treatable with catheter-based stenting where haemodynamic significance is confirmed.

Right Heart Failure Due to Chronic Pressure Overload

Progressive right ventricular dysfunction arising from sustained elevation of pulmonary artery pressure, requiring haemodynamic assessment to guide treatment and assess prognosis.

Pulmonary Hypertension Due to Left Heart Disease

The most common cause of elevated pulmonary pressures. Elevated left atrial pressure from diastolic dysfunction, mitral valve disease, or heart failure is transmitted back to the pulmonary circulation. The distinction from other causes requires precise pressure measurement at right heart catheterisation.

Resistant Systemic Hypertension

Blood pressure persistently above target despite optimal medical therapy. Secondary causes must be systematically excluded before advanced therapies such as renal denervation are considered.

Unexplained Breathlessness with Suspected Pulmonary Vascular Disease

Patients with progressive breathlessness in whom standard investigations have not identified a clear cause. Invasive assessment, including exercise of right heart catheterisation is the most sensitive investigation in this context.

Complex Blood Pressure Disorders

Advanced Diagnostic Assessment

Right Heart Catheterisation

The gold standard investigation for pulmonary hypertension and complex haemodynamic disease. Performed under local anaesthesia via venous access, it provides direct measurement of pressures throughout the right heart and pulmonary circulation, cardiac output, and pulmonary vascular resistance. These measurements are essential to classify pulmonary hypertension by cause, confirm haemodynamic severity, and guide treatment selection. Over 200 right heart catheterisations have been performed at Level 3 independent competence.

Vasoreactivity Testing

Performed during right heart catheterisation in patients with suspected pulmonary arterial hypertension. Short-acting pulmonary vasodilators are administered, and the response of the pulmonary vasculature is measured. A significant response identifies patients who may benefit from calcium channel blocker therapy and carries important prognostic implications.

Pulmonary Angiography

Imaging of the pulmonary arterial tree performed in the catheterisation laboratory, indicated when chronic thromboembolic pulmonary hypertension is suspected. Contrast is injected directly into the pulmonary arteries to define the distribution and nature of embolic obstruction.

Renal Angiography

Catheter-based imaging of the renal arteries to identify haemodynamically significant renal artery stenosis as a cause of resistant or renovascular hypertension, with stenting of confirmed significant lesions where benefit is anticipated.

Coronary Angiography

Frequently performed alongside right heart catheterisation and structural evaluation to exclude significant coronary artery disease in patients presenting with breathlessness or suspected haemodynamic cardiac disease.

Cardiac Device and Rhythm Procedures

Right Heart Catheterisation

Performed routinely as part of diagnostic evaluation for all patients with suspected pulmonary hypertension, unexplained haemodynamic abnormality, or complex valve disease.

Pulmonary Angiography

Performed in the same catheterisation session as right heart catheterisation when chronic thromboembolic pulmonary hypertension or other structural pulmonary vascular disease is suspected.

Renal Artery Angiography and Stenting

Catheter-based assessment and treatment of renal artery stenosis via arterial access, with stent deployment where haemodynamically significant stenosis is confirmed.

Renal Denervation

A catheter-based treatment for resistant hypertension after optimal medical therapy and exclusion of secondary causes. Radiofrequency or ultrasound energy disrupts renal sympathetic nerves to lower blood pressure. Supported by SPYRAL HTN-ON MED and RADIANCE II trials, with dedicated training and research experience in mineralocorticoid receptor antagonism.

Combined Cardiopulmonary Haemodynamic Assessment

Integrated evaluation of both the systemic and pulmonary circulations within a single catheterisation laboratory session, providing a comprehensive haemodynamic profile in patients with complex multi-system circulatory disease.

WHY CHOOSE DR. YASIR PARVIZ

International Expertise. Precision Cardiovascular Care.

Dr. Yasir Parviz combines interventional cardiology experience with advanced expertise in pulmonary hypertension, resistant hypertension, and invasive haemodynamic assessment. He uses direct pressure measurement and catheter-based investigation to identify the underlying cause and guide appropriate, evidence-based treatment.

200+ Right Heart Catheterisations

Pulmonary Hypertension Assessment

Resistant Hypertension Evaluation

Renal Denervation Training

Frequently Asked Questions

1. What is pulmonary hypertension and how is it different from regular high blood pressure?
Pulmonary hypertension refers specifically to elevated pressure in the arteries supplying the lungs, arising from the right side of the heart. Regular high blood pressure refers to elevated pressure in the arterial circulation supplying the rest of the body, arising from the left side of the heart. They are distinct conditions with different causes, different consequences, and entirely different treatments.
2. How is pulmonary hypertension diagnosed?
A definitive diagnosis requires right heart catheterisation, which directly measures pressure within the pulmonary arteries. Echocardiography can suggest the diagnosis and estimate pressure indirectly but cannot confirm it with the accuracy needed to guide treatment decisions or distinguish between the different underlying causes.
3. What causes resistant hypertension?
Resistant hypertension may be caused by renal artery stenosis, primary aldosteronism from an adrenal adenoma, obstructive sleep apnoea, overactivation of the sympathetic nervous system, or other secondary causes. Specialist evaluation is required to systematically identify or exclude each treatable cause before advanced therapies are considered.
4. Is right heart catheterisation safe?
Right heart catheterisation is a well-established minimally invasive procedure performed via a vein under local anaesthesia. It does not require general anaesthesia or intensive care admission. Serious complications are uncommon when performed in a specialist centre with experienced operators.
5. What is renal denervation and who is it suitable for?
Renal denervation is a catheter-based procedure that reduces sympathetic nervous system overactivity contributing to resistant hypertension by delivering controlled energy to the nerve fibres running along the renal artery walls. It is suitable for patients with documented resistant hypertension who have been optimised on medication and in whom secondary causes have been excluded. Candidate suitability is assessed individually.
6. Can pulmonary hypertension be treated?
Yes. Treatment depends entirely on the underlying cause. Pulmonary arterial hypertension is managed with targeted vasodilator therapies that can significantly improve symptoms and slow disease progression. Pulmonary hypertension due to left heart disease is addressed by treating the underlying cardiac condition. Chronic thromboembolic pulmonary hypertension may be amenable to surgical or catheter-based intervention. Accurate classification is the essential first step in every case.