Pulmonary Hypertension Flashcards

1
Q

What is pulmonary hypertension?

A

Pulmonary hypertension is a condition characterised by elevated pressure in the pulmonary arteries, leading to strain on the right side of the heart.

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2
Q

What are the normal pulmonary artery pressure values?

A

Normal pulmonary artery pressure is <25 mmHg at rest.

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3
Q

What are the main types of pulmonary hypertension?

A

The five types include pulmonary arterial hypertension (PAH), PH due to left heart disease, PH due to lung diseases, PH due to chronic thromboembolic disease, and PH with unclear mechanisms.

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4
Q

What is the most common cause of pulmonary hypertension?

A

Left heart disease is the most common cause of pulmonary hypertension.

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5
Q

What are the common symptoms of pulmonary hypertension?

A

Symptoms include dyspnoea, fatigue, chest pain, syncope, and peripheral oedema.

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6
Q

What are the signs of pulmonary hypertension on examination?

A

Signs include raised JVP, right ventricular heave, loud P2 heart sound, and signs of right heart failure such as peripheral oedema and hepatomegaly.

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7
Q

What is pulmonary arterial hypertension (PAH)?

A

PAH is a subset of pulmonary hypertension caused by structural or functional changes in the pulmonary arteries, often idiopathic or associated with conditions like connective tissue diseases.

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8
Q

What is the pathophysiology of pulmonary hypertension?

A

It involves increased pulmonary vascular resistance due to vasoconstriction, vascular remodelling, and thrombosis, leading to right ventricular strain.

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9
Q

What are the risk factors for pulmonary hypertension?

A

Risk factors include connective tissue diseases, congenital heart disease, HIV, chronic lung disease, and family history.

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10
Q

What investigations are used to diagnose pulmonary hypertension?

A

Investigations include echocardiography, right heart catheterisation, chest X-ray, ECG, and blood tests (e.g., BNP).

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11
Q

What are the echocardiographic findings in pulmonary hypertension?

A

Findings may include elevated pulmonary artery systolic pressure, right ventricular hypertrophy, and dilatation.

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12
Q

What is the gold standard for diagnosing pulmonary hypertension?

A

Right heart catheterisation is the gold standard for measuring pulmonary artery pressures and diagnosing pulmonary hypertension.

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13
Q

What are the ECG findings in pulmonary hypertension?

A

ECG may show right axis deviation, right ventricular hypertrophy, and right atrial enlargement.

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14
Q

What are the chest X-ray findings in pulmonary hypertension?

A

Findings may include enlarged pulmonary arteries, pruning of peripheral vessels, and right ventricular enlargement.

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15
Q

What are the common causes of pulmonary arterial hypertension (PAH)?

A

Causes include idiopathic PAH, connective tissue diseases, congenital heart defects, and portal hypertension.

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16
Q

What is chronic thromboembolic pulmonary hypertension (CTEPH)?

A

CTEPH is caused by unresolved pulmonary emboli leading to obstruction of pulmonary vessels and increased pulmonary artery pressure.

17
Q

What are the differential diagnoses for pulmonary hypertension?

A

Differential diagnoses include heart failure, chronic obstructive pulmonary disease (COPD), interstitial lung disease, and pulmonary embolism.

18
Q

What is the role of BNP in pulmonary hypertension?

A

BNP (B-type natriuretic peptide) levels are often elevated due to right ventricular strain and can aid in diagnosis and monitoring of pulmonary hypertension.

19
Q

How is pulmonary hypertension classified?

A

It is classified into five groups: PAH (Group 1), PH due to left heart disease (Group 2), PH due to lung disease (Group 3), CTEPH (Group 4), and PH with unclear mechanisms (Group 5).

20
Q

What is the medical management of pulmonary hypertension?

A

Management includes vasodilators (e.g., prostacyclins, endothelin receptor antagonists, PDE-5 inhibitors), oxygen therapy, and anticoagulation.

21
Q

What is the role of oxygen therapy in pulmonary hypertension?

A

Oxygen therapy improves oxygenation, reduces pulmonary vasoconstriction, and is particularly beneficial in Group 3 PH due to lung diseases.

22
Q

What surgical options are available for pulmonary hypertension?

A

Surgical options include pulmonary endarterectomy for CTEPH and lung transplantation for severe cases.

23
Q

What lifestyle modifications are recommended for pulmonary hypertension?

A

Patients should avoid heavy exertion, maintain a healthy weight, stop smoking, and avoid high altitudes.

24
Q

What is the prognosis for pulmonary hypertension?

A

Prognosis depends on the underlying cause and treatment, but it can be poor without appropriate intervention, especially in idiopathic PAH.

25
Q

What are the complications of pulmonary hypertension?

A

Complications include right heart failure, arrhythmias, and sudden cardiac death.