Pulmonary HTN Flashcards

1
Q

What are the components of the pulmonary artery and right ventricle?

A
  1. Wall of the pulmonary artery and branches are only 1/3 thickness of aorta
  2. Can handle a HUGE amount of blood flow (on the way to the alveoli)
  3. Blood flow variable and dependent on cardiac output
    *5-25 liters
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2
Q

What is the ideal or healthy pressure of the pulmonary vasculature

A
  1. Low-pressure, low resistance due to large cross sectional area
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3
Q

What is the pressure of the pulmonary artery and mean pulmonary artery

A
  1. Pulmonary artery pressure
    *systolic = 15-30mmHg (PASP)
  2. Mean pulmonary artery pressure
    *9-18mmHG (MPAP)
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4
Q

What is the Right ventricular and Right atrial pressure

A

R ventricular
*systolic = 15-30mmHG
*diastolic = 2-8mmHG
R atrial (CVP)
*2-6mmHG

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5
Q

What happens to the pressure in pulmonary HTN

A
  1. Increased pulmonary artery pressure
    *resistance is affected
    *will be a complex disease state
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6
Q

What will the systolic pulmonary artery pressure (PASP) and Mean pulmonary artery pressure (MPAP) be in pulmonary HTN

A

PASP
*greater than 25-30mmHg
MPAP
*greater than 18-20mmHG

**as pulmonary vasculature resistance increases so does MPAP

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7
Q

What are the steps leading to Cor pulmonale (right sided HF)

A
  1. Increased pulmonary vasculature resistance
  2. Increased MPAP
  3. Right ventricular hypertrophy
  4. Cor pulmonale
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8
Q

In the steps leading to cor pulmonale what happens to the cardiac output

A
  1. The cardiac output will begin to compromise and decrease
    *from increased afterload and decreased contractibility
    *tachycarida is an initial compensatory response
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9
Q

What eventually leads to right HF

A
  1. Increased afterload compromises right ventricular function and eventually results in right HF
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10
Q

What is group 1 classification of pulmonary HTN

A

Pulmonary arterial hypertension (PAH) diseases that localize directly on the pulmonary arteries
*idiopathic
*inheritable
*drug and toxin induced
*connective tissue disease, HIV infection

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11
Q

What is group 2 of pulmonary HTN classifications

A

Pulmonary venous HTN due to left heart disease
*LV systolic dysfunction
*LV diastolic dysfunction
*valvular disease

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12
Q

What is group 3 of pulmonary HTN classifications

A

Pulmonary HTN due to lung disease and / or hypoxemia
*COPD
*interstitial lung disease
*sleep-disordered breathing

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13
Q

What is group 4 of pulmonary HTN classifications

A

Pulm HTN due to pulmonary obstruction
*thromboembolism

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14
Q

What is group 5 of pulmonary HTN classifications

A

Pulm HTN with unclear or multi factorial mechanisms
*hematologic disorders
*systemic disorders

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15
Q

How to determine clinical severity based on symptoms and functional status (I and II)

A

I
*symptoms free-when physical active or resting
II
*no symptoms at rest, but normal activities such as climbing the stairs, grocery shopping or making bed, some discomfort and SOB

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16
Q

How to determine clinical severity based on symptoms and functional status (III and IV)

A

III
*resting may be symptom-free but normal chores around the house are greatly limited due to SOB
IV
*symptoms at rest and serve symptoms with an activity

17
Q

What are the risk factors for PH

A
  1. OSA
  2. Lung disease (obstructive and restrictive)
  3. Obesity
  4. Gender
    *idiopathic and heritable MC in females
  5. Pregnancy
    *women already diagnosed with PH have a much higher risk of mortality
  6. Drugs and toxins (methamphetamines)
18
Q

What happens when COPD is causing PH

A
  1. Hypoxia pulmonary vasoconstriction will redirect blood flow AWAY from the poorly ventilated areas in attempt to match up the ventilation / perfusion ratio and optimize oxygenation of blood
19
Q

What can hypoxia pulmonary vasoconstriction lead to?

A
  1. Vascular remodeling and sustained vasoconstriction
    *thickening of the media and peripheral extension of muscle into pulmonary vessels that are normally devoid of muscle
20
Q

What are the sign of symptoms of pulmonary HTN

A
  1. Exertional dyspnea and fatigue
  2. Syncope
  3. Hemoptysis
21
Q

Why is the diagnosis of pulmonary HTN delayed

A
  1. Because symptoms are attributed incorrectly
    *age, deconditioning, or a coexisting or alternate medical condition
22
Q

What will you find during the PE?

A
  1. Narrow splitting of second heart sound w/loud pulmonary component, R-sided third heart sound, systolic ejection click, tricuspid regurgitation murmur
  2. Hepatomegaly, ascities
  3. Lower extremity edema
  4. Cyanosis
23
Q

What will be on the PE (more advanced disease)

A
  1. Dyspnea at rest
  2. Chest pain, pressure
  3. Dizziness
  4. Weakness or fatigue
  5. Cyanosis
  6. Chronic cough
  7. Palpitations, tachycardia, abdominal pain
  8. Exertional syncope (severe)
24
Q

What lab studies should you conduct

A
  1. BNP (brain natriuretic peptide)
    *secreted by the ventricles in response to excessive stretching of the cardiomycytes
  2. Thyroid function
  3. Liver function
  4. Kidney function
  5. Electrolytes
    *labs may be WNL, depending on cause of Pulm HTN
25
What diagnostic tests could you conduct
1. PFT 2. CXR 3. EKG 4. Exercise testing
26
What will be on the CXR?
1. Enlargement of pulmonary, hilar vessels 2. Attenuation (pruning) of the peripheral pulmonary arterial tree 3. Advanced disease *enlargement of the right atrium and ventricles
27
What will be on the EKG
1. Right ventricular strain of hypertrophy *right axis deviation, R BBB 2. Right atrial enlargement *peaked P waves in inferior and right-sided leads
28
What imaging studies could you do?
1. Echocardiogram w/Doppler flow *right ventricular dilatation or dysfunction *elevated right systolic ventricular pressure 2. CT of chest 3. V/Q scan 4. Cardiac MRI
29
What is the gold standard for confirming Pulm HTN?
1. Right heart catherteization *can quantify / obtain pressures
30
What is the reason to conduct a left heart catheterization?
LV dysfunction or valvular disease
31
What is the primary action for treatment
1. Identify, identify cause, and aim therapy at cause
32
What is the treatment for group 1 of Pulm HTN
Pulmonary vasodilators *endothelin receptor antagonists *phosphodiesterase inhibitors *prostacyclin/prostacyclin analogue
33
What are some other treatment options
1. Calcium channel blockers 2. Digoxin 3. Diuretics 4. Anticoagulants (Warfarin, for group 4)
34
What is atrial septostomy (right to left shunt)? (Potential tx)
Want to divert blood flow to bypass the pulmonary vascular bed and enter the systemic circulation which will elevate systemic blood flow and maintaining tissue perfusion
35
What is the benefit of right to left shunt
1. Decreased pressure of the pulmonary vasculature bed, but 2. Less oxygenated blood in circulation *not curative, only for symptoms
36
What is the prognosis
Can improve with therapy (group 1) 1. Poor prognosis *Age >50 *Cor Pulmonale, RV dysfunction *male gender *functional class III or IV