SM 165a - Pulmonary HTN Flashcards

1
Q

Describe the hemodynamics of CTEPH (WHO group 4)

MAP @ rest:

PCWP:

A

WHO Group 4:

MAP @ rest: 25 mmHg

PCWP: ≤15 mmHg

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2
Q

Describe the hemodynamics of pulmonary venous hypertension (WHO group 2)

MAP @ rest:

PCWP:

mPAP @ exercise:

PVR:

A

WHO Group 2:

MAP @ rest: >25 mmHg

PCWP: 15 mmHg*

mPAP @ exercise: >30 mmHg

PVR: <3 Wood units*

* = difference between group 1 and group 2

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3
Q

Describe the hemodynamics that define pulmonary arterial hypertension (WHO group 1)

MAP @ rest:

PCWP:

mPAP @ exercise:

PVR:

A

WHO Group 1:

MAP @ rest: >25 mmHg

PCWP: ≤15 mmHg*

mPAP @ exercise: >30 mmHg

PVR: >3 wood units* - WHO Group 1 is a “high resistance” disease

* = hemodynamic differences between WHO groups 1 and 2.

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4
Q

Describe the hemodynamics of pulmonary hypertension due to lung disease (WHO group 3)

MAP @ rest:

A

WHO Group 3:

MAP @ rest: >20 mmHg

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5
Q

How would you differentiate between the following classification?

Lung disease without PH: mPAP =

Lung disease with PH: mPAP =

Lung disease with severe PH: mPAP =

A

Lung disease without PH: mPAP <25 mmHg

Lung disease with PH: mPAP >25 mmHg

Lung disease with severe PH: mPAP ≥35 mmHg OR mPAP >25 mmHG w/ low cardiac index

(Think COPD, ILD, CPFE as far as lung disease goes)

CPFE = combined pulmonary fibrosis & emphysema

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6
Q

In approaching this patient (RAP = 15 mmHg, mPAP = 49 mmHg, PCWP = 23 mmHg) with pulmonary hypertension, what would be the most appropriate first step in management?

  1. Start diuresis with a loop diuretic for heart failure
  2. Start IV epoprostenol for pulmonary vasodilation to acutely decrease mean pulmonary artery pressure
  3. Start the endothelin receptor antagonist, bosentan, to decrease pulmonary vascular resistance and decrease RV strain
  4. Start full anticoagulation with coumadin
A

a. Start diuresis with a loop diuretic for heart failure

  • PCWP ≥ 25 mmHg => pulmonary venous hypertension
    • Due to left heart failure
    • Treatment = diuresis + optimize HF medication
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7
Q

In lung disease with severe pulmonary hypertension, what is the driver of reduced exercise capacity?

A

Circulatory impairment (rather than ventilatory impariment)

Likely due to severe vascular abnormalities

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8
Q

Pulmonary hypertension that is idiopathic, heriable, or drug or toxin induced is classified as WHO group _____

(Caused by __________________)

A

Pulmonary hypertension that is idiopathic, heriable, or drug or toxin induced is classified as WHO group** **1

(Caused by pulmonary arterial hypertension)

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9
Q

What are some of the causes of WHO group 1 pulmonary hypertension?

A
  • Idiopathic
  • Heritable
  • Drug/toxin-induced
  • Associated with…
    • Connective tissue dieseases
    • HIV infection
    • Portal HTN
    • Congenital (pulmonary shunt)
    • Schistosomiasis
    • Chronic hemolytic anemia
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10
Q

What drugs target the endothelin pathway in the treatment of WHO group 1 PAH?

A
  • Ambrisentan
  • Bosentan
  • Macitentan
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11
Q

What drugs target the nitric oxide pathway in the treatment of WHO group 1 PAH?

A
  • Phosphodiesterase inhibitors
    • Sildenafil
    • Tadalafil
  • Guanylate cyclase stimulators
    • Riociguat
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12
Q

What drugs target the prostacyclin pathway in the treatment of WHO group 1 PAH?

A

Goal = increase the effects of prostacyclin

  • Epoprostenol
  • Treprostinil
  • Iloprost
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13
Q

What histological changes would you expect to see in WHO Group 1 pulmonary hypertension?

A

WHO Group 1 = Pulmonary arterial hypertension

  • Smooth muscle hypertrophy
  • Neointima formation neovascularization
  • Endothelial cell proliferation
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14
Q

What histological changes would you expect to see in WHO Group 2 pulmonary hypertension?

A

WHO Group 2 pulmonary hypertension = Pulmonary Venous Hypertension (due to left heart failure)

  • Medial thickening
  • Occlusive venopathy
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15
Q

What is the equation for pulmonary vascular resistance?

A

PVR = (mPAP - Left atrial pressure) / CO

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16
Q

What is the gold standard for diagnosing Pulmonary Hypertension?

A

Right heart catheterization

Many tests preceed this

17
Q

What is the treatment for WHO Group 1 PAH?

A

Pulmonary vasodilator therapy:
Not curative, but helps manage symptoms

  • Endothelin receptor antagonists
  • Phosphodiesterase inhibitors*
    • Inhibits the breakdown of NO
  • Soluble guanylate cyclase stimulators*
    • Stimulates NO receptors
  • Prostacyclins

*Targets the Nitric Oxide pathway

18
Q

What is the treatment for WHO group 2 PVH?

A

Optimize heart failure medications

Diuresis

Pulmonary vasodilators are contraindicated

19
Q

What is the treatment for WHO group 3 pulmonary hypertension?

A

Optimize lung disease medications

Reverse hypoxia

20
Q

What is the treatment for WHO group 4 pulmonary hypertension?

A

WHO group 4 = CTEPH

  • Anticoagulation
  • Referral for thromboendarterectomy
    • Remove the clot
  • Vasodilators
    • Bridge to surgery, or if the operation is contraindicated
21
Q

Which WHO group pulmonary hypertension is curable?

A

WHO group 4 - Chronic thromboembolic pulmonary hypertension (CTEPH)

22
Q

Which WHO group pulmonary hypertension is driven by disease at location D?

A

WHO group 2 = Pulmonary Venous Hypertension

(due to left heart failure)

23
Q

Which WHO group pulmonary hypertension is driven by disease at location C?

A

WHO group 1 = Pulmonary arterial hypertension

24
Q

Which WHO group pulmonary hypertension is driven by disease at location B?

A

WHO Group 3 = Lung Disease

25
Q

Which WHO group pulmonary hypertension is driven by disease at location A?

A

WHO group 4 = CTEPH (Chronic thromboembolic pulmonary hypertension)

26
Q

WHO group pulmonary hypertension is caused by left heart disease

A

WHO group 2 pulmonary hypertension is caused by left heart disease

27
Q

WHO group pulmonary hypertension is caused by chronic thromboembolic pulmonary hypertension

A

WHO group 4 pulmonary hypertension is caused by chronic thromboembolic pulmonary hypertension

28
Q

WHO group pulmonary hypertension is caused by pulmonary arterial hypertension

A

WHO group 1 pulmonary hypertension is caused by pulmonary arterial hypertension

29
Q

WHO group pulmonary hypertension is caused by unclear or multifactorial mechanisms

A

WHO group 5 pulmonary hypertension is caused by unclear or multifactorial mechanisms

30
Q

WHO group 1 pulmonary hypertension is caused by

A

WHO group 1 pulmonary hypertension is caused by pulmonary arterial hypertension

31
Q

WHO group 2 pulmonary hypertension is caused by

A

WHO group 2** pulmonary hypertension is caused by **left heart disease

32
Q

WHO group pulmonary hypertension is caused by lung disease and/or hypoxia

A

WHO group 3 pulmonary hypertension is caused by lung disease and/or hypoxia

33
Q

WHO group 3 pulmonary hypertension is caused by

A

WHO group 3 pulmonary hypertension is caused by lung disease and/or hypoxia

34
Q

WHO group 4 pulmonary hypertension is caused by

A

WHO group 4 pulmonary hypertension is caused by chronic thromboembolic pulmonary hypertension

35
Q

WHO group 5 pulmonary hypertension is caused by

A

WHO group 5 pulmonary hypertension is caused by unclear or multifactorial mechanisms

36
Q

WHO group pulmonary hypertension is caused by lung disease and/or hypoxia

A

WHO group 3 pulmonary hypertension is caused by lung disease and/or hypoxia

37
Q

Why is it important to correctly categorize pulmonary hypertension?

A

Therapies differ between groups - Incorrect treatments can worsen clinical status