Pulmonary Vascular Disease - Presberg Flashcards

1
Q
  1. What is the major cause of pulmonary embolism (PE)?
  2. What is a major risk factor for thromboembolism formation in the first place?
A
  1. DVT: 60-90% of PE originate in proximal deep veins of legs
  2. Thrombophilias
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2
Q

Name some mutations responsible for the thrombophilias that increase the risk of thrombosis / thromboembolism.

A

Mutation (result of mutation):

  • Prot C or S (defective)
  • ATIII (defective)
  • Factor V (un-inactivatable by Prot C)
    • aka Factor V Ledien
  • Prothrombin (activating)
  • MTHFR (some enzyme that helps with homocysteine → methionine pathway)
  • Factor VIII (activating)
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3
Q

Name some medical risks of venous thromboembolism aside from thrombophilias (think of Virchow’s Triad).

A
  • Hip or knee surgery
  • Immobility
  • CHF
  • Obesity
  • Malignancy
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4
Q

What is the prognosis of PE if untreated?

If treated?

A

Untreated: 30%

Treated: 1-3% (worse with chronic PE dur to underlying risk factors)

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5
Q

Describe some nonspecific symptoms of PE.

A
  • Dyspnea (acute or subacute)
  • Dizziness & syncope
    • massive / saddle PE
  • Pleuritic chest pain
    • infarct / bloody effusion
  • Palpitations & Tachycardia
  • Hemoptysis
    • infarct
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6
Q

What type(s) of imaging are typically used to diagnose:

  • DVT?
  • PE?
A
  • DVT
    • Doppler Ultrasound
  • PE
    • CT pulmonary angiogram
    • Ventilation perfusion scans
      • Will see mottled/patchy perfusion pattern instead of a nice solid shape
      • Some fuzz around the edges of the perfused area is normal - look for major gaps
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7
Q

What are the five groups of chronic pulmonary HTN disorders according to the WHO classification scheme?

What categorization was recently abolished?

A

I. Pulmonary Arterial HTN (PAH)

  • “Precapillary”
  • Idiopathic or caused by things not listed below
  • e.g. drugs, infections (HIV, Schistosomiasis), genetic disorder, congenital disorder, etc.

II. Pulm HTN + left heart disease

  • Most common form

III. Pulm HTN + lung diseases

  • e.g. COPD, interstitial lung diseases
  • FVC < 70%

IV. Pulm HTN + chronic thromboembolic disorders

V. Pulm HTM + Misc diseases

  • Tumors
  • Blood disorders
  • Systemic disorders (sarcoidosis, vasculitis)
  • Metabolic disorders

Primary vs. Secondary classification recently eliminated

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8
Q

What is the single most common etiology of Pulmonary HTN?

A

Left heart disease

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9
Q

What is the specific diagnostic criteria for Group I Pulmonary Arterial HTN (PAH)?

A
  • Mean pulmonary arterial pressure (mPAP) > 25mmHg at rest
  • Normal wedge pressure (PCWP)
    • Recall: PWCP estimates left heart filling pressure
    • Abnormal would likely indicate Group II
    • This is important differential as Group II is most common type
  • Not Groups II, III, IV, or V
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10
Q

What is the best noninvasive test for diagnosing PH? (Pulmonary HTN)

What findings are sought using this test?

A

Echcardiogram

Look for:

  • R atrial and ventricular changes
  • R ventricular overload
  • Estimate PA pressure
  • Congenital heart disease, PFO, or shunt
  • Pericardial effusion
    • Impacts prognosis
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11
Q

What are the specific criteria that indicate decreased RV function?

A
  • Right Atrial Pressure (RAP) > 10mmHg
  • CI < 2.2 L/min•m2
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12
Q
  1. What heritable gene mutation is often associated with cases of Group I PAH (aka idiopathic PAH or IPAH)
  2. What is the inheritance pattern?
  3. How much of IPAH is due to this?
A
  1. BMPR2 mutations
    • “Bone morphogenic protein receptor type II” (name likely not important)
    • Normal receptor helps inhibit proliferation of vascular smooth muscle - without it, overproliferation leads to PH
  2. Auto Dom w/ low penetrance
    • Pathoma: Typically seen in young females
  3. 10% of IPAH is heritable, 55% of heritable IPAH is from BMPR2
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13
Q
  1. What specific (not directly inherited) disease is also associated with Group 1 PAH?
  2. From a few slides ago: do you recall other more general causes of Group I PAH?
A
  1. Scleroderma
  2. Other causes:
    • Infection (HIV, schistosoma)
    • Drugs
    • Inherited or congenital disorder
    • Portal HTN / liver disease
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14
Q

The 5 WHO PAH Groups describe the causes of PAH.

On the other hand, the 4 WHO/NYHA PAH functional Classes describe the severity of PAH.

Describe these 4 PAH classes.

A
  • Class I
    • Sxs do not limit physical activity
    • Ordinary activity does not cause undue comfort
  • Class II
    • Slight limitation of activity
    • Comfortable at rest
    • Experiences sxs with ordinary activity
  • Class III
    • Marked limitation of activity
    • Comfortable at rest
    • Expeiences sxs with minimal activity
  • Class IV
    • Inability to carry out any activity
    • Sxs may be present at rest
    • Discomfort increased by any activity
    • Manifest signs of right heart failure
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15
Q

What vascular pathologies can be noted in Group I PAH?

Which is pathognomonic to Group I PAH? Hint: Image

A
  • Large pulm. Artery Thickening
  • Medial wall smooth muscle hypertrophy
  • Plexiform Lesion in small vessels
    • Pathognomonic
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16
Q
  1. What 3 major endothelial cell defects have been associated with PAH?
  2. What two core effects on vasculature do all three of these pathways share?
  3. Why are these defects important?
A
  1. Endothelial cell defects:
    • Decreased prostacyclin
    • Increased endothelins
    • Decreased NO Synthase
  2. All three affect:
    • degree of vascular tone
      • (prost and NO dilate, endothelins constrict)
    • level of SMC proliferation
      • (prost and NO inhibit, endothelins activate)
  3. These three pathways are implicated in PAH pathogenesis and are targets for current and emerging therapies
17
Q

Name the drug form of prostacyclin given to treat PAH.

A

Epoprostenol

18
Q

Name a endothelin receptor antagonist used to treat PAH.

A

Bosentan

(Bos-EN-t-AN is an ENdothelin receptor ANtagonoist)

19
Q

Name two drugs used to treat PAH by increased NO levels. How do they work?

A
  1. Sildenafil (Viagra!)
    • Increases cGMP
  2. Riociguat
    • soluble guanylate cyclase stimulator
    • very recent
20
Q

What is the morphology of Pulmonary Vasculitis?

A
  • Pulmonary & alveolar hemorrhage
  • Lung infiltrates
    • nodular
    • cavitary lesions
      • “gas-filled areas of the lung in the center of a nodule, mass or area of consolidation”
    • Associated with interstitial lung disease
21
Q

Name 4 types of alveolar hemorrhage syndromes

A
  1. Goodpasture’s Syndome
    • aka anti-basement membrane Ab disease / ABMAb
  2. Wegener’s Granulomatosis
    • aka ANCA-associated vasculitis
  3. Idiopathic Pulmonary Hemosiderosis
  4. Collagen vascular diseases
    • e.g. SLE
22
Q

What is the classic triad of symptoms in diagnosis of alveolar hemorrage syndromes?

A
  1. Hemoptysis
  2. Pumonary infiltrates
  3. Anemia
23
Q

What are three life-threatening complications of alveolar hemorrhage syndromes?

A
  1. Respiratory failure
  2. Acute renal failure
  3. Severe anemia
24
Q

Name some lab and imaging techniques used to diagnose the underlyign causes of alveolar hemorrage syndromes.

A
  • sputum / tracheal aspirate
  • bronchoalveolar lavage (BAL)
    • heart failure cells
  • urine (may alert you to other organ problems)
  • serial Hgb
  • Serial CXRs
  • Serology:
    • ABMAb
    • ANCA
    • ANA
  • Biopsy:
    • Lung
    • Skin (when a more systemic cause is suspected)
    • Renal (ditto)
25
Q

(Sort of review)

What drugs are often used to treated vasculitis diseases?

A

Long-term immune suppression!

  • Prednisone
  • Cyclophosphamide
  • Rituximab
    • (anti CD20 mAb → anti B-cell, if you forgot)
26
Q

Which part of the respiratory tract is affected first in Wegener’s Granulomatosis?

A

Upper respiratory tract affected before (and somewhat more often than) Lower tract