W5 Flashcards

1
Q

What is the main pathophysiological difference between an obstructive and restrictive lung condition?

A

Obstructive ==> Limitation of expiratory airflow due to abnormal airways
Restrictive ==> Limitation of inspiratory airflow due to abnormal lung tissue

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2
Q

What is COPD?

A

Chronic obstruction of expiratory airflow due to abnormalities in the airways and/or loss of alveoli tissue

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3
Q

What are the typical clinical findings in a COPD pt?

A
  • SOB
  • Incr. RR and WOB
  • Wheeze
  • Cough
  • Abnormal ausc. findings
  • Fatigue
  • Hyperinflation on CXR
  • FEV1 / FVC < 0.7
  • Hypoxemia +/- hypercapnia
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4
Q

What are the risk factors for COPD?

A
  • Smoking
  • Secondary exposure to smoke or other environmental toxins
  • Age
  • Hx of childhood respiratory infections
  • Genetics
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5
Q

What is pathophysiology for COPD?

A

Airway inflammation (from chronic exposure to risk factors) ⇒ mucus hypersecretion + alveoli tissue destruction ⇒ Decr. elastic recoil and radial traction (decr. lung compliance) + expiratory airflow obstruction ⇒ Air trapping ⇒ Hyperinflation

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6
Q

Chronic hypoxemia can lead to R sided heart failure. What is the term and pathophysiological process for this?

A

Cor pulmonale
Chronic hypoxia → Hypoxia pulmonary vasoconstriction → Pulmonary artery HT → R ventricle pathological hypertrophy → R sided diastolic dysfunction (cor pulmonale)

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7
Q

What are the complications from hyperinflated lungs

A

⇑ Alveolar dead space
V/Q mismatch
Hypoxemia
Dyspnoea
⇑ Use of accessory respiratory muscle
⇓ Use of diaphgram during ventilation

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8
Q

What is the pathophysiology of asthma?

A

Incr. airway sensitivity to stimulus ⇒ bronchial hyperactivity ⇒ mucus hypersecretion (goblet cell hypertrophy) + bronchial smooth muscle hypertrophy ⇒ Incr. airway obstruction and constriction ⇒ Decr. expir. airflow + premature airway collapse

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9
Q

Describe bronchiectasis.

A

Permanent dilation of airways

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10
Q

What is the pathophysiology of bronchiectasis?

A

Initial infection ⇒ Inflammatory and mucociliary response ⇒ Mucus hypersecretion + cilia dysfunction (impaired mucociliary clearance) ⇒ mucus plug formation ⇒ microbial colonisation ⇒ further inflammation and infection ⇒ destruction of airway elasticity and muscular components⇒ ⇓ bronchial elastic recoil ⇒ further ⇓ mucociliary clearance ⇒ cycle of chronic inflammation

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11
Q

What is the pathophysiology of cystic fibrosis?

A

CF transmembrane conductance regulator gene defect ⇒ ⇑ chloride and sodium ion uptake in epithelial cells of respiratory tract ⇒ ⇑ water reuptake into cells ⇒ ⇓ Aqueous sole layer height ⇒ ⇑ mucus viscosity and tenacity ⇒ ⇓ mucociliary clearance ⇒ Mucus plug formation ⇒ Microbial colonisation ⇒ Recurrent respiratory infection

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12
Q

What the non-respiratory complications of cystic fibrosis?

A
  • Fat malabsorption
  • Poor weight gain
  • Anemia
  • Osteopenia
  • Malnutrition
  • Cystic fibrosis diabetes
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13
Q

What is the pathophysiology of pulmonary fibrosis?

A

Irreversible accumulation of scar tissue within the lung interstitium ⇒ Thickening and rigidity of interstitium ⇒ ⇓ lung compliance + ⇑ elastic recoil ⇒ ⇓ lung expansion/capacity

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14
Q

Clubbing is a common clinical sign in chronic pulmonary diseases due to ____

A

Chronic hypoxemia

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15
Q

List 4 respiratory disease questionnaires

A
  • Chronic respiratory disease questionnaire
  • St George’s respiratory disease questionnaire
  • Nijmegen Questionnaire
  • Modified medical research council dyspnea score
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16
Q

What is dynamic hyperinflation and pathophysiology underlying it?

A

Dynamic hyperinflation ⇒ Incr. hyperinflation during physical activity
Hyperinflation ⇒ Diaphragm in a shortened position ⇒ ⇓ Contribution to ventilation ⇒ ⇑ ventilation requirements (during physical exertion) ⇒ ⇑ Expir. Flow rate demands + ⇓ time for expir. ⇒ Inability to meet demands (due expir. Flow limitations) ⇒ ⇑ hyperinflation during physical activity (dynamic hyperinflation) ⇒ ⇑ Dyspnea