Airway mucosal Function Flashcards

Week 8

1
Q

Functions of airway mucous

A

Barrier to water loss

Barrier to microbial invasion

Clearance of inhaled foreign matter

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2
Q

Mucosal dehydration consequences

A

Increased viscosity and elasticity

Adherence to airway wall (decreased ability to clear)

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3
Q

What is the Pathogenesis of ALL common airway diseases?

A

Excessive mucous = impaired clearance

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4
Q

What are the 2 principal cells of surface epithelium?

A

Ciliated

Secretory (cara/club, goblet and serous)

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5
Q

Where do we fine submucosal glands?

A

Nose, trachea and bronchi

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6
Q

What conditions lead to excessive mucous and how?

A

Smoking, infection, oxidative stress and pathogenic factors

= secretory cell hypertrophy and goblet cell hyperplasia.

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7
Q

What is the dominant variable in determining mucus clearance?

A

ASL hydration

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8
Q

Why is it important for ASL to be hydrated?

A
  • increases mucus transport rates (movement)
    • maintains PCL depth so that cilia can beat
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9
Q

Mechanism of ASL secretion

A

Epithelial cell active ion transport:

Cl and HCO3 secretion –>

CFTR inhibits ENaC activity –>

Decreased Na reabsorption –>

CFTR stimulates 2Cl channels and a Cl/HCO3 exchanger –>

Na and water follow gradient in paracellular pathways –>

Increased ASL hydration and pH.

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10
Q

What are alveolar macrophages and what occurs if they die?

A

gulf and phagocytose foreign particles and deliver to mucociliary escalator, lymphatics and blood.

die: Release trypsin –> tissue damage (digests elastin)

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11
Q

What are the consequences of Primary Cilia Dyskineses?

A

Stagnation and accumulation of mucous (early onset refractory or recurrent airway infections)

Infertility: defect in flagella of spermatozoa and cilia of uterine tubes

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12
Q

What is the mechanistic change of COPD?

A

Increased airway resistance (obstruction)

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13
Q

What are the 3 main mechanisms of airway obstruction?

A

Conditions within lumen

Causes within wall of airway

Causes outside the airway

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14
Q

What are conditions within lumen that lead to airway obstruction?

A

Partial occlusion by excessive secretions
= Chronic bronchitis and P Oedema

Aspiration of foreign material
=Localised or complete occlusion

Retained post-op secretions

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15
Q

What are the causes within wall of airway that lead to airway obstruction?

A

Contraction of bronchial SM
=Asthma

Hypertrophy of mucous glands
=Chronic bronchitis

Inflammation or oedema of airway wall
=Chronic bronchitis and asthma

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16
Q

What are the causes outside the airway that lead to airway obstruction?

A

Destruction of lung parenchyma
=Emphysema

Localised compression of bronchus
=Enlarged lymph nodes or neoplasm

Peri bronchial oedema

17
Q

What is COPD-BC?

A

Excessive production of mucus for most days for at least 3 months in a year for at least the last 2 successive years

18
Q

COPD-BC pathogenesis

A

Chronic inflammation triggered by chronic irritation via inhaled substances or infection

19
Q

treatment of COPD-BC

A

Liberal fluid intake (hydrates ASL and increases mucus clearance by decreasing mucous viscosity)

physiotherapy (move mucus)

postural changes

bronchodilators, anticholinergics, and corticosteroids

20
Q

Characteristics of CF classes I-III.

A

Classic CF, early diagnosis

Increased sweat Cl

Pancreatic insufficiency

21
Q

characteristics of CF classes IV-VI.

A

Late diagnosis

Sweat Cl near normal

Pancreatic sufficiency

22
Q

CF Pathogenesis

A

Dehydrated ASL ( increased adherence and decreased PCL depth)

Mucous hypersecretion

Acidic ASL from decreased HCO3 transport

23
Q

Clinical features of CF

A

Course crackles and bronchial auscultation

Consolidation

Fibrosis and cystic changes

24
Q

Pulmonary function impact of CF.

A

Abnormal ventilation distribution

Increased alveolar-arterial difference

Decreased FEV unresponsive to bronchodilators

Increased has trapping

Decreased exercise tolerance

25
Q

CF management

A
  • antibiotics (treat antibiotics)
  • physiotherapy and postural drainage
  • mucolytic agents
  • CFTR modulators
  • lung transplant
26
Q

what are the causes of Respiratory failure type 1

A

Ventilation/perfusion mismatch

Increased shunt

Diffusion impairment

Alveolar hypoventilation

27
Q

Features of resp failure Type 2

A

Gas exchange failure

Hypoxemia w normocapnia or hypocapnia

PaO2 < 60mmHg

28
Q

Features of Type 2 Resp Failure

A

Ventilatory failure

Hypoxemia w hypercarbia

PaO2 < 60mmHg and PaCO2 > 45mmHg

29
Q

Causes of Type 2 resp failure

A

Decreased output from central resp centres (drug overdoes, anaesthesia)

Increased dead space (COPD)

Mechanical defect in chest wall (flail chest, kyphoscoliosis)

Inspiratory muscle fatigueq