Modules 2.1 & 2.2 Flashcards

1
Q

What are the different respiratory rhythms?

A

Kussmaul: deep, laboured breathing
Cheyne-Stokes: alternating deep and shallow breathing with periods of apnoea
Ataxic: irregular breathing pattern
Apneustic: prolonged insp. phase followed by short exp. phase

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2
Q

What is Paroxysmal nocturnal dyspnoea?

A

Due to left-sided congestive heart failure.
- body fluid is redistributed during sleep, but left ventricle cannot keep up with output of right ventricle, leading to increased venous return and pulmonary oedema
- individual wakes up gasping for air and coughing

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3
Q

What is the pathway of dyspnoea?

A

Motor output: efferent signals from primary motor cortex/brainstem to muscles, feedback to senseory cortex
Chemoceptor stimulation: aortic arch and carotid bodies sensing O2 & CO2 levels, medulla sensing CO2 & H+ in CSF
Causes: HF, anemia, PE, Pluerisy, P cancer and fibrosis, pneumonia, COPD, asthma

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4
Q

What is a cough?

A
  • innate response to irration of resp. tract
  • defense mechanism to manually clearn airway of debris or pathogens
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5
Q

What are the different types of breath sounds?

A

Crackles= serous secretions
Course crackles= thicker mucous
Absence of breath= lung collapse
Wheezing/whistling= narrowing of small airway
Stridor= upper airway obstruction

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6
Q

What defines a acute, sub-acute and chronic cough?

A

Acute: <3 weeks
- infectious (viral, bronchitis), non infectious (exacerbations)
Sub-acute: 3-8 weeks
- post infection due to epi cell inflammation
Chronic: >8 weeks
- asthma, GORD, UACS, NAEB

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7
Q

What are the differences in sputum?

A

Dark-coloured: pneumococcal pneumonia
Purulent/odoured: bronchiectasis
Thick mucous: asthma/CF
Blood tinged: tumour or TB
Haemoptysis: PE

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8
Q

What is cyanosis and the differences between central and peripheral?

A
  • bluish discoloration of the skin and mucous membranes due to inc in deoxyhaemoglobin
    Central: locating around lips and tongue, o2 <85%, due to insufficient O2, dec pulmonary bf, mixing of arterial and venous blood, or polycythaemia.
    Peripheral: located in fingers and toes, blood contains greater than 5g of deoxyhaemoglobin.
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9
Q

What is the difference between hypoxia and hypoxemia?

A

Hypoxia: dec. o2 in tissues
Hypoxemia: dec. o2 in arterial blood

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10
Q

What is digital clubbing?

A
  • growth of digits due connective tissue
    proliferation and increased blood flow beneath the nail matrix.
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11
Q

What are the stages of clubbing?

A
  1. Softening of nail bed
  2. Increased angle of nail plate
  3. Inc. convexity of nail
  4. Enlargement of distal finger
  5. Glossy and striated nail
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12
Q

What is the pathophys. of digital clubbing?

A
  1. Megakaryocytes fail to fragment in the pulmonary vasculature.
  2. Unfragmented megakaryocytes enter systemic circulation.
  3. They accumulate in distal capillary beds
  4. Release growth factors: Platelet-derived growth factor (PDGF) and vascular
    endothelial growth factor (VEGF).
  5. Growth factors stimulate: Vascular and connective tissue proliferation, leading to
    the characteristic bulbous appearance.
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13
Q

What’s the difference between obstructive and restrictive diseases?

A

Obstructive: airflow limitation during exhalation, inc. lung volumes
Restrictive: lung expansion prevention during inhalation, dec. lung volumes

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14
Q

What are the normal arterial blood gas (ABG) values?

A

pH: 7.35-7.45, determines acidity levels
PaCO2: 35-45mmHg, indicates resp. component
HCO3: 22-36mmol/L, inidcates metabolic component

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15
Q

How are O2 and CO2 transported throughout the body?

A

O2: Mainly attached to haemoglobins
CO2: 7% dissolved into plasma, 23% attached to haemoglobins, 70% converted into HCO3 to enter an erythrocyte to be exchanged for Cl, converted back to CO2 to then be exhaled

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16
Q

What is the difference between hyper/hypocapnia?

A

Hyper: hypoventilation, hence inc. CO2 in body >60mmHg severe
Hypo: hyper ventilation, hence dec. CO2 in body <25mmHh severe
- alters acidity of blood in body

17
Q

What are the differences between Type I and Type II Resp failure?

A

Type I: inadequate oxygenation of blood, hypoxemia
- due to low O2 environment, impaired alveolar diffusion or ventilation perfusion mismatch
Type II: inadequate oxygenation of blood and CO2 removal capabilities
- due to ventilation failure, obstructive or musculoskeletal problems