Chest Medicine Flashcards

(51 cards)

1
Q

Airway diseases (3)

A

COPD, Asthma, Bronchiectasis

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2
Q

Respiratory Diseases of the PARENCHYMA/ INTERSTITIUM (4)

A

Fibrosis, Hypersensitivity Pneumonitis,

Emphysema, pneumonia

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3
Q

Respiratory Diseases of the Pluera

A

Pleural Effusion, Pleural thickening, Mesothelioma/Pleural malignancy

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4
Q

Vascular problems

A

PE, Pulmonary hypertension

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5
Q

Ventilation problems

A

Sleep disordered breathing, obesity hypoventilation, neuromuscular problems, thoracic cage abnormality

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6
Q

Imaging for lung diseases

A

CXR, HRCT,

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7
Q

Pulmonary function tests

A

Spirometry – FEV1/ VC/ FVC/ FEV1/VC ratio

Lung volumes – TLC/ RV

Transfer factor – TLCO/ KCO

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8
Q

Restrictive lung diseases

A

Normal FEV1/VC

Obesity, Thoracic cage abnormalities, fibrosis, neuromuscular abnormalities

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9
Q

Obstructive lung diseases

A

FEV1/VC <70%
Asthma
COPD
Bronchiectasis

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10
Q

Flow Volume loops

A

Can show if airflow is appropriate for a particular lung volume. Can give an indication of where major problem is.

Large airway obstruction- flattened exp and inspir loop,

Diffuse small airway obstruction- early peaked exp loop and normal inspir loop

Intrathoracic obstruction (mediastinal tumour) have a more pronounced affect on the expiratory than inspiratory limb

Extrathorcic obstruction (goiter) has a more pronounced affect on the inspiratory than expiratory limb

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11
Q

Lung volumes TLC & RV- Obstructive

A

TLC increases with hyperinflation, RV increases due to gas trapping

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12
Q

Lung volumes TLC & RV- Restrictive

A

TLC- reduced

RV- normal/low

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13
Q

Test of functionality of the alveolar-capillary membrane

A

Transfer factor

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14
Q

Factors affecting TLCO (5)

A
  1. Ventilation Perfusion Mismatch - common in many lung diseases
  2. Reduction in the area of alveolar-capillary membrane - e.g. emphysema
  3. Increased thickness of alveolar-capillary membrane - e.g. pulmonary fibrosis
  4. Pulmonary Blood flow - e.g. pulmonary hypertension
  5. Haemoglobin concentration - e.g. anaemia leads to a decrease in TLCO
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15
Q

KCO

A

Transfer coefficient=functionality ‘per unit volume’ of lung.

Can increase to compensate for low TLCO if extra pulmonary causes of reduced lung volume obesity, thoracic cage abnormalities etc.

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16
Q

HRCT

A

1mm slice every 10 mm, good for suspected diffuse lung conditions

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17
Q

Spiral or Helical CT

A

Less resolution but done in continuum therefore dont miss small nodules etc

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18
Q

Pneumoconiosis

A

Lung disease caused by mineral dust
Fibrogenic=coal, silica, asbestos
Non fibrogenic= Siderosis (Iron) Welders
Baritosis (Ba miners)

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19
Q

Silicosis

A
  1. Early : diffuse nodules on CXR
    Differentiate from sarcoidosis, TB, diffuse malignancy
  2. Late : solid mass / upper zone
    Differentiate from lung cancer, TB
  3. Restrictive lung function abnormality
    4.Characteristic findings on biopsy
    Dense fibrosis with birefringent particles
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20
Q

Coal workers pneumoconiosis

A

Early : diffuse nodules on CXR
Differentiate from sarcoidosis, TB, diffuse malignancy
Late : solid mass / upper zone
Differentiate from lung cancer, TB
Restrictive lung function abnormality
Characteristic findings on biopsy
Dust accumulation around terminal bronchioles with fibrosis

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21
Q

Asbestos related disease

A

Heavy exposure= Lung cancer, asbestosis

Light exposure= mesothelioma, plueral plaques (no impact on lung function), plueral fibrosis

22
Q

Transudate

A

Effusion fluid caused by changes in mechanical or oncotic pressure.

LOW protein <30g/L, LDH <200

Cardiac, renal failure, cirrhosis, ascites

23
Q

Exudate

A

Effusion fluid caused by Increased permeabiliity of cap by pleural disease

Protein>30g/L, LDH>200

Malignancy, infection, inflammation,

24
Q

Occupational asthma

A

Asthma which is caused by exposures to some agent at work (or is substantially worsened)

50% still have astham even after leaving work

Can be sensitiser (90%) Latency period between 1st exposure to a “sensitiser” and immunologically-driven symptoms

or irritant induced

25
Work related asthma
Asthma symptoms which are increased because of exposures at work (eg exercise, dust, cold)
26
Investigation of occupation asthma
``` History Skin prick tests Peak flow readings at work and home Airway responsiveness measurements Inhalational challenge test ``` Tx- as per standard BTS
27
Chronic Bronchitis
Chronic or recurrent excessive mucus secretion in the bronchial tree
28
Emphysema
An increase beyond the normal in the size of the air spaces distal to the terminal bronchiole(alveoli) accompanied by destruction of their walls and without obvious fibrosis.”
29
Cor Pulmonale
V/Q matching process constricts blood flow around areas of hypoxia, in emphysema hypoxia is everywhere=> pulomnary hypertension,
30
Type 1 Respiratory Failure
PaO2 < 8kPa Causes V/Q mismatch & shunt
31
Type 2 Respiratory Failure
PaO2 < 8 kPa on air & PaCo2 > 6 kPa Causes Hypoventilation Increase in deadspace ventilation V/Q mismatch
32
Symptoms suggestive of respiratory insufficiency
``` Breathless on exertion (dyspnoea) Breathless when lying down (orthopnoea) Poor concentration Extreme fatigue Decreased appetite Anxiety Nocturnal hypoventilation symptoms Disturbed sleep, frequent awakenings, morning headaches ```
33
Investigation of respiratory insufficiency
1. FVC / SNIP / MIP / MEP - to measure and assess inspiratory and expiratory function 2. Overnight oximetry or transcutaneous CO2 monitoring – to assess presence of nocturnal hypoventilation 3. Arterial Blood Gas analysis – to determine urgency of treatment assessment 4. Venous bicarbonate – to measure total CO2 5. Sleep studies
34
Hypoventilation
COPD OSA DMD
35
OSA
Ix Epworth sleepiness score Limited somnography Oximetry only Tx Weight loss CPAP- effective at controlling Sx
36
DMD & COPD
NIV
37
Interstitial Lung disease
An imprecise term for a range of diseases which affect the lung parenchyma with cellular infiltration of the alveoli, interstitium and distal airways, and which may progress to fibrosis
38
Types of ILD
1. Idiopathic Pulmonary Fibrosis 2. Sarcoidosis 3. Hypersensitivity Pneumonitis (EAA) 4. Pneumoconiosis 5. Connective tissue disease 6. Drug related interstitial disease
39
IPF Tx
1. Nothing 2. Best Supportive Care ie:oxygen/rehab 3. Pirfenidone/Nintedanib (expensive & rare) 4. Recruit to Clinical Trials 5. Transplant
40
IPF features Hx
- Progressive breathlessness - Dry cough - Failure to respond to treatments for other conditions
41
IPF Ex findings
- cyanosis - clubbing - fine crackles - reduced chest expansion
42
Multisystem granulomatous disease of unknown cause primarily affecting the lung
Sarcoid | No Tx or steroids if required
43
ILD Ix
CXR=> HRCT Lung Function ABG Auto antibodies and serum ACE
44
Bilateral Hilar/Mediastinal Lymphadenopathy
Sarcoid TB Lymphoma Carcinoma
45
EBUS
Used to take biopsy mediastinal lymph nodes
46
EAA (hypersensitivity Pneumonisitis
Presents with cough, breathlessness and sometimes systemic symptoms of fever, weight loss Occupation/Hobbies!
47
EAA Ex
Crackles & Also wheeze and squeaks
48
EAA Diagnosis
Usually suffice to have appropriate exposure, positive antibody response and clinical/radiological picture
49
EAA Ix
Mosaicism on HRCT (air trapping) hallmark
50
EAA Tx
Avoid antigen | Steroids
51
IPF
All lung function parameters reduced Type 1 Respiratory Failure picture