Respiratory Flashcards

0
Q

Oxygen toxicity is PCO2 >6 and pH <7.35 and what PaO2? (1)

A

PaO2 is >10kPa

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1
Q

Which device is used to deliver a fixed or precise oxygen concentration? (1)

A

Venturi

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2
Q

What conditions are at risk of oxygen toxicity? (2)

Ie chronic CO2 retainers who rely on hypoxic drive.

A

Chronic hypoxic lung disease- Patients with COPD, severe chronic asthma, bronchiectasis/CF
Obesity hypoventilation syndrome- High BMI,
Neuromuscular disease- Muscular dystrophy
Chest wall disease- kyphoscoliosis
Drugs- opioids

88-92%

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4
Q

Define respiratory failure type 1 (2)

A

PaO2 < 8kPa
PaCO2 normal or low

Due to V/Q mismatch

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5
Q

Define respiratory failure type 2. (2)

A

Low PaO2 < 8 kPa
High PaO2 >6 kPa
Caused by ventilation problems.

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6
Q

A patient is severely hypercapnic due to excessive oxygen therapy.
What action do you take? (1)

A

Reduce to 35% if patient is fully alert
Call critical care for mechanical ventilation if drowsy
Do not stop oxygen suddenly.

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7
Q

A 67 year old man is in A+E with an exacerbation of COPD.
On examination he is on 28% oxygen, sats of 85% and looks distressed.
The ABG shows;
PaO2 6.7
PaCO2 8.3
pH 7.32

What does the blood gas show? (1)
Give 2 ways to improve his oxygen saturations. (2)

A

Uncompensated respiratory acidosis
Don’t control PaCO2 by reducing O2 if already hypoxic.

Check airway and sit up
Beonchodilators
Reverse sedation
Titrate O2 to get sats up to 90% and rpt ABG (controlled oxygen therapy.
Mechanical ventilation
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8
Q

What is the aim of long term oxygen therapy? (1)

A

Delay death and cor pulmonale

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9
Q

When is long term oxygen therapy indicated? (3)

A

If PaO2 <7.3kPa
If PaO2 7.3-8kPa AND secondary polycythaemia or evidence of pulmonary hypertension.
Also nocturnal hypoventilation caused by obesity, neuromuscular/spinal/chest wall disease or obstructive sleep apnoea.

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10
Q

In an emergency if sats are 98% do you give supplementary oxygen? (1)

A

No does not help breathlessness if O2 sats are ok.

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11
Q

Where is the carina of the lungs? (1)

A

The junction of the manubrium and the 2nd right costal margin. (Level of T5)

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12
Q

Describe the basic structure of the lungs. (4)

A

The trachea extends from inferior cricoid cartilage(C6) to the carina (T5) where it divides into the left and right bronchi. The bronchi divide by dichromatour branching up to 23 times into secondary, tertiary bronchi and smaller bronchioles and terminal bronchioles and alveoli.
The left lung contains 2 lobes and a cardiac notch whereas the right lobe has 3 lobes.
The lungs are surrounded by double layer of pleura, visceral and parietal pleura, filled with a small amount of fluid.

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13
Q

What epithelium lines the airways? (2)

A

Ciliated columnar epithelium and mucous (goblet) cells

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14
Q

Describe the mucociliary escalator. (2)

A

Mucous is secreted by goblet cells (most in larger airways) and traps macrophages, bacteria and inhaled particles. Ciliated columnar epithelium then move the mucous in a cephalad direction, thus clearing the lungs.

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15
Q

Name 4 causes of breathlessness occurring chronically (onset over days or weeks). (4)

A

Asthma, COPD, ILD, Pleural effusion, cancer of the bronchus/trachea, HF, severe anaemia.

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16
Q

Name 5 causes of breathlessness occurring acutely over minutes or hours. (5)

A

Acute asthma, Exacerbation COPD, Pneumothorax, PE, Pneumonia, Hypersensitivity pneumonitis (extrinsic allergic alveolitis), Left HF, Cardiac tamponade, Hyperventilation (panic), Upper airways obstruction (foreign body, anaphylaxis)

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17
Q

Describe PND. (3)**

A

Paroxysmal nocturnal dyspnoea is a symptom of left sided HF. Patient wakes up gasping for breath and finds some relief on sitting up right.

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18
Q

Define orthopnoea. (3)**

A

Breathlessness that occurs when lying flat and is the result of abdominal contents shifting diaphragm into thorax and redistribution of blood from legs back to lungs.

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19
Q

Describe the epithelium of the alveoli. (2)

A

Consists of Type I and Type II pneumocytes. Type 1 cover approximate 95% of the alveolar surface (they are very thin and so used for gas exchange) compared to Type II that secrete surfactant and cover the remaining 5%.

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20
Q

The lungs have dual blood flow. Describe this. (2)

A

Pulmonary circulation (deoxygenated blood from Right side of heart) and Bronchial (systemic) circulation that brings oxygenated blood from the descending aorta to oxygenate the lung tissue (primarily along the larger airways).

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21
Q

Name 3 causes of a persistent cough. (3)

A

Asthma, Post-nasal drip, GORD*, ACEi, post-viral cough
Lung airway disease: COPD, bronchiectasis, foreign body, tumour.
Lung parenchymal disease: ILD, lung abscess

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22
Q

Name the muscles used in normal inspiration and expiration. (2)

A

Inspiration: diaphragm (C345), intercostal muscles (sternocleidomastoid and scalenes when in distress)
Expiration: none, it is passive relying on elastic recoil. (internal intercostals and abdominal wall become active during exercise)

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23
Q

A 55 year old man attends A+E with a first episode of sudden onset shortness of breath lasting 3 hours.
He has no PMH and quit smoking 25 years ago.
Name 4 investigations you would like to do initally. (4)

A

Bedside: Obs: (SATs, BP, RR, Pulse, Temp.) Lung FTs (peak flow, spirometry), ECG*
Bloods: ABGs, FBC, U+Es, blood glucose, Trop T, D-dimer
Imaging: CXR
, ?Echo

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24
Q

Name 4 diseases that smoking is a risk factor for. (4)

A

GI cancer: mouth, oesophagus, stomach, pancreas
Resp cancer: Larynx, bronchus.
Urogenital cancer: Bladder, Kidney, Cervix
COPD
PVD
IHD

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25
Q

Mr Smith requires a bronchoscopy for a biopsy of a mass. He is concerned about the test.
Why might a bronchoscopy be undertaken? Give 3. (3)
Name 3 medications he may recieve during the investigation. (3)

A

Diagnosis - look or biopsy, Treatment - remove foreign body or growth, BAL - lavage for washings to send for cytology
IV Midazolam, topical lidocaine anaesthesia, anti-muscarinic to reduce bronchial secretions eg atropine

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26
Q

Name 3 causes of haemoptysis. (3)
Define massive haemoptysis. (2)
Give 2 causes of massive haemopytsis. (2)

A

Bronchiectasis, Bronchial carcinoma, PE, bronchitis, pneumonia (rust coloured), abscess, TB. Rare: Wegener’s granulomatosis, bleeding disorders, Goodpasture’s syndrome.
Massive haemoptysis is more than 200ml in 24 hours.
Pulmonary TB, bronchiectasis, lung abscess or malignancy.

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27
Q

In spirometry what are the 2 most important measurements taken? (2)
What is a normal result? (1)
Give an example of a restrictive lung condition and a obstructive lung condition and the respective values. (4)
Clue: LO HR

A

FVC1 and FVC (FEV1/FVC)
Normal is 0.7
Restrictive is FEV1/FVC >0.7 eg ILD, scoliosis
Obstructive is FEV1/FVC

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28
Q

When would a pleural aspiration be undertaken? (1)

Name 2 complications of a pleural aspirate. (3)

A

Sample with fine bore needle to investigate cause of a pleural effusion, or drainage of a pleural effusion for symptom relief.
Pneumothorax, infection, damage to neurovascular bundle in subcostal groove, seeding of malignant cells along the tract with a malignant effusion.

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29
Q

Describe a V/Q scan. (3)

A

Xenon-133 is inhaled and microaggregates of albumin labelled with Technetium-99m are injected IV.
Pulmonary emboli are detected as “cold” areas on the perfusion scan in relation to the ventilation scan.
However, many lung diseases can affect both values and so V/Q scan is only useful when reported as normal (excluding PE) or reported as high probability of PE.

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30
Q

You suspect a diagnosis of lung fibrosis in a patient. What is the most appropriate imaging test for diagnosis? (1)

A

High resolution CT.

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31
Q

What is measurement of carbon monoxide transfer factor? (2)

A

Measurement of the the transfer of a low concentation of carbon monoxide added to inspired air to the hemoglobin.
Gas transfer is reduced in early emphysema and lung fibrosis.
TLCO is the absolute value, whereas KCO is the value adjusted for lung volume.

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32
Q

What does yellow/green sputum indicate? (1)

A

Infection or allergy

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33
Q

Define Peak Expiratory Flow Rate. (3)

A

Measure of maximum expiratory flow during a forced expiration after forced inspiration and measured with a peak flow meter.

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34
Q

What does pink frothy sputum indicate? (1)

A

Heart failure

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35
Q

What does rust coloured sputum indicate? (1)

A

Pneumonia

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36
Q

Define COPD. (2)

What 2 diseases are encompassed by COPD? (2)

A

Chronic obstructive pulmonary disease is characterised by poorly reversible airways obstruction thats is usually progressive and associted with persistent inflammatory response of the lungs.
Chronic bronchitis and emphysema

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37
Q

In spirometry, how can COPD and asthma be diagnosed? (2)

A

Obstructive picture ie FEV1/FVC <0.7%

Post bronchodilator will show more than 20% improvement in asthma.

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38
Q

How does cigarette smoke cause COPD? (2)

A

Smoking causes mucous cell hypertrophy and increase in neutrophils, macrophages and lymphocytes in the airways which release inflammatory mediators. This leads to amplified inflammatory process, structural changes and connective tissue breakdown (protease-anti-protease imblanace) in lung parenchyma. Emphysema.
Alpha 1 antitrypsin is major protease inhibitor, that is inactivated by cigarette smoke.

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39
Q

Describe the differences between pink puffers and blue bloaters. (2)

A

These terms describe the extremes of the spectrum.
Pink Puffers have predominantly emPhysema. Increased alveolar ventilation leaves low PaO2 and low PaCO2, they are breathless but not cyanosed.
Blue bloaters have predominantly chronic Bronchitis. Decreased alveolar ventilation leaves low PaO2 and high PaCO2, cyanosed but not breathless. They may be oedematous and have features of CO2 retention. They rely on hypoxic drive, give O2 with care.

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40
Q

Define emphysema. (2)

A

Emphysema is defined pathologically by dilataion and destruction of the lung tissue distal to the terminal bronchioles. Changes lead to loss of elastic recoil that holds the airways open during expiration and so is associated with air trapping and expiratory airflow limitation.

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41
Q

What underlying condition may cause a 35 year old to show signs of COPD? (1)

A

alpha 1 anti-trypsin deficiency

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42
Q

Describe the pathophysiology of chronic bronchitis. (3)

A

Airway narrowing caused by hypertrophy and hyperplasia of the mucous producing cells, bronchial wall inflammation and mucosal oedema. Epithelial layer may ulcerate and on healing, columnar epithelium is replaced by squamous epithelium (squamous metaplasia).

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43
Q

What is the infective agent in a common cold? (1)

A

Rhinovirus

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44
Q

In allergic rhinitis, what tests can be used to identify triggers? (2)

A
Skin prick testing
RAST testing (serum IgE levels for specific antibodies)
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45
Q

Which groups of patients should be offered the flu vaccine? (3)

A

Healthy children aged 2, 3 and 4 (live nasal injection)
Children at risk aged 2-17 (live nasal injection)
Children aged 6m-2years at risk of infection (inactive injection)
Pregnancy
Weakened immune system
Long term cardiac or respiratory problems
Over 65 years old

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46
Q

Steve, a 2 year old boy was eating some peanuts and started coughing and wheezing. Apart from inhalation, what other differential is important to consider? (1)
Anatomically where is the peanut most likely to be and why? (2)
How is the peanut best removed in an emergency or non-emergency? (2)

A

Anaphylaxis
Right bronchus, right is more vertical than the left.
Heimlich manoeuvre or bronchoscopy

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47
Q

What is the common term used to describe acute larynotracheobronchitis? (1)
What is the main infective cause? (1)
What is the management? (3)

A

Croup
Parainfluenza virus
Oxygen, oral or IM steroids, nebulised adrenaline.

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48
Q

What is the main infective cause of acute pharyngitis? (1)
What are the most common bacterial causes? (3)
How are they treated? (2)

A

Adenovirus, if more persistent and severe then may have secondary bacterial infection of Group A haemolytic streptococcus, staphylococcus aureus, haemophilus influenzae.
Treat viral causes symptomatically. Treat bacterial causes with phenoxymethylpenicillin 500mg qds for 10 days

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49
Q

What infection is oseltamivir used to treat? (1)

What is its mode of action? (1)

A
Influenza
Neuramidase inhibitor (influenza virus has H and N antigens, N=neuramidase)
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50
Q

What is the most common complication of influenza? (1)

A

Viral or secondary bacterial pneumonia

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51
Q

Name 2 signs on examination that are associated with CO2 retention. (2)

A

Warm peripheries, bounding pulse, flapping tremor of outstretched hands, confusion in severe cases.

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52
Q

In a patient with COPD, what can contribute to reduced exercise tolerance apart from decreasing lung function? (2)

A

Skeletal muscle dysfunction caused by age, malnutrition, systemic inflammation, inactivity and hypoxia)

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53
Q

Describe the spirometry results of a patient with COPD. (4)

A

FEV1/FVC: <80%) in emphysema

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54
Q

Why might a patient with COPD become polycythaemic? (1)

A

Hypoxia causes increase in RBC production.

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55
Q

How many stages of COPD are there and how are they distinguished? (4)
What symptoms would you expect at each stage? (4)

A

4
Mild: FEV1 >80% - chronic cough
Moderate: FEV1 50-80% - SOB on exertion
Severe: FEV1 30-50% - SOB on minimal exertion, may have weight loss and depression
Very severe: FEV1<30% predicted - SOB at rest

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56
Q

What age of onset of COPD would be classed as early onset? (1)
What blood test would then be indicated? (1)

A

<40 years old

Alpha-1 antitrypsin serum levels

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57
Q

Apart from doctors name 3 other professionals involved in the MDT for a patient with COPD. (3)

A

Respiratory nurse specialists, physiotherapists, occupational therapists, dietitian, palliative care.
GP and respiratory physician

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58
Q

What bronchodilator therapy may be considered for a patient with COPD? (3)
What vaccinations should a patient receive? (2)

A

Long acting antimuscarinic (tiotropium) as once daily maintenance
Short acting b2 agonist to reduce acute symptoms
Long acting b2 agonist for persistent dyspnoea

Annual flu and once-off pneumococcal vaccine.

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59
Q

How can reversibility of COPD be assessed clinically? (2)

A

2 week course of 30mg prednisolone.

Spirometry before and after, if more than 15% reversible then add in inhaled corticosteroid.

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60
Q

Which groups of patients are eligible to consider long term oxygen therapy? (2)
How are patients assessed for LTOT? (1)

A

PaO2 s made at least 3 weeks apart in a stable patient who is receiving optimum treatment.

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61
Q

Name 4 medications that may be used in the management of a patient with advanced COPD. (4)

A
Tiotropium
Salbutamol
Salmeterol
Oxygen
Prednisolone
Antibiotics
Carbocisteine
Diuretics
62
Q

What are the three criteria for diagnosing an exacerbation of COPD? (3)

A

Increased breathlessness
Increased sputum volume
Increased sputum purulence

63
Q

What is the major complication of COPD? (1)

A

Respiratory failure

64
Q

How is oxygen managed in an acute exacerbation of COPD? (2)

A

Aim for SATs of 88-92% and PaO2 >8kPa without increasing PaCO2.
Use Venturi mask at low concentration 24% to maintain respiratory drive and increase as necessary in increments following ABGs every 30-60mins if no hypoventilation, CO2 retention or worsening acidosis.

65
Q

What is the management of an acute exacerbation of COPD? (4)

A

Oxygen - controlled - SATs 88-92%
Bronchodilators - salbutamol and ipratropium 4-6 hourly
Oral prednisolone 40mg
Antibiotics if suspected infection e.g. co-amoxiclav

66
Q

If a patient with an acute exacerbation of COPD is in type 2 respiratory failure (low PaO2 and high PaCO2) how should nebulisers be given? (1)
What alternatives are there for assisting ventilation? (1)

A

Air driven nebulisers with supplementary oxygen through nasal specs if indicated.
BiPap, intubation and mechanical ventilation, Respiratory stimulants are not often used e.g. doxapram

67
Q

How is prognosis assessed in COPD? (4)

A
BODE index
BMI
Obstruction - FEV1
Dyspnoea
Exercise tolerance
68
Q

What is obstructive sleep apnoea? (2)

Who is most commonly affected? (1)

A
Repeated apnoea (cessation of breathing for more than 10 secs) as a result of obstructed upper airway during sleep.
Most commonly seen in overweight middle aged men or children with enlarged tonsils.
69
Q

Name 2 contributing factors for obstructive sleep apnoea. (2)

A

Obesity
Alcohol before bed
COPD
Also more common in hypothyroidism and acromegaly.

70
Q

Why does obstructive sleep apnoea only have symptoms at night? (1)

A

The muscles that hold the airway open during sleep are hypotonic, and the airway will remain closed until the patient wakes by the sensation of trying to breathe against a closed throat.

71
Q

How can obstructive sleep apnoea be differentiated from snoring? (2)
What is the management of sleep apnoea? (2)

A

Epworth sleepiness scale.
Home oximetry
Inpatient sleep studies

Conservative: weight loss
Medical: CPAP keeps pharyngeal walls open
Surgical: removal of large tonsils

72
Q

What is bronchiectasis? (2)

A

Permanent abnormal dilatation of the central and medium sized airways, leading to impaired clearance of bronchial secretions and risk of secondary bacterial infections and inflammation.
It may be generalised or localised to one lobe.

73
Q

What are the commonest causes of bronchiectasis? (3)

Name one rare cause. (1)

A

Idiopathic
CF
Post infection (TB, Whooping cough, pneumonia)

rare: Immunodeficiency eg AIDS, congenital ciliary defect eg Kartageners or situs invertus.

74
Q

What symptoms would suggest a diagnosis of bronchiectasis? (2)

A
Chronic productive cough*
Recurrent chest infections*
Large amounts of thick foul smelling green sputum*
Haemoptysis
SOB
Wheeze
75
Q

You are treating a woman with a chronic cough productive of green sputum. She had TB as a child.
You suspect bronchiectasis. What investigations would you undertake? (3)
What organisms are most likely to have caused her infective exacerbation? (2)

A

Bedside: Sputum culture*
Bloods: FBC, blood cultures,
Imaging: CXR, HRCT*

Staphylococcus aureus, Haemophilus influenzae, Pseudomonas aeruginosa.

76
Q

What management is used in the treatment of bronchiectasis? (3)

A

Respiratory physiotherapy techniques
Antibiotics for infections: if pseudomonas oral antibiotics will not treat, requires nebuliser or IV antibiotics e.g. Tobramycin
Inhaled or oral steroids can slow rate of progression.
Bronchodilators (beta agonists and antimuscarinics) can provide symptomatic relief if not improving FEV1.

77
Q

Name 3 complications of bronchiectasis. (3)

A
Haemopytsis
Pneumonia
Empyema
Pneumothorax
Respiratory failure
Metastatic cerebral abscess
78
Q

What is cystic fibrosis? (2)

A

Autosomal recessive disorder occurring in 1:2000 live births. Mutation of chromosome 7 that codes for cystic fibrosis transmembrane conductance regulator protein. This leads to increased viscosity of mucous produced in lungs, pancreas, GI and reproductive tracts and increased salt content in sweat glands.

79
Q

How do children with CF start with normal lungs and end in respiratory failure? (3)

A

Born with normal lung structure, however, thickened mucous is more difficult to clear from airway and frequent infections ensue. Resultant inflammatory response damaged the airway and leads to progressive bronchiectasis, airflow limitation and respiratory failure.

80
Q

What peripheral clinical sign on examination of a patient with CF is most likely? (1)

A

Finger clubbing.

81
Q

Define asthma. (3)

A

Variable, reversible airways obstruction characterised by airflow limitation, bronchial inflammation and airway hyper responsiveness.

82
Q

Describe the 2 classifications of asthma. (2)

A

Extrinsic: Atopic, allergens can be identified by positive skin prick reactions.
Intrinsic: starts in middle age with no obvious external cause.

83
Q

What is atopy? (2)

A

Combination of asthma, eczema and hay fever.

It is a term used to describe individuals who readily develop IgE antibodies against common environmental antigens.

84
Q

Describe the pathophysiology of asthma. (5)

A

STILL tO DO!!

85
Q

Having taken an FBC on an asthmatic patient, what type of white blood cells would be most raised? (1)

A

Eosinophils

86
Q

What signs would you expect to find on examination of the chest of an asthmatic? (3)

A

Palpation: Reduced chest expansion
Percussion: may be normal or hyper resonant
Auscultation: Decreased air entry, prolonged expiratory phase, bilateral expiratory polyphonic wheeze.

87
Q

What investigations may help to diagnose asthma? (3)

A
Spirometry
PEF diary - diurnal variation
Histamine challenge for bronchial hyper-responsiveness
Skin prick tests to look for allergens 
CXR in acute attack
88
Q

What non-medical management should be offered to asthmatic patients? (2)

A

Smoking cessation
Avoidance of triggers
Annual flu vaccination

89
Q

Describe the step-wise management of asthma in adults. (5)

A

Step 1: SABA prn
Step 2: + Regular ICS
Step 3: + LABA and increase ICS to 800mcg/day
if LABA not effective stop and + leukotriene antagonist or oral theophylline MR
Step 4: SABA prn + ICS + LABA
+ 6 week trial of leukotriene receptor antagonist or theophylline or oral beta2 agonist
Step 5: Regular prednisolone and refer to specialist

90
Q

What are the aims of asthma management? (3)

A

No day or night time symptoms
No exacerbations
No use of SABA
Normal lung function (PEF>80% predicted)

91
Q

When should step down of asthma medications be considered? (10

A

Every 3 months review treatment. Consider stepping down if control achieved.

92
Q

What are leukotrienes? (1)

A

Inflammatory mediators released by mast cells which cause bronchoconstriction and increased production of mucous.

93
Q

Name 4 life threatening features of asthma? (4)

A
Silent chest
Cyanosis
Poor respiratory effort
Exhaustion
Altered conscious level
Bradycardia
Hypotension
PEF < 8kPa
94
Q

Give 3 signs of severe acute asthma. (3)

A
Cannot complete sentences in one breath
RR > 25
Pulse > 110
Sats >92%
PEF 33-50%
95
Q

What is the emergency management of a moderate/severe acute asthma attack? (4)

A
Check in BNF
Oxygen to maintain sats 94-98%
Nebulised salbutamol 5mg
Iv hydrocortisone 200mg 
Antibiotics if evidence of infection
IV fluids
96
Q

Why are urea and electrolytes measured in an acute asthma attack? (1)

A

Salbutamol and steroids can cause hypokalaemia.

97
Q

What is the management of life threatening asthma attack? (4)

A
Oxygen therapy
Salbutamol nebs 5mg every 10-20 mins
Hydrocortisone IV 200mg 4hrly
Ipratropium nebs 0.5mg 4-6 hrly
Magnesium sulphate 1.2-2g IV over 20 mins
Inform ITU for possible intubation
98
Q

Define pneumonia. (1)
Name 3 causes of pneumonia. (3)
Name 3 specific bacterial causes of pneumonia. (3)

A

Inflammation of the lungs usually caused by bacteria.
Bacteria, viral, aspiration, radiotherapy
Streptococcus pneumoniae, mycoplasma pneumoniae, haemophilis influenzae, staphylococcus aureus, legionella pneumophila, coxiella burnetti, psuedomonas aeruginosa.

99
Q

A patient is diagnosed with pneumonia and you suspect a bacterrial cause.
What organism would you expect in a patient with a PMH of;
A) COPD.
B) IVDU
C) CF

A

A) haemophilus influenzae
B) staphylococcus aureus
C) psuedomonas aeruginosa

100
Q

Name 2 causes of community acquired pneumonia (2)

Name 2 causes of hospital acquired pneumonia. (2)

A

CAP: streptococcus pneumoniae, haemophilus influenza, mycoplasma pneumoniae.

HAP: gram negative enterococci, staphylococcus aureus. Pseudomonas aeruginosa.

Atypical CAP: legionella pneumophilia, pneumocystis jiroveci.

101
Q

Name 3 signs of pneumonia. (3)

A
Fever
Signs of consolidation- dull to percussion, increased tactile vocal fremitus
Pleural rub
Pleural effusion
Confusion
102
Q

How is the severity of pneumonia assessed? (4)

A
CURB 65 max score of 6
Confusion
Urea >7 mmol/L
Resp rate > 30
BP sys <60
Age over 65

0-1 treat as OP, 2 treat as IP, 3+ severe consider ITU

103
Q

What investigations would you perform in a patient in who you suspect pneumonia? (6)

A

Bedside: obs, sputum sample, urine (for legionella and pneumococcal antigen), ECG
Bloods: FBC (infection), CRP (monitor inflammatory markers), blood cultures, U&Es
Imaging: CXR

104
Q

How would you manage a patient with pneumonia on the ward?

A

Oxygen, fluids, physiotherapy to encourage coughing, analgesics.

HAP: gram negative - co-amoxiclav 500mg TDS, add in metronidazole if patient at risk of anaerobic bacteria eg long ITU stay or aspiration.

Mild CAP: amoxicillin 500mg tds
Severe CAP: IV cefuroxime and clarithromycin

105
Q

How does aspiration cause pneumonia? (2)
Which area of the lung is most likely to be affected? (1)
What sort of organisms are most likely and what antibiotic will best treat them? (2)

A

Aspiration of gastric contents causes severe destructive pneumonia due to the corrosive effect of the gastric acid.
Right lower lobe (posterior segment) due to right bronchus is more vertical.
Usually anaerobe infection. Treat with metronidazole.

106
Q

Give 2 complications of pneumonia. (2)

A

Lung abscess - localised suppuration of the lung associated with cavity formation.
Empyema - presence of pus in pleural cavity, usually from rupture of a lung abscess or bacterial spread from severe pneumonia.

107
Q

A 72 year old male attends your surgery complaining of a 3 month persistent dry cough and progressive shortness of breath on exertion.
On examination you can hear fine late inspiratory crackles.
What is your main differential? (1)

A

Interstitial lung disease.

108
Q

What is a granuloma? (2)

What disease is the most common cause of lung granulomas? (1)

A

Mass or nodule of chronic inflammatory tissue formed by the response of macrophages to a slowly soluble antigen or irritant. Characterised by the presence of epithelioid multinucleate giant cells.
Sarcoidosis

109
Q

What is sarcoidosis? (1)
How does it present? (2)
What percentage of cases are found incidentally on CXR? (1)

A

Multi-system non-caseating granulomatous disorder or unknown cause typically affecting young and middle aged adults.
Bilateral hilar lymphadenopathy, and/or pulmonary infiltrations and skin and eye lesions.
50%

110
Q

Which ethnic groups are most severely affected by sarcoidosis? (1)

A

Occurs in all ethnic groups, but African black people have a more severe disease course.

111
Q

Give 3 causes of bilateral hilar lymphadenopathy. (3)

A

Sarcoidosis, Pulmonary TB, Lymphoma, Bronchial carcinoma with secondary spread.

112
Q

How can sarcoidosis be diagnosed? (2)

What tests may help with severity/staging? (2)

A

Clinical picture and exclusion of other diseases.
Biopsy of LN’s, skin lesions or transbronchial can diagnose histologically.

Lung function tests assess severity (restrictive pattern), CXR or HRCT for staging. FBC, LFT, U+Es & Ca for abnormalities and organ involvement.

113
Q

What is the course of sarcoidosis? (2)

A

Remits spontaneously in 2 years in 70% of patients.
In 5-10% pulmonary infiltration leads to progressive fibrosis and increasing dyspnoea, cor pulmonale, respiratory failure and death. Death can also occur by hypercalciuria causing renal damage.

114
Q

Name some signs and symptoms of sarcoidosis. (6)

Clue: SARCOID

A

Skin - erythema nodosum, infiltration of scars
Arthritis- esp hands and feet
Resp - bilat hilar lymphadenopathy, pulmonary infiltrates, cough, wheeze, fine crackles on examination
Cardio - heart block, HF
Ocular - anterior uveitis, conjunctival nodules
Intracranial (brain) - meninges inflammation, seizures, hypothalamic-pituitary infiltration
Derangement of liver and renal function - granulomatous hepatitis, hepatosplenomegaly, hypercalciuria (nephrocalcinosis)

115
Q

Why can patients with sarcoidosis become hypercalcaemic? (1)

A

Sarcoid macrophages produce active vitamin D3

116
Q

How is sarcoidosis managed? (2)

A

Hilar lymphadenopathy without changes on CXR or lung function tests do not require treatment and 2/3 will spontaneously resolve.
Infiltration or abnormal lung FTs 6 months after diagnosis is treated by prednisolone reduced over 6-12 months.

117
Q

What is Wegener’s granulomatosis? (2)
Name 3 symptoms. (3)
What blood test can be helpful both diagnostically and success of treatment? (1)

A

Vasculitis of unknown aetiology. Characterised by lesions in upper respiratory tract, lungs and kidneys.
Rhinorrhoea, nasal mucosal ulceration, cough, haemoptysis and pleuritic pain.
Saddle nose, haematuria, proteinuria.
Anti-neutrophil cytoplasmic antibodies (ANCA)

118
Q

A 65 year old man presents to clinic with a 3 month history of progressive shortness of breath and non-productive cough.
On examination he has finger clubbing and fine inspiratory basal crackles.
What is the most likely diagnosis? (1)
Name 2 further differentials. (2)
What imaging would you perform and what changes would you expect to see? (4)

A

Idiopathic pulmonary fibrosis
Other ILD. Sarcoidosis, asbestosis, hypersensitivity pneumonitis.
CXR: ground glass appearance, progressing to fibrosis and honeycombing. Changes most prominent in lower lung zones.
HRCT: best. Bilateral linear opacities and honeycombing.

119
Q

What is the correct term for extrinsic allergic alveolitis? (1)
What is it? (2)

Name 2 symptoms. (2)
Describe what is seen on CXR. (2)

A

Hypersensitivity pneumonitis
Characterised by widespread diffuse inflammatory reaction in the alveoli and small airways in response to inhalation of organic dusts.
Fever, malaise, cough, SOB several hours after exposure to antigen.
CXR shows fluffy nodular shadowing => streaky shadows particualrly in upper zones.

120
Q

Give 2 causes of hypersensitivity pneumonitis. (3)
Describe changes seen on HRCT? (2)
What is the management? (2)

A

Farmers lung
Bird fanciers lung
Cheese washers lung
Wine makers lung

Reticular and nodular changes with ground glass opacity.

Avoidance of exposure to antigen. High dose prednisolone may help in early stages.

121
Q

What is Goodpasture’s syndrome? (2)

How is it treated? (1)

A

Autoimmune antibodies against basement membrane of both kidneys and lungs causing cough, haemoptysis and acute glomerularnephritis.

Steroids

122
Q

Name 3 lung diseases that can be caused by inhalation of dusts, gases, vapours and fumes at work. (3)

A

Acute bronchitis, pulmonary oedema, pulmonary fibrosis, occupational asthma*, hypersensitivity pneumonitis, bronchial carcinoma.

123
Q

You are treating an 85 year old man who has a cough productive of black sputum and breathlessness. He has never smoked but the rest of social history is unknown.
What form of ILD would you most consider? (1)

A

Pneumoconiosis
Small coal particles escape normal mucociliary clearance to reach upper lobe acinus where it causes inflammation and fibrosis.
Initially nodules but can cause progressive pulmonary fibrosis even after exposure to coal is over.

124
Q

Name 2 causes of upper lobe fibrosis and 2 causes of predominantly lower lobe fibrosis. (4)

Clue: TEARSS & ABCD

A

Upper lobe: TB, EAA, Ankylosing spondylitis, Radiation, Sarcoidosis
Lower lobe: Asbestosis, Bronchiectasis, Cryptogenic fibrosing alveolitis, Drugs (bleomycin, mtx, amiodarone, azthioprine, penicillamine)

125
Q

With regards to asbestosis, name 3 occupations at risk. (3)
Generally, what is the latency period between exposure and disease? (1)
Name 2 diseases caused by exposure to asbestos. (2)

A

Electricians, builders, plumbers, shipyard or ship engineering workers.
20-40 years between exposure and disease.
Diffuse pleural thickening, mesothelioma, asbestosis, lung cancer.

126
Q

Name the 4 types of bronchial carcinoma. (4)

A

Small cell: (25%)

Non- small cell: squamous (40%), large cell (25%) and adenocarcinoma (10%)

127
Q

Name 4 common sign and symptoms of bronchial carcinoma. (4)

A

Local effects of tumour: cough, chest pain, dyspnoea, haemoptysis
Spread in chest: pleura/ribs- pain and fractures; brachial plexus- pain in shoulder; sympathetic ganglion- Horner’s; left recurrent laryngeal nerve- hoarseness; SVC- upper limb oedema, facial congestion, distended neck veins
Mets: bone and brain- pain, spinal cord compression, seizures
General: clubbing, weight loss, malaise, lethargy

128
Q

Name 2 common sites for metastases in bronchial carcinoma. (2)

A

Bone

Brain

129
Q

Which forms of lung cancer metastasise early? (2)

A

Small and large cell.

130
Q

What cells does small cell lung carcinoma arise from? (1)

What substances can small cell carcinomas produce? (2)

A

Kulchitsky- neuroendocrine cells.

ACTH- Cushings syndrome
ADH- dilutional hyponatraemia
PTH-like - hypercalcaemia
hCG- gynaecomastia

131
Q

What is Eaton-Lambert syndrome? (2)

Which lung cancer is it most associated with? (1)

A
Paraneoplastic syndrome (60% assd with cancer)
Autoimmune production of antibodies to presynaptic membrane causing proximal muscle weakness if arms and legs.

Small cell

132
Q

How does Lambert-Eaton syndrome differ to myasthenia gravis? (2)

A

LES: auto antibodies against pre synaptic membrane.
MG: auto antibodies against post synaptic membrane.

133
Q

What investigations are useful when considering bronchial carcinoma as a diagnosis? (3)

A

Sputum- cytology
CXR- round shadow with irregular border or evidence of lobar collapse, cavitation, pleural effusion or secondary pneumonia.
Bronchoscopy- washings for cytology; biopsy for histology
Transthoracic fine needle aspiration- biopsy of peripheral lesions
CT thorax- assess for surgery and spread
PET scan- confirmation or exclusion of metastatic intrathoracic LNs

134
Q

What is staging of a cancer? (2)

What staging is used in lung cancers? (1)

A

Method to determine the extent and severity of a patient’s cancer, to determine management and prognosis.
TNM

135
Q

What primary cancers can cause lung metastases? Name 3. (3)

A
Kidney
Prostate
Breast
Bone
GIT
Cervix
Ovary
136
Q

What is a flail segment? (1)

What other injury is it associated with? (1)

A

Severe blunt trauma causes 3 or more ribs to break in 2 or more places, thus separation of part of the rib cage. Due to ambient pressures compared to those inside the lungs, the flail segment moves in a opposite manner to the rest of the rib cage. (Paradoxical breathing)

Associated with pulmonary contusion.

137
Q

Define kyphosis and scoliosis. (2)

How can they result in respiratory failure? (2)

A

Kyphosis is bowing of the thoracic spine.
Scoliosis is a curved ‘S’ shape spine.
When severe they can restrict the lung capacity.

138
Q

What is pleurisy? (1)

Name 2 causes? (2)

A

Inflammation of the pleura without effusion causing pleuritic chest pain (localised, sharp, worse on inspiration)
Pneumonia, Pulmonary infarct, Carcinoma.

139
Q

Define pleural effusion. (2)

How much fluid is required to detect a pleural effusion clinically/radiologically? (2)

A

Excessive collection of fluid in the pleural space.
500ml- clinically detected
300ml - radiologically detected

140
Q

Name 3 physical signs that would be produced by a pleural effusion? (3)
How much fluid would be required to cause these signs? (1)

A

Palpation: Reduced expansion, mediastinal shift away from effusion
Percussion: Dull (stony-dull)
Auscultation: Absent breath sounds, reduced vocal resonance

500ml

141
Q

What are the two types of pleural effusion? (2)

What criteria can be used to distinguish between the two types and when would this be required? (2)

A

Transudate: pleural fluid protein< 25g/L
Exudate: pleural fluid protein> 35g/L

Light’s criteria when fluid protein between 25-35g/L

142
Q

What are Light’s criteria (3) and what 2 samples are required? (2)

A

Pleural fluid aspirate & Venous blood sample

  1. Pleural fluid protein/serum protein>0.5
  2. Pleural fluid LDH/serum LDH>0.6
  3. Pleural fluid LDH> 2/3 upper limit of normal LDH
    One or more is suggestive of exudate.
143
Q

What are the terms for a pleural effusion filled with blood, pus and lymph fluid? (3)

A

Haemothorax; Empyema, Chylothorax.

144
Q

Name 3 causes of transdative pleural effusion and exudative pleural effusion. (6)

A

Transudate: HF, Hypoalbuminaemia, Hypothyroidism, Constrictive pericarditis, Ovarian fibroma producing right sided effusion.
Exudate: Infection, Malignancy, PE with infarction, Connective tissue disease, Mesothelioma, Sarcoidosis, Acute pancreatitis, Drugs (mtx, amiodarone)

145
Q

What is the mechanism behind a transudate or exudate? (2)

A

T: Mismatch between hydrostatic forces, favouring accumulation of fluid.
E: Damaged or altered pleura or impaired lymphatic drainage of pleural space.

146
Q

Bob is a 63 year old man who has come in with a two week history of increasing SOB and weight loss. He is a long term smoker.
On examination his left side shows reduced air entry in the middle and lower zones and stony dullness on percussion.
What do you think is the cause of his symptoms? (1)
Which direction will his trachea have moved? (1)
What is the best management step both diagnostically and therapeutically? (1)
Name 3 tests you would perform on the sample taken above? (3)

A

Pulmonary effusion secondary to bronchial carcinoma.

Trachea moves away from effusion ie to the Right

Large volume thoracocentesis (under US guidance if necessary).

Appearance, protein, LDH, glucose, pH, cytology and microscopy.

147
Q

Tom has had a large exudative pleural effusion caused by lung carcinoma. It has reoccurred twice.
How can it be prevented from reoccurring? (1)

A

Drained to dryness and filled with a sclerosing agent. eg talc, tetracycline or bleomycin.

148
Q

What is a pneumothorax? (2)

What group are prone to spontaneous pneumothorax? (1)

A

Air in the pleural space causing a partial or complete collapse of lung. It occurs spontaneously or secondary to trauma.
Tall and thin young men - rupture of pleural pleb.

149
Q

What is tension pneumothorax? (1)
What is the most common cause? (1)
What is the management? (2)

A

Nasal NIV or mechanical ventilation causes a pleural tear that acts as a one-way valve , through which air is able to pass during inspiration but not exit during expiration.
immediate decompression by needle thoracocentesis in 2nd ICS, midclavicular line, then intercostal tube drainage.

150
Q

Which way would the mediastinum shift in a pneumothorax? (1)

What would you expect with percussion? (1)

A

Away from the lesion.

Hyper-resonant

151
Q

Tim is a tall and thin 23 year old man who presents with sudden onset of pleuritic chest pain and shortness of breath.
On CXR he has a pneumothorax with a rim of air of 3cm. What is your management? (1)
His mate Rain has also some pleuritic chest pain but not SOB. On CXR the rim of air is less than 2cm.
What is your management if he is asthmatic? (1)
What is your management if he has no PMH? (1)

A

SOB and rim>2cm = aspirate

Asthmatic - may be secondary pneumothorax. Admit.

Primary-