Respiratory Flashcards

1
Q

What is pneumonia?
How does it present and what are common examination findings?

A

Pneumonia is a respiratory tract infection of the lung tissue, causing inflammation in the alveolar space.

Presenting symptoms:
Cough
Sputum production
Shortness of breath
Fever
Feeling generally unwell
Haemoptysis (coughing up blood)
Pleuritic chest pain (sharp chest pain, worse on inspiration)
Delirium (acute confusion)

Characteristic chest signs of pneumonia include:

Bronchial breath sounds (harsh inspiratory and expiratory breath sounds) due to consolidation around the airways
Focal coarse crackles caused by air passing through sputum in the airways
Dullness to percussion due to lung tissue filled with sputum or collapsed

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2
Q

What is the CURB-65 score?

A

The NICE guidelines on pneumonia (updated 2022) recommend using the CRB-65 scoring system out of hospital and CURB-65 in hospital. They suggest considering hospital assessment when the CRB-65 score is more than 0.

C – Confusion (new disorientation in person, place or time)
U – Urea > 7 mmol/L
R – Respiratory rate ≥ 30
B – Blood pressure < 90 systolic or ≤ 60 diastolic.]
65 – Age ≥ 65

The CURB-65 score predicts mortality. NICE state 0/1 is low risk (under 3%), 2 is intermediate risk (3-15%), and 3-5 is high risk (above 15%):

Score 0/1: Consider treatment at home
Score ≥ 2: Consider hospital admission
Score ≥ 3: Consider intensive care

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3
Q

What causes pneumonia?
What is atypical pneumonia?

A

The top causes of typical bacterial pneumonia are:

Streptococcus pneumoniae (most common)
Haemophilus influenzae

Atypical pneumonia is caused by organisms that cannot be cultured in the normal way or detected using a gram stain. Treatment with penicillin is ineffective. They are treated with macrolides (e.g., clarithromycin), fluoroquinolones (e.g., levofloxacin) and tetracyclines (e.g., doxycycline).

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4
Q

What is asthma?

A

Asthma is a chronic inflammatory airway disease leading to variable airway obstruction. The smooth muscle in the airways is hypersensitive and responds to stimuli by constricting and causing airflow obstruction. This bronchoconstriction is reversible with bronchodilators, such as inhaled salbutamol.

Asthma is one of several atopic conditions, including eczema, hay fever and food allergies. Patients with one of these conditions are more likely to have others. These conditions characteristically run in families.

Asthma typically presents in childhood. However, it can present at any age. Adult-onset asthma refers to asthma presenting in adulthood. Occupational asthma refers to asthma caused by environmental triggers in the workplace.

The severity of symptoms of asthma varies enormously between individuals. Acute asthma exacerbations involve rapidly worsening symptoms and can quickly become life-threatening.

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5
Q

How does asthma present and what are typical triggers?

A

Symptoms are episodic, meaning there are periods where the symptoms are worse and better. There is diurnal variability, meaning the symptoms fluctuate at different times of the day, typically worse at night.

Typical symptoms are:

Shortness of breath
Chest tightness
Dry cough
Wheeze

Symptoms should improve with bronchodilators. No response to bronchodilators reduces the likelihood of asthma.

Patients may have a history of other atopic conditions, such as eczema, hayfever and food allergies. They often have a family history of asthma or atopy.

Examination is generally normal when the patient is well. A key finding with asthma is a widespread “polyphonic” expiratory wheeze.

Certain environmental triggers can exacerbate the symptoms of asthma. These vary between individuals:

Infection
Night-time or early morning
Exercise
Animals
Cold, damp or dusty air
Strong emotions

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6
Q

What are investigations done for asthma?

A

Spirometry is the test used to establish objective measures of lung function. It involves different breathing exercises into a machine that measures volumes of air and flow rates and produces a report. A FEV1:FVC ratio of less than 70% suggests obstructive pathology (e.g., asthma or COPD).

Reversibility testing involves giving a bronchodilator (e.g., salbutamol) before repeating the spirometry to see if this impacts the results. NICE says a greater than 12% increase in FEV1 on reversibility testing supports a diagnosis of asthma.

Fractional exhaled nitric oxide (FeNO) measures the concentration of nitric oxide exhaled by the patient. Nitric oxide is a marker of airway inflammation. The test involves a steady exhale for around 10 seconds into a device that measures FeNO. NICE say a level above 40 ppb is a positive test result, supporting a diagnosis. Smoking can lower the FeNO, making the results unreliable.

Peak flow variability is measured by keeping a peak flow diary with readings at least twice daily over 2 to 4 weeks. NICE says a peak flow variability of more than 20% is a positive test result, supporting a diagnosis.

Direct bronchial challenge testing is the opposite of reversibility testing. Inhaled histamine or methacholine is used to stimulate bronchoconstriction, reducing the FEV1 in patients with asthma. NICE say a PC20 (provocation concentration of methacholine causing a 20% reduction in FEV1) of 8 mg/ml or less is a positive test result.

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7
Q

What is the long term management of asthma?

A

1) Short-acting beta-2 agonist inhaler (e.g. salbutamol) as required
2) Inhaled corticosteroid (low dose) taken regularly
3) Leukotriene receptor antagonist (e.g., montelukast) taken regularly
4) Long-acting beta-2 agonists (e.g., salmeterol) taken regularly
5) Consider changing to a maintenance and reliever therapy (MART) regime
6) Increase the inhaled corticosteroid to a moderate dose
7) Consider high-dose inhaled corticosteroid or additional drugs (e.g., LAMA or theophylline)
8) Specialist management (e.g., oral corticosteroids)

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8
Q

What is acute exacerbation of asthma?

A

acute exacerbation of asthma involves a rapid deterioration in symptoms. Any typical asthma triggers, such as infection, exercise or cold weather, could set off an acute exacerbation.

Presenting features of an acute exacerbation are:

Progressively shortness of breath
Use of accessory muscles
Raised respiratory rate (tachypnoea)
Symmetrical expiratory wheeze on auscultation
The chest can sound “tight” on auscultation, with reduced air entry throughout

On arterial blood gas analysis, patients initially have respiratory alkalosis, as a raised respiratory rate (tachypnoea) causes a drop in CO2. A normal pCO2 or low pO2 (hypoxia) is a concerning sign, as it means they are getting tired, indicating life-threatening asthma. Respiratory acidosis due to high pCO2 is a very bad sign.

Grading Acute Asthma
Moderate exacerbation features:

Peak flow 50 – 75% best or predicted

Severe exacerbation features:

Peak flow 33-50% best or predicted
Respiratory rate above 25
Heart rate above 110
Unable to complete sentences

Life-threatening exacerbation features:

Peak flow less than 33%
Oxygen saturations less than 92%
PaO2 less than 8 kPa
Becoming tired
Confusion or agitation
No wheeze or silent chest
Haemodynamic instability (shock)

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9
Q

What is the management for patients with acute exacerbations of asthma?

A

Patients with an acute exacerbation of asthma can deteriorate quickly. Acute asthma is potentially life-threatening. Treatment should be aggressive and they should be escalated early to seniors and intensive care. Treatment decisions, particularly intravenous aminophylline, salbutamol and magnesium, should involve experienced seniors.

Mild exacerbations may be treated with:

Inhaled beta-2 agonists (e.g., salbutamol) via a spacer
Quadrupled dose of their inhaled corticosteroid (for up to 2 weeks)
Oral steroids (prednisolone) if the higher ICS is inadequate
Antibiotics only if there is convincing evidence of bacterial infection
Follow-up within 48 hours

Moderate exacerbations may additionally be treated with:

Consider hospital admission
Nebulised beta-2 agonists (e.g., salbutamol)
Steroids (e.g., oral prednisolone or IV hydrocortisone)

Severe exacerbations may additionally be treated with:

Hospital admission
Oxygen to maintain sats 94-98%
Nebulised ipratropium bromide
IV magnesium sulphate
IV salbutamol
IV aminophylline

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10
Q

how are obstructive and restrictive lung diseases diagnosed?

A

Obstructive lung disease is diagnosed when the FEV1 is less than 70% of the FVC, meaning a FEV1:FVC ratio of less than 70%. This suggests that obstruction is slowing the air passage out of the lungs. The person may have a relatively good lung volume, but air can only move slowly in and out of the lungs due to obstruction.

In asthma, the obstruction is a narrowed airway due to bronchoconstriction. In COPD, there is chronic airway and lung damage, causing obstruction. You can test the reversibility of this obstruction by giving a bronchodilator (e.g., salbutamol). The obstructive picture is typically reversible in asthma but less so in COPD.

In restrictive lung disease:

FEV1 and FVC are equally reduced
FEV1:FVC ratio greater than 70%

Restrictive lung disease limits the ability of the lungs to expand and fill with air. The lungs are restricted from effectively expanding. This is different from obstructive lung disease, where there is obstructed airflow.

Restriction of lung expansion leads to inadequate ventilation of the alveoli and insufficient blood oxygenation.

The FEV1:FVC ratio is normal or raised in restrictive lung disease without obstructive pathology affecting airflow through the airways. The FVC is reduced due to the restriction of lung expansion and capacity.

Restrictive lung disease includes conditions that limit how well the chest wall and lungs can expand, for example:

Interstitial lung disease, such as idiopathic pulmonary fibrosis
Sarcoidosis
Obesity
Motor neurone disease
Scoliosis

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11
Q

What is COPD and how does it present?

A

Chronic obstructive pulmonary disease (COPD) involves a long-term, progressive condition involving airway obstruction, chronic bronchitis and emphysema. It is almost always the result of smoking and is largely preventable. While it is not reversible, it is treatable.

Damage to the lung tissues obstructs the flow of air through the airways. Chronic bronchitis refers to long-term symptoms of a cough and sputum production due to inflammation in the bronchi. Emphysema involves damage and dilatation of the alveolar sacs and alveoli, decreasing the surface area for gas exchange.

Unlike asthma, airway obstruction is minimally reversible with bronchodilators, such as salbutamol. Patients are susceptible to exacerbations, during which their lung function worsens. Exacerbations triggered by infection are called infective exacerbations of COPD.

Presentation
A typical presentation of COPD is a long-term smoker with persistent symptoms of:

Shortness of breath
Cough
Sputum production
Wheeze
Recurrent respiratory infections, particularly in winter

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12
Q

What is the long term management of COPD?

A

Continuing smoking will progressively worsen lung function and prognosis. Smoking cessation services are available.

Patients should have the pneumococcal and annual flu vaccine.

Pulmonary rehabilitation involves a multidisciplinary approach to help improve function and quality of life, including physical training and education.

Initial medical treatment recommended by the NICE guidelines (updated 2019) involves:

Short-acting beta-2 agonists (e.g., salbutamol)
Short-acting muscarinic antagonists (e.g., ipratropium bromide)

The second step, when symptoms or exacerbations are still a problem, is determined by whether there are asthmatic or steroid-responsive features, measured by:

Previous diagnosis of asthma or atopy
Variation in FEV1 of more than 400mls
Diurnal variability in peak flow of more than 20%
Raised blood eosinophil count

Where there are no asthmatic or steroid-responsive features, treatment is a combination of:

Long-acting beta agonist (LABA)
Long-acting muscarinic antagonist (LAMA)
Anoro Ellipta, Ultibro Breezhaler and DuaKlir Genuair are examples of LABA and LAMA combination inhalers.

Where there are asthmatic or steroid-responsive features, treatment is a combination of:

Long-acting beta agonist (LABA)
Inhaled corticosteroid (ICS)
Fostair, Symbicort and Seretide are examples of LABA and ICS combination inhalers.

The final inhaler step is a combination of a LABA, LAMA and ICS. Trimbow, Trelegy Ellipta and Trixeo Aerosphere are examples of LABA, LAMA and ICS combination inhalers.

In more severe cases, additional options (guided by a specialist) are:

Nebulisers (e.g., salbutamol or ipratropium)
Oral theophylline
Oral mucolytic therapy to break down sputum (e.g., carbocisteine)
Prophylactic antibiotics (e.g., azithromycin)
Oral corticosteroids (e.g., prednisolone)
Oral phosphodiesterase-4 inhibitors (e.g., roflumilast)
Long-term oxygen therapy at home
Lung volume reduction surgery (removing damaged lung tissue to improve the function of healthier tissue)
Palliative care (opiates and other drugs may be used to help breathlessness)

Patients taking azithromycin need ECG and liver function monitoring before and during treatment.

Long-term oxygen therapy (LTOT) is used for severe COPD with chronic hypoxia (sats < 92%), polycythaemia, cyanosis or cor pulmonale. Smoking is a contraindication due to the fire risk.

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13
Q

What is the management of an acute exacerbation of COPD?

A

First-line medical treatment of an acute exacerbation of COPD involves:

Regular inhalers or nebulisers (e.g., salbutamol and ipratropium)
Steroids (e.g., prednisolone 30 mg once daily for 5 days)
Antibiotics if there is evidence of infection

Respiratory physiotherapy can be used to help clear sputum.

Additional options in severe cases include:

IV aminophylline
Non-invasive ventilation (NIV)
Intubation and ventilation with admission to intensive care

Doxapram may be used as a respiratory stimulant where NIV or intubation is not appropriate.

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14
Q

What is bronchiectasis and what are the causes?

A

Bronchiectasis involves permanent dilation of the bronchi, the large airways that transport air to the lungs. Sputum collects and organisms grow in the wide tubes, resulting in a chronic cough, continuous sputum production and recurrent infections.

Bronchiectasis results from damage to the airways. Potential causes of this damage include:

Idiopathic (no apparent cause)
Pneumonia
Whooping cough (pertussis)
Tuberculosis
Alpha-1-antitrypsin deficiency
Connective tissue disorders (e.g., rheumatoid arthritis)
Cystic fibrosis
Yellow nail syndrome

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15
Q

What are symptoms and signs of bronchiectasis?
What investigations would you do?

A

Key presenting symptoms are:

Shortness of breath
Chronic productive cough
Recurrent chest infections
Weight loss

Signs of bronchiectasis on examination include:

Sputum pot by the bedside
Oxygen therapy (if needed)
Weight loss (cachexia)
Finger clubbing
Signs of cor pulmonale (e.g., raised JVP and peripheral oedema)
Scattered crackles throughout the chest that change or clear with coughing
Scattered wheezes and squeaks

Sputum culture is used to identify colonising and infective organisms. The most common infective organisms are:

Haemophilus influenza
Pseudomonas aeruginosa

Chest x-ray findings include:

Tram-track opacities (parallel markings of a side-view of the dilated airway)
Ring shadows (dilated airways seen end-on)

High-resolution CT (HRCT) is the test of choice for establishing the diagnosis.

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16
Q

What is the management for bronchiectasis?

A

General management involves:

Vaccines (e.g., pneumococcal and influenza)
Respiratory physiotherapy to help clear sputum
Pulmonary rehabilitation
Long-term antibiotics (e.g., azithromycin) for frequent exacerbations (e.g., 3 or more per year)
Inhaled colistin for Pseudomonas aeruginosa colonisation
Long-acting bronchodilators may be considered for breathlessness
Long-term oxygen therapy in patients with reduced oxygen saturation
Surgical lung resection may be considered for specific areas of disease
Lung transplant is an option for end-stage disease

17
Q

What is ILD?

A

Interstitial lung disease includes many conditions that cause inflammation and fibrosis of the lung parenchyma (lung tissue). Fibrosis involves the replacement of elastic and functional lung tissue with non-functional scar tissue.

The conditions we will cover here are::

Idiopathic pulmonary fibrosis (the most important to remember)
Secondary pulmonary fibrosis
Hypersensitivity pneumonitis
Cryptogenic organising pneumonia
Asbestosis

Presentation
The key presenting features are:

Shortness of breath on exertion
Dry cough
Fatigue

18
Q

How would you diagnose ILD?

A

Diagnosis of interstitial lung disease involves:

Clinical features
High-resolution CT scan (HRCT) of the thorax (showing a typical “ground glass” appearance)
Spirometry

Spirometry may be normal or show a restrictive pattern:

FEV1 and FVC are equally reduced
FEV1:FVC ratio greater than 70%

Other investigations where there is doubt about the diagnosis include:

Lung biopsy
Bronchoalveolar lavage

19
Q

What drugs can cause pulmonary fibrosis
What conditions can cause pulmonary fibrosis secondarily?

A

Several drugs can cause pulmonary fibrosis:

Amiodarone (also causes grey/blue skin)
Cyclophosphamide
Methotrexate
Nitrofurantoin

Pulmonary fibrosis can occur secondary to other conditions:

Alpha-1 antitrypsin deficiency
Rheumatoid arthritis
Systemic lupus erythematosus (SLE)
Systemic sclerosis
Sarcoidosis

20
Q

What is hypersensitivity pneumonitis?

A

Hypersensitivity pneumonitis, also called extrinsic allergic alveolitis, involves type III and type IV hypersensitivity reaction to an environmental allergen. Inhalation of allergens in patients sensitised to that allergen causes an immune response, leading to inflammation and damage to the lung tissue.

Bronchoalveolar lavage is performed during a bronchoscopy procedure. The airways are washed with sterile saline to gather cells, after which the fluid is collected and analysed. Raised lymphocytes (lymphocytosis) are suggestive of hypersensitivity pneumonitis.

Management involves removing the allergen, oxygen where necessary and steroids.

Examples of specific causes:

Bird-fancier’s lung is a reaction to bird droppings
Farmer’s lung is a reaction to mouldy spores in hay
Mushroom worker’s lung is a reaction to specific mushroom antigens
Malt worker’s lung is a reaction to mould on barley

21
Q

What is asbestosis?

A

Asbestosis refers to lung fibrosis related to asbestos exposure. Asbestos is fibrogenic, meaning it causes lung fibrosis. It is also oncogenic, meaning it causes cancer. The effects of asbestos usually take several decades to develop. Asbestos inhalation causes several problems:

Lung fibrosis
Pleural thickening and pleural plaques
Adenocarcinoma
Mesothelioma

22
Q

What is cryptogenic organising pneumonia?

A

Cryptogenic organising pneumonia was previously known as bronchiolitis obliterans organising pneumonia. It involves a focal area of inflammation of the lung tissue. It can be idiopathic or triggered by infection, inflammatory disorders, medications, radiation, environmental toxins, or allergens.

Presentation is similar to infectious pneumonia, with shortness of breath, cough, fever and lethargy. Inspiratory crackles may be heard on auscultation.

Chest x-ray findings are also similar to pneumonia, with a focal consolidation. A lung biopsy is the definitive investigation. Diagnosis is often delayed due to the similarities to infectious pneumonia.

Treatment is with systemic corticosteroids.

23
Q

What is the general management for ILD?

A

Generally, there is a poor prognosis and limited management options in interstitial lung disease, and treatment is primarily supportive. Options include:

Remove or treat the underlying cause
Home oxygen where there is hypoxia
Stop smoking
Physiotherapy and pulmonary rehabilitation
Pneumococcal and flu vaccine
Advanced care planning and palliative care where appropriate
Lung transplant is an option, but the risks and benefits need careful consideration

24
Q

What causes a pleural effusion?
How does it present on examination?
What would you see on X-ray?
What’s the treatment?

A

Exudative causes are related to inflammation. The inflammation results in protein leaking out of the tissues into the pleural space (ex- meaning moving out of). The top causes are:

Cancer (e.g., lung cancer or mesothelioma)
Infection (e.g., pneumonia or tuberculosis)
Rheumatoid arthritis

Transudative causes relate to fluid moving across or shifting into the pleural space (trans- meaning moving across):

Congestive cardiac failure
Hypoalbuminaemia
Hypothyroidism
Meigs syndrome

Presentation
The typical presenting symptom is shortness of breath.

Examination findings are:

Dullness to percussion over the effusion
Reduced breath sounds
Tracheal deviation away from the effusion in very large effusions

Investigations
Chest x-ray findings are:

Blunting of the costophrenic angle
Fluid in the lung fissures
Larger effusions will have a meniscus (a curving upwards where it meets the chest wall and mediastinum)
Tracheal and mediastinal deviation away from the effusion in very large effusions

Treatment
Diagnosing and treating the underlying cause is the mainstay of management.

Conservative management may be appropriate as small effusions will resolve with treatment of the underlying cause. More significant effusions often need aspiration or drainage.

Pleural aspiration involves sticking a needle through the chest wall into the effusion and aspirating the fluid. Aspiration can temporarily relieve the pressure, but the effusion may recur, and further drainage may be required.

Chest drain can be used to drain the effusion and prevent it from recurring.

25
Q

What are the signs of a tension pneumothorax?
What is the management?

A

Signs of Tension Pneumothorax:

Tracheal deviation away from the side of the pneumothorax
Reduced air entry on the affected side
Increased resonance to percussion on the affected side
Tachycardia
Hypotension

Management is a chest drain

26
Q

What is a PE?
What are the risk factors?
How does it present?

A

Pulmonary embolism (PE) describes a blood clot (thrombus) in the pulmonary arteries. An embolus is a thrombus that has travelled in the blood, often from a deep vein thrombosis (DVT) in a leg. The thrombus will block the blood flow to the lung tissue and strain the right side of the heart. DVTs and PEs are collectively known as venous thromboembolism (VTE).

Risk factors:

Immobility
Recent surgery
Long-haul travel
Pregnancy
Hormone therapy with oestrogen (e.g., combined oral contraceptive pill or hormone replacement therapy)
Malignancy
Polycythaemia (raised haemoglobin)
Systemic lupus erythematosus
Thrombophilia

Presenting features include:

Shortness of breath
Cough
Haemoptysis (coughing up blood)
Pleuritic chest pain (sharp pain on inspiration)
Hypoxia
Tachycardia
Raised respiratory rate
Low-grade fever
Haemodynamic instability causing hypotension

27
Q

What investigations would you do for a potential PE?

How would a patient with a PE ABG look like?

A

A chest x-ray is usually normal in a pulmonary embolism but is required to rule out other pathology.

The Wells score is used when considering pulmonary embolism. The outcome decides the next step:

Likely: perform a CT pulmonary angiogram (CTPA) or alternative imaging (see below)
Unlikely: perform a d-dimer, and if positive, perform a CTPA

ABG:

Patients with a pulmonary embolism often have respiratory alkalosis on an ABG. Hypoxia causes a raised respiratory rate. Breathing fast means they “blow off” extra CO2. A low CO2 means the blood becomes alkalotic. The other main cause of respiratory alkalosis is hyperventilation syndrome. Patients with PE will have a low pO2, whereas patients with hyperventilation syndrome will have a high pO2.

28
Q

What is sarcoidosis?
How does it present?

A

Sarcoidosis is a chronic granulomatous disorder. Granulomas are inflammatory nodules full of macrophages. The cause of these granulomas is unknown.

It is usually associated with respiratory symptoms but has many extra-pulmonary manifestations, such as erythema nodosum and lymphadenopathy. Symptoms can vary dramatically from asymptomatic to severe or life-threatening.

Sarcoidosis can affect anyone. It seems to be slightly more common in:

Aged 20-39 or around 60
Women
Black ethnic origin

TOM TIP: The typical MCQ exam patient is a 20-40 year old black female presenting with a dry cough and shortness of breath. They may have nodules on their shins, suggesting erythema nodosum.

Skin Features
Less than half of patients with sarcoidosis have skin involvement. However, these findings are worth remembering for exams.

Erythema nodosum is characterised by nodules of inflamed subcutaneous fat on the shins. Inflammation of fat is called panniculitis. Erythema nodosum presents as raised, red, tender, painful, subcutaneous nodules across both shins. Over time the nodules settle and appear as bruises. There are many causes of erythema nodosum.

Lupus pernio is specific to sarcoidosis and presents with raised purple skin lesions, often on the cheeks and nose.

Systemic Symptoms:
Fever
Fatigue
Weight loss

29
Q

What are the investigations for Sarcoidosis?
What is the management?

A

The blood test findings to remember are:

Raised angiotensin-converting enzyme (ACE) (often used as a screening test)
Raised calcium (hypercalcaemia)

Imaging
Various imaging investigations may be performed:

Chest x-ray may show hilar lymphadenopathy
High-resolution CT scanning may show hilar lymphadenopathy and pulmonary nodules
MRI can show central nervous system involvement
PET scan can show active inflammation in affected areas

Other tests may be used to determine which organs are affected:

U&Es for kidney involvement
Urine albumin-creatinine ratio to look for proteinuria
LFTs for liver involvement
Ophthalmology assessment for eye involvement
ECG and echocardiogram for heart involvement
Ultrasound for liver and kidney involvement

Management
Conservative management is considered in patients with no or mild symptoms.

Oral steroids (for 6-24 months) are usually first-line where treatment is required. Bisphosphonates protect against osteoporosis whilst on long-term steroids.

Methotrexate is a second-line option.

Lung transplant is rarely required in severe pulmonary disease.

30
Q

What are the different histological types of lung cancer?
How does lung cancer present?

A

The histological types of lung cancer can be broadly divided into:

Small-cell lung cancer (SCLC) (around 20%)
Non-small-cell lung cancer (around 80%)

Non-small-cell lung cancer can be further divided into:

Adenocarcinoma (around 40% of total lung cancers)
Squamous cell carcinoma (around 20% of total lung cancers)
Large-cell carcinoma (around 10% of total lung cancers)
Other types (around 10% of total lung cancers)

Small-cell lung cancer cells contain neurosecretory granules that release neuroendocrine hormones. SCLC may be responsible for various paraneoplastic syndromes.

Mesothelioma is a lung malignancy affecting the mesothelial cells of the pleura. It is strongly linked to asbestos inhalation. There is a substantial latent period between exposure to asbestos and the development of mesothelioma of up to 45 years. The prognosis is very poor. Chemotherapy can improve survival, but it is essentially palliative.

Presenting features of lung cancer include:

Shortness of breath
Cough
Haemoptysis (coughing up blood)
Finger clubbing
Recurrent pneumonia
Weight loss
Lymphadenopathy – often supraclavicular nodes are the first to be found on examination

31
Q

What is spirometry?

A

Spirometry is the test used to establish objective measures of lung function. It involves different breathing exercises into a machine that measures volumes of air and flow rates and produces a report. Reversibility testing involves giving a bronchodilator (e.g., salbutamol) before repeating the spirometry to see if this impacts the results.

Forced expiratory volume in 1 second (FEV1) is the air a person can forcefully exhale in 1 second. This measures how easily air can flow out of the lungs. It is reduced with airflow obstruction.

Forced vital capacity (FVC) is the total air a person can exhale after a full inhalation. This measures the total volume of air that the person can take into their lungs. It is reduced with restricted lung capacity.