Respiratory Flashcards

(148 cards)

1
Q

What is an ABG?

A

Measures blood gas tension values of arterial PO2 and PCO2 and blood’s pH

Arterial O2 saturation can be determined

Requires a small volume of blood be drawn from radial artery with syringe and thin needle

Sometimes femoral artery or arterial catheter

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2
Q

What are the indications for an ABG?

A
  • Respiratory failure
  • Identification of acid-base disorders
  • Any severe illness which may lead to a metabolic acidosis: cardiac/liver/renal/multiorgan failure, hyperglycaemic states in DM, sepsis, burns, poisons/toxins
  • Ventilated patients
  • Sleep studies
  • Severely unwell patients - affects prognosis
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3
Q

What are the possible complications of an ABG?

A
  • Local haematoma
  • Arterial vasospasm
  • Arterial occlusion
  • Air or thrombus embolism
  • LA anaphylactic reaction
  • Infection at puncture site
  • Needle stick injury to healthcare professional
  • Vessel laceration
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4
Q

What is aspergillus lung disease?

A

Lung disease associated with Aspergillus fungal infection

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5
Q

Summarise the epidemiology of aspergillus lung disease

A

Uncommon

Mainly occurs in elderly and immunocompromised

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6
Q

Explain the aetiology of aspergillus lung disease

A

Inhalation of Aspergillus spores can produce 3 different clinical pictures:
1. Aspergilloma - growth of an A. fumigates mycetoma ball in pre-existing lung cavity (eg post-TB, old infarct or abscess)

  1. Allergic bronchopulmonary aspergillosis (ABPA) - colonisation of airways by Aspergillus –> IgE/G-mediated immune responses; occurs in asthmatics; release of proteolytic enzymes, mycotoxins and antibodies –> airway damage + central bronchiectasis
  2. Invasive aspergillosis - invasion of aspergillus into lung tissue and fungal dissemination in immunosuppressed patients
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7
Q

What are the risk factors for aspergillus lung disease?

A

Asthma
CF
Elderly
Immunocompromised

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8
Q

What are the presenting symptoms of aspergillus lung disease?

A

Aspergilloma:
Asymptomatic
Haemoptysis - potentially massive

ABPA:
Difficult to control asthma
Recurrent episodes of pneumonia w wheeze, cough, fever, and malaise

Invasive aspergillosis:
Dyspnoea
Rapid deterioration
Septic picture

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9
Q

What are the signs O/E of aspergillus lung disease?

A
Tracheal deviation (only w v large aspergillomas)
Dullness in affected lung
Reduced breath sounds
Wheeze (in ABPA)
Cyanosis (in invasive aspergillosis)
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10
Q

How is aspergillus lung disease investigated?

A

Aspergilloma:

  1. CXR - upper zone round mass w crescent of air around
  2. CT/MRI if CXR unclear

ABPA:

  1. Immediate skin test reactivity to Aspergillus antigens
  2. Eosinophilia
  3. Raised total serum IgE
  4. Raised specific serum IgE and IgG to A. fumigatus
  5. CXR
  6. CT
  7. Lung function tests

Invasive aspergillosis:

  1. Culture/histo or bronchoalveolar lavage fluid/sputum - Aspergillus
  2. Chest CT - nodules surrounded by ground-glass appearance (halo sign)
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11
Q

What does a CXR of ABPA show?

A

Transient patchy shadows
Collapse
Distended mucous-filled bronchi

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12
Q

What does a CT of ABPA show?

A

Lung infiltrates

Central bronchiectasis

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13
Q

What do lung function tests in ABPA show?

A

Reversible airflow limitation

Reduced lung volumes/gas transfer

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14
Q

What does a CXR of aspergilloma show?

A

Round mass with a crescent of air around it in upper zones

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15
Q

What does a chest CT of invasive aspergillosis show?

A

Nodules surrounded by ground-glass appearance (halo sign)

Due to haemorrhage into tissue surrounding fungal invasion

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16
Q

What is asthma?

A

Chronic inflammatory airway disease characterised by variable reversible airway obstruction, airway hyper-responsiveness and bronchial inflammation

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17
Q

Summarise the epidemiology of asthma

A

10% of children
5% of adults
Increasing prevalence

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18
Q

Explain the aetiology of asthma

A

Genetic factors:
FHx
Atopy

Environmental factors:
House dust mites
Pollen
Pets
Cigarette smoke
Viral RTIs
Aspergillus fumigatus spores
Occupational allergens
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19
Q

What are the presenting symptoms of asthma?

A

Recurrent episodes
Wheeze
SOB
Cough (worse in morning and at night)

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20
Q

What are the signs O/E of asthma?

A
General inspection:
May be normal
Nasal polyposis
Tachypnoea
Use of accessory muscles
Prolonged expiratory phase
Hyper-inflated chest

Auscultation:
Wheeze (polyphonic)

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21
Q

What are the precipitating factors of asthma?

A
Cold
Viral infection
Drugs - B blockers, NSAIDs
Exercise
Emotions
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22
Q

How is asthma investigated?

A
  1. FEV1/FVC ratio <80% of predicted
  2. FEV1 <80% of predicted
  3. Reduced peak expiratory flow rate
  4. CXR - normal or hyper-inflated
  5. FBC - normal or raised eosinophils and/or neutrophilia
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23
Q

What are the possible complications of asthma?

A

Exacerbations - asthma attacks
Airway remodelling
Oral candidiasis, dysphonia, and oesophageal candidiasis secondary to ICS use

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24
Q

What is bronchiectasis?

A

Lung airway disease characterised by chronic bronchial dilation, impaired mucociliary clearance and frequent bacterial infections

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25
Summarise the epidemiology of bronchiectasis
Most often arises initially in childhood Incidence has decreased with use of ABx 1/1000 per year
26
Explain the aetiology of bronchiectasis
Chronic lung inflammation --> fibrosis + permananet dilation of bronchi --> mucus pooling --> predisposes to further cycles of infection, damage, and fibrosis of bronchial walls Causes: Idiopathic (50%) Post-infections - eg pneumonia, whooping cough, TB Host-defence defects - eg Kartagener's syndrome, CF Obstruction of bronchi - eg foreign body, enlarged LNs GORD Inflammatory disorders - eg RA
27
What are the presenting symptoms of bronchiectasis?
Productive cough w purulent sputum or haemoptysis Breathlessness Chest pain Malaise Fever Weight loss Symptoms usually begin after acute respiratory illness
28
What are the signs O/E of bronchiectasis?
Clubbing Coarse crepitations (usually at lung bases) that shift with coughing Wheeze
29
How is bronchiectasis investigated?
Sputum: Culture and sensitivity ``` CXR: Dilated bronchi - tramline shadows (parallel lines from hilum to diaphragm) Fibrosis Atelectasis Pneumonic consolidations May be normal ``` High-res CT: Best diagnostic method Dilated bronchi w thickened walls
30
How is bronchiectasis managed?
Conservative: Maintain hydration Flu vaccination Physiotherapy - enable sputum and mucus clearance Medical: Acute exacerbation - 2 IV ABx which cover Pseudomonas aeruginosa Prophylactic ABx w >3 exacerbations/yr ICS eg fluticasone - to reduce inflammation and sputum volume Bronchodilators Surgical: Bronchial artery embolisation - if life-threatening haemoptysis Localised resection Lung/heart-lung transplantation
31
What are the possible complications of bronchiectasis?
``` Life-threatening haemoptysis Persistent infections Empyema Respiratory failure Cor pulmonale Multi-organ abscesses ```
32
What is the prognosis of bronchiectasis?
Most patients continue to have symptoms after 10 years
33
Which organisms commonly cause bronchiectasis?
``` Pseudomonas aeruginosa Haemophilus influenzae Staphylococcus aureus Streptococcus pneumoniae Klebsiella Mycobacteria ```
34
What is extrinsic allergic alveolitis?
Interstitial inflammatory disease of the distal gas-exchanging parts of the lung AKA hypersensitivity pneumonitis
35
Summarise the epidemiology of extrinsic allergic alveolitis
Uncommon 2% of occupational lung disease 50% of reported cases affect farm workers Geographical variation
36
Explain the aetiology of extrinsic allergic alveolitis
Inhalation of antigenic dusts induce a hypersensitivity response in susceptible individuals Antigenic dusts include microbes and animal proteins Eg Farmer's Lung - mouldy hay containing thermophilic actinomycetes Pigeon Fancier's Lung - blood on bird feathers and excreta Maltworker's Lung - barley/maltings containing Aspergillus clavatus
37
What are the risk factors for extrinsic allergic alveolitis?
Smoking Viral infection Exposure to avian protein/mould/bacterial antigen Exposure todiisocyanate Exposure to acid anhydride antigen Exposure to metal-working fluid Nitrofurantoin, methotrexate, roxithomycin, rituximab Herbal supplements with ayurvedic medicine
38
What are the presenting symptoms of extrinsic allergic alveolitis?
``` Dyspnoea Non-productive/productive cough Fever/chills Malaise Weight loss/anorexia ```
39
What are the signs O/E of extrinsic allergic alveolitis?
Acute: Rapid shallow breathing Pyrexia Inspiratory crepitations Chronic: Fine inspiratory crepitations Clubbing
40
How is extrinsic allergic alveolitis investigated?
1. Bloods FBC - neutrophilia, lymphopenia ABG - reduced PO2 + PCO2 2. Serology - IgG to fungal/avian antigens 3. CXR - often normal in acute episodes - fibrosis in chronic 4. High-rest CT thorax - patchy 'ground glass' shadowing and nodules 5. Lung function tests - restrictive defect (low FEV1, low FVC) - preserved or increased FEV1:FVC - reduced TLC 6. Bronchoalveolar lavage - increased cellularity - biopsy
41
What is idiopathic pulmonary fibrosis?
Inflammatory condition of the lung resulting in fibrosis of the alveoli and interstitium
42
Summarise the epidemiology of idiopathic pulmonary fibrosis
Rare 6/100,000 More common in males
43
Explain the aetiology of idiopathic pulmonary fibrosis
Genetically predisposed host (e.g. surfactant protein mutations); recurrent alveolar damage results in cytokine release, activating fibroblasts, differentiating into myofibroblasts and increased collagen synthesis Drugs can produce similar illnesses (bleomycin, methotrexate, amiodarone)
44
What are the risk factors for idiopathic pulmonary fibrosis?
Smoking Occupational exposure to metal or wood Chronic microaspiration Animal and vegetable dusts
45
What are the presenting symptoms of idiopathic pulmonary fibrosis?
Gradual-onset, progressive SOB on exertion Dry cough No wheeze Symptoms may be preceded by viral-type illness
46
What are the signs O/E of idiopathic pulmonary fibrosis?
Clubbing Bibasal fine late inspiratory crackles Signs of RHF in advanced disease
47
How is idiopathic pulmonary fibrosis investigated?
Bloods: ABG - normal early, PO2 decreases w exercise, normal PCO2, rises in late disease ANA/RF - 1/3 pts +ve CXR: Normal at presentation Early disease - ground glass shadowing Later disease - reticulonodular shadowing, signs of cor pulmonale, honeycombing High-res CT: More sensitive in early disease than CXR - ground- glass ``` Lung function tests: Restrictive features - reduced FEV1 and FVC, w preserved or increased FEV1:FVC Decreased lung volumes Decreased lung compliance Decreased TLC ``` Lung biopsy - gold standard for diagnosis
48
What is obstructive sleep apnoea?
A disease characterised by recurrent prolapse of the pharyngeal airway and apnoea (cessation of airflow > 10s) during sleep, followed by arousal from sleep AKA Pickwickian Syndrome
49
Summarise the epidemiology of obstructive sleep apnoea
Common 5-20% of men > 35 years 2-5% of women > 35 years Prevalence increases with age
50
Explain the aetiology of obstructive sleep apnoea
Occurs due to narrowing of the upper airways because of the collapse of soft tissues of the pharynx Due to decreased tone of pharyngeal dilators during sleep
51
What are the risk factors for obstructive sleep apnoea?
``` Weight gain Smoking Alcohol Sedative use Enlarged tonsils and adenoids in children Macroglossia Marfan's syndrome Craniofacial abnormalities ```
52
What are the presenting symptoms of obstructive sleep apnoea?
``` Excessive daytime sleepiness Unrefreshing or restless sleep Morning headaches Dry mouth Difficulty concentration Irritability and mood changes Partner reporting snoring, nocturnal apnoeic episodes or nocturnal choking ```
53
What are the signs O/E of obstructive sleep apnoea?
``` Large tongue Enlarged tonsils Long or thick uvula Retognathia (pulled back jaws) Neck circumference > 42 in males/40 in females Obesity Hypertension ```
54
How is obstructive sleep apnoea investigated?
Sleep study - monitor airflow, respiratory effort, pulse oximetry and HR Bloods - TFTs, ABG
55
What is pneumoconicoses?
Fibrosing interstitial lung disease
56
What are the risk factors for pneumoconicoses?
Occupational exposure to silica, coal, beryllium High cumulative dose of inhaled silica or coal Cigarette smoking Chronic beryllium disease: glutamic acid at position 69 of the HLA-DP1 beta chain
57
What is presenting symptoms of pneumoconicoses?
``` Insidious onset SOB Dyspnoea on exertion Dry cough Black sputum (melanoptysis) Pleuritic chest pain ```
58
What are the signs O/E of pneumoconicoses?
Normal chest exam Silicosis: decreased breath sounds, signs of RHF Asbestosis: Bi-basal, inspiratory crepitations Clubbing Signs of pleural effusion or RHF (cor pulmonale)
59
How is pneumoconicoses investigated?
1. CXR Simple: micronodular mottling Complicated: nodular opacities in upper zones, micronodular shadowing, eggshell calcification of hilar LNs (characteristic of silicosis), bilateral lower zone reticulonodular shadowing and pleural plaques (in asbestosis) 2. CT scan - fibrotic changes 3. Bronchoscopy 4. Lung function tests - restrictive pattern (reduced FEV1 and FVC)
60
What is sarcoidosis?
A chronic gramulomatous disorder of unknown aetiology, commonly affecting the lungs, skin, and eyes. Characterised by accumulation of lymphocytes and macrophages and the formation of non-caseating granulomas in the lungs and other organs.
61
What are the risk factors for sarcoidosis?
Age 20-40 years FHx sarcoidosis Scandinavian origin
62
What are the presenting symptoms of sarcoidosis?
``` Cough Dyspnoea Chronic fatigue Arthralgia Wheeze Rhonchi - bronchospasm Photophobia Red painful eye Blurred vision ```
63
What are the signs O/E of sarcoidosis?
Lymphadenopathy | Red eye
64
How is sarcoidosis investigated?
1. CXR Hilar and/or paratracheal adenopathy with upper lobe predominant, bilateral infiltrates; pleural effusions (rare) and egg shell calcifications (very rare) ``` 2. Bloods FBC: anaemia, leukopenia Serum urea: elevated Creatinine: elevated Liver enzymes: elevated Serum Ca: elevated ``` 3. Lung function tests Restrictive/obstructive/mixed pattern 4. ECG - conduction defects 5. Purified protein derivative of tuberculin (PPD) - negative
65
What is tuberculosis?
Granulomatous disease caused by Mycobacterium tuberculosis
66
Summarise the epidemiology of tuberculosis
Annual mortality = 3 million (95% in developing countries) Annual UK incidence = 6000 Asian immigrants are highest risk group in UK
67
What are the presenting symptoms of tuberculosis?
``` Primary TB: Mostly asymptomatic Fever Malaise Cough Wheeze Erythema nodosum Phlyctenular conjunctivitus ``` ``` Miliary TB: Fever Weight loss Meningitis Yellow caseous tubercles spread to other organs ``` Post-primary TB: Fever/night sweats Malaise
68
What are the risk factors for tuberculosis?
``` Exposure to infection Born in Asia, Latin America, Africa HIV infection Immunosuppressive medicines: systemic CS, TNF-alpha antagonists Silicosis 30x risk Apical fibrosis ```
69
Explain the aetiology of tuberculosis
Infection by Mycobacterium tuberculosis (IC organism) | Survives after being phagocytosed by macrophages
70
What are the signs and symptoms of primary TB?
``` Mostly asymptomatic Fever Malaise Cough Wheeze Erythema nodosum Phlyctenular conjunctivitus ```
71
What are the signs and symptoms of miliary TB?
Fever Weight loss Meningitis Yellow caseous tubercles spread to other organs
72
How is tuberculosis investigated?
1. CXR: abnormal typical for TB; abnormal atypical for TB; or normal 2. Sputum acid-fast bacilli smear: positive for acid-fast bacilli 3. Sputum culture: positive; no growth; or other mycobacteria 4. FBC: raised WBC, low Hb 5. Nucleic acid amplification tests: +ve for M tuberculosis
73
What are the signs of symptoms of post-primary TB?
``` Fever Night sweats Malaise Weight loss Breathlessness Cough Sputum Haemoptysis Pleuritic chest pain Signs of pleural effusion Collapse Consolidation Fibrosis ```
74
What causes miliary TB?
Haematogenous dissemination of TB
75
What causes post-primary TB?
Reinfection or reactivation of TB
76
What is primary TB?
Initial infection may be pulmonary or, more rarely, gastrointestinal
77
What are the gastrointestinal signs and symptoms of TB?
``` Subacute obstruction Change in bowel habit Weight loss Peritonitis Ascites ```
78
What are the gastrointestinal signs and symptoms of TB?
``` Subacute obstruction Change in bowel habit Weight loss Peritonitis Ascites ```
79
What is pneumonia?
Infection of distal lung parenchyma
80
Summarise the epidemiology of pneumonia
5-11/1000 | Community-acquired pneumonia is responsible for > 60,000 deaths per year in UK
81
What are the risk factors for pneumonia?
``` Age Smoking Alcohol Pre-existing lung disease Immunodeficiency Contact with patients with pneumonia ```
82
What are the presenting symptoms of pneumonia?
``` Fever Rigors Sweating Malaise Cough Sputum Breathlessness Pleuritic chest pain Confusion ```
83
What are the signs O/E of pneumonia?
``` Pyrexia Respiratory distress Tachypnoea Tachycardia Hypotension Cyanosis Decreased chest expansion Dull to percuss over affected area Increased tactile vocal fremitus over affected area Bronchial breathing over affected area Coarse crepitations on affected side ```
84
How is pneumonia investigated?
``` 1. Bloods FBC - raised WCC U+Es LFTs Culture ABG - assess pulmonary function Film - Mycoplasma causes red cell agglutination ``` 2. CXR Lobar or patchy shadowing Pleural efusion Note: Klebsiella often affect upper lobes May detect complications, eg lung abscess 3. Sputum/pleural fluid - MC&S 4. Urine - Penumococcus and Legionella antigens 5. Atypical viral serology 6. Bronchoscopy and bronchoalveolar lavage - if Penumocystis carinii pneumonia suspected, or if pneumonia fails to resolve
85
How is pneumonia managed?
1. Assess severity using BTS guidelines 2. Empirical ABx - oral amoxicillin (0 markers) - oral/IV amoxicillin + erythromycin (1 marker) - IV cefurozime/cefotaxime/co-amoxiclav + erythromycin (>1 marker) - add metronidazole if: aspiration, lung abscess, empyema - switch to appropriate antibiotic based on sensitivity 3. Supportive treatment - oxygen - IV fluids - CPAP, BiPAP, ITU care for resp failure - surgical drainage for abscess/empyema 4. Discharge planning If 2+ features of clinical instability present (high temp, tachycardia, tachypnoea, hypotension, low O2 sats) - high risk of readmission and mortality Consider other causes if pneumonia not resolving
86
What are the possible complications of pneumonia?
``` Pleural effusion Epyema Localised suppuration, eg abscess - swinging fever, persistent pneumonia, copious/foul-smelling sputum Septic shock ARDS Acute renal failure ```
87
What is the prognosis of pneumonia?
Most resolve with Tx within 1-3 weeks Severe pneumonia has high mortality
88
How can pneumonia be characterised?
``` Community-acquired Hospital-acquired/nosocomial Aspiration Pneumonia in the immunocompromised Typical Atypical (Mycoplasma, Chlamydia, Legionella) ```
89
What are the atypical pneumonia symptoms?
Headache Myalgia Diarrhoea/abdo pain Dry cough
90
What is the CURB-65 score?
Used to assess severity of pneumonia ``` Confusion < 8 AMTS Urea > 7 mmol/L Respiratory rate > 30/min Blood pressure: systolic < 90mmHg or diastolic < 60mmHg Age > 65 years ```
91
How can pneumonia be prevented?
Pneumococcal vaccine Haemophilus influenzae type B vaccine Given to high risk groups, eg elderly, spenectomy
92
How can pneumonia be prevented?
Pneumococcal vaccine Haemophilus influenzae type B vaccine Given to high risk groups, eg elderly, splenectomy
93
What is pneumothorax?
Air in the pleural space
94
Summarise the epidemiology of pneumothorax
Annual incidence: 9/100,000 20-40yos 4x more common in males
95
Explain the aetiology of pneumothorax
Spontaneous: - occurs in people w typically normal lungs - typically in tall, thin males - probably caused by rupture of subpleural bleb Secondary: - pre-existing lung disease, eg COPD, asthma, TB Traumatic: - penetrating injury to chest - often iatrogenic, eg during jugular venous cannulation, thoracocentesis
96
What are the risk factors for pneumothorax?
``` Smoking FHx Tall and slender <40yo Recent invasive medical procedure Chest trauma Acute severe asthma COPD TB AIDS-related Pneumocystis jirovecii infection CF Lymphangioleiomyomatosis Birt-Hogg-Dube syndrome Pulmonary Langerhans cell histiocytosis Erdheim-Chester disease ```
97
What are the presenting symptoms of pneumothorax?
May be asymptomatic if small Sudden-onset breathlessness Pleuritic chest pain Distress w rapid shallow breathing in tension pneumothorax
98
What are the signs O/E of pneumothorax?
``` No signs if small Signs of respiratory distress Reduced expansion Hyper-resonance to percussion Reduced breath sounds ``` ``` Tension pneumothorax: Severe resp distress Tachycardia Hypotension Cyanosis Distended neck veins Tracheal deviation away from side of pneumothorax ```
99
How is pneumothorax investigated?
CXR: - dark area of film w no lung markings - fluid level may be seen if there is any bleeding ABG: check for hypoxaemia
100
How is pneumothorax managed?
Oxygen Chest-tube thoracostomy Immediate needle decompression (tension) Suction
101
What are the possible complications of pneumothorax?
Recurrent pneumothoraces | Bronchopleural fistula
102
What is the prognosis of pneumothorax?
20% have another pneumothorax | Frequency increases w repeated pneumothoraces
103
What is pulmonary embolism?
Occlusion of pulmonary vessels, most commonly by a thrombus that has travelled to the pulmonary vascular system from another site
104
Summarise the epidemiology of pulmonary embolism
``` Relatively common (especially in hospitalised patients) Occur in 10-20% of patients with confirmed proximal DVT ```
105
Explain the aetiology of pulmonary embolism
Thrombus 95% arise from DVT in lower limbs Rarely arises in right atrium (in AF patients) ``` Other causes of embolus: Amniotic fluid Air Fat Tumour Mycotic ```
106
What are the risk factors for pulmonary embolism?
``` Surgical patients Immobility Obesity OCP Heart failure Malignancy ```
107
What are the presenting symptoms of pulmonary embolism?
Depends on site and size of embolus Small - may be asymptomatic Moderate - sudden onset SOB, cough, haemoptysis, pleuritic chest pain Large (or proximal) - as above + severe central pleuritic chest pain, shock, collapse, acute RHF, sudden death Multiple small recurrent - symptoms of pulmonary HTN
108
What are the signs O/E of pulmonary embolism?
Small - often no clinical signs, may be some tachycardia and tachypnoea Moderate - tachypnoea, tachycardia, pleural rub, low O2 sats despite supplementation Massive - shock, cyanosis, signs of right heart strain (raised JVP, left parasternal heave, accentuated S2) Multiple recurrent PE - signs of pulmonary HTN, signs of RHF
109
How is pulmonary embolism investigated?
Well's Score used to determine best investigation for PE Low probability (Wells 4 or less) - use D-dimer High probability (Wells>4) - requires imaging (CTPA) Also: Bloods - ABG, thrombophilia screen ECG - normal, tachycardia, right axis deviation or RBBB, S1Q3T3 pattern CXR - often normal but helps exclude other diagnoses VQ scan - shows areas of mismatch --> infarcted lung Doppler US of lower limb - VTE Echocardiography - may show right heart strain
110
How is pulmonary embolism managed?
Primary prevention: Compression stockings Heparin prophylaxis for those at risk Good mobilisation and adequate hydration ``` If haemodynamically stable: O2 Anticoagulation w heparin or LMWH Switch over to oral warfarin for at least 3 months Maintain INR 2-3 Analgesia ``` If haemodynamically unstable (massive PE): Resuscitate O2 IV fluids Thrombolysis with tPA considered if cardiac arrest imminent Surgical/radiological: Embolectomy IVC filtres - sometimes used for recurrent PEs despite adequate anticoagulation/when CI
111
What are the possible complications of pulmonary embolism?
Death Pulmonary infarction Pulmonary hypertension Right heart failure
112
What is the prognosis of pulmonary embolism?
30% mortality in those left untreated 8% mortality with treatment Increased risk of future thromboembolic disease
113
What is lung cancer?
Primary malignant neoplasm of the lung Small cell - 20% Non-small cell - 80%
114
Summarise the epidemiology of lung cancer
Most common fatal cancer in the west 18% of cancer mortality worldwide 3x more common in males
115
What are the risk factors for lung cancer?
Smoking Asbestos exposure Other occupational exposure: polycyclic hydrocarbons, nickel, radon Atmospheric pollution
116
What are the presenting symptoms of lung cancer?
May be asymptomatic Primary: Cough, haemoptysis, chest pain, recurrent pneumonia Local invasion: Brachial plexus invasion --> shoulder/arm pain Left recurrent laryngeal nerve invasion --> hoarse voice and bovine cough Dysphagia Arrhytmias Horner's syndrome ``` Metastatic disease/paraneoplastic phenomenon: Weight loss Fatigue Fractures Bone pain ```
117
What are the presenting symptoms of lung cancer?
May be asymptomatic Primary: Cough, haemoptysis, chest pain, recurrent pneumonia Local invasion: Brachial plexus invasion --> shoulder/arm pain Left recurrent laryngeal nerve invasion --> hoarse voice and bovine cough Dysphagia Arrhytmias Horner's syndrome ``` Metastatic disease/paraneoplastic phenomenon: Weight loss Fatigue Fractures Bone pain ```
118
What are the signs O/E of lung cancer?
May be NO SIGNS Fixed monophonic wheeze (single obstruction) Signs of lobar collapse or pleural effusion Signs of metastases - Virchow's node
119
What is COPD?
Chronic, progressive lung disorder characterised by airflow obstruction that is not fully reversible, with the following: Chronic bronchitis - chronic cough and sputum production on most days for at least 3 months per year over 2 consecutive years Emphysema - pathological diagnosis of permanent destructive enlargement of air spaces distal to terminal bronchioles
120
Summarise the epidemiology of COPD
Very common - 8% prevalence Presents in middle age or later More common in males Increasingly common in females
121
What are the risk factors for COPD?
Smoking
122
What are the presenting symptoms of COPD?
``` Chronic cough Sputum production SOB Some wheeze Reduced exercise tolerance ```
123
What are the signs O/E of COPD?
General inspection: Tar staining Cyanosis Barrel chest Palpation: Reduced expansion Percussion: Hyper-resonance Auscultation: Reduced air mvmt Wheezing Coarse crackles (hair-like) Other: Signs of RHF
124
How is COPD investigated?
Spirometry and lung function tests: Obstructive picture - reduced PEFR, FEV1:FVC, increased lung volumes, decreased CO gas transfer coefficient ``` CXR: May appear normal Hyperinflation (>6 anterior ribs, flattened diaphragm) Reduced peripheral lung markings Elongated cardiac silhouette ``` Bloods: FBC - increased Hb and hct due to secondary polycythaemia ABG: hypoxia, normal/raised PCO2 ECG and echocardiogram: check for cor pulmonale Sputum and blood cultures: useful in acute infective exacerbations A1 antitrypsin levels (deficiency)
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What are the possible complications of COPD?
``` Acute respiratory failure Infections Pulmonary hypertension Right heart failure Pneumothorax - secondary to bullae rupture Secondary polycythaemia ```
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What is the prognosis of COPD?
High morbidity 3-year surivial of 90% if < 60 years, FEV1 > 50% predicted 3-year survival of 75% if > 60 years, FEV1: 40-49% predicted
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What is asbestosis?
Diffuse interstitial fibrosis of the lung as a consequence of exposure to asbestos fibres
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Explain the aetiology of asbestosis
Inhalation of asbestos fibres A fibrous silicate, a naturally occurring mineral The more asbestos inhaled, the greater the risk of developing asbestosis
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What are the risk factors for asbestosis?
Cumulative dose of inhaled asbestos | Smoking (reduces ability of lung to clear asbestos fibres)
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What are the presenting symptoms of asbestosis?
SOB on exertion | Dry, non-productive cough
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What are the signs O/E of asbestosis?
Dyspnoea Crackles - initially at bases Clubbing in advanced disease
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How is asbestosis investigated?
1. CXR: PA and lateral Lower zone linear interstitial fibrosis; progressively involves entire lung; pleural thickening 2. Lung function tests Restrictive changes May have obstructive picture - esp if Hx of asbestos exposure and smoking
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What is mesothelioma?
An aggressive epithelial neoplasm arising from the lining of the lung, abdomen, pericardium, or tunica vaginalis
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Summarise the epidemiology of mesothelioma
More common in men and white people Typically occurs in 60-90yos In UK, incidence increasing rapidly since 60s Country-to-country variation due to disparities in asbestos use and regulation
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Explain the aetiology of mesothelioma
Asbestos exposure Dose-response relationship Latency period between exposure and development of malignancy = 20-40 years Also: Radiotherapy Genetic - BAP1 mutation, SV-40
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What are the risk factors of mesothelioma?
Asbestos exposure 60-85 yo due to latency period (20-40 years) Male FHx
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What are the presenting symptoms of mesothelioma?
Increasing SOB Chest pain Dry, non-productive cough Constitutional: fever, fatigue, sweats, weight loss
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What are the signs O/E of mesothelioma?
Laboured breathing Diminished breath sounds (due to effusion, trapped lung, bronchial obstruction) Dullness to percussion (effusion)
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How is mesothelioma investigated?
1. CXR - unilateral pleural effusion - irregular pleural thickening - reduced lung volumes - parenchymal changes, eg lower zone linear interstitial fibrosis 2. Chest CT - pleural thickening and/or discrete pleural plaques - pleural and/or pericardial effusions - enlarged hilar and/or mediastinal LNs - chest wall invasion and/or spread along needle tracts 3. Thoracentesis - exudate - malignant cells in pleural fluid
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How is asthma managed?
1. SABA - salbutamol 2. SABA + ICS - salbutamol + beclomethasone 3. LABA + ICS - salmeterol + beclomethasone 4. Trials - theophylline, oral beta-agonists, oral leukotriene receptor agonists (Montelukast) 5. Oral CS
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How is an acute asthma attack investigated?
PEF Moderate = 50-75% Acute-severe = 33-50 Life-threatening = <33 Near fatal = raised pCO2
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How is an acute asthma attack managed?
1. Basic obs - HR, SpO2 2. Measure and record PEF 3. O2 saturation and maintain SpO2 at 94-98% 4. ABG 5. Serum K and glucose Repeat ABG if PaO2 <8kPa, unless SpO2 >92%; or initial PaCO2 is normal or raised; or if patient deteriorates
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How is chronic COPD managed?
1. SABA or SAMA - salbutamol or ipratroprium bromide - MILD 2. Add LABA or LAMA - salmeterol or tiotropium - MODERATE 3. LAMA + LABA or LABA + ICS - symbicort (budesonide (ICS) and formoterol (LABA)) - SEVERE 4. LAMA + LABA + ICS - VERY SEVERE ``` Also: Smoking cessation Annual flu vaccine Pneumoccocal vaccine Long term O2 therapy Lung volume reduction surgery ```
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What are the long-term O2 therapy guidelines?
pO2 < 7.3kPa and one of the following: - secondary polycythaemia - nocturnal hypoxaemia - peripheral oedema - pulmonary HTN
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How do you manage an infective exacerbation of asthma?
1. O2 2. Neb salbutamol 5mg/Neb ipratropium bromide 0.5mg 3. Oral prednisolone 40-50mg + IV hydrocortisone 100mg 4. IV magnesium sulphate + SENIOR HELP 5. IV aminophylline 6. ITU + intubation
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How do you manage an infective exacerbation of COPD?
1. (Blue Venturi) 24% O2 2. Neb salbutamol 5mg, neb ipratropium bromide 0.5mg 3. Oral prednisolone 40-50mg, IV hydrocortisone 200mg 4. IV amoxicillin 5. 500mg IV aminophylline 6. BiPAP (NIV)
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How is the severity of COPD classified?
``` FEV1 % > 80% - mild 50-79% - moderate 30-49% - severe < 30% very severe ```
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What are the respiratory causes of clubbing?
Malignancy Empyema lung abscess ILD CF